BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 29923336)

  • 1. Germline genetic variants were interactively associated with somatic alterations in gastric cancer.
    Zhang X; Wang Y; Tian T; Zhou G; Jin G
    Cancer Med; 2018 Aug; 7(8):3912-3920. PubMed ID: 29923336
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Interaction analysis between germline susceptibility loci and somatic alterations in lung cancer.
    Wang Y; Wang C; Zhang J; Zhu M; Zhang X; Li Z; Dai J; Ma H; Hu Z; Jin G; Shen H
    Int J Cancer; 2018 Aug; 143(4):878-885. PubMed ID: 29492964
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Interaction analysis between germline genetic variants and somatic mutations in head and neck cancer.
    Feng G; Feng H; Qi Y; Wang T; Ni N; Wu J; Yuan H
    Oral Oncol; 2022 May; 128():105859. PubMed ID: 35428027
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A computational approach to distinguish somatic vs. germline origin of genomic alterations from deep sequencing of cancer specimens without a matched normal.
    Sun JX; He Y; Sanford E; Montesion M; Frampton GM; Vignot S; Soria JC; Ross JS; Miller VA; Stephens PJ; Lipson D; Yelensky R
    PLoS Comput Biol; 2018 Feb; 14(2):e1005965. PubMed ID: 29415044
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Exome-wide analysis of bi-allelic alterations identifies a Lynch phenotype in The Cancer Genome Atlas.
    Buckley AR; Ideker T; Carter H; Harismendy O; Schork NJ
    Genome Med; 2018 Sep; 10(1):69. PubMed ID: 30217226
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Common Germline Risk Variants Impact Somatic Alterations and Clinical Features across Cancers.
    Namba S; Saito Y; Kogure Y; Masuda T; Bondy ML; Gharahkhani P; Gockel I; Heider D; Hillmer A; Jankowski J; MacGregor S; Maj C; Melin B; Ostrom QT; Palles C; Schumacher J; Tomlinson I; Whiteman DC; Okada Y; Kataoka K
    Cancer Res; 2023 Jan; 83(1):20-27. PubMed ID: 36286845
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Integrating germline and somatic variation information using genomic data for the discovery of biomarkers in prostate cancer.
    Mamidi TKK; Wu J; Hicks C
    BMC Cancer; 2019 Mar; 19(1):229. PubMed ID: 30871495
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genomic characterization of biliary tract cancers identifies driver genes and predisposing mutations.
    Wardell CP; Fujita M; Yamada T; Simbolo M; Fassan M; Karlic R; Polak P; Kim J; Hatanaka Y; Maejima K; Lawlor RT; Nakanishi Y; Mitsuhashi T; Fujimoto A; Furuta M; Ruzzenente A; Conci S; Oosawa A; Sasaki-Oku A; Nakano K; Tanaka H; Yamamoto Y; Michiaki K; Kawakami Y; Aikata H; Ueno M; Hayami S; Gotoh K; Ariizumi SI; Yamamoto M; Yamaue H; Chayama K; Miyano S; Getz G; Scarpa A; Hirano S; Nakamura T; Nakagawa H
    J Hepatol; 2018 May; 68(5):959-969. PubMed ID: 29360550
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Germline and Somatic Genetic Variants in the p53 Pathway Interact to Affect Cancer Risk, Progression, and Drug Response.
    Zhang P; Kitchen-Smith I; Xiong L; Stracquadanio G; Brown K; Richter PH; Wallace MD; Bond E; Sahgal N; Moore S; Nornes S; De Val S; Surakhy M; Sims D; Wang X; Bell DA; Zeron-Medina J; Jiang Y; Ryan AJ; Selfe JL; Shipley J; Kar S; Pharoah PD; Loveday C; Jansen R; Grochola LF; Palles C; Protheroe A; Millar V; Ebner DV; Pagadala M; Blagden SP; Maughan TS; Domingo E; Tomlinson I; Turnbull C; Carter H; Bond GL
    Cancer Res; 2021 Apr; 81(7):1667-1680. PubMed ID: 33558336
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Whole genome sequencing identifies rare germline variants enriched in cancer related genes in first degree relatives of familial pancreatic cancer patients.
