BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 33130899)

  • 21. Disease-associated non-coding variants alter NKX2-5 DNA-binding affinity.
    Peña-Martínez EG; Rivera-Madera A; Pomales-Matos DA; Sanabria-Alberto L; Rosario-Cañuelas BM; Rodríguez-Ríos JM; Carrasquillo-Dones EA; Rodríguez-Martínez JA
    Biochim Biophys Acta Gene Regul Mech; 2023 Mar; 1866(1):194906. PubMed ID: 36690178
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Partitioned glioma heritability shows subtype-specific enrichment in immune cells.
    Ostrom QT; Edelson J; Byun J; Han Y; Kinnersley B; Melin B; Houlston RS; Monje M; ; Walsh KM; Amos CI; Bondy ML
    Neuro Oncol; 2021 Aug; 23(8):1304-1314. PubMed ID: 33743008
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genome-wide association study identifies multiple susceptibility loci for glioma.
    Kinnersley B; Labussière M; Holroyd A; Di Stefano AL; Broderick P; Vijayakrishnan J; Mokhtari K; Delattre JY; Gousias K; Schramm J; Schoemaker MJ; Fleming SJ; Herms S; Heilmann S; Schreiber S; Wichmann HE; Nöthen MM; Swerdlow A; Lathrop M; Simon M; Bondy M; Sanson M; Houlston RS
    Nat Commun; 2015 Oct; 6():8559. PubMed ID: 26424050
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Bioinformatics pipeline to guide post-GWAS studies in Alzheimer's: A new catalogue of disease candidate short structural variants.
    Lutz MW; Chiba-Falek O
    Alzheimers Dement; 2023 Sep; 19(9):4094-4109. PubMed ID: 37253165
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Common genetic variants with fetal effects on birth weight are enriched for proximity to genes implicated in rare developmental disorders.
    Beaumont RN; Mayne IK; Freathy RM; Wright CF
    Hum Mol Genet; 2021 May; 30(11):1057-1066. PubMed ID: 33682876
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Beyond Endometriosis Genome-Wide Association Study: From Genomics to Phenomics to the Patient.
    Zondervan KT; Rahmioglu N; Morris AP; Nyholt DR; Montgomery GW; Becker CM; Missmer SA
    Semin Reprod Med; 2016 Jul; 34(4):242-54. PubMed ID: 27513026
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prioritizing Cardiovascular Disease-Associated Variants Altering NKX2-5 Binding through an Integrative Computational Approach.
    Peña-Martínez EG; Pomales-Matos DA; Rivera-Madera A; Messon-Bird JL; Medina-Feliciano JG; Sanabria-Alberto L; Barreiro-Rosario AC; Rodriguez-Rios JM; Rodríguez-Martínez JA
    medRxiv; 2023 Sep; ():. PubMed ID: 37693486
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Perturbation of the insomnia WDR90 GWAS locus pinpoints rs3752495 as a causal variant influencing distal expression of neighboring gene, PIG-Q.
    Sonti S; Littleton SH; Pahl MC; Zimmerman AJ; Chesi A; Palermo J; Lasconi C; Brown EB; Pippin JA; Wells AD; Doldur-Balli F; Pack AI; Gehrman PR; Keene AC; Grant SFA
    Sleep; 2024 Apr; ():. PubMed ID: 38571402
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Integrative single-nucleus multi-omics analysis prioritizes candidate cis and trans regulatory networks and their target genes in Alzheimer's disease brains.
    Gamache J; Gingerich D; Shwab EK; Barrera J; Garrett ME; Hume C; Crawford GE; Ashley-Koch AE; Chiba-Falek O
    Cell Biosci; 2023 Oct; 13(1):185. PubMed ID: 37789374
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Coexistence of Multiple Functional Variants and Genes Underlies Genetic Risk Locus 11p11.2 of Alzheimer's Disease.
    Xu M; Liu Q; Bi R; Li Y; Li H; Kang WB; Yan Z; Zheng Q; Sun C; Ye M; Xiang BL; Luo XJ; Li M; Zhang DF; Yao YG
    Biol Psychiatry; 2023 Nov; 94(9):743-759. PubMed ID: 37290560
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.
    Chen XF; Guo MR; Duan YY; Jiang F; Wu H; Dong SS; Zhou XR; Thynn HN; Liu CC; Zhang L; Guo Y; Yang TL
    JCI Insight; 2020 Sep; 5(17):. PubMed ID: 32879140
    [TBL] [Abstract][Full Text] [Related]  

