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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 1
2002 2
2003 4
2004 6
2005 8
2006 2
2007 14
2008 20
2009 30
2010 39
2011 36
2012 34
2013 47
2014 57
2015 34
2016 39
2017 36
2018 35
2019 30
2020 33
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2022 34
2023 28
2024 14

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535 results

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Page 1
An Overview of the Main Genetic, Epigenetic and Environmental Factors Involved in Autism Spectrum Disorder Focusing on Synaptic Activity.
Masini E, Loi E, Vega-Benedetti AF, Carta M, Doneddu G, Fadda R, Zavattari P. Masini E, et al. Int J Mol Sci. 2020 Nov 5;21(21):8290. doi: 10.3390/ijms21218290. Int J Mol Sci. 2020. PMID: 33167418 Free PMC article. Review.
Autism spectrum disorder (ASD) is a neurodevelopmental disorder that affects social interaction and communication, with restricted interests, activity and behaviors. ...
Autism spectrum disorder (ASD) is a neurodevelopmental disorder that affects social interaction and communication, with …
Genetic correlates of phenotypic heterogeneity in autism.
Warrier V, Zhang X, Reed P, Havdahl A, Moore TM, Cliquet F, Leblond CS, Rolland T, Rosengren A; EU-AIMS LEAP; iPSYCH-Autism Working Group; Spectrum 10K and APEX Consortia; Rowitch DH, Hurles ME, Geschwind DH, Børglum AD, Robinson EB, Grove J, Martin HC, Bourgeron T, Baron-Cohen S. Warrier V, et al. Nat Genet. 2022 Sep;54(9):1293-1304. doi: 10.1038/s41588-022-01072-5. Epub 2022 Jun 2. Nat Genet. 2022. PMID: 35654973 Free PMC article.
Furthermore, in autistic individuals without co-occurring intellectual disability (ID), autism PGS are overinherited by autistic females compared to males. Finally, we observed higher SNP heritability for autistic males and for autistic i …
Furthermore, in autistic individuals without co-occurring intellectual disability (ID), autism PGS are overinherited by aut …
SHANK1 polymorphisms and SNP-SNP interactions among SHANK family: A possible cue for recognition to autism spectrum disorder in infant age.
Qiu S, Li Y, Bai Y, Shi J, Cui H, Gu Y, Ren Y, Zhao Q, Zhang K, Lu M, Wang Y, Li Y, Zhong W, Zhu X, Liu Y, Cheng Y, Qiao Y, Liu Y. Qiu S, et al. Autism Res. 2019 Mar;12(3):375-383. doi: 10.1002/aur.2065. Epub 2019 Jan 10. Autism Res. 2019. PMID: 30629339
Autism spectrum disorder (ASD) is a serious lifelong neurodevelopmental disorder. ...These SHANK1 variants may not affect the susceptibility to ASD in Chinese Han population. SNP-SNP interactions in SHANK family may confer ASD risk. Autism …
Autism spectrum disorder (ASD) is a serious lifelong neurodevelopmental disorder. ...These SHANK1 variants may not affe …
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
Cross-Disorder Group of the Psychiatric Genomics Consortium. Cross-Disorder Group of the Psychiatric Genomics Consortium. Lancet. 2013 Apr 20;381(9875):1371-1379. doi: 10.1016/S0140-6736(12)62129-1. Epub 2013 Feb 28. Lancet. 2013. PMID: 23453885 Free PMC article.
We aimed to identify specific variants underlying genetic effects shared between the five disorders in the Psychiatric Genomics Consortium: autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disord …
We aimed to identify specific variants underlying genetic effects shared between the five disorders in the Psychiatric Genomics Consortium: …
Autism, DRD3 and repetitive and stereotyped behavior, an overview of the current knowledge.
Staal WG. Staal WG. Eur Neuropsychopharmacol. 2015 Sep;25(9):1421-6. doi: 10.1016/j.euroneuro.2014.08.011. Epub 2014 Sep 1. Eur Neuropsychopharmacol. 2015. PMID: 25224105 Review.