    Tan M; Brusgaard K; Gerdes AM; Mortensen MB; Detlefsen S; Schaffalitzky de Muckadell OB; Joergensen MT
    Clin Genet; 2021 Nov; 100(5):551-562. PubMed ID: 34313325
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association Analysis of Driver Gene-Related Genetic Variants Identified Novel Lung Cancer Susceptibility Loci with 20,871 Lung Cancer Cases and 15,971 Controls.
    Wang Y; Gorlova OY; Gorlov IP; Zhu M; Dai J; Albanes D; Lam S; Tardon A; Chen C; Goodman GE; Bojesen SE; Landi MT; Johansson M; Risch A; Wichmann HE; Bickeboller H; Christiani DC; Rennert G; Arnold SM; Brennan P; Field JK; Shete S; Le Marchand L; Melander O; Brunnstrom H; Liu G; Hung RJ; Andrew AS; Kiemeney LA; Zienolddiny S; Grankvist K; Johansson M; Caporaso NE; Woll PJ; Lazarus P; Schabath MB; Aldrich MC; Stevens VL; Ma H; Jin G; Hu Z; Amos CI; Shen H
    Cancer Epidemiol Biomarkers Prev; 2020 Jul; 29(7):1423-1429. PubMed ID: 32277007
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Haplotype-resolved germline and somatic alterations in renal medullary carcinomas.
    Tan KT; Kim H; Carrot-Zhang J; Zhang Y; Kim WJ; Kugener G; Wala JA; Howard TP; Chi YY; Beroukhim R; Li H; Ha G; Alper SL; Perlman EJ; Mullen EA; Hahn WC; Meyerson M; Hong AL
    Genome Med; 2021 Jul; 13(1):114. PubMed ID: 34261517
    [TBL] [Abstract][Full Text] [Related]  

  • 14. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing.
    Koboldt DC; Zhang Q; Larson DE; Shen D; McLellan MD; Lin L; Miller CA; Mardis ER; Ding L; Wilson RK
    Genome Res; 2012 Mar; 22(3):568-76. PubMed ID: 22300766
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Allele-specific expression: applications in cancer and technical considerations.
    Robles-Espinoza CD; Mohammadi P; Bonilla X; Gutierrez-Arcelus M
    Curr Opin Genet Dev; 2021 Feb; 66():10-19. PubMed ID: 33383480
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exploring the link between germline and somatic genetic alterations in breast carcinogenesis.
    Bonifaci N; Górski B; Masojć B; Wokołorczyk D; Jakubowska A; Dębniak T; Berenguer A; Serra Musach J; Brunet J; Dopazo J; Narod SA; Lubiński J; Lázaro C; Cybulski C; Pujana MA
    PLoS One; 2010 Nov; 5(11):e14078. PubMed ID: 21124932
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations.
    Yehia L; Ni Y; Sesock K; Niazi F; Fletcher B; Chen HJL; LaFramboise T; Eng C
    PLoS Genet; 2018 Apr; 14(4):e1007352. PubMed ID: 29684080
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exome Array Analysis Identifies Variants in SPOCD1 and BTN3A2 That Affect Risk for Gastric Cancer.
    Zhu M; Yan C; Ren C; Huang X; Zhu X; Gu H; Wang M; Wang S; Gao Y; Ji Y; Miao X; Yang M; Chen J; Du J; Huang T; Jiang Y; Dai J; Ma H; Zhou J; Wang Z; Hu Z; Ji G; Zhang Z; Shen H; Shi Y; Jin G
    Gastroenterology; 2017 Jun; 152(8):2011-2021. PubMed ID: 28246015
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Constructing germline research cohorts from the discarded reads of clinical tumor sequences.
    Gusev A; Groha S; Taraszka K; Semenov YR; Zaitlen N
    Genome Med; 2021 Nov; 13(1):179. PubMed ID: 34749793
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A method to reduce ancestry related germline false positives in tumor only somatic variant calling.
    Halperin RF; Carpten JD; Manojlovic Z; Aldrich J; Keats J; Byron S; Liang WS; Russell M; Enriquez D; Claasen A; Cherni I; Awuah B; Oppong J; Wicha MS; Newman LA; Jaigge E; Kim S; Craig DW
    BMC Med Genomics; 2017 Oct; 10(1):61. PubMed ID: 29052513
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.