BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

442 related articles for article (PubMed ID: 32596782)

  • 21. Actionable Genes, Core Databases, and Locus-Specific Databases.
    Pinard A; Miltgen M; Blanchard A; Mathieu H; Desvignes JP; Salgado D; Fabre A; Arnaud P; Barré L; Krahn M; Grandval P; Olschwang S; Zaffran S; Boileau C; Béroud C; Collod-Béroud G
    Hum Mutat; 2016 Dec; 37(12):1299-1307. PubMed ID: 27600092
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Pitfalls in the interpretation of CFTR variants in the context of incidental findings.
    Boussaroque A; Bergougnoux A; Raynal C; Audrézet MP; Sasorith S; Férec C; Bienvenu T; Girodon E
    Hum Mutat; 2019 Dec; 40(12):2239-2246. PubMed ID: 31350925
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Pathway networks generated from human disease phenome.
    Cirincione AG; Clark KL; Kann MG
    BMC Med Genomics; 2018 Sep; 11(Suppl 3):75. PubMed ID: 30255817
    [TBL] [Abstract][Full Text] [Related]  

  • 24. HAEdb: a novel interactive, locus-specific mutation database for the C1 inhibitor gene.
    Kalmár L; Hegedüs T; Farkas H; Nagy M; Tordai A
    Hum Mutat; 2005 Jan; 25(1):1-5. PubMed ID: 15580551
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Ten years of DICER1 mutations: Provenance, distribution, and associated phenotypes.
    de Kock L; Wu MK; Foulkes WD
    Hum Mutat; 2019 Nov; 40(11):1939-1953. PubMed ID: 31342592
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project.
    Cotton RG; Al Aqeel AI; Al-Mulla F; Carrera P; Claustres M; Ekong R; Hyland VJ; Macrae FA; Marafie MJ; Paalman MH; Patrinos GP; Qi M; Ramesar RS; Scott RJ; Sijmons RH; Sobrido MJ; Vihinen M;
    Genet Med; 2009 Dec; 11(12):843-9. PubMed ID: 20010362
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database.
    Peltomäki P; Vasen H
    Dis Markers; 2004; 20(4-5):269-76. PubMed ID: 15528792
    [TBL] [Abstract][Full Text] [Related]  

  • 28. DNA mutation motifs in the genes associated with inherited diseases.
    Růžička M; Kulhánek P; Radová L; Čechová A; Špačková N; Fajkusová L; Réblová K
    PLoS One; 2017; 12(8):e0182377. PubMed ID: 28767725
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics.
    Cooper DN; Chen JM; Ball EV; Howells K; Mort M; Phillips AD; Chuzhanova N; Krawczak M; Kehrer-Sawatzki H; Stenson PD
    Hum Mutat; 2010 Jun; 31(6):631-55. PubMed ID: 20506564
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Epimutations and cancer predisposition: importance and mechanisms.
    Hesson LB; Hitchins MP; Ward RL
    Curr Opin Genet Dev; 2010 Jun; 20(3):290-8. PubMed ID: 20359882
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multiple endocrine neoplasia type 1 (MEN1): An update of 208 new germline variants reported in the last nine years.
    Concolino P; Costella A; Capoluongo E
    Cancer Genet; 2016; 209(1-2):36-41. PubMed ID: 26767918
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Saccharomyces genome database informs human biology.
    Skrzypek MS; Nash RS; Wong ED; MacPherson KA; Hellerstedt ST; Engel SR; Karra K; Weng S; Sheppard TK; Binkley G; Simison M; Miyasato SR; Cherry JM
    Nucleic Acids Res; 2018 Jan; 46(D1):D736-D742. PubMed ID: 29140510
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Substantial batch effects in TCGA exome sequences undermine pan-cancer analysis of germline variants.
    Rasnic R; Brandes N; Zuk O; Linial M
    BMC Cancer; 2019 Aug; 19(1):783. PubMed ID: 31391007
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing.
    Mandelker D; Zhang L; Kemel Y; Stadler ZK; Joseph V; Zehir A; Pradhan N; Arnold A; Walsh MF; Li Y; Balakrishnan AR; Syed A; Prasad M; Nafa K; Carlo MI; Cadoo KA; Sheehan M; Fleischut MH; Salo-Mullen E; Trottier M; Lipkin SM; Lincoln A; Mukherjee S; Ravichandran V; Cambria R; Galle J; Abida W; Arcila ME; Benayed R; Shah R; Yu K; Bajorin DF; Coleman JA; Leach SD; Lowery MA; Garcia-Aguilar J; Kantoff PW; Sawyers CL; Dickler MN; Saltz L; Motzer RJ; O'Reilly EM; Scher HI; Baselga J; Klimstra DS; Solit DB; Hyman DM; Berger MF; Ladanyi M; Robson ME; Offit K
    JAMA; 2017 Sep; 318(9):825-835. PubMed ID: 28873162
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Kidney gene database: a curated and integrated database of genes involved in kidney disease.
    Zhao H; Li LC; Okino ST; Kane CJ; Carroll PR; Dahiya R
    J Urol; 2004 Dec; 172(6 Pt 1):2344-6. PubMed ID: 15538263
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Go!Poly: A gene-oriented polymorphism database.
    Zhang G; Zhang S; Chen W; Qiu W; Wu H; Wang J; Luo J; Gu X; Cotton RG
    Hum Mutat; 2001 Nov; 18(5):382-7. PubMed ID: 11668631
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Revealing the human mutome.
    Chen JM; Férec C; Cooper DN
    Clin Genet; 2010 Oct; 78(4):310-20. PubMed ID: 20569258
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Characterization of germline mutations in familial lung cancer from the Chinese population.
    Kanwal M; Ding XJ; Ma ZH; Li LW; Wang P; Chen Y; Huang YC; Cao Y
    Gene; 2018 Jan; 641():94-104. PubMed ID: 29054765
    [TBL] [Abstract][Full Text] [Related]  

  • 39. ssSNPTarget: genome-wide splice-site Single Nucleotide Polymorphism database.
    Yang JO; Kim WY; Bhak J
    Hum Mutat; 2009 Dec; 30(12):E1010-20. PubMed ID: 19760752
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancers.
    Lipkin SM; Wang V; Stoler DL; Anderson GR; Kirsch I; Hadley D; Lynch HT; Collins FS
    Hum Mutat; 2001 May; 17(5):389-96. PubMed ID: 11317354
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 23.