176 related articles for article (PubMed ID: 33431980)
1. Exploring the biological role of postzygotic and germinal de novo mutations in ASD.
Alonso-Gonzalez A; Calaza M; Amigo J; González-Peñas J; Martínez-Regueiro R; Fernández-Prieto M; Parellada M; Arango C; Rodriguez-Fontenla C; Carracedo A
Sci Rep; 2021 Jan; 11(1):319. PubMed ID: 33431980
[TBL] [Abstract][Full Text] [Related]
2. Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder.
Lim ET; Uddin M; De Rubeis S; Chan Y; Kamumbu AS; Zhang X; D'Gama AM; Kim SN; Hill RS; Goldberg AP; Poultney C; Minshew NJ; Kushima I; Aleksic B; Ozaki N; Parellada M; Arango C; Penzol MJ; Carracedo A; Kolevzon A; Hultman CM; Weiss LA; Fromer M; Chiocchetti AG; Freitag CM; ; Church GM; Scherer SW; Buxbaum JD; Walsh CA
Nat Neurosci; 2017 Sep; 20(9):1217-1224. PubMed ID: 28714951
[TBL] [Abstract][Full Text] [Related]
3.
Alonso-Gonzalez A; Rodriguez-Fontenla C; Carracedo A
Front Genet; 2018; 9():406. PubMed ID: 30298087
[TBL] [Abstract][Full Text] [Related]
4. Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder.
Takata A; Miyake N; Tsurusaki Y; Fukai R; Miyatake S; Koshimizu E; Kushima I; Okada T; Morikawa M; Uno Y; Ishizuka K; Nakamura K; Tsujii M; Yoshikawa T; Toyota T; Okamoto N; Hiraki Y; Hashimoto R; Yasuda Y; Saitoh S; Ohashi K; Sakai Y; Ohga S; Hara T; Kato M; Nakamura K; Ito A; Seiwa C; Shirahata E; Osaka H; Matsumoto A; Takeshita S; Tohyama J; Saikusa T; Matsuishi T; Nakamura T; Tsuboi T; Kato T; Suzuki T; Saitsu H; Nakashima M; Mizuguchi T; Tanaka F; Mori N; Ozaki N; Matsumoto N
Cell Rep; 2018 Jan; 22(3):734-747. PubMed ID: 29346770
[TBL] [Abstract][Full Text] [Related]
5. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
Chen R; Davis LK; Guter S; Wei Q; Jacob S; Potter MH; Cox NJ; Cook EH; Sutcliffe JS; Li B
Mol Autism; 2017; 8():14. PubMed ID: 28344757
[TBL] [Abstract][Full Text] [Related]
6. Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders.
Li J; Wang L; Guo H; Shi L; Zhang K; Tang M; Hu S; Dong S; Liu Y; Wang T; Yu P; He X; Hu Z; Zhao J; Liu C; Sun ZS; Xia K
Mol Psychiatry; 2017 Sep; 22(9):1282-1290. PubMed ID: 28831199
[TBL] [Abstract][Full Text] [Related]
7. Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction.
Marco EJ; Aitken AB; Nair VP; da Gente G; Gerdes MR; Bologlu L; Thomas S; Sherr EH
BMC Med Genomics; 2018 May; 11(1):50. PubMed ID: 29801487
[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. Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database.
Li J; Cai T; Jiang Y; Chen H; He X; Chen C; Li X; Shao Q; Ran X; Li Z; Xia K; Liu C; Sun ZS; Wu J
Mol Psychiatry; 2016 Feb; 21(2):290-7. PubMed ID: 25849321
[TBL] [Abstract][Full Text] [Related]
10. Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort.
