Home About us Editorial board Ahead of print Browse Articles Search Submit article Instructions Subscribe Contacts Login 
  • Users Online: 535
  • Home
  • Print this page
  • Email this page


 
Previous article Browse articles Next article 
REVIEW ARTICLE
J Res Med Sci 2017,  22:27

Environmental factors influencing the risk of autism


1 Division of Genetics, Department of Biology, Faculty of Science, Tarbiat Modares University, Tehran, Iran
2 Division of Genetics, Department of Biology, Faculty of Science, Isfahan University, Isfahan, Iran
3 Cellular and Molecular Research Center, Shahrekord University of Medical Sciences, Shahrekord; Genetic and Identification Lab, Legal Medicine Center, Isfahan, Iran
4 Department of Psychiatry, School of Medicine, Isfahan University of Medical Sciences, Noor Hospital, Isfahan, Iran

Date of Submission06-Jun-2016
Date of Decision06-Nov-2016
Date of Acceptance16-Nov-2016
Date of Web Publication16-Feb-2017

Correspondence Address:
Mojgan Karahmadi
Department of Psychiatry, School of Medicine, Isfahan University of Medical Sciences, Noor Hospital, Isfahan
Iran
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/1735-1995.200272

Rights and Permissions
  Abstract 

Autism is a developmental disability with age of onset in childhood (under 3 years old), which is characterized by definite impairments in social interactions, abnormalities in speech, and stereotyped pattern of behaviors. Due to the progress of autism in recent decades, a wide range of studies have been done to identify the etiological factors of autism. It has been found that genetic and environmental factors are both involved in autism pathogenesis. Hence, in this review article, a set of environmental factors involved in the occurrence of autism has been collected, and finally, some practical recommendations for reduction of the risk of this devastating disease in children are represented.

Keywords: Autism, environmental factors, etiological factors


How to cite this article:
Karimi P, Kamali E, Mousavi SM, Karahmadi M. Environmental factors influencing the risk of autism. J Res Med Sci 2017;22:27

How to cite this URL:
Karimi P, Kamali E, Mousavi SM, Karahmadi M. Environmental factors influencing the risk of autism. J Res Med Sci [serial online] 2017 [cited 2023 Jun 2];22:27. Available from: https://www.jmsjournal.net/text.asp?2017/22/1/27/200272


  Introduction Top


Autism described by Asperger (in 1938) and Kanner (in 1943)[1] is a severe neurodevelopmental disorder and belongs to autism spectrum disorders (ASDs), including autism, Asperger syndrome, Rett syndrome, unidentified pervasive developmental disorders, and childhood disintegrative disorder.[2],[3] Autism is 4–5 times more common among boys than girls.[4],[5],[6] The most prominent clinical and phenotypic features of autism are extensive disabilities in social and behavioral communications, language impairment or inability to speak, and strong tendency toward stereotyped and repetitive patterns of behavior.[7],[8] Regarding statistical reports, the prevalence of autism had increased from 4–5 cases per 10,000 children in 1980s to 30–60 cases in 1990s,[9] and through astonishing increase, there are about 8.0 per 1000 children aged 8 years in 2004 and 9.0 per 1000 in 2006 or 1 in every 110 children aged 8 years in 2006. In 2012, a combined ASD prevalence of 11.3 per 1000 children aged 8 years or 1 in 88 children was published by the Autism and Developmental Disabilities Monitoring Network.[7],[10] With regard to its progressive increase over the last two decades,[11] and lack of effective treatment, and moreover, the difficulties imposed on the society and families of autistic children, the importance of investigation on causes of this disease and effort to prevent it become clear. There is growing body of evidence about genetic factors enrolment which is supporting autism etiology through genetic mutations (e.g., heritability and twins).[12],[13] According to the important role of epigenetics in autism etiology, a lot of genes have been studied, and in some cases, opposite results obtained.[14],[15] Studying identical twins and lack of complete concordance among them and excessive genetic studies with no conclusive results unveils the importance of environmental risk factors and their role in etiology of autism.[16],[17] Hence, the interactions between susceptible genes and environmental factors have been proposed as the major mechanism of autism etiology.[18],[19]

Currently, epigenetic and its complex mechanisms are presented as the most momentous mediator in the environment and genome interactions.[20] Environmental factors can affect the quality and quantity of gene expression without changing the DNA sequence through epigenetic mechanisms, including DNA methylation, changes in histone proteins, and expression of noncoding RNAs. This way, they can be transferred to the next cellular generation or even the next organism generation.[20],[21] As a result, exposure to harmful environmental factors can change the expression of developmental key genes in critical periods of embryo formation and increases the risk of genomic imprinting diseases such as autism.[22],[23]

None of the environmental factors is sufficient to yield autism, but rather a collection of them can be involved in the incidence of autism.[24] In this article, regarding mother and child exposure time to risk factors, they are divided into prenatal, natal, and postnatal risk factors.


  Prenatal Risk Factors Top


Physical, mental, and psychological health and financial state throughout the pregnancy are important factors affecting fetal development and health. An unhealthy mother who is not mentally and physically healthy and well nourished might be unable to have a healthy neonate. A set of prenatal risk factors which increase a child's susceptibility to autism is presented in [Table 1].
Table 1: Prenatal risk factors

Click here to view


Parental age

Advanced parental age (particularly paternal age) has been identified as one of the most important risk factors of autism.[25],[26],[27],[28],[29] In many studies, maternal and paternal age older than or equal to 34 years has been found associated with increased risk of autism in their offspring; however, in other studies, the relationship between child autism and the age of both parents[30] or even the age of one parent [24],[31],[32],[33],[34] is rejected. Intriguingly, the relationship between increased risk of autism and elevated paternal age has been approved in most studies.[28],[32],[33],[34],[35],[36],[37],[38],[39],[40] Particularly, a study was conducted among Iranian people in 2010 to explore the presence or absence of association between parental age and risk of autism. Based on this study, autism risk increases by 29% for every 10-year elevation in fathers' age. In other words, fathers aged between 34 and 39 had a nearly two-fold greater risk, and those who are older than 40 have more than two-fold (2.58) greater risk to have an affected child in comparison to who ones aged 25-29 years old.[38] In other studies in Japan [34] and China,[40] similar relationships were explored between paternal age and increased risk of autism. Lack of any correlation between maternal age and susceptibility of autism in these three mentioned studies has critical importance. The probable explanation for this phenomenon is the formation of de novo mutations in germline cells and modifications in DNA methylation, which can result in general epigenetic alterations in the expression of neural development genes and, finally, disorders in sperm genomic imprinting. As a result, the probability of neural impairments, such as autism, would be increased.[28],[36],[37] Advanced paternal age also affects immune system function and, consequently, the development of the nervous system.[35]

In studies that increase in maternal age manifests a correlation with autism,[24],[30],[31],[41],[42],[43],[44] chromosomal abnormalities and trinucleotide repeat expansion in the ovule,[42] and increase in the obstetric intervention [43] may be proposed as probable reasons. On the other hand, being small for gestational age can increase the risk of autism due to lack of physical maturity, inability, and poor maternal cares. Mothers who are younger than 20 may be exposed to intrauterine growth retardation of fetus and preterm birth, which both of them are potent for, associated with increased risk of autism.[30],[31],[41]

Maternal physical health

Metabolic syndrome, bleeding, and mother infection during pregnancy are some of mother's physical diseases which are related to child autism.[45] Maternal bleeding during pregnancy which is associated with a significant 81% elevated risk of autism,[26] and metabolic syndrome, including diabetes,[26],[46],[47] hypertension,[31],[48] and obesity,[48],[49] paves the way for hypoxia (deficiency of oxygen) in utero[46] which results in deficient brain development and induction of myelination changes, membrane adhesion, and deficiency in hippocampal neurons (a brain area which is highly involved in autism).[23],[50] Maternal viral infections in the first trimester of pregnancy, including rubella,[51],[52],[53] measles, mumps, chicken pox,[45],[51] influenza,[45],[51],[54] herpes,[51],[55] pneumonia, syphilis, varicella zoster,[55] and cytomegalovirus [45],[56] and bacterial infections in the second trimester which require hospitalization, increase the risk of autism in embryo.[51] Such relationship is due to abnormal maternal immune activation and, consequently, elevated levels of inflammatory cytokines which affect the embryonic brain development and increase the risk of autism and other neuropathophysiological status.[57],[58]

Maternal mental health

According to the importance and impact of family unit, parental behavior, and their communication patterns on the formation of children's personality and emotions,[59] the association between parental psychiatric history and risk of child mental disorders, especially autism, is obvious. For example, the association of parental psychiatric history such as schizophrenia with a nearly three-fold increased risk of autism [30],[60],[61],[62],[63] or the relationship between mother's depression,[20],[60],[61],[62],[63] anxiety,[40], 61, [64],[65],[66],[67],[68],[69],[70] and personality disorders [60] and susceptibility to autism has been proved in many studies.

In addition to mothers who have experienced mental illnesses throughout their lives and are recognized as mentally illness, those who undergo mental problems such as depression, anxiety, and considerable stress during 21–32 weeks of gestation, a period of heightened plasticity for fetal formation and development [71] can have irremediable effects, through epigenetic mechanism, on the expression of fetus stress response genes, the genes involved in neurobiology, metabolism, and physiology that can persist across the lifespan.[70] Mother's inappropriate psychological state, especially great and long-lasting stresses [72] which may result in some other personality disorders such as aggression in mothers,[73] can expose the fetus to elevated levels of cortisol through interrupting mother's HPA axis, amplifying adrenal steroids such as cortisol and increasing placental permeability to these hormones, basically. Consequently, fetal developmental programming (through epigenome) would be highly affected, and through interrupting the fetal stress response system, the way for different physical and mental impairments including autism would be paved.[20] On the other hand, rates of subclinical anxiety problems are increased among males and siblings in middle childhood.[74]

Maternal prenatal medication use

Maternal prenatal medication use can be associated with a 46% increased risk of fetus autism.[26] Researches about different kinds of drugs have revealed a significant 68% increased risk of autism in relation to prenatal psychiatric medication use.[26] The negative effect of prenatal medication use is caused by their placental crossing and disturbing fetal development, based on many studies. For example, use of antiepileptic drugs, as well as valproic acid, leads to fetal valproate syndrome, increases oxidative stress and varied gene expression pattern, and subsequently results in developmental delays, deficient motor activities and social behaviors, and finally, postnatal growth alterations.[45],[75],[76] Moreover, it is confirmed that paracetamol (acetaminophen), which is widely used as an analgesic/antipyretic drug, can induce apoptosis and necrosis that are observed in autistic brains. In addition, paracetamol (acetaminophen) induces oxidative stress and immune dysregulation in humans.[77] Furthermore, positive connection between antidepressant medications and autism has been demonstrated in many studies.[78],[79],[80] The relationship between susceptibility to autism and taking some other medications has been identified, such as thalidomide, a painkiller,[81] misoprostol, a prostaglandin analog drug for the prevention and treatment of gastric ulcers,[82] in the first trimester, and β2-adrenergic agonists such as terbutaline to treat asthma.[83],[84]

Familial socioeconomic status

Considering economic, social, educational, and psychological aspects of family's life, autistic children and their families are of poor state, mainly.[85] Basically, these families inevitably experience unhealthy, inappropriate sociality and unrehabilitated life conditions because of financial problems, occupational and psychological stresses.[86],[87],[88] Inaccessibility to health care and recreational facilities represented in infection and impaired physical health.[89] Furthermore, exposure to stress and anxiety (such as shared living place with couple's families) imposes psychological tension for the parents, especially pregnant mother, and increasing susceptibility to child autism during pregnancy.[40],[65],[66]

On the other hand, isolation of mother and breakdown in communications and social interactions can negatively affect her psychological state and endanger both mother and embryo's health.[90] There are numerous researches evaluating the relationship between parental education and risk of child autism and have variable conclusions which confirmed the correlation between low level of parental education and risk of autism,[85] and some others indicate strength correlation between highly educated parents and incidence of autism.[91],[92],[93]