The SNP rs167771 of the dopamine-3-receptor gene (DRD3) has been associated with autism spectrum disorder (ASD) in samples from the United Kingdom, The Netherlands and Spain. ...To conclude, striatum abnormalities in autism are associated with repetiti …
The SNP rs167771 of the dopamine-3-receptor gene (DRD3) has been associated with autism spectrum disorder (ASD) in samp …
Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.
Weiss LA. Weiss LA. Expert Rev Mol Diagn. 2009 Nov;9(8):795-803. doi: 10.1586/erm.09.59. Expert Rev Mol Diagn. 2009. PMID: 19895225 Review.
Autism and related traits are highly heritable but cannot be explained by currently known genetic risk factors. Therefore, the advent of genome-wide single nucleotide polymorphism (SNP) and copy number variant (CNV) microarray technologies heralded identification of …
Autism and related traits are highly heritable but cannot be explained by currently known genetic risk factors. Therefore, the advent …
The Autism Genome Project: goals and strategies.
Hu-Lince D, Craig DW, Huentelman MJ, Stephan DA. Hu-Lince D, et al. Am J Pharmacogenomics. 2005;5(4):233-46. doi: 10.2165/00129785-200505040-00004. Am J Pharmacogenomics. 2005. PMID: 16078860 Review.
Autism is a complex neurodevelopmental disorder with a broad spectrum of symptoms and varying severity. Currently, no biological diagnosis exists. Although there has been a significant increase in autism genetics research recently, validated susceptibility ge …
Autism is a complex neurodevelopmental disorder with a broad spectrum of symptoms and varying severity. Currently, no biologic …
High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families.
AlAyadhi LY, Hashmi JA, Iqbal M, Albalawi AM, Samman MI, Elamin NE, Bashir S, Basit S. AlAyadhi LY, et al. Neuroscience. 2016 Dec 17;339:561-570. doi: 10.1016/j.neuroscience.2016.10.030. Epub 2016 Oct 19. Neuroscience. 2016. PMID: 27771533
Here, we report CNVs identified using Illumina Human Omni 2.5M oligonucleotide microarrays in 11 multiplex families with autism spectrum disorder (ASD) referred to Autism Research and Treatment Center (ART) and Madinah Maternity and Children Hospital (MMCH). …
Here, we report CNVs identified using Illumina Human Omni 2.5M oligonucleotide microarrays in 11 multiplex families with autism spect …
The genetics of Autism Spectrum Disorders--a guide for clinicians.
Heil KM, Schaaf CP. Heil KM, et al. Curr Psychiatry Rep. 2013 Jan;15(1):334. doi: 10.1007/s11920-012-0334-3. Curr Psychiatry Rep. 2013. PMID: 23250815 Review.
Recent advances in genetic testing technology have made chromosome microarray analysis (CMA) a first-tier clinical diagnostic test for Autism Spectrum Disorders (ASDs). Two main types of microarrays are available, single nucleotide polymorphism (SNP) arrays and arra …
Recent advances in genetic testing technology have made chromosome microarray analysis (CMA) a first-tier clinical diagnostic test for Au …
Analysis of the SNP rs3747333 and rs3747334 in NLGN4X gene in autism spectrum disorder: a meta-analysis.
Sun H, Yang Y, Zhang L, Wu H, Zhang H, Li H. Sun H, et al. Ann Gen Psychiatry. 2019 May 21;18:6. doi: 10.1186/s12991-019-0227-5. eCollection 2019. Ann Gen Psychiatry. 2019. PMID: 31139237 Free PMC article.
BACKGROUND: The SNP rs3747333 and rs3747334 in Neuroligin 4X (NLGN4X) gene have been demonstrated to be associated with the susceptibility to Autism spectrum disorder (ASDs; MIM 209850), but the results are inconsistent. ...
BACKGROUND: The SNP rs3747333 and rs3747334 in Neuroligin 4X (NLGN4X) gene have been demonstrated to be associated with the susceptib …
535 results