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.
264 related articles for article (PubMed ID: 35172496)
21. Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals. Kuusisto KM; Bebel A; Vihinen M; Schleutker J; Sallinen SL Breast Cancer Res; 2011 Feb; 13(1):R20. PubMed ID: 21356067 [TBL] [Abstract][Full Text] [Related]
22. Genetic Predisposition to Breast and Ovarian Cancers: How Many and Which Genes to Test? Angeli D; Salvi S; Tedaldi G Int J Mol Sci; 2020 Feb; 21(3):. PubMed ID: 32046255 [TBL] [Abstract][Full Text] [Related]
23. Pathogenicity Reclassification of Genetic Variants Related to Early-Onset Breast Cancer among Women of Mongoloid Origin. Gervas P; Molokov A; Babyshkina N; Kiselev A; Zarubin A; Yumov E; Pisareva L; Choynzonov E; Cherdyntseva N Asian Pac J Cancer Prev; 2022 Jun; 23(6):2027-2033. PubMed ID: 35763645 [TBL] [Abstract][Full Text] [Related]
24. Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria. Hoyer J; Vasileiou G; Uebe S; Wunderle M; Kraus C; Fasching PA; Thiel CT; Hartmann A; Beckmann MW; Lux MP; Reis A BMC Cancer; 2018 Sep; 18(1):926. PubMed ID: 30257646 [TBL] [Abstract][Full Text] [Related]
25. Clinical utility of hereditary cancer panel testing: Impact of PALB2, ATM, CHEK2, NBN, BRIP1, RAD51C, and RAD51D results on patient management and adherence to provider recommendations. Vysotskaia V; Kaseniit KE; Bucheit L; Ready K; Price K; Johansen Taber K Cancer; 2020 Feb; 126(3):549-558. PubMed ID: 31682005 [TBL] [Abstract][Full Text] [Related]
26. Prevalence of Pathogenic Germline Mutations in 13 Hereditary Cancer-Related Genes in Breast Cancer Patients in Narathiwat Province, Thailand. Sukpan P; Kanokwiroon K; Sriplung H; Laochareonsuk W; Choochuen P; Auseng N; Wanawanakorn K; Sangkhathat S Asian Pac J Cancer Prev; 2023 Feb; 24(2):525-530. PubMed ID: 36853301 [TBL] [Abstract][Full Text] [Related]
27. Contribution of Massive Parallel Sequencing to Diagnosis of Hereditary Ovarian Cancer in the Czech Republic. Soukupová J; Lhotová K; Zemánková P; Vočka M; Janatová M; Stolařová L; Borecká M; Kleiblová P; Macháčková E; Foretová L; Koudová M; Lhota F; Tavandzis S; Zikán M; Stránecký V; Veselá K; Panczak A; Kotlas J; Kleibl Z Klin Onkol; 2019; 32(Supplementum2):72-78. PubMed ID: 31409082 [TBL] [Abstract][Full Text] [Related]
28. Hereditary genes and SNPs associated with breast cancer. Mahdi KM; Nassiri MR; Nasiri K Asian Pac J Cancer Prev; 2013; 14(6):3403-9. PubMed ID: 23886119 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. Recurrent Mutations in Łukomska A; Menkiszak J; Gronwald J; Tomiczek-Szwiec J; Szwiec M; Jasiówka M; Blecharz P; Kluz T; Stawicka-Niełacna M; Mądry R; Białkowska K; Prajzendanc K; Kluźniak W; Cybulski C; Dębniak T; Huzarski T; Tołoczko-Grabarek A; Byrski T; Baszuk P; Narod SA; Lubiński J; Jakubowska A Cancers (Basel); 2021 Feb; 13(4):. PubMed ID: 33670479 [TBL] [Abstract][Full Text] [Related]
31. Frequency of Pathogenic Germline Mutations in Early and Late Onset Familial Breast Cancer Patients Using Multi-Gene Panel Sequencing: An Egyptian Study. Nassar A; Zekri AN; Kamel MM; Elberry MH; Lotfy MM; Seadawy MG; Hassan ZK; Soliman HK; Lymona AM; Youssef ASE Genes (Basel); 2022 Dec; 14(1):. PubMed ID: 36672847 [TBL] [Abstract][Full Text] [Related]