  Natal Risk Factors Top


[Table 2] suggests natal risk factors which increase the fetal risk of autism. Abnormal gestational age, preterm (<35 weeks) and postterm pregnancy (>42 weeks), is associated with a significantly increased risk of autism.[30],[40],[47],[92],[94],[95] Prenatal risk factors such as bleeding during pregnancy and natal risk factors such as fetal complications including fetal distress, umbilical-cord complications such as fetal nuchal cord and cesarean delivery (26% increased risk of autism)[47] are all involved in hypoxia (lack of oxygen) and consequently increasing susceptibility to child autism.[31],[42],[47],[95] Fetal nuchal cord occurred significantly more frequent among children with autism (23.2%) regarding the controls (6.3%) and it causes fetal deficiency in blood, oxygen, and nutrition, which would affect fetal brain development and results in damage to the newborn central nervous system if the inadequate blood flow is severe or enough long-lasting.[40] Three brain regions, including basal ganglia, hippocampus, and lateral ventricles, are highly vulnerable to hypoxia.[42] Autistic children's brain exhibit larger lateral ventricles, morphological hippocampal abnormalities, and increased dopaminergic activity (what hypoxia causes).[96]
Table 2: Natal risk factors

Click here to view


Postnatal risk factors: Lesser

Postnatal risk factors have crucial roles in susceptibility to autism, and a set of them is mentioned in [Table 3]. Low birth weight, jaundice, and postnatal infection are some of the most significant risk factors. A neonate with birth weight, which is the result of three potential factors (genetic growth potential, duration of pregnancy and rate of fetal growth)[30] minor than 2500 g considered as low birth weight and associated with a two-fold increase in the risk of autism.[31],[47],[93],[97],[98] Postnatal jaundice is a result of high bilirubin production caused by increased breakdown of fetal erythrocytes and a low hepatic excretory capacity resulting from general immaturity of the liver and it can be associated with death during a sensitive period (around the 40 weeks of pregnancy) or susceptibility to mental disorders, especially a four-fold increase in autism if survive.[30],[40],[47],[99],[100] In addition to prenatal maternal infection during pregnancy, postnatal infections such as meningitis [55] mumps, varicella, unknown fever, and ear infections [101] on the first 30 days of life are correlated with high risk of autism.[102],[103]
Table 3: Postnatal risk factors

Click here to view



  Protective or Autism-Unrelated Factors Top


Among the environmental factors which are probable to cause autism, vaccines can be noted. Epidemiological studies have found no association between measles, measles, as well as mumps, vaccines (as environmental risk factors), and increased risk of autism.[101],[104] Contrary to directly related or unrelated factors to autism, some factors have protective roles. Unsaturated fatty acids can be cited as these factors. The biological effects of such fatty acids, such as linoleic acid, omega-3, and omega-6, on the retinal and brain development in utero,[105] signal transduction, gene expression, and as components of cell membranes [106],[107] in the first 2 months of pregnancy (the most critical period of embryonic physical development) are highly important to such an extent that high maternal intake of omega-6 and linoleic acid is inversely associated with ASD risk in offspring, corresponding to a 34% reduction in autism risk, and in contrary, lower than 5% of ω-3 fatty acid intake had significant increase in offspring ASD risk. Therefore, fatty acids consumption of different diets has an inverse effect on risk of autism.[108] In addition to unsaturated fatty acids, taking folic acid 3 months before pregnancy and during the 1st month of pregnancy can provide protection against autism in mothers and infants who have one copy of MTHFR 677 C>T allele at least. Maternal folic acid supplementation intake during early pregnancy is associated with less behavioral problems in offspring at 18 months age,[109] reduced risk of severe language delay at age 3,[110] improved verbal and attention competence at 4 years,[111] subordinate scores of childhood hyperactivity at age 8 years,[112] and particularly decrease the risk of autism.[113]


  Discussion Top


Autism is a multifactorial neurodevelopmental disorder which is caused by genetic and environmental factors. The prevalence of autism has been increased over the last decades. About every disorder, prevention is more important than cure. Among the risk factors of autism, environmental ones attracted the attention of most of the scientists because prevention is possible by avoiding from them.

There are a lot of environmental risk factors which influence autism pathogenesis by their epigenetic effects. These factors are divided into three categories, included prenatal, natal, and postnatal risk factors. Each category allocates to the specific period of neonate development. A collection of these factors is involved in the pathogenesis of autism. A comprehensive list of these factors is collected in this review. Regarding these factors, it would be essential to point out some requirements to prevent child autism. The following advice and suggestions are useful for parents to pass the highly significant period of pregnancy with confidence, especially those who have had experience of autistic children, and are about to prevent giving birth to another suffered infant.

Recommendations

  1. Advanced parental age (particularly paternal age) has important role in autism incidence in their neonate;[25],[26],[27],[28],[29], [32],[33],[34],[35],[36],[37],[38],[39],[40], [114],[115] therefore, it is suggested that the best time to have a child (especially for father) is under the age of 35
  2. Families with more than one autistic child would have increased risk to have an affected infant because the presence of more than one older affected sibling causes a two-fold increase in the risk of autism in the next children. These families are further at risk regarding those who have only one autistic child (32.2% of multiplex vs. 13.5% of simplex).[116],[117] Therefore, genetic consultation is strongly suggested to families with more than two autistic children who decided to have more children
  3. Considering the fact that autistic children are typically the primary child of their family and there is a significant (61%) increase in risk for first-born children compared with next children; if the first child of a family is autistic and the second child is unaffected, it will be less probable to have another autistic child.[26],[53],[55],[56],[118],[119] However, such a relationship has not been observed in other studies [30],[31],[97],[120],[121]
  4. Although the severity of autism is higher in the female gender, the prevalence of autism in boys is 3–4 folds greater than girls.[4],[6] Hence, sex determination test is highly recommended to parents who are in danger for autism, to increase the probability of having healthy baby girls
  5. The investigation of families and relatives of both autistic and healthy children has revealed the fact that familial psychiatric history is more common among autistic children's families and relatives with regard to healthy children;[30],[60] hence, in addition to genetic susceptibility, environmental factors are also involved in the incidence of such diseases and make mental problems appear in children differently from their parents.[61] As a result, regarding the strong association between parental psychiatric history and higher risk of autism in their children [30],[62],[63] and, generally, the impact of parental behavior on children's personality and mental health,[59] parents will be advised to complete their treatment and recovery periods before pregnancy
  6. Due to the direct effect of maternal emotional state on fetal health, mothers must avoid occupational and mental stresses. Mothers, who tolerate mental stresses such as family problems, stressful living places, financial problems, and loneliness, expose their children to different learning and mental problems such as autism [20],[40],[64],[86],[90],[93],[122]
  7. Mother exposure to some chemicals such as pesticides, air and water pollutants, and heavy metals and other chemicals can affect fetal health negatively through epigenetic alterations of gene expression and neurodevelopmental process such as changing neuronal migration.[20],[123],[124] Consequently, parents must care about where they choose to live that be far from environmental pollutions and recreational and clinical facilities must be available. Moreover, newborns must not be exposed to trihalomethane, tetrachloroethylene, trichloroethylene, and other chemicals [101]
  8. The quality of mother–infant interactions during the postnatal period has great importance; that's why mothers are supposed to provide proper care for their children. The absence of such emotional mother–infant relation has a great effect on the postnatal development of neural and signaling pathways in addition to affecting secretion of some hormones such as dopamine, oxytocin, and serotonin.[64],[125] They all can be involved in susceptibility to autism
  9. Due to side effects of mother's prenatal medication that is mentioned previously,[26] it is highly recommended that mothers should avoid taking any medication during pregnancy. Moreover, without prescription, the children must not be given medications such as paracetamol (acetaminophen) for pain and fever management following vaccinations in early infancy [77],[126],[127].
  10. Maternal smoking and alcohol consumption should be strictly forbidden during pregnancy, because in various studies, it has been proved that prenatal maternal smoking or even passive smoking includes polycyclic aromatic hydrocarbons, metals, and other chemicals with known adverse health effects, which may cause fetal hypoxia and affect fetal brain development.[31],[40],[49],[128],[129] Although in some studies, the connection between maternal smoking and risk of ASD has been rejected [130]
  11. Natural childbirth has priority over cesarean section because cesarean is especially prevalent among mothers who give birth to autistic children [47]
  12. Regarding the protective properties of unsaturated fatty acids [105],[106],[107],[108] and folic acid [109],[110],[111],[112],[113], in addition, the effects of iron deficiency, folate, methionine,[50], 113, [131],[132],[133] and vitamins [134],[135],[136],[137],[138],[139] on susceptibility to autism highlight the importance of an appropriate diet during pregnancy. Considering the profound impacts of different vitamins on physical health, the impact of Vitamin D on significant biological processes such as DNA repair and its anti-inflammatory quality on brain tissue,[134],[135],[137],[139] and the roles of vitamin A and other vitamins in brain development,[53] it is better to eat foods enriched with different vitamins and iron in addition to taking vitamin supplements and folic acid during pregnancy. Furthermore, eating foods such as fish which is enriched with omega-3 and other unsaturated fatty acids help in the normal development of the embryo. Appropriate postnatal care prevents the problems with lack of Vitamin D and other crucial components [136],[138]
  13. Pregnancy obesity (>90 kg) and excessive weight gain during pregnancy are significantly associated with the incidence of autism;[48],[129] therefore, mothers who are more susceptible to autism should be very careful about their dietary to prevent weight gain during pregnancy.
  14. Based on some studies, prolonged exposure to elevated temperature during pregnancy and susceptibility to child autism are related.[47] Therefore, mothers must avoid taking long saunas and other forms of exposure
  15. Due to the negative impacts of activation and aberrations of the maternal and fetal immune systems and increased level of cytokines on neural development of embryos and infants, mothers must care about their health during pregnancy as well as their newborn's health to stop probable infections, especially in the 1st month of infant lives.[45],[49],[77],[99],[101],[108],[122]



  Conclusion Top


Given that autism is an epigenetic disorder in which environmental risk factors are the most momentous mediators in its pathogenesis, detection of these factors can help parents avoid the danger of autism onset in their children. By following the mentioned tips, parents can provide a lower risk condition for the outbreak of autism.

Financial support and sponsorship

This study was supported by Isfahan University of Medical Sciences.

Conflicts of interest

There are no conflicts of interest.


