165 related articles for article (PubMed ID: 27197284)
1. Association of Common Susceptibility Variants of Pancreatic Cancer in Higher-Risk Patients: A PACGENE Study.
Childs EJ; Chaffee KG; Gallinger S; Syngal S; Schwartz AG; Cote ML; Bondy ML; Hruban RH; Chanock SJ; Hoover RN; Fuchs CS; Rider DN; Amundadottir LT; Stolzenberg-Solomon R; Wolpin BM; Risch HA; Goggins MG; Petersen GM; Klein AP
Cancer Epidemiol Biomarkers Prev; 2016 Jul; 25(7):1185-91. PubMed ID: 27197284
[TBL] [Abstract][Full Text] [Related]
2. Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer.
Childs EJ; Mocci E; Campa D; Bracci PM; Gallinger S; Goggins M; Li D; Neale RE; Olson SH; Scelo G; Amundadottir LT; Bamlet WR; Bijlsma MF; Blackford A; Borges M; Brennan P; Brenner H; Bueno-de-Mesquita HB; Canzian F; Capurso G; Cavestro GM; Chaffee KG; Chanock SJ; Cleary SP; Cotterchio M; Foretova L; Fuchs C; Funel N; Gazouli M; Hassan M; Herman JM; Holcatova I; Holly EA; Hoover RN; Hung RJ; Janout V; Key TJ; Kupcinskas J; Kurtz RC; Landi S; Lu L; Malecka-Panas E; Mambrini A; Mohelnikova-Duchonova B; Neoptolemos JP; Oberg AL; Orlow I; Pasquali C; Pezzilli R; Rizzato C; Saldia A; Scarpa A; Stolzenberg-Solomon RZ; Strobel O; Tavano F; Vashist YK; Vodicka P; Wolpin BM; Yu H; Petersen GM; Risch HA; Klein AP
Nat Genet; 2015 Aug; 47(8):911-6. PubMed ID: 26098869
[TBL] [Abstract][Full Text] [Related]
3. Statewide Retrospective Review of Familial Pancreatic Cancer in Delaware, and Frequency of Genetic Mutations in Pancreatic Cancer Kindreds.
Catts ZA; Baig MK; Milewski B; Keywan C; Guarino M; Petrelli N
Ann Surg Oncol; 2016 May; 23(5):1729-35. PubMed ID: 26727920
[TBL] [Abstract][Full Text] [Related]
4. Identification of germline genetic mutations in patients with pancreatic cancer.
Salo-Mullen EE; O'Reilly EM; Kelsen DP; Ashraf AM; Lowery MA; Yu KH; Reidy DL; Epstein AS; Lincoln A; Saldia A; Jacobs LM; Rau-Murthy R; Zhang L; Kurtz RC; Saltz L; Offit K; Robson ME; Stadler ZK
Cancer; 2015 Dec; 121(24):4382-8. PubMed ID: 26440929
[TBL] [Abstract][Full Text] [Related]
5. Mutation analysis of the PALB2 gene in unselected pancreatic cancer patients in the Czech Republic.
Borecka M; Zemankova P; Vocka M; Soucek P; Soukupova J; Kleiblova P; Sevcik J; Kleibl Z; Janatova M
Cancer Genet; 2016 May; 209(5):199-204. PubMed ID: 27106063
[TBL] [Abstract][Full Text] [Related]
6. The Role of
Pilarski R
Am Soc Clin Oncol Educ Book; 2019 Jan; 39():79-86. PubMed ID: 31099688
[TBL] [Abstract][Full Text] [Related]
7. Association of breast cancer susceptibility variants with risk of pancreatic cancer.
Couch FJ; Wang X; McWilliams RR; Bamlet WR; de Andrade M; Petersen GM
Cancer Epidemiol Biomarkers Prev; 2009 Nov; 18(11):3044-8. PubMed ID: 19843670
[TBL] [Abstract][Full Text] [Related]
8. PALB2 analysis in BRCA2-like families.
Adank MA; van Mil SE; Gille JJ; Waisfisz Q; Meijers-Heijboer H
Breast Cancer Res Treat; 2011 Jun; 127(2):357-62. PubMed ID: 20582465
[TBL] [Abstract][Full Text] [Related]
9. Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic Cancer.
