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 *

213 related articles for article (PubMed ID: 33539344)

  • 21. 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]  

  • 22. Genomic selection signatures in autism spectrum disorder identifies cognitive genomic tradeoff and its relevance in paradoxical phenotypes of deficits versus potentialities.
    Prakash A; Banerjee M
    Sci Rep; 2021 May; 11(1):10245. PubMed ID: 33986442
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD.
    Guo W; Samuels JF; Wang Y; Cao H; Ritter M; Nestadt PS; Krasnow J; Greenberg BD; Fyer AJ; McCracken JT; Geller DA; Murphy DL; Knowles JA; Grados MA; Riddle MA; Rasmussen SA; McLaughlin NC; Nurmi EL; Askland KD; Cullen BA; Piacentini J; Pauls DL; Bienvenu OJ; Stewart SE; Goes FS; Maher B; Pulver AE; Valle D; Mattheisen M; Qian J; Nestadt G; Shugart YY
    Eur Neuropsychopharmacol; 2017 Jul; 27(7):657-666. PubMed ID: 28641744
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genome-wide association analysis of autism identified multiple loci that have been reported as strong signals for neuropsychiatric disorders.
    Xia L; Ou J; Li K; Guo H; Hu Z; Bai T; Zhao J; Xia K; Zhang F
    Autism Res; 2020 Mar; 13(3):382-396. PubMed ID: 31647196
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Influence of tissue context on gene prioritization for predicted transcriptome-wide association studies.
    Li B; Veturi Y; Bradford Y; Verma SS; Verma A; Lucas AM; Haas DW; Ritchie MD
    Pac Symp Biocomput; 2019; 24():296-307. PubMed ID: 30864331
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Unveiling promising drug targets for autism spectrum disorder: insights from genetics, transcriptomics, and proteomics.
    Jiang R; Huang W; Qiu X; Chen J; Luo R; Zeng R; Tong S; Lyu Y; Sun P; Lian Q; Leung FW; Liu Y; Sha W; Chen H
    Brief Bioinform; 2024 May; 25(4):. PubMed ID: 39038939
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
    Casey JP; Magalhaes T; Conroy JM; Regan R; Shah N; Anney R; Shields DC; Abrahams BS; Almeida J; Bacchelli E; Bailey AJ; Baird G; Battaglia A; Berney T; Bolshakova N; Bolton PF; Bourgeron T; Brennan S; Cali P; Correia C; Corsello C; Coutanche M; Dawson G; de Jonge M; Delorme R; Duketis E; Duque F; Estes A; Farrar P; Fernandez BA; Folstein SE; Foley S; Fombonne E; Freitag CM; Gilbert J; Gillberg C; Glessner JT; Green J; Guter SJ; Hakonarson H; Holt R; Hughes G; Hus V; Igliozzi R; Kim C; Klauck SM; Kolevzon A; Lamb JA; Leboyer M; Le Couteur A; Leventhal BL; Lord C; Lund SC; Maestrini E; Mantoulan C; Marshall CR; McConachie H; McDougle CJ; McGrath J; McMahon WM; Merikangas A; Miller J; Minopoli F; Mirza GK; Munson J; Nelson SF; Nygren G; Oliveira G; Pagnamenta AT; Papanikolaou K; Parr JR; Parrini B; Pickles A; Pinto D; Piven J; Posey DJ; Poustka A; Poustka F; Ragoussis J; Roge B; Rutter ML; Sequeira AF; Soorya L; Sousa I; Sykes N; Stoppioni V; Tancredi R; Tauber M; Thompson AP; Thomson S; Tsiantis J; Van Engeland H; Vincent JB; Volkmar F; Vorstman JA; Wallace S; Wang K; Wassink TH; White K; Wing K; Wittemeyer K; Yaspan BL; Zwaigenbaum L; Betancur C; Buxbaum JD; Cantor RM; Cook EH; Coon H; Cuccaro ML; Geschwind DH; Haines JL; Hallmayer J; Monaco AP; Nurnberger JI; Pericak-Vance MA; Schellenberg GD; Scherer SW; Sutcliffe JS; Szatmari P; Vieland VJ; Wijsman EM; Green A; Gill M; Gallagher L; Vicente A; Ennis S
    Hum Genet; 2012 Apr; 131(4):565-79. PubMed ID: 21996756
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families.
    Al-Sarraj Y; Al-Dous E; Taha RZ; Ahram D; Alshaban F; Tolfat M; El-Shanti H; Albagha OME
    Genes (Basel); 2021 May; 12(5):. PubMed ID: 34069769
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism.
    Matoba N; Liang D; Sun H; Aygün N; McAfee JC; Davis JE; Raffield LM; Qian H; Piven J; Li Y; Kosuri S; Won H; Stein JL
    Transl Psychiatry; 2020 Aug; 10(1):265. PubMed ID: 32747698
    [TBL] [Abstract][Full Text] [Related]  

