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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

470 related articles for article (PubMed ID: 23966865)

  • 1. Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.
    He X; Sanders SJ; Liu L; De Rubeis S; Lim ET; Sutcliffe JS; Schellenberg GD; Gibbs RA; Daly MJ; Buxbaum JD; State MW; Devlin B; Roeder K
    PLoS Genet; 2013; 9(8):e1003671. PubMed ID: 23966865
    [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. 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]  

  • 4. Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.
    Liu L; Sabo A; Neale BM; Nagaswamy U; Stevens C; Lim E; Bodea CA; Muzny D; Reid JG; Banks E; Coon H; Depristo M; Dinh H; Fennel T; Flannick J; Gabriel S; Garimella K; Gross S; Hawes A; Lewis L; Makarov V; Maguire J; Newsham I; Poplin R; Ripke S; Shakir K; Samocha KE; Wu Y; Boerwinkle E; Buxbaum JD; Cook EH; Devlin B; Schellenberg GD; Sutcliffe JS; Daly MJ; Gibbs RA; Roeder K
    PLoS Genet; 2013 Apr; 9(4):e1003443. PubMed ID: 23593035
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A framework for the interpretation of de novo mutation in human disease.
    Samocha KE; Robinson EB; Sanders SJ; Stevens C; Sabo A; McGrath LM; Kosmicki JA; Rehnström K; Mallick S; Kirby A; Wall DP; MacArthur DG; Gabriel SB; DePristo M; Purcell SM; Palotie A; Boerwinkle E; Buxbaum JD; Cook EH; Gibbs RA; Schellenberg GD; Sutcliffe JS; Devlin B; Roeder K; Neale BM; Daly MJ
    Nat Genet; 2014 Sep; 46(9):944-50. PubMed ID: 25086666
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
    O'Roak BJ; Deriziotis P; Lee C; Vives L; Schwartz JJ; Girirajan S; Karakoc E; Mackenzie AP; Ng SB; Baker C; Rieder MJ; Nickerson DA; Bernier R; Fisher SE; Shendure J; Eichler EE
    Nat Genet; 2011 Jun; 43(6):585-9. PubMed ID: 21572417
    [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. Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.
    Jiang YH; Yuen RK; Jin X; Wang M; Chen N; Wu X; Ju J; Mei J; Shi Y; He M; Wang G; Liang J; Wang Z; Cao D; Carter MT; Chrysler C; Drmic IE; Howe JL; Lau L; Marshall CR; Merico D; Nalpathamkalam T; Thiruvahindrapuram B; Thompson A; Uddin M; Walker S; Luo J; Anagnostou E; Zwaigenbaum L; Ring RH; Wang J; Lajonchere C; Wang J; Shih A; Szatmari P; Yang H; Dawson G; Li Y; Scherer SW
    Am J Hum Genet; 2013 Aug; 93(2):249-63. PubMed ID: 23849776
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Towards a molecular characterization of autism spectrum disorders: an exome sequencing and systems approach.
    An JY; Cristino AS; Zhao Q; Edson J; Williams SM; Ravine D; Wray J; Marshall VM; Hunt A; Whitehouse AJ; Claudianos C
    Transl Psychiatry; 2014 Jun; 4(6):e394. PubMed ID: 24893065
    [TBL] [Abstract][Full Text] [Related]  

  • 10. De novo missense variants disrupting protein-protein interactions affect risk for autism through gene co-expression and protein networks in neuronal cell types.
    Chen S; Wang J; Cicek E; Roeder K; Yu H; Devlin B
    Mol Autism; 2020 Oct; 11(1):76. PubMed ID: 33032641
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Exome sequencing reveals new causal mutations in children with epileptic encephalopathies.
    Veeramah KR; Johnstone L; Karafet TM; Wolf D; Sprissler R; Salogiannis J; Barth-Maron A; Greenberg ME; Stuhlmann T; Weinert S; Jentsch TJ; Pazzi M; Restifo LL; Talwar D; Erickson RP; Hammer MF
    Epilepsia; 2013 Jul; 54(7):1270-81. PubMed ID: 23647072
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chromosomal microarray and whole-exome sequence analysis in Taiwanese patients with autism spectrum disorder.
    Chang YS; Lin CY; Huang HY; Chang JG; Kuo HT
    Mol Genet Genomic Med; 2019 Dec; 7(12):e996. PubMed ID: 31595719
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes.
    Feliciano P; Zhou X; Astrovskaya I; Turner TN; Wang T; Brueggeman L; Barnard R; Hsieh A; Snyder LG; Muzny DM; Sabo A; ; Gibbs RA; Eichler EE; O'Roak BJ; Michaelson JJ; Volfovsky N; Shen Y; Chung WK
    NPJ Genom Med; 2019; 4():19. PubMed ID: 31452935
    [TBL] [Abstract][Full Text] [Related]  

  • 16. De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.
    Babbs C; Lloyd D; Pagnamenta AT; Twigg SR; Green J; McGowan SJ; Mirza G; Naples R; Sharma VP; Volpi EV; Buckle VJ; Wall SA; Knight SJ; ; Parr JR; Wilkie AO
    J Med Genet; 2014 Nov; 51(11):737-47. PubMed ID: 25228304
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dendritic Spine in Autism Genetics: Whole-Exome Sequencing Identifying De Novo Variant of
    Xie Y; Wang H; Hu B; Zhang X; Liu A; Cai C; Li S; Chen C; Wang Z; Yin Z; Wang M
    Children (Basel); 2022 Dec; 10(1):. PubMed ID: 36670631
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.
    Nguyen HT; Bryois J; Kim A; Dobbyn A; Huckins LM; Munoz-Manchado AB; Ruderfer DM; Genovese G; Fromer M; Xu X; Pinto D; Linnarsson S; Verhage M; Smit AB; Hjerling-Leffler J; Buxbaum JD; Hultman C; Sklar P; Purcell SM; Lage K; He X; Sullivan PF; Stahl EA
    Genome Med; 2017 Dec; 9(1):114. PubMed ID: 29262854
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Whole-genome sequencing of quartet families with autism spectrum disorder.
    Yuen RK; Thiruvahindrapuram B; Merico D; Walker S; Tammimies K; Hoang N; Chrysler C; Nalpathamkalam T; Pellecchia G; Liu Y; Gazzellone MJ; D'Abate L; Deneault E; Howe JL; Liu RS; Thompson A; Zarrei M; Uddin M; Marshall CR; Ring RH; Zwaigenbaum L; Ray PN; Weksberg R; Carter MT; Fernandez BA; Roberts W; Szatmari P; Scherer SW
    Nat Med; 2015 Feb; 21(2):185-91. PubMed ID: 25621899
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.
    Kenny EM; Cormican P; Furlong S; Heron E; Kenny G; Fahey C; Kelleher E; Ennis S; Tropea D; Anney R; Corvin AP; Donohoe G; Gallagher L; Gill M; Morris DW
    Mol Psychiatry; 2014 Aug; 19(8):872-9. PubMed ID: 24126926
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.