BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

352 related articles for article (PubMed ID: 33300042)

  • 21. An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci.
    Mountjoy E; Schmidt EM; Carmona M; Schwartzentruber J; Peat G; Miranda A; Fumis L; Hayhurst J; Buniello A; Karim MA; Wright D; Hercules A; Papa E; Fauman EB; Barrett JC; Todd JA; Ochoa D; Dunham I; Ghoussaini M
    Nat Genet; 2021 Nov; 53(11):1527-1533. PubMed ID: 34711957
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A comprehensive integrated post-GWAS analysis of Type 1 diabetes reveals enhancer-based immune dysregulation.
    Kim SS; Hudgins AD; Yang J; Zhu Y; Tu Z; Rosenfeld MG; DiLorenzo TP; Suh Y
    PLoS One; 2021; 16(9):e0257265. PubMed ID: 34529725
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Epigenomic and Transcriptomic Prioritization of Candidate Obesity-Risk Regulatory GWAS SNPs.
    Zhang X; Li TY; Xiao HM; Ehrlich KC; Shen H; Deng HW; Ehrlich M
    Int J Mol Sci; 2022 Jan; 23(3):. PubMed ID: 35163195
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Interrogation of human hematopoiesis at single-cell and single-variant resolution.
    Ulirsch JC; Lareau CA; Bao EL; Ludwig LS; Guo MH; Benner C; Satpathy AT; Kartha VK; Salem RM; Hirschhorn JN; Finucane HK; Aryee MJ; Buenrostro JD; Sankaran VG
    Nat Genet; 2019 Apr; 51(4):683-693. PubMed ID: 30858613
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Systematic tissue-specific functional annotation of the human genome highlights immune-related DNA elements for late-onset Alzheimer's disease.
    Lu Q; Powles RL; Abdallah S; Ou D; Wang Q; Hu Y; Lu Y; Liu W; Li B; Mukherjee S; Crane PK; Zhao H
    PLoS Genet; 2017 Jul; 13(7):e1006933. PubMed ID: 28742084
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Comprehensive functional annotation of susceptibility variants associated with asthma.
    Gautam Y; Afanador Y; Ghandikota S; Mersha TB
    Hum Genet; 2020 Aug; 139(8):1037-1053. PubMed ID: 32240371
    [TBL] [Abstract][Full Text] [Related]  

  • 27. IMPACT: Genomic Annotation of Cell-State-Specific Regulatory Elements Inferred from the Epigenome of Bound Transcription Factors.
    Amariuta T; Luo Y; Gazal S; Davenport EE; van de Geijn B; Ishigaki K; Westra HJ; Teslovich N; Okada Y; Yamamoto K; ; Price AL; Raychaudhuri S
    Am J Hum Genet; 2019 May; 104(5):879-895. PubMed ID: 31006511
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Deep learning predicts DNA methylation regulatory variants in the human brain and elucidates the genetics of psychiatric disorders.
    Zhou J; Chen Q; Braun PR; Perzel Mandell KA; Jaffe AE; Tan HY; Hyde TM; Kleinman JE; Potash JB; Shinozaki G; Weinberger DR; Han S
    Proc Natl Acad Sci U S A; 2022 Aug; 119(34):e2206069119. PubMed ID: 35969790
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Pinpointing miRNA and genes enrichment over trait-relevant tissue network in Genome-Wide Association Studies.
    Li B; Dong J; Yu J; Fan Y; Shang L; Zhou X; Bai Y
    BMC Med Genomics; 2020 Dec; 13(Suppl 11):191. PubMed ID: 33371893
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The genomic signature of trait-associated variants.
    Kindt AS; Navarro P; Semple CA; Haley CS
    BMC Genomics; 2013 Feb; 14():108. PubMed ID: 23418889
    [TBL] [Abstract][Full Text] [Related]  

  • 31. CAUSEL: an epigenome- and genome-editing pipeline for establishing function of noncoding GWAS variants.
    Spisák S; Lawrenson K; Fu Y; Csabai I; Cottman RT; Seo JH; Haiman C; Han Y; Lenci R; Li Q; Tisza V; Szállási Z; Herbert ZT; Chabot M; Pomerantz M; Solymosi N; ; Gayther SA; Joung JK; Freedman ML
    Nat Med; 2015 Nov; 21(11):1357-63. PubMed ID: 26398868
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Integrative analysis of 3604 GWAS reveals multiple novel cell type-specific regulatory associations.
    Breeze CE; Haugen E; Reynolds A; Teschendorff A; van Dongen J; Lan Q; Rothman N; Bourque G; Dunham I; Beck S; Stamatoyannopoulos J; Franceschini N; Berndt SI
    Genome Biol; 2022 Jan; 23(1):13. PubMed ID: 34996498
    [TBL] [Abstract][Full Text] [Related]  

  • 33. DIVAN: accurate identification of non-coding disease-specific risk variants using multi-omics profiles.
    Chen L; Jin P; Qin ZS
    Genome Biol; 2016 Dec; 17(1):252. PubMed ID: 27923386
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A Multi-omic Integrative Scheme Characterizes Tissues of Action at Loci Associated with Type 2 Diabetes.
    Torres JM; Abdalla M; Payne A; Fernandez-Tajes J; Thurner M; Nylander V; Gloyn AL; Mahajan A; McCarthy MI
    Am J Hum Genet; 2020 Dec; 107(6):1011-1028. PubMed ID: 33186544
    [TBL] [Abstract][Full Text] [Related]  

  • 35. GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits.
    Huang D; Yi X; Zhang S; Zheng Z; Wang P; Xuan C; Sham PC; Wang J; Li MJ
    Nucleic Acids Res; 2018 Jul; 46(W1):W114-W120. PubMed ID: 29771388
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Chromatin accessibility and gene expression during adipocyte differentiation identify context-dependent effects at cardiometabolic GWAS loci.
    Perrin HJ; Currin KW; Vadlamudi S; Pandey GK; Ng KK; Wabitsch M; Laakso M; Love MI; Mohlke KL
    PLoS Genet; 2021 Oct; 17(10):e1009865. PubMed ID: 34699533
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Cascading epigenomic analysis for identifying disease genes from the regulatory landscape of GWAS variants.
    Ng B; Casazza W; Kim NH; Wang C; Farhadi F; Tasaki S; Bennett DA; De Jager PL; Gaiteri C; Mostafavi S
    PLoS Genet; 2021 Nov; 17(11):e1009918. PubMed ID: 34807913
    [TBL] [Abstract][Full Text] [Related]  

  • 38. HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease.
    Ward LD; Kellis M
    Nucleic Acids Res; 2016 Jan; 44(D1):D877-81. PubMed ID: 26657631
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Parsing the Functional Impact of Noncoding Genetic Variants in the Brain Epigenome.
    Powell SK; O'Shea C; Brennand KJ; Akbarian S
    Biol Psychiatry; 2021 Jan; 89(1):65-75. PubMed ID: 33131715
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Quantifying functional impact of non-coding variants with multi-task Bayesian neural network.
    Xu C; Liu Q; Zhou J; Xie M; Feng J; Jiang T
    Bioinformatics; 2020 Mar; 36(5):1397-1404. PubMed ID: 31693090
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.