BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

652 related articles for article (PubMed ID: 32372567)

  • 21. 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]  

  • 22. Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk.
    Salyakina D; Cukier HN; Lee JM; Sacharow S; Nations LD; Ma D; Jaworski JM; Konidari I; Whitehead PL; Wright HH; Abramson RK; Williams SM; Menon R; Haines JL; Gilbert JR; Cuccaro ML; Pericak-Vance MA
    PLoS One; 2011; 6(10):e26049. PubMed ID: 22016809
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders.
    Glessner JT; Khan ME; Chang X; Liu Y; Otieno FG; Lemma M; Slaby I; Hain H; Mentch F; Li J; Kao C; Sleiman PMA; March ME; Connolly J; Hakonarson H
    J Neurodev Disord; 2023 Apr; 15(1):14. PubMed ID: 37120522
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Synergistic interactions between Drosophila orthologues of genes spanned by de novo human CNVs support multiple-hit models of autism.
    Grice SJ; Liu JL; Webber C
    PLoS Genet; 2015 Mar; 11(3):e1004998. PubMed ID: 25816101
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Finding underlying genetic mechanisms of two patients with autism spectrum disorder carrying familial apparently balanced chromosomal translocations.
    Toraman B; Bilginer SÇ; Hesapçıoğlu ST; Göker Z; Soykam HO; Ergüner B; Dinçer T; Yıldız G; Ünsal S; Kasap BK; Kandil S; Kalay E
    J Gene Med; 2021 Apr; 23(4):e3322. PubMed ID: 33591602
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Copy number variations independently induce autism spectrum disorder.
    Yingjun X; Haiming Y; Mingbang W; Liangying Z; Jiaxiu Z; Bing S; Qibin Y; Xiaofang S
    Biosci Rep; 2017 Aug; 37(4):. PubMed ID: 28533427
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.
    Siu MT; Butcher DT; Turinsky AL; Cytrynbaum C; Stavropoulos DJ; Walker S; Caluseriu O; Carter M; Lou Y; Nicolson R; Georgiades S; Szatmari P; Anagnostou E; Scherer SW; Choufani S; Brudno M; Weksberg R
    Clin Epigenetics; 2019 Jul; 11(1):103. PubMed ID: 31311581
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Clinical and molecular characterization of three genomic rearrangements at chromosome 22q13.3 associated with autism spectrum disorder.
    Chen CH; Chen HI; Liao HM; Chen YJ; Fang JS; Lee KF; Gau SS
    Psychiatr Genet; 2017 Feb; 27(1):23-33. PubMed ID: 27846046
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study.
    Abdi M; Aliyev E; Trost B; Kohailan M; Aamer W; Syed N; Shaath R; Gandhi GD; Engchuan W; Howe J; Thiruvahindrapuram B; Geng M; Whitney J; Syed A; Lakshmi J; Hussein S; Albashir N; Hussein A; Poggiolini I; Elhag SF; Palaniswamy S; Kambouris M; de Fatima Janjua M; Tahir MOE; Nazeer A; Shahwar D; Azeem MW; Mokrab Y; Aati NA; Akil A; Scherer SW; Kamal M; Fakhro KA
    Genome Med; 2023 Oct; 15(1):81. PubMed ID: 37805537
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
    Lionel AC; Crosbie J; Barbosa N; Goodale T; Thiruvahindrapuram B; Rickaby J; Gazzellone M; Carson AR; Howe JL; Wang Z; Wei J; Stewart AF; Roberts R; McPherson R; Fiebig A; Franke A; Schreiber S; Zwaigenbaum L; Fernandez BA; Roberts W; Arnold PD; Szatmari P; Marshall CR; Schachar R; Scherer SW
    Sci Transl Med; 2011 Aug; 3(95):95ra75. PubMed ID: 21832240
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder.
    Mahjani B; De Rubeis S; Gustavsson Mahjani C; Mulhern M; Xu X; Klei L; Satterstrom FK; Fu J; Talkowski ME; Reichenberg A; Sandin S; Hultman CM; Grice DE; Roeder K; Devlin B; Buxbaum JD
    Mol Autism; 2021 Oct; 12(1):65. PubMed ID: 34615535
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Copy number and sequence variants implicate APBA2 as an autism candidate gene.
    Babatz TD; Kumar RA; Sudi J; Dobyns WB; Christian SL
    Autism Res; 2009 Dec; 2(6):359-64. PubMed ID: 20029827
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Copy number variations in Japanese children with autism spectrum disorder.
    Sakamoto Y; Shimoyama S; Furukawa T; Adachi M; Takahashi M; Mikami T; Kuribayashi M; Osato A; Tsushima D; Saito M; Ueno S; Nakamura K
    Psychiatr Genet; 2021 Jun; 31(3):79-87. PubMed ID: 33591083
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Identification of Developmental and Behavioral Markers Associated With Genetic Abnormalities in Autism Spectrum Disorder.
    Bishop SL; Farmer C; Bal V; Robinson EB; Willsey AJ; Werling DM; Havdahl KA; Sanders SJ; Thurm A
    Am J Psychiatry; 2017 Jun; 174(6):576-585. PubMed ID: 28253736
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genomic architecture of autism from comprehensive whole-genome sequence annotation.
    Trost B; Thiruvahindrapuram B; Chan AJS; Engchuan W; Higginbotham EJ; Howe JL; Loureiro LO; Reuter MS; Roshandel D; Whitney J; Zarrei M; Bookman M; Somerville C; Shaath R; Abdi M; Aliyev E; Patel RV; Nalpathamkalam T; Pellecchia G; Hamdan O; Kaur G; Wang Z; MacDonald JR; Wei J; Sung WWL; Lamoureux S; Hoang N; Selvanayagam T; Deflaux N; Geng M; Ghaffari S; Bates J; Young EJ; Ding Q; Shum C; D'Abate L; Bradley CA; Rutherford A; Aguda V; Apresto B; Chen N; Desai S; Du X; Fong MLY; Pullenayegum S; Samler K; Wang T; Ho K; Paton T; Pereira SL; Herbrick JA; Wintle RF; Fuerth J; Noppornpitak J; Ward H; Magee P; Al Baz A; Kajendirarajah U; Kapadia S; Vlasblom J; Valluri M; Green J; Seifer V; Quirbach M; Rennie O; Kelley E; Masjedi N; Lord C; Szego MJ; Zawati MH; Lang M; Strug LJ; Marshall CR; Costain G; Calli K; Iaboni A; Yusuf A; Ambrozewicz P; Gallagher L; Amaral DG; Brian J; Elsabbagh M; Georgiades S; Messinger DS; Ozonoff S; Sebat J; Sjaarda C; Smith IM; Szatmari P; Zwaigenbaum L; Kushki A; Frazier TW; Vorstman JAS; Fakhro KA; Fernandez BA; Lewis MES; Weksberg R; Fiume M; Yuen RKC; Anagnostou E; Sondheimer N; Glazer D; Hartley DM; Scherer SW
    Cell; 2022 Nov; 185(23):4409-4427.e18. PubMed ID: 36368308
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Two de novo variations identified by massively parallel sequencing in 13 Chinese families with children diagnosed with autism spectrum disorder.
    Li SJ; Yu SS; Luo HY; Li X; Rao B; Wang Y; Li ZZ; Liu G; Zou LP; Zhang JS; Feng C; Liu J; Liu JW; Hu N; Chen XQ; Yu SY; Li K; He MW; Yu XG; Wang J; Guo SL; Chen ZY; Zhang L; Ma L
    Clin Chim Acta; 2018 Apr; 479():144-147. PubMed ID: 29366832
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 33.