130 related articles for article (PubMed ID: 35428027)
1. 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]
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. 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]
4. Germline variants in DNA repair genes are associated with young-onset head and neck cancer.
Cury SS; Miranda PM; Marchi FA; Canto LMD; Chulam TC; Petersen AH; Aagaard MM; Pinto CAL; Kowalski LP; Rogatto SR
Oral Oncol; 2021 Nov; 122():105545. PubMed ID: 34598035
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.
Currás-Freixes M; Inglada-Pérez L; Mancikova V; Montero-Conde C; Letón R; Comino-Méndez I; Apellániz-Ruiz M; Sánchez-Barroso L; Aguirre Sánchez-Covisa M; Alcázar V; Aller J; Álvarez-Escolá C; Andía-Melero VM; Azriel-Mira S; Calatayud-Gutiérrez M; Díaz JÁ; Díez-Hernández A; Lamas-Oliveira C; Marazuela M; Matias-Guiu X; Meoro-Avilés A; Patiño-García A; Pedrinaci S; Riesco-Eizaguirre G; Sábado-Álvarez C; Sáez-Villaverde R; Sainz de Los Terreros A; Sanz Guadarrama Ó; Sastre-Marcos J; Scolá-Yurrita B; Segura-Huerta Á; Serrano-Corredor Mde L; Villar-Vicente MR; Rodríguez-Antona C; Korpershoek E; Cascón A; Robledo M
J Med Genet; 2015 Oct; 52(10):647-56. PubMed ID: 26269449
[TBL] [Abstract][Full Text] [Related]
9. Germline mutation in RNASEL predicts increased risk of head and neck, uterine cervix and breast cancer.
Madsen BE; Ramos EM; Boulard M; Duda K; Overgaard J; Nordsmark M; Wiuf C; Hansen LL
PLoS One; 2008 Jun; 3(6):e2492. PubMed ID: 18575592
[TBL] [Abstract][Full Text] [Related]
10. A Multiethnic Germline-Somatic Association Database Deciphers Multilayered and Interconnected Genetic Mutations in Cancer.
Xin J; Mo Z; Chai R; Hua W; Wang J
Cancer Res; 2024 Feb; 84(3):364-371. PubMed ID: 38016109
[TBL] [Abstract][Full Text] [Related]
11. Integrating Germline and Somatic Mutation Information for the Discovery of Biomarkers in Triple-Negative Breast Cancer.
Wu J; Mamidi TKK; Zhang L; Hicks C
Int J Environ Res Public Health; 2019 Mar; 16(6):. PubMed ID: 30909550
[TBL] [Abstract][Full Text] [Related]
12. Association between germline variants and somatic mutations in colorectal cancer.
Barfield R; Qu C; Steinfelder RS; Zeng C; Harrison TA; Brezina S; Buchanan DD; Campbell PT; Casey G; Gallinger S; Giannakis M; Gruber SB; Gsur A; Hsu L; Huyghe JR; Moreno V; Newcomb PA; Ogino S; Phipps AI; Slattery ML; Thibodeau SN; Trinh QM; Toland AE; Hudson TJ; Sun W; Zaidi SH; Peters U
Sci Rep; 2022 Jun; 12(1):10207. PubMed ID: 35715570
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. NF-κB1 Intronic Region Polymorphisms as Risk Factor for Head and Neck Cancer in HPV-Infected Population from Pakistan.
Sarwar S; Tareen MU; Sabir M; Sultan A; Malik SA
Curr Mol Med; 2022; 22(1):74-82. PubMed ID: 33653249
[TBL] [Abstract][Full Text] [Related]
16. Codon-level co-occurrences of germline variants and somatic mutations in cancer are rare but often lead to incorrect variant annotation and underestimated impact prediction.
Koire A; Kim YW; Wang J; Katsonis P; Jin H; Lichtarge O
PLoS One; 2017; 12(3):e0174766. PubMed ID: 28350864
[TBL] [Abstract][Full Text] [Related]
17. Comprehensive Study of Germline Mutations and Double-Hit Events in Esophageal Squamous Cell Cancer.
Zeng B; Huang P; Du P; Sun X; Huang X; Fang X; Li L
Front Oncol; 2021; 11():637431. PubMed ID: 33889545
[TBL] [Abstract][Full Text] [Related]
18. Frequency of pathogenic germline variants in cancer susceptibility genes in 1336 renal cell carcinoma cases.
Yngvadottir B; Andreou A; Bassaganyas L; Larionov A; Cornish AJ; Chubb D; Saunders CN; Smith PS; Zhang H; Cole Y; Research Consortium GE; Larkin J; Browning L; Turajlic S; Litchfield K; Houlston RS; Maher ER
Hum Mol Genet; 2022 Aug; 31(17):3001-3011. PubMed ID: 35441217
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Integrative and comparative genomic analysis of HPV-positive and HPV-negative head and neck squamous cell carcinomas.
Seiwert TY; Zuo Z; Keck MK; Khattri A; Pedamallu CS; Stricker T; Brown C; Pugh TJ; Stojanov P; Cho J; Lawrence MS; Getz G; Brägelmann J; DeBoer R; Weichselbaum RR; Langerman A; Portugal L; Blair E; Stenson K; Lingen MW; Cohen EE; Vokes EE; White KP; Hammerman PS
Clin Cancer Res; 2015 Feb; 21(3):632-41. PubMed ID: 25056374
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