  Authors' Contribution Top


  • PK, EK, SMM contributed in the conception of the work, conducting the study, revising the draft, approval of the final version of the manuscript, and agreed for all aspects of the work. PK contributed in the conception of the work, revising the draft, approval of the final version of the manuscript, and agreed for all aspects of the work
  • MK contributed in the conception of the work, conducting the study, revising the draft, approval of the final version of the manuscript, and agreed for all aspects of the work.
[186]

 
  References Top

1.
Lyons V, Fitzgerald M. Asperger (1906-1980) and Kanner (1894-1981), the two pioneers of autism. J Autism Dev Disord 2007;37:2022-3.  Back to cited text no. 1
    
2.
Volkmar FR, State M, Klin A. Autism and autism spectrum disorders: Diagnostic issues for the coming decade. J Child Psychol Psychiatry 2009;50:108-15.  Back to cited text no. 2
    
3.
Paris P. Autism Spectrum Disorders: Phenotypes, Mechanisms and Treatments. Switzerland: 2015. DOI:10.1159/isbn.978-3-318-02602-3.  Back to cited text no. 3
    
4.
Kinney DK, Munir KM, Crowley DJ, Miller AM. Prenatal stress and risk for autism. Neurosci Biobehav Rev 2008;32:1519-32.  Back to cited text no. 4
    
5.
Elsabbagh M, Divan G, Koh YJ, Kim YS, Kauchali S, Marcín C, et al. Global prevalence of autism and other pervasive developmental disorders. Autism Res 2012;5:160-79.  Back to cited text no. 5
    
6.
Werling DM, Geschwind DH. Sex differences in autism spectrum disorders. Curr Opin Neurol 2013;26:146-53.  Back to cited text no. 6
    
7.
Rapin I. The autistic-spectrum disorders. N Engl J Med 2002;347:302-3.  Back to cited text no. 7
    
8.
Developmental, D.M.N.S.Y. and I. Principal. Prevalence of autism spectrum disorder among children aged 8 years-autism and developmental disabilities monitoring network, 11 sites, United States, 2010. Morbidity and mortality weekly report. Vol. 63. Surveillance summaries, Washington, DC: 2002. p. 1.  Back to cited text no. 8
    
9.
Bertrand J, Mars A, Boyle C, Bove F, Yeargin-Allsopp M, Decoufle P. Prevalence of autism in a United States population: The Brick Township, New Jersey, investigation. Pediatrics 2001;108:1155-61.  Back to cited text no. 9
    
10.
Volkmar FR, Pauls D. Autism. Lancet 2003;362:1133-41.  Back to cited text no. 10
    
11.
Centers for Disease Control and Prevention. Prevalence of autism spectrum disorders- autism and developmental disabilities monitoring network, 14 sites, united states, 2008. MMWR 2012;61(3):1-19.  Back to cited text no. 11
    
12.
Weiss LA, Arking DE; Gene Discovery Project of Johns Hopkins and the Autism Consortium, Daly MJ, Chakravarti A. A genome-wide linkage and association scan reveals novel loci for autism. Nature 2009;461:802-8.  Back to cited text no. 12
    
13.
Folstein SE, Rosen-Sheidley B. Genetics of autism: Complex aetiology for a heterogeneous disorder. Nat Rev Genet 2001;2:943-55.  Back to cited text no. 13
    
14.
Musavi SM, Kamali E, Karahmadi M, Salehi M. RORA and autism in Isfahan population: A complicated epigenetic relationship. Cell J (Yakhteh) 2016;18:540-6.  Back to cited text no. 14
    
15.
Nguyen A, Rauch TA, Pfeifer GP, Hu VW. Global methylation profiling of lymphoblastoid cell lines reveals epigenetic contributions to autism spectrum disorders and a novel autism candidate gene, RORA, whose protein product is reduced in autistic brain. FASEB J 2010;24:3036-51.  Back to cited text no. 15
    
16.
Ronald A, Hoekstra RA. Autism spectrum disorders and autistic traits: A decade of new twin studies. Am J Med Genet B Neuropsychiatr Genet 2011;156B: 255-74.  Back to cited text no. 16
    
17.
Hallmayer J, Cleveland S, Torres A, Phillips J, Cohen B, Torigoe T, et al. Genetic heritability and shared environmental factors among twin pairs with autism. Arch Gen Psychiatry 2011;68:1095-102.  Back to cited text no. 17
    
18.
Herbert MR. Contributions of the environment and environmentally vulnerable physiology to autism spectrum disorders. Curr Opin Neurol 2010;23:103-10.  Back to cited text no. 18
    
19.
Deth R, Muratore C, Benzecry J, Power-Charnitsky VA, Waly M. How environmental and genetic factors combine to cause autism: A redox/methylation hypothesis. Neurotoxicology 2008;29:190-201.  Back to cited text no. 19
    
20.
Perera F, Herbstman J. Prenatal environmental exposures, epigenetics, and disease. Reprod Toxicol 2011;31:363-73.  Back to cited text no. 20
    
21.
Bollati V, Baccarelli A. Environmental epigenetics. Heredity (Edinb) 2010;105:105-12.  Back to cited text no. 21
    
22.
Foley DL, Craig JM, Morley R, Olsson CA, Dwyer T, Smith K, et al. Prospects for epigenetic epidemiology. Am J Epidemiol 2009;169:389-400.  Back to cited text no. 22
    
23.
Wang SC, Oelze B, Schumacher A. Age-specific epigenetic drift in late-onset Alzheimer's disease. PLoS One 2008;3:e2698.  Back to cited text no. 23
    
24.
Glasson EJ, Bower C, Petterson B, de Klerk N, Chaney G, Hallmayer JF. Perinatal factors and the development of autism: A population study. Arch Gen Psychiatry 2004;61:618-27.  Back to cited text no. 24
    
25.
Durkin MS, Maenner MJ, Newschaffer CJ, Lee LC, Cunniff CM, Daniels JL, et al. Advanced parental age and the risk of autism spectrum disorder. Am J Epidemiol 2008;168:1268-76.  Back to cited text no. 25
    
26.
Gardener H, Spiegelman D, Buka SL. Prenatal risk factors for autism: Comprehensive meta-analysis. Br J Psychiatry 2009;195:7-14.  Back to cited text no. 26
    
27.
Lee BK, McGrath JJ. Advancing parental age and autism: Multifactorial pathways. Trends Mol Med 2015;21:118-25.  Back to cited text no. 27
    
28.
Parner ET, Baron-Cohen S, Lauritsen MB, Jørgensen M, Schieve LA, Yeargin-Allsopp M, et al. Parental age and autism spectrum disorders. Ann Epidemiol 2012;22:143-50.  Back to cited text no. 28
    
29.
Shelton JF, Tancredi DJ, Hertz-Picciotto I. Independent and dependent contributions of advanced maternal and paternal ages to autism risk. Autism Res 2010;3:30-9.  Back to cited text no. 29
    
30.
Larsson HJ, Eaton WW, Madsen KM, Vestergaard M, Olesen AV, Agerbo E, et al. Risk factors for autism: Perinatal factors, parental psychiatric history, and socioeconomic status. Am J Epidemiol 2005;161:916-25.  Back to cited text no. 30
    
31.
Hultman CM, Sparén P, Cnattingius S. Perinatal risk factors for infantile autism. Epidemiology 2002;13:417-23.  Back to cited text no. 31
    
32.
Lauritsen MB, Pedersen CB, Mortensen PB. Effects of familial risk factors and place of birth on the risk of autism: A nationwide register-based study. J Child Psychol Psychiatry 2005;46:963-71.  Back to cited text no. 32
    
33.
Reichenberg A, Gross R, Weiser M, Bresnahan M, Silverman J, Harlap S, et al. Advancing paternal age and autism. Arch Gen Psychiatry 2006;63:1026-32.  Back to cited text no. 33
    
34.
Tsuchiya KJ, Takagai S, Kawai M, Matsumoto H, Nakamura K, Minabe Y, et al. Advanced paternal age associated with an elevated risk for schizophrenia in offspring in a Japanese population. Schizophr Res 2005;76:337-42.  Back to cited text no. 34
    
35.
Alter MD, Kharkar R, Ramsey KE, Craig DW, Melmed RD, Grebe TA, et al. Autism and increased paternal age related changes in global levels of gene expression regulation. PLoS One 2011;6:e16715.  Back to cited text no. 35
    
36.
Hultman CM, Sandin S, Levine SZ, Lichtenstein P, Reichenberg A. Advancing paternal age and risk of autism: New evidence from a population-based study and a meta-analysis of epidemiological studies. Mol Psychiatry 2011;16:1203-12.  Back to cited text no. 36
    
37.
Kong A, Frigge ML, Masson G, Besenbacher S, Sulem P, Magnusson G, et al. Rate of de novo mutations and the importance of father's age to disease risk. Nature 2012;488:471-5.  Back to cited text no. 37
    
38.
Sasanfar R, Haddad SA, Tolouei A, Ghadami M, Yu D, Santangelo SL. Paternal age increases the risk for autism in an Iranian population sample. Mol Autism 2010;1:2.  Back to cited text no. 38
    
39.
van Balkom ID, Bresnahan M, Vuijk PJ, Hubert J, Susser E, Hoek HW. Paternal age and risk of autism in an ethnically diverse, non-industrialized setting: Aruba. PLoS One 2012;7:e45090.  Back to cited text no. 39
    
40.
Zhang X, Lv CC, Tian J, Miao RJ, Xi W, Hertz-Picciotto I, et al. Prenatal and perinatal risk factors for autism in China. J Autism Dev Disord 2010;40:1311-21.  Back to cited text no. 40
    
41.
Hultman CM, Sparén P. Autism – Prenatal insults or an epiphenomenon of a strongly genetic disorder? Lancet 2004;364:485-7.  Back to cited text no. 41
    
42.
Kolevzon A, Gross R, Reichenberg A. Prenatal and perinatal risk factors for autism: A review and integration of findings. Arch Pediatr Adolesc Med 2007;161:326-33.  Back to cited text no. 42
    
43.
Rosenthal AN, Paterson-Brown S. Is there an incremental rise in the risk of obstetric intervention with increasing maternal age? Br J Obstet Gynaecol 1998;105:1064-9.  Back to cited text no. 43
    
44.
Sandin S, Hultman CM, Kolevzon A, Gross R, MacCabe JH, Reichenberg A. Advancing maternal age is associated with increasing risk for autism: A review and meta-analysis. J Am Acad Child Adolesc Psychiatry 2012;51:477-86.e1.  Back to cited text no. 44
    
45.
Ornoy A, Weinstein-Fudim L, Ergaz Z. Prenatal factors associated with autism spectrum disorder (ASD). Reprod Toxicol 2015;56:155-69.  Back to cited text no. 45
    
46.
Eidelman AI, Samueloff A. The pathophysiology of the fetus of the diabetic mother. In: Seminars in Perinatology. Seminars in perinatology 2002;26(3):232-36. [DOI:http://dx.doi.org/10.1053/sper.2002.34215].  Back to cited text no. 46
    
47.
Gardener H, Spiegelman D, Buka SL. Perinatal and neonatal risk factors for autism: A comprehensive meta-analysis. Pediatrics 2011;128:344-55.  Back to cited text no. 47
    
48.
Krakowiak P, Walker CK, Bremer AA, Baker AS, Ozonoff S, Hansen RL, et al. Maternal metabolic conditions and risk for autism and other neurodevelopmental disorders. Pediatrics 2012;129:e1121-8.  Back to cited text no. 48
    
49.
Guinchat V, Thorsen P, Laurent C, Cans C, Bodeau N, Cohen D. Pre-, peri- and neonatal risk factors for autism. Acta Obstet Gynecol Scand 2012;91:287-300.  Back to cited text no. 49
    
50.
Georgieff MK. The effect of maternal diabetes during pregnancy on the neurodevelopment of offspring. Minn Med 2006;89:44-7.  Back to cited text no. 50
    
51.
Deykin EY, MacMahon B. Viral exposure and autism. Am J Epidemiol 1979;109:628-38.  Back to cited text no. 51
    
52.
Libbey JE, Sweeten TL, McMahon WM, Fujinami RS. Autistic disorder and viral infections. J Neurovirol 2005;11:1-10.  Back to cited text no. 52
    
53.
London EA. The environment as an etiologic factor in autism: A new direction for research. Environ Health Perspect 2000;108 Suppl 3:401-4.  Back to cited text no. 53
    
54.
Atladóttir HÓ, Henriksen TB, Schendel DE, Parner ET. Autism after infection, febrile episodes, and antibiotic use during pregnancy: An exploratory study. Pediatrics 2012;130:e1447-54.  Back to cited text no. 54
    
55.
Gillberg C, Coleman M. The Biology of the Autistic Syndromes. Vol. 25. London, UK: Cambridge University Press; 2000. p. 340.  Back to cited text no. 55
    
56.
Yamashita Y, Fujimoto C, Nakajima E, Isagai T, Matsuishi T. Possible association between congenital cytomegalovirus infection and autistic disorder. J Autism Dev Disord 2003;33:455-9.  Back to cited text no. 56
    
57.
Croen LA, Grether JK, Yoshida CK, Odouli R, Van de Water J. Maternal autoimmune diseases, asthma and allergies, and childhood autism spectrum disorders: A case-control study. Arch Pediatr Adolesc Med 2005;159:151-7.  Back to cited text no. 57
    
58.
Elovitz MA, Brown AG, Breen K, Anton L, Maubert M, Burd I. Intrauterine inflammation, insufficient to induce parturition, still evokes fetal and neonatal brain injury. Int J Dev Neurosci 2011;29:663-71.  Back to cited text no. 58
    
59.
Karahmadi M. Parental interaction patterns in children with attention deficit hyperactive disorder and control group. J Res Med Sci 2007;12:143-6.  Back to cited text no. 59
    