  • 32. FORGEdb: a tool for identifying candidate functional variants and uncovering target genes and mechanisms for complex diseases.
    Breeze CE; Haugen E; Gutierrez-Arcelus M; Yao X; Teschendorff A; Beck S; Dunham I; Stamatoyannopoulos J; Franceschini N; Machiela MJ; Berndt SI
    Genome Biol; 2024 Jan; 25(1):3. PubMed ID: 38167104
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Gaining insight into metabolic diseases from human genetic discoveries.
    Claussnitzer M; Susztak K
    Trends Genet; 2021 Dec; 37(12):1081-1094. PubMed ID: 34315631
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A multilayered post-GWAS assessment on genetic susceptibility to pancreatic cancer.
    López de Maturana E; Rodríguez JA; Alonso L; Lao O; Molina-Montes E; Martín-Antoniano IA; Gómez-Rubio P; Lawlor R; Carrato A; Hidalgo M; Iglesias M; Molero X; Löhr M; Michalski C; Perea J; O'Rorke M; Barberà VM; Tardón A; Farré A; Muñoz-Bellvís L; Crnogorac-Jurcevic T; Domínguez-Muñoz E; Gress T; Greenhalf W; Sharp L; Arnes L; Cecchini L; Balsells J; Costello E; Ilzarbe L; Kleeff J; Kong B; Márquez M; Mora J; O'Driscoll D; Scarpa A; Ye W; Yu J; ; García-Closas M; Kogevinas M; Rothman N; Silverman DT; ; Albanes D; Arslan AA; Beane-Freeman L; Bracci PM; Brennan P; Bueno-de-Mesquita B; Buring J; Canzian F; Du M; Gallinger S; Gaziano JM; Goodman PJ; Gunter M; LeMarchand L; Li D; Neale RE; Peters U; Petersen GM; Risch HA; Sánchez MJ; Shu XO; Thornquist MD; Visvanathan K; Zheng W; Chanock SJ; Easton D; Wolpin BM; Stolzenberg-Solomon RZ; Klein AP; Amundadottir LT; Marti-Renom MA; Real FX; Malats N
    Genome Med; 2021 Feb; 13(1):15. PubMed ID: 33517887
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Annotating functional effects of non-coding variants in neuropsychiatric cell types by deep transfer learning.
    Lai B; Qian S; Zhang H; Zhang S; Kozlova A; Duan J; Xu J; He X
    PLoS Comput Biol; 2022 May; 18(5):e1010011. PubMed ID: 35576194
    [TBL] [Abstract][Full Text] [Related]  

  • 36. High-throughput identification of noncoding functional SNPs via type IIS enzyme restriction.
    Li G; Martínez-Bonet M; Wu D; Yang Y; Cui J; Nguyen HN; Cunin P; Levescot A; Bai M; Westra HJ; Okada Y; Brenner MB; Raychaudhuri S; Hendrickson EA; Maas RL; Nigrovic PA
    Nat Genet; 2018 Aug; 50(8):1180-1188. PubMed ID: 30013183
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Integrated Functional Genomic Analysis Enables Annotation of Kidney Genome-Wide Association Study Loci.
    Sieber KB; Batorsky A; Siebenthall K; Hudkins KL; Vierstra JD; Sullivan S; Sur A; McNulty M; Sandstrom R; Reynolds A; Bates D; Diegel M; Dunn D; Nelson J; Buckley M; Kaul R; Sampson MG; Himmelfarb J; Alpers CE; Waterworth D; Akilesh S
    J Am Soc Nephrol; 2019 Mar; 30(3):421-441. PubMed ID: 30760496
    [TBL] [Abstract][Full Text] [Related]  

  • 38. HiChIP-based Epigenomic Footprinting Identifies a Promoter Variant of UXS1 that Confers Genetic Susceptibility to Gastroesophageal Cancer.
    Gnanapragasam A; Kirbizakis E; Li A; White KH; Mortenson KL; Cavalcante de Moura J; Jawhar W; Yan Y; Falter R; Russett C; Giannias B; Camilleri-Broët S; Bertos N; Cools-Lartigue J; Garzia L; Sangwan V; Ferri LE; Zhang X; Bailey SD
    Cancer Res; 2024 May; ():. PubMed ID: 38748784
    [TBL] [Abstract][Full Text] [Related]  

  • 39. NetREm: Network Regression Embeddings reveal cell-type transcription factor coordination for gene regulation.
    Khullar S; Huang X; Ramesh R; Svaren J; Wang D
    bioRxiv; 2024 May; ():. PubMed ID: 37961577
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Motif-Raptor: a cell type-specific and transcription factor centric approach for post-GWAS prioritization of causal regulators.
    Yao Q; Ferragina P; Reshef Y; Lettre G; Bauer DE; Pinello L
    Bioinformatics; 2021 Aug; 37(15):2103-2111. PubMed ID: 33532840
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.