Hu C; Hart SN; Polley EC; Gnanaolivu R; Shimelis H; Lee KY; Lilyquist J; Na J; Moore R; Antwi SO; Bamlet WR; Chaffee KG; DiCarlo J; Wu Z; Samara R; Kasi PM; McWilliams RR; Petersen GM; Couch FJ
JAMA; 2018 Jun; 319(23):2401-2409. PubMed ID: 29922827
[TBL] [Abstract][Full Text] [Related]
10. Inherited predisposition to pancreatic adenocarcinoma: role of family history and germ-line p16, BRCA1, and BRCA2 mutations.
Lal G; Liu G; Schmocker B; Kaurah P; Ozcelik H; Narod SA; Redston M; Gallinger S
Cancer Res; 2000 Jan; 60(2):409-16. PubMed ID: 10667595
[TBL] [Abstract][Full Text] [Related]
11. BRCA2 germline mutations in familial pancreatic carcinoma.
Hahn SA; Greenhalf B; Ellis I; Sina-Frey M; Rieder H; Korte B; Gerdes B; Kress R; Ziegler A; Raeburn JA; Campra D; Grützmann R; Rehder H; Rothmund M; Schmiegel W; Neoptolemos JP; Bartsch DK
J Natl Cancer Inst; 2003 Feb; 95(3):214-21. PubMed ID: 12569143
[TBL] [Abstract][Full Text] [Related]
12. DNA mismatch repair network gene polymorphism as a susceptibility factor for pancreatic cancer.
Dong X; Li Y; Chang P; Hess KR; Abbruzzese JL; Li D
Mol Carcinog; 2012 Jun; 51(6):491-9. PubMed ID: 21681824
[TBL] [Abstract][Full Text] [Related]
13. Variants associated with susceptibility to pancreatic cancer and melanoma do not reciprocally affect risk.
Wu L; Goldstein AM; Yu K; Yang XR; Rabe KG; Arslan AA; Canzian F; Wolpin BM; Stolzenberg-Solomon R; Amundadottir LT; Petersen GM
Cancer Epidemiol Biomarkers Prev; 2014 Jun; 23(6):1121-4. PubMed ID: 24642353
[TBL] [Abstract][Full Text] [Related]
14. Evaluation of the contribution of the three breast cancer susceptibility genes CHEK2, STK11, and PALB2 in non-BRCA1/2 French Canadian families with high risk of breast cancer.
Guénard F; Pedneault CS; Ouellette G; Labrie Y; Simard J; ; Durocher F
Genet Test Mol Biomarkers; 2010 Aug; 14(4):515-26. PubMed ID: 20722467
[TBL] [Abstract][Full Text] [Related]
15. Polymorphic variants in hereditary pancreatic cancer genes are not associated with pancreatic cancer risk.
McWilliams RR; Bamlet WR; de Andrade M; Rider DN; Couch FJ; Cunningham JM; Matsumoto ME; Rabe KG; Hammer TJ; Petersen GM
Cancer Epidemiol Biomarkers Prev; 2009 Sep; 18(9):2549-52. PubMed ID: 19690177
[TBL] [Abstract][Full Text] [Related]
16. Low penetrance breast cancer predisposition SNPs are site specific.
Mcinerney N; Colleran G; Rowan A; Walther A; Barclay E; Spain S; Jones AM; Tuohy S; Curran C; Miller N; Kerin M; Tomlinson I; Sawyer E
Breast Cancer Res Treat; 2009 Sep; 117(1):151-9. PubMed ID: 19005751
[TBL] [Abstract][Full Text] [Related]
17. Genetic variants of the peroxisome proliferator-activated receptor (PPAR) signaling pathway genes and risk of pancreatic cancer.
Liu X; Qian D; Liu H; Abbruzzese JL; Luo S; Walsh KM; Wei Q
Mol Carcinog; 2020 Aug; 59(8):930-939. PubMed ID: 32367578
[TBL] [Abstract][Full Text] [Related]
18. Common variants in mismatch repair genes and risk of invasive ovarian cancer.
Song H; Ramus SJ; Quaye L; DiCioccio RA; Tyrer J; Lomas E; Shadforth D; Hogdall E; Hogdall C; McGuire V; Whittemore AS; Easton DF; Ponder BA; Kjaer SK; Pharoah PD; Gayther SA
Carcinogenesis; 2006 Nov; 27(11):2235-42. PubMed ID: 16774946
[TBL] [Abstract][Full Text] [Related]