60.
Bölte S, Knecht S, Poustka F. A case-control study of personality style and psychopathology in parents of subjects with autism. J Autism Dev Disord 2007;37:243-50.  Back to cited text no. 60
    
61.
Daniels JL, Forssen U, Hultman CM, Cnattingius S, Savitz DA, Feychting M, et al. Parental psychiatric disorders associated with autism spectrum disorders in the offspring. Pediatrics 2008;121:e1357-62.  Back to cited text no. 61
    
62.
Fish B, Marcus J, Hans SL, Auerbach JG, Perdue S. Infants at risk for schizophrenia: Sequelae of a genetic neurointegrative defect. A review and replication analysis of pandysmaturation in the Jerusalem Infant Development Study. Arch Gen Psychiatry 1992;49:221-35.  Back to cited text no. 62
    
63.
Wolff S, Narayan S, Moyes B. Personality characteristics of parents of autistic children: A controlled study. J Child Psychol Psychiatry 1988;29:143-53.  Back to cited text no. 63
    
64.
Gudsnuk K, Champagne FA. Epigenetic influence of stress and the social environment. Ilar J 2012;53:279-88. [doi: 10.1093/ilar.53.3-4.279].  Back to cited text no. 64
    
65.
Ladd CO, Huot RL, Thrivikraman KV, Nemeroff CB, Plotsky PM. Long-term adaptations in glucocorticoid receptor and mineralocorticoid receptor mRNA and negative feedback on the hypothalamo-pituitary-adrenal axis following neonatal maternal separation. Biol Psychiatry 2004;55:367-75.  Back to cited text no. 65
    
66.
Maccari S, Darnaudery M, Morley-Fletcher S, Zuena AR, Cinque C, Van Reeth O. Prenatal stress and long-term consequences: Implications of glucocorticoid hormones. Neurosci Biobehav Rev 2003;27:119-27.  Back to cited text no. 66
    
67.
Mueller BR, Bale TL. Sex-specific programming of offspring emotionality after stress early in pregnancy. J Neurosci 2008;28:9055-65.  Back to cited text no. 67
    
68.
O'Donnell K, O'Connor TG, Glover V. Prenatal stress and neurodevelopment of the child: Focus on the HPA axis and role of the placenta. Dev Neurosci 2009;31:285-92.  Back to cited text no. 68
    
69.
Sabih F, Sajid WB. There is significant stress among parents having children with autism. J Rawalpindi Med 2008;33:214-6.  Back to cited text no. 69
    
70.
Weinstock M. The long-term behavioural consequences of prenatal stress. Neurosci Biobehav Rev 2008;32:1073-86.  Back to cited text no. 70
    
71.
Beversdorf DQ, Manning SE, Hillier A, Anderson SL, Nordgren RE, Walters SE, et al. Timing of prenatal stressors and autism. J Autism Dev Disord 2005;35:471-8.  Back to cited text no. 71
    
72.
Musavi SM, Kamali E, Karimi P, Fatahi F, Chaleshtari MH, Salehi M. Autism and ENVIRONMENT in Isfahan area: Severe and Scheduled Prenatal Stresses at Spotlight! Archive of Iranian Medicine, 2016. [under review].  Back to cited text no. 72
    
73.
Karahmadi M, Esmaeili DN. Aggression and some of its demographic correlates in nurses of pediatric wards in hospitals affi liated to Isfahan Medical University. J Res Behav Sci 2007; 5(1):33-7.  Back to cited text no. 73
    
74.
Shivers CM, Deisenroth LK, Taylor JL. Patterns and predictors of anxiety among siblings of children with autism spectrum disorders. J Autism Dev Disord 2013;43:1336-46.  Back to cited text no. 74
    
75.
Narita M, Oyabu A, Imura Y, Kamada N, Yokoyama T, Tano K, et al. Nonexploratory movement and behavioral alterations in a thalidomide or valproic acid-induced autism model rat. Neurosci Res 2010;66:2-6.  Back to cited text no. 75
    
76.
Ornoy A. Valproic acid in pregnancy: How much are we endangering the embryo and fetus? Reprod Toxicol 2009;28:1-10.  Back to cited text no. 76
    
77.
Bauer AZ, Kriebel D. Prenatal and perinatal analgesic exposure and autism: An ecological link. Environ Health 2013;12:41.  Back to cited text no. 77
    
78.
Gidaya NB, Lee BK, Burstyn I, Yudell M, Mortensen EL, Newschaffer CJ. In utero exposure to selective serotonin reuptake inhibitors and risk for autism spectrum disorder. J Autism Dev Disord 2014;44:2558-67.  Back to cited text no. 78
    
79.
Harrington RA, Lee LC, Crum RM, Zimmerman AW, Hertz-Picciotto I. Prenatal SSRI use and offspring with autism spectrum disorder or developmental delay. Pediatrics 2014;133:e1241-8.  Back to cited text no. 79
    
80.
Rai D, Lee BK, Dalman C, Golding J, Lewis G, Magnusson C. Parental depression, maternal antidepressant use during pregnancy, and risk of autism spectrum disorders: Population based case-control study. BMJ 2013;346:f2059.  Back to cited text no. 80
    
81.
Ito T, Ando H, Suzuki T, Ogura T, Hotta K, Imamura Y, et al. Identification of a primary target of thalidomide teratogenicity. Science 2010;327:1345-50.  Back to cited text no. 81
    
82.
Bandim JM, Ventura LO, Miller MT, Almeida HC, Costa AE. Autism and Möbius sequence: An exploratory study of children in Northeastern Brazil. Arq Neuropsiquiatr 2003;61:181-5.  Back to cited text no. 82
    
83.
Witter FR, Zimmerman AW, Reichmann JP, Connors SL. In utero beta 2 adrenergic agonist exposure and adverse neurophysiologic and behavioral outcomes. Am J Obstet Gynecol 2009;201:553-9.  Back to cited text no. 83
    
84.
Zerrate MC, Pletnikov M, Connors SL, Vargas DL, Seidler FJ, Zimmerman AW, et al. Neuroinflammation and behavioral abnormalities after neonatal terbutaline treatment in rats: Implications for autism. J Pharmacol Exp Ther 2007;322:16-22.  Back to cited text no. 84
    
85.
Lee LC, Harrington RA, Louie BB, Newschaffer CJ. Children with autism: Quality of life and parental concerns. J Autism Dev Disord 2008;38:1147-60.  Back to cited text no. 85
    
86.
Adler NE, Newman K. Socioeconomic disparities in health: Pathways and policies. Health Aff (Millwood) 2002;21:60-76.  Back to cited text no. 86
    
87.
Durkin MS, Maenner MJ, Meaney FJ, Levy SE, DiGuiseppi C, Nicholas JS, et al. Socioeconomic inequality in the prevalence of autism spectrum disorder: Vidence from a U.S. cross-sectional study. PLoS One 2010;5:e11551.  Back to cited text no. 87
    
88.
Finegan JA, Quarrington B. Pre-, peri-, and neonatal factors and infantile autism. J Child Psychol Psychiatry 1979;20:119-28.  Back to cited text no. 88
    
89.
Kaczynski AT, Henderson KA. Parks and recreation settings and active living: A review of associations with physical activity function and intensity. J Phys Act Health 2008;5:619-32.  Back to cited text no. 89
    
90.
Samadi SA, McConkey R. Autism in developing countries: Lessons from iran. Autism Res Treat 2011;2011:145359.  Back to cited text no. 90
    
91.
Croen LA, Grether JK, Selvin S. Descriptive epidemiology of autism in a California population: Who is at risk? J Autism Dev Disord 2002;32:217-24.  Back to cited text no. 91
    
92.
Hvidtjørn D, Grove J, Schendel D, Schieve LA, Sværke C, Ernst E, et al. Risk of autism spectrum disorders in children born after assisted conception: A population-based follow-up study. J Epidemiol Community Health 2011;65:497-502.  Back to cited text no. 92
    
93.
King MD, Bearman PS. Socioeconomic status and the increased prevalence of autism in California. Am Sociol Rev 2011;76:320-46.  Back to cited text no. 93
    
94.
Buchmayer S, Johansson S, Johansson A, Hultman CM, Sparén P, Cnattingius S. Can association between preterm birth and autism be explained by maternal or neonatal morbidity? Pediatrics 2009;124:e817-25.  Back to cited text no. 94
    
95.
Maimburg RD, Vaeth M. Perinatal risk factors and infantile autism. Acta Psychiatr Scand 2006;114:257-64.  Back to cited text no. 95
    
96.
Previc FH. Prenatal influences on brain dopamine and their relevance to the rising incidence of autism. Med Hypotheses 2007;68:46-60.  Back to cited text no. 96
    
97.
Eaton WW, Mortensen PB, Thomsen PH, Frydenberg M. Obstetric complications and risk for severe psychopathology in childhood. J Autism Dev Disord 2001;31:279-85.  Back to cited text no. 97
    
98.
Schendel D, Bhasin TK. Birth weight and gestational age characteristics of children with autism, including a comparison with other developmental disabilities. Pediatrics 2008;121:1155-64.  Back to cited text no. 98
    
99.
Maimburg RD, Bech BH, Vaeth M, Møller-Madsen B, Olsen J. Neonatal jaundice, autism, and other disorders of psychological development. Pediatrics 2010;126:872-8.  Back to cited text no. 99
    
100.
Maimburg RD, Vaeth M, Schendel DE, Bech BH, Olsen J, Thorsen P. Neonatal jaundice: A risk factor for infantile autism? Paediatr Perinat Epidemiol 2008;22:562-8.  Back to cited text no. 100
    
101.
Newschaffer CJ, Fallin D, Lee NL. Heritable and nonheritable risk factors for autism spectrum disorders. Epidemiol Rev 2002;24:137-53.  Back to cited text no. 101
    
102.
Rosen NJ, Yoshida CK, Croen LA. Infection in the first 2 years of life and autism spectrum disorders. Pediatrics 2007;119:e61-9.  Back to cited text no. 102
    
103.
Li Q, Cheung C, Wei R, Hui ES, Feldon J, Meyer U, et al. Prenatal immune challenge is an environmental risk factor for brain and behavior change relevant to schizophrenia: Evidence from MRI in a mouse model. PLoS One 2009;4:e6354.  Back to cited text no. 103
    
104.
Taylor B, Miller E, Lingam R, Andrews N, Simmons A, Stowe J. Measles, mumps, and rubella vaccination and bowel problems or developmental regression in children with autism: Population study. BMJ 2002;324:393-6.  Back to cited text no. 104
    
105.
Haggarty P. Effect of placental function on fatty acid requirements during pregnancy. Eur J Clin Nutr 2004;58:1559-70.  Back to cited text no. 105
    
106.
Casper RC. Nutrients, neurodevelopment, and mood. Curr Psychiatry Rep 2004;6:425-9.  Back to cited text no. 106
    
107.
Deckelbaum RJ, Worgall TS, Seo T. n-3 fatty acids and gene expression. Am J Clin Nutr 2006;83 6 Suppl: 1520S-5S.  Back to cited text no. 107
    
108.
Lyall K, Munger KL, O'Reilly ÉJ, Santangelo SL, Ascherio A. Maternal dietary fat intake in association with autism spectrum disorders. Am J Epidemiol 2013;178:209-20.  Back to cited text no. 108
    
109.
Roza SJ, van Batenburg-Eddes T, Steegers EA, Jaddoe VW, Mackenbach JP, Hofman A, et al. Maternal folic acid supplement use in early pregnancy and child behavioural problems: The Generation R Study. Br J Nutr 2010;103:445-52.  Back to cited text no. 109
    
110.
Roth C, Magnus P, Schjølberg S, Stoltenberg C, Surén P, McKeague IW, et al. Folic acid supplements in pregnancy and severe language delay in children. JAMA 2011;306:1566-73.  Back to cited text no. 110
    
111.
Julvez J, Fortuny J, Mendez M, Torrent M, Ribas-Fitó N, Sunyer J. Maternal use of folic acid supplements during pregnancy and four-year-old neurodevelopment in a population-based birth cohort. Paediatr Perinat Epidemiol 2009;23:199-206.  Back to cited text no. 111
    
