BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

888 related articles for article (PubMed ID: 33374967)

  • 1. 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]  

  • 2. 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]  

  • 3. Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.
    Kim DS; Burt AA; Ranchalis JE; Wilmot B; Smith JD; Patterson KE; Coe BP; Li YK; Bamshad MJ; Nikolas M; Eichler EE; Swanson JM; Nigg JT; Nickerson DA; Jarvik GP;
    Am J Med Genet B Neuropsychiatr Genet; 2017 Jun; 174(4):381-389. PubMed ID: 28332277
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing.
    Wu J; Yu P; Jin X; Xu X; Li J; Li Z; Wang M; Wang T; Wu X; Jiang Y; Cai W; Mei J; Min Q; Xu Q; Zhou B; Guo H; Wang P; Zhou W; Hu Z; Li Y; Cai T; Wang Y; Xia K; Jiang YH; Sun ZS
    J Genet Genomics; 2018 Oct; 45(10):527-538. PubMed ID: 30392784
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic factors contributing to autism spectrum disorder in Williams-Beuren syndrome.
    Codina-Sola M; Costa-Roger M; Pérez-García D; Flores R; Palacios-Verdú MG; Cusco I; Pérez-Jurado LA
    J Med Genet; 2019 Dec; 56(12):801-808. PubMed ID: 31413120
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families.
    Al-Mubarak B; Abouelhoda M; Omar A; AlDhalaan H; Aldosari M; Nester M; Alshamrani HA; El-Kalioby M; Goljan E; Albar R; Subhani S; Tahir A; Asfahani S; Eskandrani A; Almusaiab A; Magrashi A; Shinwari J; Monies D; Al Tassan N
    Sci Rep; 2017 Jul; 7(1):5679. PubMed ID: 28720891
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Novel rare missense variations and risk of autism spectrum disorder: whole-exome sequencing in two families with affected siblings and a two-stage follow-up study in a Japanese population.
    Egawa J; Watanabe Y; Wang C; Inoue E; Sugimoto A; Sugiyama T; Igeta H; Nunokawa A; Shibuya M; Kushima I; Orime N; Hayashi T; Okada T; Uno Y; Ozaki N; Someya T
    PLoS One; 2015; 10(3):e0119413. PubMed ID: 25806950
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder.
    Mirzaa GM; Chong JX; Piton A; Popp B; Foss K; Guo H; Harripaul R; Xia K; Scheck J; Aldinger KA; Sajan SA; Tang S; Bonneau D; Beck A; White J; Mahida S; Harris J; Smith-Hicks C; Hoyer J; Zweier C; Reis A; Thiel CT; Jamra RA; Zeid N; Yang A; Farach LS; Walsh L; Payne K; Rohena L; Velinov M; Ziegler A; Schaefer E; Gatinois V; Geneviève D; Simon MEH; Kohler J; Rotenberg J; Wheeler P; Larson A; Ernst ME; Akman CI; Westman R; Blanchet P; Schillaci LA; Vincent-Delorme C; Gripp KW; Mattioli F; Guyader GL; Gerard B; Mathieu-Dramard M; Morin G; Sasanfar R; Ayub M; Vasli N; Yang S; Person R; Monaghan KG; Nickerson DA; van Binsbergen E; Enns GM; Dries AM; Rowe LJ; Tsai ACH; Svihovec S; Friedman J; Agha Z; Qamar R; Rodan LH; Martinez-Agosto J; Ockeloen CW; Vincent M; Sunderland WJ; Bernstein JA; ; Eichler EE; Vincent JB; ; Bamshad MJ
    Genet Med; 2020 Mar; 22(3):538-546. PubMed ID: 31723249
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene.
    Patowary A; Won SY; Oh SJ; Nesbitt RR; Archer M; Nickerson D; Raskind WH; Bernier R; Lee JE; Brkanac Z
    Transl Psychiatry; 2019 Jan; 9(1):4. PubMed ID: 30664616
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.
    Guo H; Peng Y; Hu Z; Li Y; Xun G; Ou J; Sun L; Xiong Z; Liu Y; Wang T; Chen J; Xia L; Bai T; Shen Y; Tian Q; Hu Y; Shen L; Zhao R; Zhang X; Zhang F; Zhao J; Zou X; Xia K
    Sci Rep; 2017 Mar; 7():44155. PubMed ID: 28281572
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of a de novo FOXP1 mutation and incidental discovery of inherited genetic variants contributing to a case of autism spectrum disorder and epilepsy.
    Jay K; Mitra A; Harding T; Matthes D; Van Ness B
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00751. PubMed ID: 31111659
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder.
    Hashimoto R; Nakazawa T; Tsurusaki Y; Yasuda Y; Nagayasu K; Matsumura K; Kawashima H; Yamamori H; Fujimoto M; Ohi K; Umeda-Yano S; Fukunaga M; Fujino H; Kasai A; Hayata-Takano A; Shintani N; Takeda M; Matsumoto N; Hashimoto H
    J Hum Genet; 2016 Mar; 61(3):199-206. PubMed ID: 26582266
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 45.