434 related articles for article (PubMed ID: 31491383)
1. 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]
2. Whole Exome Sequencing Identifies Novel De Novo Variants Interacting with Six Gene Networks in Autism Spectrum Disorder.
Kim N; Kim KH; Lim WJ; Kim J; Kim SA; Yoo HJ
Genes (Basel); 2020 Dec; 12(1):. PubMed ID: 33374967
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Genetic contributions to autism spectrum disorder.
Havdahl A; Niarchou M; Starnawska A; Uddin M; van der Merwe C; Warrier V
Psychol Med; 2021 Oct; 51(13):2260-2273. PubMed ID: 33634770
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. The contributions of rare inherited and polygenic risk to ASD in multiplex families.
Cirnigliaro M; Chang TS; Arteaga SA; Pérez-Cano L; Ruzzo EK; Gordon A; Bicks LK; Jung JY; Lowe JK; Wall DP; Geschwind DH
Proc Natl Acad Sci U S A; 2023 Aug; 120(31):e2215632120. PubMed ID: 37506195
[TBL] [Abstract][Full Text] [Related]
7. Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.
Leppa VM; Kravitz SN; Martin CL; Andrieux J; Le Caignec C; Martin-Coignard D; DyBuncio C; Sanders SJ; Lowe JK; Cantor RM; Geschwind DH
Am J Hum Genet; 2016 Sep; 99(3):540-554. PubMed ID: 27569545
[TBL] [Abstract][Full Text] [Related]
8. Elevated polygenic burden for autism is associated with differential DNA methylation at birth.
Hannon E; Schendel D; Ladd-Acosta C; Grove J; ; Hansen CS; Andrews SV; Hougaard DM; Bresnahan M; Mors O; Hollegaard MV; Bækvad-Hansen M; Hornig M; Mortensen PB; Børglum AD; Werge T; Pedersen MG; Nordentoft M; Buxbaum J; Daniele Fallin M; Bybjerg-Grauholm J; Reichenberg A; Mill J
Genome Med; 2018 Mar; 10(1):19. PubMed ID: 29587883
[TBL] [Abstract][Full Text] [Related]
9. Identification of common genetic risk variants for autism spectrum disorder.
Grove J; Ripke S; Als TD; Mattheisen M; Walters RK; Won H; Pallesen J; Agerbo E; Andreassen OA; Anney R; Awashti S; Belliveau R; Bettella F; Buxbaum JD; Bybjerg-Grauholm J; Bækvad-Hansen M; Cerrato F; Chambert K; Christensen JH; Churchhouse C; Dellenvall K; Demontis D; De Rubeis S; Devlin B; Djurovic S; Dumont AL; Goldstein JI; Hansen CS; Hauberg ME; Hollegaard MV; Hope S; Howrigan DP; Huang H; Hultman CM; Klei L; Maller J; Martin J; Martin AR; Moran JL; Nyegaard M; Nærland T; Palmer DS; Palotie A; Pedersen CB; Pedersen MG; dPoterba T; Poulsen JB; Pourcain BS; Qvist P; Rehnström K; Reichenberg A; Reichert J; Robinson EB; Roeder K; Roussos P; Saemundsen E; Sandin S; Satterstrom FK; Davey Smith G; Stefansson H; Steinberg S; Stevens CR; Sullivan PF; Turley P; Walters GB; Xu X; ; ; ; ; Stefansson K; Geschwind DH; Nordentoft M; Hougaard DM; Werge T; Mors O; Mortensen PB; Neale BM; Daly MJ; Børglum AD
Nat Genet; 2019 Mar; 51(3):431-444. PubMed ID: 30804558
[TBL] [Abstract][Full Text] [Related]
10. Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism.
Du Y; Li Z; Liu Z; Zhang N; Wang R; Li F; Zhang T; Jiang Y; Zhi X; Wang Z; Wu J
Genet Med; 2020 Jan; 22(1):170-180. PubMed ID: 31332282
[TBL] [Abstract][Full Text] [Related]
11. [Genetic analyses for identifying molecular mechanisms in autism spectrum disorders].
Chiocchetti A; Klauck SM
Z Kinder Jugendpsychiatr Psychother; 2011 Mar; 39(2):101-11. PubMed ID: 21442598
[TBL] [Abstract][Full Text] [Related]
12. The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
Merikangas AK; Segurado R; Heron EA; Anney RJ; Paterson AD; Cook EH; Pinto D; Scherer SW; Szatmari P; Gill M; Corvin AP; Gallagher L
Mol Psychiatry; 2015 Nov; 20(11):1366-72. PubMed ID: 25421404
[TBL] [Abstract][Full Text] [Related]
13. Genetic research in autism spectrum disorders.
Robinson EB; Neale BM; Hyman SE
Curr Opin Pediatr; 2015 Dec; 27(6):685-91. PubMed ID: 26371945
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Whole-genome sequencing in a family with twin boys with autism and intellectual disability suggests multimodal polygenic risk.
McKenna B; Koomar T; Vervier K; Kremsreiter J; Michaelson JJ
Cold Spring Harb Mol Case Stud; 2018 Dec; 4(6):. PubMed ID: 30559312
[TBL] [Abstract][Full Text] [Related]
16. Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder.
Wang L; Zhang Y; Li K; Wang Z; Wang X; Li B; Zhao G; Fang Z; Ling Z; Luo T; Xia L; Li Y; Guo H; Hu Z; Li J; Sun Z; Xia K
Mol Autism; 2020 Oct; 11(1):75. PubMed ID: 33023636
[TBL] [Abstract][Full Text] [Related]
17. Genetic architecture in autism spectrum disorder.
Devlin B; Scherer SW
Curr Opin Genet Dev; 2012 Jun; 22(3):229-37. PubMed ID: 22463983
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Integrated Systems Analysis Explores Dysfunctional Molecular Modules and Regulatory Factors in Children with Autism Spectrum Disorder.
Gao H; Zhong J; Huang Q; Wu X; Mo X; Lu L; Liang H
J Mol Neurosci; 2021 Feb; 71(2):358-368. PubMed ID: 32653993
[TBL] [Abstract][Full Text] [Related]
20. Progress in the genetics of autism spectrum disorder.
Woodbury-Smith M; Scherer SW
Dev Med Child Neurol; 2018 May; 60(5):445-451. PubMed ID: 29574884
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
