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 *

195 related articles for article (PubMed ID: 24885908)

  • 1. Changing genetic paradigms: creating next-generation genetic databases as tools to understand the emerging complexities of genotype/phenotype relationships.
    Gottlieb B; Beitel LK; Trifiro M
    Hum Genomics; 2014 May; 8(1):9. PubMed ID: 24885908
    [TBL] [Abstract][Full Text] [Related]  

  • 2. From phenotyping to genotyping - bioinformatics for the busy clinician.
    Reches A; Weiss K; Bazak L; Baris Feldman H; Maya I
    Eur J Med Genet; 2019 Aug; 62(8):103689. PubMed ID: 31226441
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gene mutation spectrum and genotype-phenotype correlation in a cohort of Chinese osteogenesis imperfecta patients revealed by targeted next generation sequencing.
    Liu Y; Asan ; Ma D; Lv F; Xu X; Wang J; Xia W; Jiang Y; Wang O; Xing X; Yu W; Wang J; Sun J; Song L; Zhu Y; Yang H; Wang J; Li M
    Osteoporos Int; 2017 Oct; 28(10):2985-2995. PubMed ID: 28725987
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotype-genotype comorbidity analysis of patients with rare disorders provides insight into their pathological and molecular bases.
    Díaz-Santiago E; Jabato FM; Rojano E; Seoane P; Pazos F; Perkins JR; Ranea JAG
    PLoS Genet; 2020 Oct; 16(10):e1009054. PubMed ID: 33001999
    [TBL] [Abstract][Full Text] [Related]  

  • 5. ncRPheno: a comprehensive database platform for identification and validation of disease related noncoding RNAs.
    Zhang W; Yao G; Wang J; Yang M; Wang J; Zhang H; Li W
    RNA Biol; 2020 Jul; 17(7):943-955. PubMed ID: 32122231
    [TBL] [Abstract][Full Text] [Related]  

  • 6. OPENING THE DOOR TO THE LARGE SCALE USE OF CLINICAL LAB MEASURES FOR ASSOCIATION TESTING: EXPLORING DIFFERENT METHODS FOR DEFINING PHENOTYPES.
    Bauer CR; Lavage D; Snyder J; Leader J; Mahoney JM; Pendergrass SA
    Pac Symp Biocomput; 2017; 22():356-367. PubMed ID: 27896989
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotype databases for genetic screens in human cells.
    Rauscher B; Valentini E; Hardeland U; Boutros M
    J Biotechnol; 2017 Nov; 261():63-69. PubMed ID: 28625679
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Bioinformatics for personal genome interpretation.
    Capriotti E; Nehrt NL; Kann MG; Bromberg Y
    Brief Bioinform; 2012 Jul; 13(4):495-512. PubMed ID: 22247263
    [TBL] [Abstract][Full Text] [Related]  

  • 9. VarElect: the phenotype-based variation prioritizer of the GeneCards Suite.
    Stelzer G; Plaschkes I; Oz-Levi D; Alkelai A; Olender T; Zimmerman S; Twik M; Belinky F; Fishilevich S; Nudel R; Guan-Golan Y; Warshawsky D; Dahary D; Kohn A; Mazor Y; Kaplan S; Iny Stein T; Baris HN; Rappaport N; Safran M; Lancet D
    BMC Genomics; 2016 Jun; 17 Suppl 2(Suppl 2):444. PubMed ID: 27357693
    [TBL] [Abstract][Full Text] [Related]  

  • 10. AraPheno and the AraGWAS Catalog 2020: a major database update including RNA-Seq and knockout mutation data for Arabidopsis thaliana.
    Togninalli M; Seren Ü; Freudenthal JA; Monroe JG; Meng D; Nordborg M; Weigel D; Borgwardt K; Korte A; Grimm DG
    Nucleic Acids Res; 2020 Jan; 48(D1):D1063-D1068. PubMed ID: 31642487
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genotype-based databases for variants causing rare diseases.
    Lanthaler B; Wieser S; Deutschmann A; Schossig A; Fauth C; Zschocke J; Witsch-Baumgartner M
    Gene; 2014 Oct; 550(1):136-40. PubMed ID: 25111118
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Dual Model for Prioritizing Cancer Mutations in the Non-coding Genome Based on Germline and Somatic Events.
    Li J; Poursat MA; Drubay D; Motz A; Saci Z; Morillon A; Michiels S; Gautheret D
    PLoS Comput Biol; 2015 Nov; 11(11):e1004583. PubMed ID: 26588488
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Transgenerational inheritance: how impacts to the epigenetic and genetic information of parents affect offspring health.
    Xavier MJ; Roman SD; Aitken RJ; Nixon B
    Hum Reprod Update; 2019 Sep; 25(5):518-540. PubMed ID: 31374565
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic Determinants of Epigenetic Patterns: Providing Insight into Disease.
    Cazaly E; Charlesworth J; Dickinson JL; Holloway AF
    Mol Med; 2015 Mar; 21(1):400-9. PubMed ID: 25822796
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Applications of bioinformatics to non-coding RNAs in the era of next-generation sequencing.
    Cheng C; Moore J; Greene C
    Pac Symp Biocomput; 2014; ():412-6. PubMed ID: 24297566
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Phenotype-loci associations in networks of patients with rare disorders: application to assist in the diagnosis of novel clinical cases.
    Bueno A; Rodríguez-López R; Reyes-Palomares A; Rojano E; Corpas M; Nevado J; Lapunzina P; Sánchez-Jiménez F; Ranea JAG
    Eur J Hum Genet; 2018 Oct; 26(10):1451-1461. PubMed ID: 29946186
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CNCDatabase: a database of non-coding cancer drivers.
    Liu EM; Martinez-Fundichely A; Bollapragada R; Spiewack M; Khurana E
    Nucleic Acids Res; 2021 Jan; 49(D1):D1094-D1101. PubMed ID: 33095860
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Detecting statistical interaction between somatic mutational events and germline variation from next-generation sequence data.
    Hu H; Huff CD
    Pac Symp Biocomput; 2014; ():51-62. PubMed ID: 24297533
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Impact of germline and somatic missense variations on drug binding sites.
    Yan C; Pattabiraman N; Goecks J; Lam P; Nayak A; Pan Y; Torcivia-Rodriguez J; Voskanian A; Wan Q; Mazumder R
    Pharmacogenomics J; 2017 Mar; 17(2):128-136. PubMed ID: 26810135
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 10.