193 related articles for article (PubMed ID: 35410794)
1. Rare variants and the oligogenic architecture of autism.
Wang T; Zhao PA; Eichler EE
Trends Genet; 2022 Sep; 38(9):895-903. PubMed ID: 35410794
[TBL] [Abstract][Full Text] [Related]
2. Genomic Patterns of De Novo Mutation in Simplex Autism.
Turner TN; Coe BP; Dickel DE; Hoekzema K; Nelson BJ; Zody MC; Kronenberg ZN; Hormozdiari F; Raja A; Pennacchio LA; Darnell RB; Eichler EE
Cell; 2017 Oct; 171(3):710-722.e12. PubMed ID: 28965761
[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. Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.
Guo H; Wang T; Wu H; Long M; Coe BP; Li H; Xun G; Ou J; Chen B; Duan G; Bai T; Zhao N; Shen Y; Li Y; Wang Y; Zhang Y; Baker C; Liu Y; Pang N; Huang L; Han L; Jia X; Liu C; Ni H; Yang X; Xia L; Chen J; Shen L; Li Y; Zhao R; Zhao W; Peng J; Pan Q; Long Z; Su W; Tan J; Du X; Ke X; Yao M; Hu Z; Zou X; Zhao J; Bernier RA; Eichler EE; Xia K
Mol Autism; 2018; 9():64. PubMed ID: 30564305
[TBL] [Abstract][Full Text] [Related]
5. Three generation families: Analysis of de novo variants in autism.
Costa CIS; da Silva Campos G; da Silva Montenegro EM; Wang JYT; Scliar M; Monfardini F; Zachi EC; Lourenço NCV; Chan AJS; Pereira SL; Engchuan W; Thiruvahindrapuram B; Zarrei M; Scherer SW; Passos-Bueno MR
Eur J Hum Genet; 2023 Sep; 31(9):1017-1022. PubMed ID: 37280359
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Recent ultra-rare inherited variants implicate new autism candidate risk genes.
Wilfert AB; Turner TN; Murali SC; Hsieh P; Sulovari A; Wang T; Coe BP; Guo H; Hoekzema K; Bakken TE; Winterkorn LH; Evani US; Byrska-Bishop M; Earl RK; Bernier RA; ; Zody MC; Eichler EE
Nat Genet; 2021 Aug; 53(8):1125-1134. PubMed ID: 34312540
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Neale BM; Kou Y; Liu L; Ma'ayan A; Samocha KE; Sabo A; Lin CF; Stevens C; Wang LS; Makarov V; Polak P; Yoon S; Maguire J; Crawford EL; Campbell NG; Geller ET; Valladares O; Schafer C; Liu H; Zhao T; Cai G; Lihm J; Dannenfelser R; Jabado O; Peralta Z; Nagaswamy U; Muzny D; Reid JG; Newsham I; Wu Y; Lewis L; Han Y; Voight BF; Lim E; Rossin E; Kirby A; Flannick J; Fromer M; Shakir K; Fennell T; Garimella K; Banks E; Poplin R; Gabriel S; DePristo M; Wimbish JR; Boone BE; Levy SE; Betancur C; Sunyaev S; Boerwinkle E; Buxbaum JD; Cook EH; Devlin B; Gibbs RA; Roeder K; Schellenberg GD; Sutcliffe JS; Daly MJ
Nature; 2012 Apr; 485(7397):242-5. PubMed ID: 22495311
[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. A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A.
Jiang YH; Sahoo T; Michaelis RC; Bercovich D; Bressler J; Kashork CD; Liu Q; Shaffer LG; Schroer RJ; Stockton DW; Spielman RS; Stevenson RE; Beaudet AL
Am J Med Genet A; 2004 Nov; 131(1):1-10. PubMed ID: 15389703
[TBL] [Abstract][Full Text] [Related]
12. No evidence that common genetic risk variation is shared between schizophrenia and autism.
Vorstman JA; Anney RJ; Derks EM; Gallagher L; Gill M; de Jonge MV; van Engeland H; Kahn RS; Ophoff RA;
Am J Med Genet B Neuropsychiatr Genet; 2013 Jan; 162B(1):55-60. PubMed ID: 23193033
[TBL] [Abstract][Full Text] [Related]
13. Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations.
Toma C; Torrico B; Hervás A; Valdés-Mas R; Tristán-Noguero A; Padillo V; Maristany M; Salgado M; Arenas C; Puente XS; Bayés M; Cormand B
Mol Psychiatry; 2014 Jul; 19(7):784-90. PubMed ID: 23999528
[TBL] [Abstract][Full Text] [Related]
14. Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance.
Lubbe SJ; Escott-Price V; Gibbs JR; Nalls MA; Bras J; Price TR; Nicolas A; Jansen IE; Mok KY; Pittman AM; Tomkins JE; Lewis PA; Noyce AJ; Lesage S; Sharma M; Schiff ER; Levine AP; Brice A; Gasser T; Hardy J; Heutink P; Wood NW; Singleton AB; Williams NM; Morris HR;
Hum Mol Genet; 2016 Dec; 25(24):5483-5489. PubMed ID: 27798102
[TBL] [Abstract][Full Text] [Related]
15. DE NOVO MUTATIONS IN AUTISM IMPLICATE THE SYNAPTIC ELIMINATION NETWORK.
Venkataraman GR; O'Connell C; Egawa F; Kashef-Haghighi D; Wall DP
Pac Symp Biocomput; 2017; 22():521-532. PubMed ID: 27897003
[TBL] [Abstract][Full Text] [Related]
16. Comparative analysis of the autism‑related variants between different autistic children in a family pedigree.
Shen L; Li P; Zheng T; Luo M; Zhang S; Huang Y; Hu Y; Li H
Mol Med Rep; 2021 Oct; 24(4):. PubMed ID: 34368859
[TBL] [Abstract][Full Text] [Related]
17. Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.
Philippi A; Tores F; Carayol J; Rousseau F; Letexier M; Roschmann E; Lindenbaum P; Benajjou A; Fontaine K; Vazart C; Gesnouin P; Brooks P; Hager J
BMC Med Genet; 2007 Dec; 8():74. PubMed ID: 18053270
[TBL] [Abstract][Full Text] [Related]
18. A strategy to identify de novo mutations in common disorders such as autism and schizophrenia.
Julie G; Hamdan FF; Rouleau GA
J Vis Exp; 2011 Jun; (52):. PubMed ID: 21712793
[TBL] [Abstract][Full Text] [Related]
19. De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Sanders SJ; Murtha MT; Gupta AR; Murdoch JD; Raubeson MJ; Willsey AJ; Ercan-Sencicek AG; DiLullo NM; Parikshak NN; Stein JL; Walker MF; Ober GT; Teran NA; Song Y; El-Fishawy P; Murtha RC; Choi M; Overton JD; Bjornson RD; Carriero NJ; Meyer KA; Bilguvar K; Mane SM; Sestan N; Lifton RP; Günel M; Roeder K; Geschwind DH; Devlin B; State MW
Nature; 2012 Apr; 485(7397):237-41. PubMed ID: 22495306
[TBL] [Abstract][Full Text] [Related]
20. Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes.
Torrico B; Shaw AD; Mosca R; Vivó-Luque N; Hervás A; Fernàndez-Castillo N; Aloy P; Bayés M; Fullerton JM; Cormand B; Toma C
J Psychiatry Neurosci; 2019 Sep; 44(5):350-359. PubMed ID: 31094488
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