32. Clinical and genetic characterization of hereditary breast cancer in a Chinese population. Jian W; Shao K; Qin Q; Wang X; Song S; Wang X Hered Cancer Clin Pract; 2017; 15():19. PubMed ID: 29093764 [TBL] [Abstract][Full Text] [Related]
33. Time to incorporate germline multigene panel testing into breast and ovarian cancer patient care. Graffeo R; Livraghi L; Pagani O; Goldhirsch A; Partridge AH; Garber JE Breast Cancer Res Treat; 2016 Dec; 160(3):393-410. PubMed ID: 27734215 [TBL] [Abstract][Full Text] [Related]
34. Investigating the prevalence of pathogenic variants in Saudi Arabian patients with familial cancer using a multigene next generation sequencing panel. AlHarbi M; Mobark NA; AlJabarat WAR; ElBardis H; AlSolme E; Hamdan AB; AlFakeeh AH; AlMushawah F; AlHarthi F; AlSharm AA; Balbaid AAO; AlJohani N; Zhou AY; Robinson HA; Alqahtani SA; Abedalthagafi M Oncotarget; 2023 Jun; 14():580-594. PubMed ID: 37306523 [TBL] [Abstract][Full Text] [Related]
35. Evaluation of AlphaFold structure-based protein stability prediction on missense variations in cancer. Keskin Karakoyun H; Yüksel ŞK; Amanoglu I; Naserikhojasteh L; Yeşilyurt A; Yakıcıer C; Timuçin E; Akyerli CB Front Genet; 2023; 14():1052383. PubMed ID: 36896237 [TBL] [Abstract][Full Text] [Related]
36. Age of ovarian cancer diagnosis among BRIP1, RAD51C, and RAD51D mutation carriers identified through multi-gene panel testing. Cummings S; Roman SS; Saam J; Bernhisel R; Brown K; Lancaster JM; Usha L J Ovarian Res; 2021 Apr; 14(1):61. PubMed ID: 33926482 [TBL] [Abstract][Full Text] [Related]
37. Inherited DNA-repair gene mutations in African American men with prostate cancer. Sartor O; Yang S; Ledet E; Moses M; Nicolosi P Oncotarget; 2020 Jan; 11(4):440-442. PubMed ID: 32064047 [TBL] [Abstract][Full Text] [Related]
38. Mutations in ATM, NBN and BRCA2 predispose to aggressive prostate cancer in Poland. Wokołorczyk D; Kluźniak W; Huzarski T; Gronwald J; Szymiczek A; Rusak B; Stempa K; Gliniewicz K; Kashyap A; Morawska S; Dębniak T; Jakubowska A; Szwiec M; Domagała P; Lubiński J; Narod SA; Akbari MR; Cybulski C; Int J Cancer; 2020 Nov; 147(10):2793-2800. PubMed ID: 32875559 [TBL] [Abstract][Full Text] [Related]
39. Frequency of mutations in a large series of clinically ascertained ovarian cancer cases tested on multi-gene panels compared to reference controls. Lilyquist J; LaDuca H; Polley E; Davis BT; Shimelis H; Hu C; Hart SN; Dolinsky JS; Couch FJ; Goldgar DE Gynecol Oncol; 2017 Nov; 147(2):375-380. PubMed ID: 28888541 [TBL] [Abstract][Full Text] [Related]
40. Association of Family Cancer History With Pathogenic Variants in Specific Breast Cancer Susceptibility Genes. Kurian AW; Abrahamse P; Ward KC; Hamilton AS; Deapen D; Berek JS; Hoang L; Yussuf A; Dolinsky J; Brown K; Slavin T; Hofer TP; Katz SJ JCO Precis Oncol; 2021; 5():. PubMed ID: 34977446 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]