112.
Schlotz W, Jones A, Phillips DI, Gale CR, Robinson SM, Godfrey KM. Lower maternal folate status in early pregnancy is associated with childhood hyperactivity and peer problems in offspring. J Child Psychol Psychiatry 2010;51:594-602.  Back to cited text no. 112
    
113.
Schmidt RJ, Tancredi DJ, Ozonoff S, Hansen RL, Hartiala J, Allayee H, et al. Maternal periconceptional folic acid intake and risk of autism spectrum disorders and developmental delay in the CHARGE (CHildhood Autism Risks from Genetics and Environment) case-control study. Am J Clin Nutr 2012;96:80-9.  Back to cited text no. 113
    
114.
Grether JK, Anderson MC, Croen LA, Smith D, Windham GC. Risk of autism and increasing maternal and paternal age in a large North American population. Am J Epidemiol 2009;170:1118-26.  Back to cited text no. 114
    
115.
King MD, Fountain C, Dakhlallah D, Bearman PS. Estimated autism risk and older reproductive age. Am J Public Health 2009;99:1673-9.  Back to cited text no. 115
    
116.
Ozonoff S, Young GS, Carter A, Messinger D, Yirmiya N, Zwaigenbaum L, et al. Recurrence risk for autism spectrum disorders: A Baby Siblings Research Consortium study. Pediatrics 2011;128:e488-95.  Back to cited text no. 116
    
117.
Constantino JN, Zhang Y, Frazier T, Abbacchi AM, Law P. Sibling recurrence and the genetic epidemiology of autism. Am J Psychiatry 2010;167:1349-56.  Back to cited text no. 117
    
118.
Bolton PF, Murphy M, Macdonald H, Whitlock B, Pickles A, Rutter M. Obstetric complications in autism: Consequences or causes of the condition? J Am Acad Child Adolesc Psychiatry 1997;36:272-81.  Back to cited text no. 118
    
119.
Brown GE, Jones SD, MacKewn AS, Plank EJ. An exploration of possible pre- and postnatal correlates of autism: A pilot survey. Psychol Rep 2008;102:273-82.  Back to cited text no. 119
    
120.
Lord C, Mulloy C, Wendelboe M, Schopler E. Pre- and perinatal factors in high-functioning females and males with autism. J Autism Dev Disord 1991;21:197-209.  Back to cited text no. 120
    
121.
Piven J, Simon J, Chase GA, Wzorek M, Landa R, Gayle J, et al. The etiology of autism: Pre-, peri- and neonatal factors. J Am Acad Child Adolesc Psychiatry 1993;32:1256-63.  Back to cited text no. 121
    
122.
Dietert RR, Dietert JM, Dewitt JC. Environmental risk factors for autism. Emerg Health Threats J 2011;4:7111.  Back to cited text no. 122
    
123.
Pavanello S, Bollati V, Pesatori AC, Kapka L, Bolognesi C, Bertazzi PA, et al. Global and gene-specific promoter methylation changes are related to anti-B[a] PDE-DNA adduct levels and influence micronuclei levels in polycyclic aromatic hydrocarbon-exposed individuals. Int J Cancer 2009;125:1692-7.  Back to cited text no. 123
    
124.
Shelton JF, Geraghty EM, Tancredi DJ, Delwiche LD, Schmidt RJ, Ritz B, et al. Neurodevelopmental disorders and prenatal residential proximity to agricultural pesticides: The CHARGE study. Environ Health Perspect 2014;122:1103-9.  Back to cited text no. 124
    
125.
Curley JP, Jensen CL, Mashoodh R, Champagne FA. Social influences on neurobiology and behavior: Epigenetic effects during development. Psychoneuroendocrinology 2011;36:352-71.  Back to cited text no. 125
    
126.
Becker KG, Schultz ST. Similarities in features of autism and asthma and a possible link to acetaminophen use. Med Hypotheses 2010;74:7-11.  Back to cited text no. 126
    
127.
Schultz ST, Klonoff-Cohen HS, Wingard DL, Akshoomoff NA, Macera CA, Ji M. Acetaminophen (paracetamol) use, measles-mumps-rubella vaccination, and autistic disorder: The results of a parent survey. Autism 2008;12:293-307.  Back to cited text no. 127
    
128.
Wright RJ. Moving towards making social toxins mainstream in children's environmental health. Curr Opin Pediatr 2009;21:222-9.  Back to cited text no. 128
    
129.
Xiao R, Sorensen TK, Williams MA, Luthy DA. Influence of pre-eclampsia on fetal growth. J Matern Fetal Neonatal Med 2003;13:157-62.  Back to cited text no. 129
    
130.
Rosen BN, Lee BK, Lee NL, Yang Y, Burstyn I. Maternal smoking and autism spectrum disorder: A meta-analysis. J Autism Dev Disord 2015;45:1689-98.  Back to cited text no. 130
    
131.
James SJ, Melnyk S, Jernigan S, Pavliv O, Trusty T, Lehman S, et al. A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism. Am J Med Genet B Neuropsychiatr Genet 2010;153B: 1209-20.  Back to cited text no. 131
    
132.
Main PA, Angley MT, Thomas P, O'Doherty CE, Fenech M. Folate and methionine metabolism in autism: A systematic review. Am J Clin Nutr 2010;91:1598-620.  Back to cited text no. 132
    
133.
Ramaekers VT, Blau N, Sequeira JM, Nassogne MC, Quadros EV. Folate receptor autoimmunity and cerebral folate deficiency in low-functioning autism with neurological deficits. Neuropediatrics 2007;38:276-81.  Back to cited text no. 133
    
134.
Fernell E, Barnevik-Olsson M, Bågenholm G, Gillberg C, Gustafsson S, Sääf M. Serum levels of 25-hydroxyvitamin D in mothers of Swedish and of Somali origin who have children with and without autism. Acta Paediatr 2010;99:743-7.  Back to cited text no. 134
    
135.
Grant WB, Soles CM. Epidemiologic evidence supporting the role of maternal Vitamin D deficiency as a risk factor for the development of infantile autism. Dermatoendocrinol 2009;1:223-8.  Back to cited text no. 135
    
136.
Kalueff AV, Tuohimaa P. Neurosteroid hormone Vitamin D and its utility in clinical nutrition. Curr Opin Clin Nutr Metab Care 2007;10:12-9.  Back to cited text no. 136
    
137.
Kinney DK, Barch DH, Chayka B, Napoleon S, Munir KM. Environmental risk factors for autism: Do they help cause de novo genetic mutations that contribute to the disorder? Med Hypotheses 2010;74:102-6.  Back to cited text no. 137
    
138.
Levenson CW, Figueirôa SM. Gestational Vitamin D deficiency: Long-term effects on the brain. Nutr Rev 2008;66:726-9.  Back to cited text no. 138
    
139.
Moore M, Piazza A, Nolan Y, Lynch MA. Treatment with dexamethasone and Vitamin D3 attenuates neuroinflammatory age-related changes in rat hippocampus. Synapse 2007;61:851-61.  Back to cited text no. 139
    
140.
Zwaigenbaum L, Szatmari P, Jones MB, Bryson SE, MacLean JE, Mahoney WJ, et al. Pregnancy and birth complications in autism and liability to the broader autism phenotype. J Am Acad Child Adolesc Psychiatry 2002;41:572-9.  Back to cited text no. 140
    
141.
MacKinnon DP, Krull JL, Lockwood CM. Equivalence of the mediation, confounding and suppression effect. Prev Sci 2000;1:173-81.  Back to cited text no. 141
    
142.
Mann JR, McDermott S, Bao H, Hardin J, Gregg A. Pre-eclampsia, birth weight, and autism spectrum disorders. J Autism Dev Disord 2010;40:548-54.  Back to cited text no. 142
    
143.
Dodds L, Fell DB, Shea S, Armson BA, Allen AC, Bryson S. The role of prenatal, obstetric and neonatal factors in the development of autism. J Autism Dev Disord 2011;41:891-902.  Back to cited text no. 143
    
144.
Atladóttir HO, Pedersen MG, Thorsen P, Mortensen PB, Deleuran B, Eaton WW, et al. Association of family history of autoimmune diseases and autism spectrum disorders. Pediatrics 2009;124:687-94.  Back to cited text no. 144
    
145.
Atladóttir HO, Thorsen P, Østergaard L, Schendel DE, Lemcke S, Abdallah M, et al. Maternal infection requiring hospitalization during pregnancy and autism spectrum disorders. J Autism Dev Disord 2010;40:1423-30.  Back to cited text no. 145
    
146.
Hastings RP, Brown T. Behavior problems of children with autism, parental self-efficacy, and mental health. Am J Ment Retard 2002;107:222-32.  Back to cited text no. 146
    
147.
Li J, Vestergaard M, Obel C, Christensen J, Precht DH, Lu M, et al. A nationwide study on the risk of autism after prenatal stress exposure to maternal bereavement. Pediatrics 2009;123:1102-7.  Back to cited text no. 147
    
148.
Arndt TL, Stodgell CJ, Rodier PM. The teratology of autism. Int J Dev Neurosci 2005;23:189-99.  Back to cited text no. 148
    
149.
Rutter M. Incidence of autism spectrum disorders: Changes over time and their meaning. Acta Paediatr 2005;94:2-15.  Back to cited text no. 149
    
150.
Kocijan-Hercigonja D, Remeta D, Orehovac M, Brkljacic D. Prenatal, perinatal and neonatal factors in infantile autism. Acta Med Croatica 1991;45:357-62.  Back to cited text no. 150
    
151.
Enstrom AM, Onore CE, van de Water JA, Ashwood P. Differential monocyte responses to TLR ligands in children with autism spectrum disorders. Brain Behav Immun 2010;24:64-71.  Back to cited text no. 151
    
152.
Torres AR. Is fever suppression involved in the etiology of autism and neurodevelopmental disorders? BMC Pediatr 2003;3:9.  Back to cited text no. 152
    
153.
Adams JB, Baral M, Geis E, Mitchell J, Ingram J, Hensley A, et al. The severity of autism is associated with toxic metal body burden and red blood cell glutathione levels. J Toxicol 2009;2009:532640.  Back to cited text no. 153
    
154.
Baccarelli A, Bollati V. Epigenetics and environmental chemicals. Curr Opin Pediatr 2009;21:243-51.  Back to cited text no. 154
    
155.
Kern JK, Grannemann BD, Trivedi MH, Adams JB. Sulfhydryl-reactive metals in autism. J Toxicol Environ Health A 2007;70:715-21.  Back to cited text no. 155
    
156.
D'Amelio M, Ricci I, Sacco R, Liu X, D'Agruma L, Muscarella LA, et al. Paraoxonase gene variants are associated with autism in North America, but not in Italy: Possible regional specificity in gene-environment interactions. Mol Psychiatry 2005;10:1006-16.  Back to cited text no. 156
    
157.
Windham G, Fenster L. Environmental contaminants and pregnancy outcomes. Fertil Steril 2008;89 2 Suppl: e111-6.  Back to cited text no. 157
    
158.
Choi H, Rauh V, Garfinkel R, Tu Y, Perera FP. Prenatal exposure to airborne polycyclic aromatic hydrocarbons and risk of intrauterine growth restriction. Environ Health Perspect 2008;116:658-65.  Back to cited text no. 158
    
159.
Salam MT, Millstein J, Li YF, Lurmann FW, Margolis HG, Gilliland FD. Birth outcomes and prenatal exposure to ozone, carbon monoxide, and particulate matter: Results from the Children's Health Study. Environ Health Perspect 2005;113:1638-44.  Back to cited text no. 159
    
160.
Johnson-Restrepo B, Kannan K. An assessment of sources and pathways of human exposure to polybrominated diphenyl ethers in the United States. Chemosphere 2009;76:542-8.  Back to cited text no. 160
    
161.
Costa LG, Giordano G, Tagliaferri S, Caglieri A, Mutti A. Polybrominated diphenyl ether (PBDE) flame retardants: Environmental contamination, human body burden and potential Adverse health effects. Acta Biomed 2008;79:172-83.  Back to cited text no. 161
    