19. The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes.
Slavin TP; Neuhausen SL; Nehoray B; Niell-Swiller M; Solomon I; Rybak C; Blazer K; Adamson A; Yang K; Sand S; Guerrero-Llamas N; Castillo D; Herzog J; Wu X; Tao S; Raja S; Chung V; Singh G; Nadesan S; Brown S; Cruz-Correa M; Petersen GM; Weitzel J;
Fam Cancer; 2018 Apr; 17(2):235-245. PubMed ID: 28687971
[TBL] [Abstract][Full Text] [Related]
20. Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
Michailidou K; Hall P; Gonzalez-Neira A; Ghoussaini M; Dennis J; Milne RL; Schmidt MK; Chang-Claude J; Bojesen SE; Bolla MK; Wang Q; Dicks E; Lee A; Turnbull C; Rahman N; ; Fletcher O; Peto J; Gibson L; Dos Santos Silva I; Nevanlinna H; Muranen TA; Aittomäki K; Blomqvist C; Czene K; Irwanto A; Liu J; Waisfisz Q; Meijers-Heijboer H; Adank M; ; van der Luijt RB; Hein R; Dahmen N; Beckman L; Meindl A; Schmutzler RK; Müller-Myhsok B; Lichtner P; Hopper JL; Southey MC; Makalic E; Schmidt DF; Uitterlinden AG; Hofman A; Hunter DJ; Chanock SJ; Vincent D; Bacot F; Tessier DC; Canisius S; Wessels LF; Haiman CA; Shah M; Luben R; Brown J; Luccarini C; Schoof N; Humphreys K; Li J; Nordestgaard BG; Nielsen SF; Flyger H; Couch FJ; Wang X; Vachon C; Stevens KN; Lambrechts D; Moisse M; Paridaens R; Christiaens MR; Rudolph A; Nickels S; Flesch-Janys D; Johnson N; Aitken Z; Aaltonen K; Heikkinen T; Broeks A; Veer LJ; van der Schoot CE; Guénel P; Truong T; Laurent-Puig P; Menegaux F; Marme F; Schneeweiss A; Sohn C; Burwinkel B; Zamora MP; Perez JI; Pita G; Alonso MR; Cox A; Brock IW; Cross SS; Reed MW; Sawyer EJ; Tomlinson I; Kerin MJ; Miller N; Henderson BE; Schumacher F; Le Marchand L; Andrulis IL; Knight JA; Glendon G; Mulligan AM; ; ; Lindblom A; Margolin S; Hooning MJ; Hollestelle A; van den Ouweland AM; Jager A; Bui QM; Stone J; Dite GS; Apicella C; Tsimiklis H; Giles GG; Severi G; Baglietto L; Fasching PA; Haeberle L; Ekici AB; Beckmann MW; Brenner H; Müller H; Arndt V; Stegmaier C; Swerdlow A; Ashworth A; Orr N; Jones M; Figueroa J; Lissowska J; Brinton L; Goldberg MS; Labrèche F; Dumont M; Winqvist R; Pylkäs K; Jukkola-Vuorinen A; Grip M; Brauch H; Hamann U; Brüning T; ; Radice P; Peterlongo P; Manoukian S; Bonanni B; Devilee P; Tollenaar RA; Seynaeve C; van Asperen CJ; Jakubowska A; Lubinski J; Jaworska K; Durda K; Mannermaa A; Kataja V; Kosma VM; Hartikainen JM; Bogdanova NV; Antonenkova NN; Dörk T; Kristensen VN; Anton-Culver H; Slager S; Toland AE; Edge S; Fostira F; Kang D; Yoo KY; Noh DY; Matsuo K; Ito H; Iwata H; Sueta A; Wu AH; Tseng CC; Van Den Berg D; Stram DO; Shu XO; Lu W; Gao YT; Cai H; Teo SH; Yip CH; Phuah SY; Cornes BK; Hartman M; Miao H; Lim WY; Sng JH; Muir K; Lophatananon A; Stewart-Brown S; Siriwanarangsan P; Shen CY; Hsiung CN; Wu PE; Ding SL; Sangrajrang S; Gaborieau V; Brennan P; McKay J; Blot WJ; Signorello LB; Cai Q; Zheng W; Deming-Halverson S; Shrubsole M; Long J; Simard J; Garcia-Closas M; Pharoah PD; Chenevix-Trench G; Dunning AM; Benitez J; Easton DF
Nat Genet; 2013 Apr; 45(4):353-61, 361e1-2. PubMed ID: 23535729
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