da Silva Montenegro EM; Costa CS; Campos G; Scliar M; de Almeida TF; Zachi EC; Silva IMW; Chan AJS; Zarrei M; Lourenço NCV; Yamamoto GL; Scherer S; Passos-Bueno MR
Autism Res; 2020 Feb; 13(2):199-206. PubMed ID: 31696658
[TBL] [Abstract][Full Text] [Related]
11. Non-coding de novo mutations in chromatin interactions are implicated in autism spectrum disorder.
Kim IB; Lee T; Lee J; Kim J; Lee S; Koh IG; Kim JH; An JY; Lee H; Kim WK; Ju YS; Cho Y; Yu SJ; Kim SA; Oh M; Han DW; Kim E; Choi JK; Yoo HJ; Lee JH
Mol Psychiatry; 2022 Nov; 27(11):4680-4694. PubMed ID: 35840799
[TBL] [Abstract][Full Text] [Related]
12. Identification of De Novo JAK2 and MAPK7 Mutations Related to Autism Spectrum Disorder Using Whole-Exome Sequencing in a Chinese Child and Adolescent Trio-Based Sample.
Jiao J; Zhang M; Yang P; Huang Y; Hu X; Cai J; Yang C; Situ M; Zhang H; Fu L; Guo K; Huang Y
J Mol Neurosci; 2020 Feb; 70(2):219-229. PubMed ID: 31838722
[TBL] [Abstract][Full Text] [Related]
13. Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder.
Krupp DR; Barnard RA; Duffourd Y; Evans SA; Mulqueen RM; Bernier R; Rivière JB; Fombonne E; O'Roak BJ
Am J Hum Genet; 2017 Sep; 101(3):369-390. PubMed ID: 28867142
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Genome-wide characteristics of
Yuen RK; Merico D; Cao H; Pellecchia G; Alipanahi B; Thiruvahindrapuram B; Tong X; Sun Y; Cao D; Zhang T; Wu X; Jin X; Zhou Z; Liu X; Nalpathamkalam T; Walker S; Howe JL; Wang Z; MacDonald JR; Chan A; D'Abate L; Deneault E; Siu MT; Tammimies K; Uddin M; Zarrei M; Wang M; Li Y; Wang J; Wang J; Yang H; Bookman M; Bingham J; Gross SS; Loy D; Pletcher M; Marshall CR; Anagnostou E; Zwaigenbaum L; Weksberg R; Fernandez BA; Roberts W; Szatmari P; Glazer D; Frey BJ; Ring RH; Xu X; Scherer SW
NPJ Genom Med; 2016 Aug; 1():160271-1602710. PubMed ID: 27525107
[No Abstract] [Full Text] [Related]
16. 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]
17. 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]
18.
Luo T; Li K; Ling Z; Zhao G; Li B; Wang Z; Wang X; Han Y; Xia L; Zhang Y; Zhou Q; Fang Z; Wang Y; Chen Q; Zhou X; Pan H; Zhao Y; Wang Y; Dong L; Huang Y; Hu Z; Pan Q; Xia K; Li J
Comput Struct Biotechnol J; 2021; 19():1414-1422. PubMed ID: 33777337
[TBL] [Abstract][Full Text] [Related]
19. Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders.
Li K; Fang Z; Zhao G; Li B; Chen C; Xia L; Wang L; Luo T; Wang X; Wang Z; Zhang Y; Jiang Y; Pan Q; Hu Z; Guo H; Tang B; Liu C; Sun Z; Xia K; Li J
J Autism Dev Disord; 2022 Mar; 52(3):1299-1313. PubMed ID: 33970367
[TBL] [Abstract][Full Text] [Related]
20. De novo genic mutations among a Chinese autism spectrum disorder cohort.
Wang T; Guo H; Xiong B; Stessman HA; Wu H; Coe BP; Turner TN; Liu Y; Zhao W; Hoekzema K; Vives L; Xia L; Tang M; Ou J; Chen B; Shen Y; Xun G; Long M; Lin J; Kronenberg ZN; Peng Y; Bai T; Li H; Ke X; Hu Z; Zhao J; Zou X; Xia K; Eichler EE
Nat Commun; 2016 Nov; 7():13316. PubMed ID: 27824329
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