162.
Luginaah IN, Lee KS, Abernathy TJ, Sheehan D, Webster G. Trends and variations in perinatal mortality and low birthweight: The contribution of socio-economic factors. Can J Public Health 1999;90:377-81.  Back to cited text no. 162
    
163.
Sampson RJ, Morenoff JD, Gannon-Rowley T, Assessing “neighborhood effects”: Social processes and new directions in research. Ann Rev Sociol 2002;28:443-78.  Back to cited text no. 163
    
164.
Currenti SA. Understanding and determining the etiology of autism. Cell Mol Neurobiol 2010;30:161-71.  Back to cited text no. 164
    
165.
Martin JA, Hamilton BE, Sutton PD, Ventura SJ, Menacker F, Kirmeyer S, et al. Births: Final Data for 2006. National Vital Statistics Reports. Vol. 57. Hyattsville, MD: National Center for Health Statistics; 2009.  Back to cited text no. 165
    
166.
Brimacombe M, Ming X, Lamendola M. Prenatal and birth complications in autism. Matern Child Health J 2007;11:73-9.  Back to cited text no. 166
    
167.
Bilder D, Pinborough-Zimmerman J, Miller J, McMahon W. Prenatal, perinatal, and neonatal factors associated with autism spectrum disorders. Pediatrics 2009;123:1293-300.  Back to cited text no. 167
    
168.
Sugie Y, Sugie H, Fukuda T, Ito M. Neonatal factors in infants with autistic disorder and typically developing infants. Autism 2005;9:487-94.  Back to cited text no. 168
    
169.
Burstyn I, Sithole F, Zwaigenbaum L. Autism spectrum disorders, maternal characteristics and obstetric complications among singletons born in Alberta, Canada. Chronic Dis Can 2010;30:125-34.  Back to cited text no. 169
    
170.
Stein D, Weizman A, Ring A, Barak Y. Obstetric complications in individuals diagnosed with autism and in healthy controls. Compr Psychiatry 2006;47:69-75.  Back to cited text no. 170
    
171.
Laxer G, Rey M, Ritvo ER. A comparison of potentially pathologic factors in European children with autism, Down's syndrome, and multiple physical handicaps. J Autism Dev Disord 1988;18:309-13.  Back to cited text no. 171
    
172.
Timonen-Soivio L, Vanhala R, Malm H, Leivonen S, Jokiranta E, Hinkka-Yli-Salomäki S, et al. The association between congenital anomalies and autism spectrum disorders in a Finnish national birth cohort. Dev Med Child Neurol 2015;57:75-80.  Back to cited text no. 172
    
173.
Juul-Dam N, Townsend J, Courchesne E. Prenatal, perinatal, and neonatal factors in autism, pervasive developmental disorder-not otherwise specified, and the general population. Pediatrics 2001;107:E63.  Back to cited text no. 173
    
174.
Haglund NG, Källén KB. Risk factors for autism and Asperger syndrome. Perinatal factors and migration. Autism 2011;15:163-83.  Back to cited text no. 174
    
175.
Karmel BZ, Gardner JM, Meade LS, Cohen IL, London E, Flory MJ, et al. Early medical and behavioral characteristics of NICU infants later classified with ASD. Pediatrics 2010;126:457-67.  Back to cited text no. 175
    
176.
Schendel DE, Autry A, Wines R, Moore C. The co-occurrence of autism and birth defects: Prevalence and risk in a population-based cohort. Dev Med Child Neurol 2009;51:779-86.  Back to cited text no. 176
    
177.
Williams K, Helmer M, Duncan GW, Peat JK, Mellis CM. Perinatal and maternal risk factors for autism spectrum disorders in New South Wales, Australia. Child Care Health Dev 2008;34:249-56.  Back to cited text no. 177
    
178.
Croen LA, Yoshida CK, Odouli R, Newman TB. Neonatal hyperbilirubinemia and risk of autism spectrum disorders. Pediatrics 2005;115:e135-8.  Back to cited text no. 178
    
179.
Badawi N, Dixon G, Felix JF, Keogh JM, Petterson B, Stanley FJ, et al. Autism following a history of newborn encephalopathy: More than a coincidence? Dev Med Child Neurol 2006;48:85-9.  Back to cited text no. 179
    
180.
Dawson S, Glasson EJ, Dixon G, Bower C. Birth defects in children with autism spectrum disorders: A population-based, nested case-control study. Am J Epidemiol 2009;169:1296-303.  Back to cited text no. 180
    
181.
Tripi G, Roux S, Canziani T, Bonnet Brilhault F, Barthélémy C, Canziani F. Minor physical anomalies in children with autism spectrum disorder. Early Hum Dev 2008;84:217-23.  Back to cited text no. 181
    
182.
Mason-Brothers A, Ritvo ER, Pingree C, Petersen PB, Jenson WR, McMahon WM, et al. The UCLA-University of Utah epidemiologic survey of autism: Prenatal, perinatal, and postnatal factors. Pediatrics 1990;86:514-9.  Back to cited text no. 182
    
183.
Atladóttir HO, Thorsen P, Schendel DE, Østergaard L, Lemcke S, Parner ET. Association of hospitalization for infection in childhood with diagnosis of autism spectrum disorders: A Danish cohort study. Arch Pediatr Adolesc Med 2010;164:470-7.  Back to cited text no. 183
    
184.
Bryson SE, Smith IM, Eastwood D. Obstetrical suboptimality in autistic children. J Am Acad Child Adolesc Psychiatry 1988;27:418-22.  Back to cited text no. 184
    
185.
Gillberg C, Gillberg IC. Infantile autism: A total population study of reduced optimality in the pre-, peri-, and neonatal period. J Autism Dev Disord 1983;13:153-66.  Back to cited text no. 185
    
186.
Deykin EY, MacMahon B. Pregnancy, delivery, and neonatal complications among autistic children. Am J Dis Child 1980;134:860-4.  Back to cited text no. 186
    



 
 
    Tables

  [Table 1], [Table 2], [Table 3]


