These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
159 related articles for article (PubMed ID: 38072246)
1. Editorial: Mitochondrial Gene Variations Increase Autism Risk: Uncovering the Complex Polygenetic Landscape of Autism. Frye RE J Am Acad Child Adolesc Psychiatry; 2024 Aug; 63(8):775-777. PubMed ID: 38072246 [TBL] [Abstract][Full Text] [Related]
2. Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank. Yap CX; Alvares GA; Henders AK; Lin T; Wallace L; Farrelly A; McLaren T; Berry J; Vinkhuyzen AAE; Trzaskowski M; Zeng J; Yang Y; Cleary D; Grove R; Hafekost C; Harun A; Holdsworth H; Jellett R; Khan F; Lawson L; Leslie J; Levis Frenk M; Masi A; Mathew NE; Muniandy M; Nothard M; Visscher PM; Dawson PA; Dissanayake C; Eapen V; Heussler HS; Whitehouse AJO; Wray NR; Gratten J Mol Autism; 2021 Feb; 12(1):12. PubMed ID: 33568206 [TBL] [Abstract][Full Text] [Related]
3. Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees. Woodbury-Smith M; Zarrei M; Wei J; Thiruvahindrapuram B; O'Connor I; Paterson AD; Yuen RKC; Dastan J; Stavropoulos DJ; Howe JL; Thompson A; Parlier M; Fernandez B; Piven J; Anagnostou E; Scherer SW; Vieland VJ; Szatmari P Am J Med Genet B Neuropsychiatr Genet; 2020 Jul; 183(5):268-276. PubMed ID: 32372567 [TBL] [Abstract][Full Text] [Related]
4. A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex. Antaki D; Guevara J; Maihofer AX; Klein M; Gujral M; Grove J; Carey CE; Hong O; Arranz MJ; Hervas A; Corsello C; Vaux KK; Muotri AR; Iakoucheva LM; Courchesne E; Pierce K; Gleeson JG; Robinson EB; Nievergelt CM; Sebat J Nat Genet; 2022 Sep; 54(9):1284-1292. PubMed ID: 35654974 [TBL] [Abstract][Full Text] [Related]
5. The landscape of copy number variations in Finnish families with autism spectrum disorders. Kanduri C; Kantojärvi K; Salo PM; Vanhala R; Buck G; Blancher C; Lähdesmäki H; Järvelä I Autism Res; 2016 Jan; 9(1):9-16. PubMed ID: 26052927 [TBL] [Abstract][Full Text] [Related]
6. Neuropsychopathology of Autism Spectrum Disorder: Complex Interplay of Genetic, Epigenetic, and Environmental Factors. Bhandari R; Paliwal JK; Kuhad A Adv Neurobiol; 2020; 24():97-141. PubMed ID: 32006358 [TBL] [Abstract][Full Text] [Related]
7. Epigenetics of autism-related impairment: copy number variation and maternal infection. Mazina V; Gerdts J; Trinh S; Ankenman K; Ward T; Dennis MY; Girirajan S; Eichler EE; Bernier R J Dev Behav Pediatr; 2015; 36(2):61-7. PubMed ID: 25629966 [TBL] [Abstract][Full Text] [Related]
8. Identification of de novo Mutations in the Chinese Autism Spectrum Disorder Cohort via Whole-Exome Sequencing Unveils Brain Regions Implicated in Autism. Yuan B; Wang M; Wu X; Cheng P; Zhang R; Zhang R; Yu S; Zhang J; Du Y; Wang X; Qiu Z Neurosci Bull; 2023 Oct; 39(10):1469-1480. PubMed ID: 36881370 [TBL] [Abstract][Full Text] [Related]
9. The genetics of autism. Muhle R; Trentacoste SV; Rapin I Pediatrics; 2004 May; 113(5):e472-86. PubMed ID: 15121991 [TBL] [Abstract][Full Text] [Related]
10. Exome Sequencing of Two Siblings with Sporadic Autism Spectrum Disorder and Severe Speech Sound Disorder Suggests Pleiotropic and Complex Effects. Peter B; Dinu V; Liu L; Huentelman M; Naymik M; Lancaster H; Vose C; Schrauwen I Behav Genet; 2019 Jul; 49(4):399-414. PubMed ID: 30949922 [TBL] [Abstract][Full Text] [Related]
11. Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants. Siu MT; Butcher DT; Turinsky AL; Cytrynbaum C; Stavropoulos DJ; Walker S; Caluseriu O; Carter M; Lou Y; Nicolson R; Georgiades S; Szatmari P; Anagnostou E; Scherer SW; Choufani S; Brudno M; Weksberg R Clin Epigenetics; 2019 Jul; 11(1):103. PubMed ID: 31311581 [TBL] [Abstract][Full Text] [Related]
12. Diversity and Classification of Genetic Variations in Autism Spectrum Disorder. Kereszturi É Int J Mol Sci; 2023 Nov; 24(23):. PubMed ID: 38069091 [TBL] [Abstract][Full Text] [Related]
13. The Yin and Yang of Autism Genetics: How Rare De Novo and Common Variations Affect Liability. Chaste P; Roeder K; Devlin B Annu Rev Genomics Hum Genet; 2017 Aug; 18():167-187. PubMed ID: 28426285 [TBL] [Abstract][Full Text] [Related]
14. Integrative analysis prioritised oxytocin-related biomarkers associated with the aetiology of autism spectrum disorder. Wang T; Zhao T; Liu L; Teng H; Fan T; Li Y; Wang Y; Li J; Xia K; Sun Z EBioMedicine; 2022 Jul; 81():104091. PubMed ID: 35665681 [TBL] [Abstract][Full Text] [Related]
15. Getting to the Cores of Autism. Iakoucheva LM; Muotri AR; Sebat J Cell; 2019 Sep; 178(6):1287-1298. PubMed ID: 31491383 [TBL] [Abstract][Full Text] [Related]
16. SHANK3 variant as a cause of nonsyndromal autism in an 11-year-old boy and a review of published literature. Kanani F; Study D; Balasubramanian M Clin Dysmorphol; 2018 Oct; 27(4):113-115. PubMed ID: 29939863 [TBL] [Abstract][Full Text] [Related]
17. Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations. Dou Y; Yang X; Li Z; Wang S; Zhang Z; Ye AY; Yan L; Yang C; Wu Q; Li J; Zhao B; Huang AY; Wei L Hum Mutat; 2017 Aug; 38(8):1002-1013. PubMed ID: 28503910 [TBL] [Abstract][Full Text] [Related]