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 *

155 related articles for article (PubMed ID: 37547663)

  • 1. The Impact of Genomic Variation on Function (IGVF) Consortium.
    IGVF Consortium
    ArXiv; 2023 Jul; ():. PubMed ID: 37547663
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genome-wide enhancer maps link risk variants to disease genes.
    Nasser J; Bergman DT; Fulco CP; Guckelberger P; Doughty BR; Patwardhan TA; Jones TR; Nguyen TH; Ulirsch JC; Lekschas F; Mualim K; Natri HM; Weeks EM; Munson G; Kane M; Kang HY; Cui A; Ray JP; Eisenhaure TM; Collins RL; Dey K; Pfister H; Price AL; Epstein CB; Kundaje A; Xavier RJ; Daly MJ; Huang H; Finucane HK; Hacohen N; Lander ES; Engreitz JM
    Nature; 2021 May; 593(7858):238-243. PubMed ID: 33828297
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genomic approaches for understanding the genetics of complex disease.
    Lowe WL; Reddy TE
    Genome Res; 2015 Oct; 25(10):1432-41. PubMed ID: 26430153
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities.
    Falk MJ; Shen L; Gonzalez M; Leipzig J; Lott MT; Stassen AP; Diroma MA; Navarro-Gomez D; Yeske P; Bai R; Boles RG; Brilhante V; Ralph D; DaRe JT; Shelton R; Terry SF; Zhang Z; Copeland WC; van Oven M; Prokisch H; Wallace DC; Attimonelli M; Krotoski D; Zuchner S; Gai X; ; ; ; ; ;
    Mol Genet Metab; 2015 Mar; 114(3):388-96. PubMed ID: 25542617
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An encyclopedia of enhancer-gene regulatory interactions in the human genome.
    Gschwind AR; Mualim KS; Karbalayghareh A; Sheth MU; Dey KK; Jagoda E; Nurtdinov RN; Xi W; Tan AS; Jones H; Ma XR; Yao D; Nasser J; Avsec Ž; James BT; Shamim MS; Durand NC; Rao SSP; Mahajan R; Doughty BR; Andreeva K; Ulirsch JC; Fan K; Perez EM; Nguyen TC; Kelley DR; Finucane HK; Moore JE; Weng Z; Kellis M; Bassik MC; Price AL; Beer MA; Guigó R; Stamatoyannopoulos JA; Lieberman Aiden E; Greenleaf WJ; Leslie CS; Steinmetz LM; Kundaje A; Engreitz JM
    bioRxiv; 2023 Nov; ():. PubMed ID: 38014075
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Moving toward a system genetics view of disease.
    Sieberts SK; Schadt EE
    Mamm Genome; 2007 Jul; 18(6-7):389-401. PubMed ID: 17653589
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Disease-associated variants in different categories of disease located in distinct regulatory elements.
    Ma M; Ru Y; Chuang LS; Hsu NY; Shi LS; Hakenberg J; Cheng WY; Uzilov A; Ding W; Glicksberg BS; Chen R
    BMC Genomics; 2015; 16 Suppl 8(Suppl 8):S3. PubMed ID: 26110593
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Disease-associated genetic variants in the regulatory regions of human genes: mechanisms of action on transcription and genomic resources for dissecting these mechanisms.
    Ignatieva EV; Matrosova EA
    Vavilovskii Zhurnal Genet Selektsii; 2021 Feb; 25(1):18-29. PubMed ID: 34541447
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Annotation of functional variation in personal genomes using RegulomeDB.
    Boyle AP; Hong EL; Hariharan M; Cheng Y; Schaub MA; Kasowski M; Karczewski KJ; Park J; Hitz BC; Weng S; Cherry JM; Snyder M
    Genome Res; 2012 Sep; 22(9):1790-7. PubMed ID: 22955989
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The role of the toxicologic pathologist in the post-genomic era(#).
    Maronpot RR
    J Toxicol Pathol; 2013 Jun; 26(2):105-10. PubMed ID: 23914052
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Computational approaches to identify functional genetic variants in cancer genomes.
    Gonzalez-Perez A; Mustonen V; Reva B; Ritchie GR; Creixell P; Karchin R; Vazquez M; Fink JL; Kassahn KS; Pearson JV; Bader GD; Boutros PC; Muthuswamy L; Ouellette BF; Reimand J; Linding R; Shibata T; Valencia A; Butler A; Dronov S; Flicek P; Shannon NB; Carter H; Ding L; Sander C; Stuart JM; Stein LD; Lopez-Bigas N;
    Nat Methods; 2013 Aug; 10(8):723-9. PubMed ID: 23900255
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Balancing selection on genomic deletion polymorphisms in humans.
    Aqil A; Speidel L; Pavlidis P; Gokcumen O
    Elife; 2023 Jan; 12():. PubMed ID: 36625544
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Primary transcripts: From the discovery of RNA processing to current concepts of gene expression - Review.
    Scherrer K
    Exp Cell Res; 2018 Dec; 373(1-2):1-33. PubMed ID: 30266658
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of sequence determinants of enhancer function using natural genetic variation.
    Yang MG; Ling E; Cowley CJ; Greenberg ME; Vierbuchen T
    Elife; 2022 Aug; 11():. PubMed ID: 36043696
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness.
    Kowalczyk A; Chikina M; Clark N
    Elife; 2022 Nov; 11():. PubMed ID: 36342464
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Deep sequencing of Danish Holstein dairy cattle for variant detection and insight into potential loss-of-function variants in protein coding genes.
    Das A; Panitz F; Gregersen VR; Bendixen C; Holm LE
    BMC Genomics; 2015 Dec; 16():1043. PubMed ID: 26645365
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High-Resolution Regulatory Maps Connect Vascular Risk Variants to Disease-Related Pathways.
    Åkerborg Ö; Spalinskas R; Pradhananga S; Anil A; Höjer P; Poujade FA; Folkersen L; Eriksson PP; Sahlén P
    Circ Genom Precis Med; 2019 Mar; 12(3):e002353. PubMed ID: 30786239
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals.
    Battle A; Mostafavi S; Zhu X; Potash JB; Weissman MM; McCormick C; Haudenschild CD; Beckman KB; Shi J; Mei R; Urban AE; Montgomery SB; Levinson DF; Koller D
    Genome Res; 2014 Jan; 24(1):14-24. PubMed ID: 24092820
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prioritization of genes driving congenital phenotypes of patients with de novo genomic structural variants.
    Middelkamp S; Vlaar JM; Giltay J; Korzelius J; Besselink N; Boymans S; Janssen R; de la Fonteijne L; van Binsbergen E; van Roosmalen MJ; Hochstenbach R; Giachino D; Talkowski ME; Kloosterman WP; Cuppen E
    Genome Med; 2019 Dec; 11(1):79. PubMed ID: 31801603
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.