This article has been cited by
1 Parenting Challenges in Families of Children with a Diagnosis of Autism Spectrum Disorder: A Qualitative Research Study in Istanbul
Mustafa Rfat, Orhan Koçak, Büsra Uzun
Global Social Welfare. 2023;
[Pubmed] | [DOI]
2 Sex differences in antioxidant defence and the regulation of redox homeostasis in physiology and pathology
Jessica Tiberi, Valeriana Cesarini, Roberta Stefanelli, Sonia Canterini, Maria Teresa Fiorenza, Piergiorgio La Rosa
Mechanisms of Ageing and Development. 2023; : 111802
[Pubmed] | [DOI]
3 Assessment of vulnerability dimensions considering Family History and environmental interplay in Autism Spectrum Disorder
Anita Brito, Felipe Franco, Helena Brentani, Patrícia Cristina Baleeiro Beltrão-Braga
BMC Psychiatry. 2023; 23(1)
[Pubmed] | [DOI]
4 Effects of an 8-week multimodal exercise program on ground reaction forces and plantar pressure during walking in boys with autism spectrum disorder
Mahrokh Dehghani, Amir Ali Jafarnezhadgero, Mohamad Abdollahpour Darvishani, Shirin Aali, Urs Granacher
Trials. 2023; 24(1)
[Pubmed] | [DOI]
5 Disentangling disorder-specific variation is key for precision psychiatry in autism
Aidas Aglinskas, Emily Schwartz, Stefano Anzellotti
Frontiers in Behavioral Neuroscience. 2023; 17
[Pubmed] | [DOI]
6 Evaluation of a “Picture Assisted Illustration Reinforcement” (PAIR) System for Oral Hygiene in Children with Autism: A Double-Blind Randomized Controlled Trial
Atrey J. Pai Khot, Abhra Roy Choudhury, Anil V. Ankola, Roopali M. Sankeshwari, Vinuta Hampiholi, Mamata Hebbal, Sagar Jalihal, Ram Surath Kumar, Laxmi Kabra, Sree Lalita Kotha
Children. 2023; 10(2): 369
[Pubmed] | [DOI]
7 PCDH19 in Males: Are Hemizygous Variants Linked to Autism?
Eliane Chouery, Jana Makhlouf, Wassim Daoud Khatoun, Cybel Mehawej, Andre Megarbane
Genes. 2023; 14(3): 598
[Pubmed] | [DOI]
8 Intestinal Barrier Dysfunction and Microbiota–Gut–Brain Axis: Possible Implications in the Pathogenesis and Treatment of Autism Spectrum Disorder
Vanessa Nadia Dargenio, Costantino Dargenio, Stefania Castellaneta, Andrea De Giacomo, Marianna Laguardia, Federico Schettini, Ruggiero Francavilla, Fernanda Cristofori
Nutrients. 2023; 15(7): 1620
[Pubmed] | [DOI]
9 The Human Gut Microbiome as a Potential Factor in Autism Spectrum Disorder
Amani Alharthi, Safiah Alhazmi, Najla Alburae, Ahmed Bahieldin
International Journal of Molecular Sciences. 2022; 23(3): 1363
[Pubmed] | [DOI]
10 Metal Profiles in Autism Spectrum Disorders: A Crosstalk between Toxic and Essential Metals
Anna Blazewicz, Andreas M. Grabrucker
International Journal of Molecular Sciences. 2022; 24(1): 308
[Pubmed] | [DOI]
11 Chemical Modulators for Targeting Autism Spectrum Disorders: From Bench to Clinic
Songhyun Lim, Sanghee Lee
Molecules. 2022; 27(16): 5088
[Pubmed] | [DOI]
12 Early Prediction and Evaluation of Risk of Autism Spectrum Disorders
Nada S Ashmawi, Manal A Hammoda
Cureus. 2022;
[Pubmed] | [DOI]
13 Epigenome-Wide Analysis Reveals DNA Methylation Alteration in ZFP57 and Its Target RASGFR2 in a Mexican Population Cohort with Autism
Queletzu Aspra, Brenda Cabrera-Mendoza, Mirna Edith Morales-Marín, Carla Márquez, Carlos Chicalote, Ana Ballesteros, Miriam Aguilar, Xochitl Castro, Amalia Gómez-Cotero, Ana María Balboa-Verduzco, Lilia Albores-Gallo, Omar Nafate-López, Carlos Alfonso Marcín-Salazar, Patricia Sánchez, Nuria Lanzagorta-Piñol, Fernando Omar López-Armenta, Humberto Nicolini
Children. 2022; 9(4): 462
[Pubmed] | [DOI]
14 Neuronal Cell Adhesion Molecules May Mediate Neuroinflammation in Autism Spectrum Disorder
Madeline Eve, Josan Gandawijaya, Liming Yang, Asami Oguro-Ando
Frontiers in Psychiatry. 2022; 13
[Pubmed] | [DOI]
15 Drosophila Model for Studying Gut Microbiota in Behaviors and Neurodegenerative Diseases
Meng-Hsuan Chiang, Shuk-Man Ho, Hui-Yu Wu, Yu-Chun Lin, Wan-Hua Tsai, Tony Wu, Chih-Ho Lai, Chia-Lin Wu
Biomedicines. 2022; 10(3): 596
[Pubmed] | [DOI]
16 Neuroinflammation in autism spectrum disorders: potential target for mesenchymal stem cell-based therapy
Rebecca S. Y. Wong
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery. 2022; 58(1)
[Pubmed] | [DOI]
17 Excessive audio–visual stimulation leads to impaired social behaviour with an effect on amygdala: Early life excessive exposure to digital devices in male rats
Monireh Mansouri, Hamidreza Pouretemad, Mohammadreza Bigdeli, Maryam Ardalan
European Journal of Neuroscience. 2022;
[Pubmed] | [DOI]
18 The Promise of DNA Methylation in Understanding Multigenerational Factors in Autism Spectrum Disorders
Julia S. Mouat, Janine M. LaSalle
Frontiers in Genetics. 2022; 13
[Pubmed] | [DOI]
19 Could neutrophil extracellular traps drive the development of autism?
Michal Pastorek, Diana Drobná, Peter Celec
Medical Hypotheses. 2022; : 110929
[Pubmed] | [DOI]
20 Early-onset of social communication and locomotion activity in F2 pups of a valproic acid-induced mouse model of autism
Chiharu Tsuji, Kazumi Furuhara, Ryuko Mizutani, Kana Minami, Pinyue Fu, Jing Zhong, Haruhiro Higashida, Shigeru Yokoyama, Takahiro Tsuji
Neuroscience Letters. 2022; : 136827
[Pubmed] | [DOI]
21 Shank postsynaptic scaffolding proteins in autism spectrum disorder: Mouse models and their dysfunctions in behaviors, synapses, and molecules
Sunmin Jung, Mikyoung Park
Pharmacological Research. 2022; 182: 106340
[Pubmed] | [DOI]
22 Genetics of autism spectrum disorders and future direction
Yuka Yasuda, Junya Matsumoto, Kenichiro Miura, Naomi Hasegawa, Ryota Hashimoto
Journal of Human Genetics. 2022;
[Pubmed] | [DOI]
23 Nitric oxide pathway as a plausible therapeutic target in autism spectrum disorders
Rishab Mehta, Anurag Kuhad, Ranjana Bhandari
Expert Opinion on Therapeutic Targets. 2022;
[Pubmed] | [DOI]
24 Pre/post-natal exposure to microplastic as a potential risk factor for autism spectrum disorder
Javeria Zaheer, Hyeongi Kim, In Ok Ko, Eun-Kyeong Jo, Eui-Ju Choi, Hae-June Lee, Insop Shim, Hyun-jeong Woo, Jonghoon Choi, Gun-Ha Kim, Jin Su Kim
Environment International. 2022; 161: 107121
[Pubmed] | [DOI]
25 Fermented foods: an update on evidence-based health benefits and future perspectives
Iñaki Diez-Ozaeta, Oihana Juaristi Astiazaran
Food Research International. 2022; : 111133
[Pubmed] | [DOI]
26 Critical Evaluation of Valproic Acid-Induced Rodent Models of Autism: Current and Future Perspectives
Sweety Mehra, Aitizaz Ul Ahsan, Era Seth, Mani Chopra
Journal of Molecular Neuroscience. 2022;
[Pubmed] | [DOI]
27 Influence of Gestational Chlorpyrifos Exposure on ASD-like Behaviors in an fmr1-KO Rat Model
Cristian Perez-Fernandez, María Matamala Montoya, Miguel Morales-Navas, Laia Guardia-Escote, María Cabré, María Teresa Colomina, Estela Giménez, Fernando Sánchez-Santed
Molecular Neurobiology. 2022;
[Pubmed] | [DOI]
28 Evaluation of p21 expression and related autism-like behavior in Bisphenol-A exposed offspring of Wistar albino rats
Syna Pervaiz Singha, Samreen Memon, Umbreen Bano, Amir Derick Isaac, Muhammad Yaqoob Shahani
Birth Defects Research. 2022;
[Pubmed] | [DOI]
29 How to Minimize the Impact of Experts’ Non-rational Beliefs on Their Judgments on Autism
Maciej Wodzinski, Marcin Rzadeczka, Marcin Moskalewicz
Community Mental Health Journal. 2022;
[Pubmed] | [DOI]
30 Modification of the toxic effects of methylmercury and thimerosal by testosterone and estradiol in SH-SY5Y neuroblastoma cell line
Selinay Basak Erdemli-Köse, Anil Yirün, Aylin Balci-Özyurt, Pinar Erkekoglu
Journal of Applied Toxicology. 2021;
[Pubmed] | [DOI]
31 An ethical analysis of divergent clinical approaches to the application of genetic testing for autism and schizophrenia
E. Morris,M. O’Donovan,A. Virani,J. Austin
Human Genetics. 2021;
[Pubmed] | [DOI]
32 2D:4D Ratio and Autism Spectrum Disorder in Brunei Darussalam
Shirley H. F. Lee,Syahiirah Abd Aziz,Mawarni Hamid,Ya Chee Lim,David Koh,Li Ling Chaw
Journal of Autism and Developmental Disorders. 2021;
[Pubmed] | [DOI]
33 Maternal rheumatoid arthritis during pregnancy and neurodevelopmental disorders in offspring: a systematic review
SS Knudsen,AFVH Thomsen,BW Deleuran,BH Bech
Scandinavian Journal of Rheumatology. 2021; : 1
[Pubmed] | [DOI]
34 A systematic review and meta-analysis of the association between maternal polycystic ovary syndrome and neuropsychiatric disorders in children
Pallavi Dubey, Bhaskar Thakur, Sheryl Rodriguez, Jessika Cox, Sheralyn Sanchez, Anacani Fonseca, Sireesha Reddy, Deborah Clegg, Alok Kumar Dwivedi
Translational Psychiatry. 2021; 11(1)
[Pubmed] | [DOI]
35 In utero exposure to ritodrine during pregnancy and risk of autism in their offspring until 8 years of age
Jungsoo Chae,Geum Joon Cho,Min-Jeong Oh,KeonVin Park,Sung Won Han,Suk-Joo Choi,Soo-young Oh,Cheong-Rae Roh
Scientific Reports. 2021; 11(1)
[Pubmed] | [DOI]
36 Longitudinal study of stool-associated microbial taxa in sibling pairs with and without autism spectrum disorder
Christine Tataru, Austin Martin, Kaitlyn Dunlap, Marie Peras, Brianna S. Chrisman, Erica Rutherford, Grace E. Deitzler, Alexandra Phillips, Xiaochen Yin, Kayleen Sabino, Roberta L. Hannibal, Wiputra Hartono, Michelle Lin, Edward Raack, Yonggan Wu, Todd Z. DeSantis, Shoko Iwai, Dennis P. Wall, Maude M. David
ISME Communications. 2021; 1(1)
[Pubmed] | [DOI]
37 Awareness and risk factors of autism spectrum disorder in an Egyptian population
Nagwa Abdel Meguid,Neveen Hassan Nashaat,Amal Elsaeid,Massimiliano Peana,Ahmed Elnahry,Geir Bjørklund
Research in Autism Spectrum Disorders. 2021; 84: 101781
[Pubmed] | [DOI]
38 Microbiota and Microglia Interactions in ASD
Marcela Davoli-Ferreira,Carolyn A. Thomson,Kathy D. McCoy
Frontiers in Immunology. 2021; 12
[Pubmed] | [DOI]
39 COMPULSORY VACCINATION FOR CHILDREN: VIOLATION OF HUMAN RIGHTS?
Siti Fazilah Abdul Shukor, Nurul Jannah Mustafa Khan, Farahdilah Ghazali
UUM Journal of Legal Studies. 2021; 12(Number 2): 115
[Pubmed] | [DOI]
40 Neural Mechanisms Underlying Repetitive Behaviors in Rodent Models of Autism Spectrum Disorders
Tanya Gandhi,Charles C. Lee
Frontiers in Cellular Neuroscience. 2021; 14
[Pubmed] | [DOI]
41 Editorial: Autism Signaling Pathways
Yi-Ping Hsueh,Yu-Chih Lin
Frontiers in Cellular Neuroscience. 2021; 15
[Pubmed] | [DOI]
42 Altering the gut microbiome to potentially modulate behavioral manifestations in autism spectrum disorders: A systematic review
Camron Davies,Dibyanshi Mishra,Rebecca S. Eshraghi,Jeenu Mittal,Rahul Sinha,Erdogan Bulut,Rahul Mittal,Adrien A. Eshraghi
Neuroscience & Biobehavioral Reviews. 2021; 128: 549
[Pubmed] | [DOI]
43 Gene–Environment Interactions in Developmental Neurotoxicity: a Case Study of Synergy between Chlorpyrifos and CHD8 Knockout in Human BrainSpheres
Sergio Modafferi,Xiali Zhong,Andre Kleensang,Yohei Murata,Francesca Fagiani,David Pamies,Helena T. Hogberg,Vittorio Calabrese,Herbert Lachman,Thomas Hartung,Lena Smirnova
Environmental Health Perspectives. 2021; 129(7): 077001
[Pubmed] | [DOI]
44 Use of probiotics in pediatric patients with autism spectrum disorder: a systematic review
Matheus Alves Alvares, Mayco José Reinaldi Serra, Isabella Delgado, Joyce Canato de Carvalho, Thaís Campanhã Cury Sotine, Youssef Adef Ali, Marcella Rocha Machado de Oliveira, Vera Esteves Vagnozzi Rullo
Revista da Associação Médica Brasileira. 2021; 67(10): 1503
[Pubmed] | [DOI]
45 Nutritional Status of Pre-school Children and Determinant Factors of Autism: A Case-Control Study
Hana Alkhalidy,Amal Abushaikha,Khadeejah Alnaser,Mohammad D. Obeidat,Islam Al-Shami
Frontiers in Nutrition. 2021; 8
[Pubmed] | [DOI]
46 Microbiome-Specific Statistical Modeling Identifies Interplay Between Gastrointestinal Microbiome and Neurobehavioral Outcomes in Patients With Autism: A Case Control Study