  • 31. An integrative analysis of non-coding regulatory DNA variations associated with autism spectrum disorder.
    Williams SM; An JY; Edson J; Watts M; Murigneux V; Whitehouse AJO; Jackson CJ; Bellgrove MA; Cristino AS; Claudianos C
    Mol Psychiatry; 2019 Nov; 24(11):1707-1719. PubMed ID: 29703944
    [TBL] [Abstract][Full Text] [Related]  

  • 32. KnockoffHybrid: A knockoff framework for hybrid analysis of trio and population designs in genome-wide association studies.
    Yang Y; Wang Q; Wang C; Buxbaum J; Ionita-Laza I
    Am J Hum Genet; 2024 Jul; 111(7):1448-1461. PubMed ID: 38821058
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Understanding the impact of SNPs associated with autism spectrum disorder on biological pathways in the human fetal and adult cortex.
    Golovina E; Fadason T; Lints TJ; Walker C; Vickers MH; O'Sullivan JM
    Sci Rep; 2021 Aug; 11(1):15867. PubMed ID: 34354167
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study.
    Cao C; Wang J; Kwok D; Cui F; Zhang Z; Zhao D; Li MJ; Zou Q
    Nucleic Acids Res; 2022 Jan; 50(D1):D1123-D1130. PubMed ID: 34669946
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification of common genetic risk variants for autism spectrum disorder.
    Grove J; Ripke S; Als TD; Mattheisen M; Walters RK; Won H; Pallesen J; Agerbo E; Andreassen OA; Anney R; Awashti S; Belliveau R; Bettella F; Buxbaum JD; Bybjerg-Grauholm J; Bækvad-Hansen M; Cerrato F; Chambert K; Christensen JH; Churchhouse C; Dellenvall K; Demontis D; De Rubeis S; Devlin B; Djurovic S; Dumont AL; Goldstein JI; Hansen CS; Hauberg ME; Hollegaard MV; Hope S; Howrigan DP; Huang H; Hultman CM; Klei L; Maller J; Martin J; Martin AR; Moran JL; Nyegaard M; Nærland T; Palmer DS; Palotie A; Pedersen CB; Pedersen MG; dPoterba T; Poulsen JB; Pourcain BS; Qvist P; Rehnström K; Reichenberg A; Reichert J; Robinson EB; Roeder K; Roussos P; Saemundsen E; Sandin S; Satterstrom FK; Davey Smith G; Stefansson H; Steinberg S; Stevens CR; Sullivan PF; Turley P; Walters GB; Xu X; ; ; ; ; Stefansson K; Geschwind DH; Nordentoft M; Hougaard DM; Werge T; Mors O; Mortensen PB; Neale BM; Daly MJ; Børglum AD
    Nat Genet; 2019 Mar; 51(3):431-444. PubMed ID: 30804558
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Comprehensive Integrative Analyses Identify TIGD5 rs75547282 as a Risk Variant for Autism Spectrum Disorder.
    Xie X; Li L; Wu H; Hou F; Chen Y; Xue Q; Zhou Y; Zhang J; Gong J; Song R
    Autism Res; 2021 Apr; 14(4):631-644. PubMed ID: 33393181
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.
    Leppa VM; Kravitz SN; Martin CL; Andrieux J; Le Caignec C; Martin-Coignard D; DyBuncio C; Sanders SJ; Lowe JK; Cantor RM; Geschwind DH
    Am J Hum Genet; 2016 Sep; 99(3):540-554. PubMed ID: 27569545
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia.
    Liu J; Li S; Li X; Li W; Yang Y; Guo S; Lv L; Xiao X; Yao YG; Guan F; Li M; Luo XJ
    BMC Med; 2021 Aug; 19(1):177. PubMed ID: 34380480
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Integrative analysis of transcriptome-wide association study and mRNA expression profile identified candidate genes and pathways associated with aortic aneurysm and dissection.
    Zhang Y; Li L; Ma L
    Gene; 2022 Jan; 808():145993. PubMed ID: 34626721
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.