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 *

165 related articles for article (PubMed ID: 26504140)

  • 21. Potpourri: An Epistasis Test Prioritization Algorithm via Diverse SNP Selection.
    Caylak G; Tastan O; Cicek AE
    J Comput Biol; 2021 Apr; 28(4):365-377. PubMed ID: 33275856
    [No Abstract]   [Full Text] [Related]  

  • 22. Integrative Tissue-Specific Functional Annotations in the Human Genome Provide Novel Insights on Many Complex Traits and Improve Signal Prioritization in Genome Wide Association Studies.
    Lu Q; Powles RL; Wang Q; He BJ; Zhao H
    PLoS Genet; 2016 Apr; 12(4):e1005947. PubMed ID: 27058395
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Improved integrative framework combining association data with gene expression features to prioritize Crohn's disease genes.
    Ning K; Gettler K; Zhang W; Ng SM; Bowen BM; Hyams J; Stephens MC; Kugathasan S; Denson LA; Schadt EE; Hoffman GE; Cho JH
    Hum Mol Genet; 2015 Jul; 24(14):4147-57. PubMed ID: 25935003
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Interpreting coronary artery disease GWAS results: A functional genomics approach assessing biological significance.
    Hartmann K; Seweryn M; Sadee W
    PLoS One; 2022; 17(2):e0244904. PubMed ID: 35192625
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Uncovering networks from genome-wide association studies via circular genomic permutation.
    Cabrera CP; Navarro P; Huffman JE; Wright AF; Hayward C; Campbell H; Wilson JF; Rudan I; Hastie ND; Vitart V; Haley CS
    G3 (Bethesda); 2012 Sep; 2(9):1067-75. PubMed ID: 22973544
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies.
    Joehanes R; Zhang X; Huan T; Yao C; Ying SX; Nguyen QT; Demirkale CY; Feolo ML; Sharopova NR; Sturcke A; Schäffer AA; Heard-Costa N; Chen H; Liu PC; Wang R; Woodhouse KA; Tanriverdi K; Freedman JE; Raghavachari N; Dupuis J; Johnson AD; O'Donnell CJ; Levy D; Munson PJ
    Genome Biol; 2017 Jan; 18(1):16. PubMed ID: 28122634
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetic control of gene expression at novel and established chronic obstructive pulmonary disease loci.
    Castaldi PJ; Cho MH; Zhou X; Qiu W; Mcgeachie M; Celli B; Bakke P; Gulsvik A; Lomas DA; Crapo JD; Beaty TH; Rennard S; Harshfield B; Lange C; Singh D; Tal-Singer R; Riley JH; Quackenbush J; Raby BA; Carey VJ; Silverman EK; Hersh CP
    Hum Mol Genet; 2015 Feb; 24(4):1200-10. PubMed ID: 25315895
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Two-stage genome-wide methylation profiling in childhood-onset Crohn's Disease implicates epigenetic alterations at the VMP1/MIR21 and HLA loci.
    Adams AT; Kennedy NA; Hansen R; Ventham NT; OʼLeary KR; Drummond HE; Noble CL; El-Omar E; Russell RK; Wilson DC; Nimmo ER; Hold GL; Satsangi J
    Inflamm Bowel Dis; 2014 Oct; 20(10):1784-93. PubMed ID: 25144570
    [TBL] [Abstract][Full Text] [Related]  

  • 30. DeepPerVar: a multi-modal deep learning framework for functional interpretation of genetic variants in personal genome.
    Wang Y; Chen L
    Bioinformatics; 2022 Dec; 38(24):5340-5351. PubMed ID: 36271868
    [TBL] [Abstract][Full Text] [Related]  

  • 31. HapBoost: a fast approach to boosting haplotype association analyses in genome-wide association studies.
    Wan X; Yang C; Yang Q; Zhao H; Yu W
    IEEE/ACM Trans Comput Biol Bioinform; 2013; 10(1):207-12. PubMed ID: 23702557
    [TBL] [Abstract][Full Text] [Related]  

  • 32. PExFInS: An Integrative Post-GWAS Explorer for Functional Indels and SNPs.
    Cheng Z; Chu H; Fan Y; Li C; Song YQ; Zhou J; Yuen KY
    Sci Rep; 2015 Nov; 5():17302. PubMed ID: 26612672
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS.
    Wang Y; Thompson WK; Schork AJ; Holland D; Chen CH; Bettella F; Desikan RS; Li W; Witoelar A; Zuber V; Devor A; ; ; Nöthen MM; Rietschel M; Chen Q; Werge T; Cichon S; Weinberger DR; Djurovic S; O'Donovan M; Visscher PM; Andreassen OA; Dale AM
    PLoS Genet; 2016 Jan; 12(1):e1005803. PubMed ID: 26808560
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Haplotypes in the expression quantitative trait locus of interleukin-1β gene are associated with schizophrenia.
    Yoshida M; Shiroiwa K; Mouri K; Ishiguro H; Supriyanto I; Ratta-Apha W; Eguchi N; Okazaki S; Sasada T; Fukutake M; Hashimoto T; Inada T; Arinami T; Shirakawa O; Hishimoto A
    Schizophr Res; 2012 Sep; 140(1-3):185-91. PubMed ID: 22804923
    [TBL] [Abstract][Full Text] [Related]  

  • 35. CandiSNPer: a web tool for the identification of candidate SNPs for causal variants.
    Schmitt AO; Assmus J; Bortfeldt RH; Brockmann GA
    Bioinformatics; 2010 Apr; 26(7):969-70. PubMed ID: 20172942
    [TBL] [Abstract][Full Text] [Related]  

  • 36. SNPsnap: a Web-based tool for identification and annotation of matched SNPs.
    Pers TH; Timshel P; Hirschhorn JN
    Bioinformatics; 2015 Feb; 31(3):418-20. PubMed ID: 25316677
    [TBL] [Abstract][Full Text] [Related]  

  • 37. An integrative functional genomics approach for discovering biomarkers in schizophrenia.
    Vawter MP; Mamdani F; Macciardi F
    Brief Funct Genomics; 2011 Nov; 10(6):387-99. PubMed ID: 22155586
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. The genome-wide risk alleles for psychiatric disorders at 3p21.1 show convergent effects on mRNA expression, cognitive function, and mushroom dendritic spine.
    Yang Z; Zhou D; Li H; Cai X; Liu W; Wang L; Chang H; Li M; Xiao X
    Mol Psychiatry; 2020 Jan; 25(1):48-66. PubMed ID: 31723243
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Alzheimer's Disease Risk Polymorphisms Regulate Gene Expression in the ZCWPW1 and the CELF1 Loci.
    Karch CM; Ezerskiy LA; Bertelsen S; ; Goate AM
    PLoS One; 2016; 11(2):e0148717. PubMed ID: 26919393
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.