Minshi Huang, Jun Liu, Kevin Liu, Jierong Chen, Zhen Wei, Zhe Feng, Yuyu Wu, Michelle Fong, Ruiyi Tian, Bryan Wang, Christoph Budjan, Patrick Zhuang, Guobin Wan, Xue-Jun Kong
Frontiers in Psychiatry. 2021; 12
[Pubmed] | [DOI]
47 Exploring the Association of Autism Spectrum Disorders and Constipation through Analysis of the Gut Microbiome
Shih-Chen Fu,Chung-Han Lee,Hsiuying Wang
International Journal of Environmental Research and Public Health. 2021; 18(2): 667
[Pubmed] | [DOI]
48 Relationship between Autism Spectrum Disorder and Pesticides: A Systematic Review of Human and Preclinical Models
Judit Biosca-Brull,Cristian Pérez-Fernández,Santiago Mora,Beatriz Carrillo,Helena Pinos,Nelida Maria Conejo,Paloma Collado,Jorge L. Arias,Fernando Martín-Sánchez,Fernando Sánchez-Santed,Maria Teresa Colomina
International Journal of Environmental Research and Public Health. 2021; 18(10): 5190
[Pubmed] | [DOI]
49 Prenatal Adversity Alters the Epigenetic Profile of the Prefrontal Cortex: Sexually Dimorphic Effects of Prenatal Alcohol Exposure and Food-Related Stress
Alexandre A. Lussier, Tamara S. Bodnar, Michelle Moksa, Martin Hirst, Michael S. Kobor, Joanne Weinberg
Genes. 2021; 12(11): 1773
[Pubmed] | [DOI]
50 Patient-Derived Induced Pluripotent Stem Cells (iPSCs) and Cerebral Organoids for Drug Screening and Development in Autism Spectrum Disorder: Opportunities and Challenges
Chiara Villa,Romina Combi,Donatella Conconi,Marialuisa Lavitrano
Pharmaceutics. 2021; 13(2): 280
[Pubmed] | [DOI]
51 In Silico Exploration of the Potential Role of Acetaminophen and Pesticides in the Etiology of Autism Spectrum Disorder
Tristan Furnary,Rolando Garcia-Milian,Zeyan Liew,Shannon Whirledge,Vasilis Vasiliou
Toxics. 2021; 9(5): 97
[Pubmed] | [DOI]
52 Epileptic Encephalopathies in Children with Autistic Spectrum Disorders: from Molecular Genetic Diagnostics to Target Therapy
?.?. ????????, ?.?. ??????????, ?.?. ????
??????????, ???????????? ? ??????????? ??????????. 2021; (2): 249
[Pubmed] | [DOI]
53 Genetic and Epigenetic Etiology Underlying Autism Spectrum Disorder
Sang Hoon Yoon,Joonhyuk Choi,Won Ji Lee,Jeong Tae Do
Journal of Clinical Medicine. 2020; 9(4): 966
[Pubmed] | [DOI]
54 The Dual-Active Histamine H3 Receptor Antagonist and Acetylcholine Esterase Inhibitor E100 Alleviates Autistic-Like Behaviors and Oxidative Stress in Valproic Acid Induced Autism in Mice
Nermin Eissa,Sheikh Azimullah,Petrilla Jayaprakash,Richard L. Jayaraj,David Reiner,Shreesh K. Ojha,Rami Beiram,Holger Stark,Dorota Lazewska,Katarzyna Kiec-Kononowicz,Bassem Sadek
International Journal of Molecular Sciences. 2020; 21(11): 3996
[Pubmed] | [DOI]
55 Risk and Protective Factors in Autism Spectrum Disorders: A Case Control Study in the Lebanese Population
Perla Gerges,Tania Bitar,Mirna Hawat,Abbas Alameddine,Michel Soufia,Christian R. Andres,Walid Hleihel
International Journal of Environmental Research and Public Health. 2020; 17(17): 6323
[Pubmed] | [DOI]
56 Aberrantly High Levels of Somatic LINE-1 Expression and Retrotransposition in Human Neurological Disorders
Diane M. Terry,Scott E. Devine
Frontiers in Genetics. 2020; 10
[Pubmed] | [DOI]
57 Vitamin C Attenuates Oxidative Stress and Behavioral Abnormalities Triggered by Fipronil and Pyriproxyfen Insecticide Chronic Exposure on Zebrafish Juvenile
Madalina Andreea Robea,Roxana Jijie,Mircea Nicoara,Gabriel Plavan,Alin Stelian Ciobica,Carmen Solcan,Gilbert Audira,Chung-Der Hsiao,Stefan-Adrian Strungaru
Antioxidants. 2020; 9(10): 944
[Pubmed] | [DOI]
58 Studying the evolution of miasm in autism spectrum disorders: A case series
Sunita Bhanudas Nikumbh
Journal of Integrated Standardized Homoeopathy. 2020; 3: 43
[Pubmed] | [DOI]
59 Maternal excessive gestational weight gain as a risk factor for autism spectrum disorder in offspring: a systematic review
Sorayya Kheirouri,Mohammad Alizadeh
BMC Pregnancy and Childbirth. 2020; 20(1)
[Pubmed] | [DOI]
60 Association between neighbourhood socioeconomic status and developmental vulnerability of kindergarten children with Autism Spectrum Disorder: A population level study
Ayesha Siddiqua,Eric Duku,Kathy Georgiades,Ronit Mesterman,Magdalena Janus
SSM - Population Health. 2020; : 100662
[Pubmed] | [DOI]
61 Adjusting for allometric scaling in ABIDE I challenges subcortical volume differences in autism spectrum disorder
Camille Michèle Williams,Hugo Peyre,Roberto Toro,Anita Beggiato,Franck Ramus
Human Brain Mapping. 2020;
[Pubmed] | [DOI]
62 Healing autism spectrum disorder with cannabinoids: a neuroinflammatory story
Emilia Carbone,Antonia Manduca,Claudia Cacchione,Stefano Vicari,Viviana Trezza
Neuroscience & Biobehavioral Reviews. 2020;
[Pubmed] | [DOI]
63 Knowledge and Awareness of Ear Protection Devices for Sound Sensitivity by Individuals With Autism Spectrum Disorders
Dorothy Neave-DiToro,Akiko Fuse,Michael Bergen
Language, Speech, and Hearing Services in Schools. 2020; : 1
[Pubmed] | [DOI]
64 Gastrointestinal involvement of autism spectrum disorder: focus on gut microbiota.
Carlo Romano Settanni,Stefano Bibbò,Gianluca Ianiro,Emanuele Rinninella,Marco Cintoni,Maria Cristina Mele,Giovanni Cammarota,Antonio Gasbarrini
Expert Review of Gastroenterology & Hepatology. 2020;
[Pubmed] | [DOI]
65 Autistic-Like Behaviours and Associated Brain Structural Plasticity are Modulated by Oxytocin in Maternally Separated Rats
Monireh Mansouri,Hamidreza Pouretemad,Mehrdad Roghani,Gregers Wegener,Maryam Ardalan
Behavioural Brain Research. 2020; : 112756
[Pubmed] | [DOI]
66 Environment-Wide Association Study ( E n WAS ) of Prenatal and Perinatal Factors Associated With Autistic Traits: A Population-Based Study
Masoud Amiri,Sander Lamballais,Eloy Geenjaar,Laura M. E. Blanken,Hanan El Marroun,Henning Tiemeier,Tonya White
Autism Research. 2020;
[Pubmed] | [DOI]
67 Probing disrupted neurodevelopment in autism using human stem cell-derived neurons and organoids: An outlook into future diagnostics and drug development
Guang Yang,Alex Shcheglovitov
Developmental Dynamics. 2019;
[Pubmed] | [DOI]
68 A Novel Approach to Dysmorphology to Enhance the Phenotypic Classification of Autism Spectrum Disorder in the Study to Explore Early Development
Stuart K. Shapira,Lin H. Tian,Arthur S. Aylsworth,Ellen R. Elias,Julie E. Hoover-Fong,Naomi J. L. Meeks,Margaret C. Souders,Anne C.-H. Tsai,Elaine H. Zackai,Aimee A. Alexander,Marshalyn Yeargin-Allsopp,Laura A. Schieve
Journal of Autism and Developmental Disorders. 2019;
[Pubmed] | [DOI]
69 Increased Risk of Atopic Diseases in the Siblings of Patients with Autism Spectrum Disorder: A Nationwide Population-Based Cohort Study
Ying-Xiu Dai,Ying-Hsuan Tai,Yun-Ting Chang,Tzeng-Ji Chen,Mu-Hong Chen
Journal of Autism and Developmental Disorders. 2019;
[Pubmed] | [DOI]
70 The dual-active histamine H3 receptor antagonist and acetylcholine esterase inhibitor E100 ameliorates stereotyped repetitive behavior and neuroinflammation in sodium valproate induced autism in mice
Nermin Eissa,Sheikh Azimullah,Petrilla Jayaprakash,Richard L. Jayaraj,David Reiner,Shreesh K. Ojha,Rami Beiram,Holger Stark,Dorota Lazewska,Katarzyna Kiec-Kononowicz,Bassem Sadek
Chemico-Biological Interactions. 2019; : 108775
[Pubmed] | [DOI]
71 Probiotic Therapy for Treating Behavioral and Gastrointestinal Symptoms in Autism Spectrum Disorder: A Systematic Review of Clinical Trials
Jun Liu,Guo-bing Wan,Ming-shi Huang,George Agyapong,Tian-le Zou,Xue-ying Zhang,Yen-Wenn Liu,Yi-qing Song,Ying-Chieh Tsai,Xue-jun Kong
Current Medical Science. 2019; 39(2): 173
[Pubmed] | [DOI]
72 Canonical Babbling: A Marker for Earlier Identification of Late Detected Developmental Disorders?
Sigrun Lang,Katrin D. Bartl-Pokorny,Florian B. Pokorny,Dunia Garrido,Nivedita Mani,Annette V. Fox-Boyer,Dajie Zhang,Peter B. Marschik
Current Developmental Disorders Reports. 2019;
[Pubmed] | [DOI]
73 Polyphenols as food bioactive compounds in the context of Autism Spectrum Disorders: a critical mini-review
Diana Serra,Leonor M. Almeida,Teresa C.P. Dinis
Neuroscience & Biobehavioral Reviews. 2019;
[Pubmed] | [DOI]
74 Glutamate Signaling Defects in Propionic Acid Orally Administered to Juvenile Rats as an Experimental Animal Model of Autism
E. Al-Suwailem,S. Abdi,R. S. Bhat,A. El-Ansary
Neurochemical Journal. 2019; 13(1): 90
[Pubmed] | [DOI]
75 Epilepsy and Neurodevelopmental Outcomes in Children With Etiologically Diagnosed Central Nervous System Infections: A Retrospective Cohort Study
Chien-Heng Lin,Wei-De Lin,I-Ching Chou,Inn-Chi Lee,Syuan-Yu Hong
Frontiers in Neurology. 2019; 10
[Pubmed] | [DOI]
76 NRXN1 Deletion and Exposure to Methylmercury Increase Astrocyte Differentiation by Different Notch-Dependent Transcriptional Mechanisms
Marilena Raciti,Jahan Salma,Stefan Spulber,Giulia Gaudenzi,Zahra Khalajzeyqami,Mirko Conti,Britt-Marie Anderlid,Anna Falk,Ola Hermanson,Sandra Ceccatelli
Frontiers in Genetics. 2019; 10
[Pubmed] | [DOI]
77 Genetic Causes and Modifiers of Autism Spectrum Disorder
Lauren Rylaarsdam,Alicia Guemez-Gamboa
Frontiers in Cellular Neuroscience. 2019; 13
[Pubmed] | [DOI]
78 Sex-Dependent Effects of Perinatal Inflammation on the Brain: Implication for Neuro-Psychiatric Disorders
Maryam Ardalan,Tetyana Chumak,Zinaida Vexler,Carina Mallard
International Journal of Molecular Sciences. 2019; 20(9): 2270
[Pubmed] | [DOI]
79 Glycan Mimetics from Natural Products: New Therapeutic Opportunities for Neurodegenerative Disease
Wenyue Wang,Sandeep Gopal,Roger Pocock,Zhicheng Xiao
Molecules. 2019; 24(24): 4604
[Pubmed] | [DOI]
80 New and Preliminary Evidence on Altered Oral and Gut Microbiota in Individuals with Autism Spectrum Disorder (ASD): Implications for ASD Diagnosis and Subtyping Based on Microbial Biomarkers
Xuejun Kong,Jun Liu,Murat Cetinbas,Ruslan Sadreyev,Madelyn Koh,Hui Huang,Adetaye Adeseye,Puhan He,Junli Zhu,Hugh Russell,Clara Hobbie,Kevi Liu,Andrew B. Onderdonk
Nutrients. 2019; 11(9): 2128
[Pubmed] | [DOI]
81 Sex-specific Behavioral Features of Rodent Models of Autism Spectrum Disorder
Se Jin Jeon,Edson Luck Gonzales,Darine Froy N. Mabunga,Schley T. Valencia,Do Gyeong Kim,Yujeong Kim,Keremkleroo Jym L. Adil,Dongpil Shin,Donghyun Park,Chan Young Shin
Experimental Neurobiology. 2018; 27(5): 321
[Pubmed] | [DOI]
82 One Health, Fermented Foods, and Gut Microbiota
Victoria Bell,Jorge Ferrão,Lígia Pimentel,Manuela Pintado,Tito Fernandes
Foods. 2018; 7(12): 195
[Pubmed] | [DOI]
83 UBE3A and Its Link With Autism
Naman Vatsa,Nihar Ranjan Jana
Frontiers in Molecular Neuroscience. 2018; 11
[Pubmed] | [DOI]
84 Sex-specific autistic endophenotypes induced by prenatal exposure to valproic acid involve anandamide signalling
Francesca Melancia,Sara Schiavi,Michela Servadio,Veronica Cartocci,Patrizia Campolongo,Maura Palmery,Valentina Pallottini,Viviana Trezza
British Journal of Pharmacology. 2018;
[Pubmed] | [DOI]
85 Diet: the keystone of autism spectrum disorder?
S. Peretti,M. Mariano,C. Mazzocchetti,M. Mazza,M. C. Pino,A. Verrotti Di Pianella,M. Valenti
Nutritional Neuroscience. 2018; : 1
[Pubmed] | [DOI]
86 Application of Human-Induced Pluripotent Stem Cells (hiPSCs) to Study Synaptopathy of Neurodevelopmental Disorders
Xuting Shen,Hoi Ting Yeung,Kwok-On Lai
Developmental Neurobiology. 2018;
[Pubmed] | [DOI]



 

Top
Previous article  Next article
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
Abstract
Introduction
Prenatal Risk Fa...
Natal Risk Factors
Protective or Au...
Discussion
Conclusion
Authors' Con...
References
Article Tables

 Article Access Statistics
    Viewed20620    
    Printed131    
    Emailed0    
    PDF Downloaded2598    
    Comments [Add]    
    Cited by others 86    

Recommend this journal