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.
191 related articles for article (PubMed ID: 36605468)
1. Genetic, Surgical and Oncological Approach to Breast Cancer, with Subaşıoğlu A; Güç ZG; Gür EÖ; Tekindal MA; Atahan MK Eur J Breast Health; 2023 Jan; 19(1):55-69. PubMed ID: 36605468 [TBL] [Abstract][Full Text] [Related]
2. Prevalence and spectrum of germline rare variants in BRCA1/2 and PALB2 among breast cancer cases in Sarawak, Malaysia. Yang XR; Devi BCR; Sung H; Guida J; Mucaki EJ; Xiao Y; Best A; Garland L; Xie Y; Hu N; Rodriguez-Herrera M; Wang C; Jones K; Luo W; Hicks B; Tang TS; Moitra K; Rogan PK; Dean M Breast Cancer Res Treat; 2017 Oct; 165(3):687-697. PubMed ID: 28664506 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Detection of Germline Variants in 450 Breast/Ovarian Cancer Families with a Multi-Gene Panel Including Coding and Regulatory Regions. Guglielmi C; Scarpitta R; Gambino G; Conti E; Bellè F; Tancredi M; Cervelli T; Falaschi E; Cosini C; Aretini P; Congregati C; Marino M; Patruno M; Pilato B; Spina F; Balestrino L; Tenedini E; Carnevali I; Cortesi L; Tagliafico E; Tibiletti MG; Tommasi S; Ghilli M; Vivanet C; Galli A; Caligo MA Int J Mol Sci; 2021 Jul; 22(14):. PubMed ID: 34299313 [TBL] [Abstract][Full Text] [Related]
5. Frequency of pathogenic germline variants in BRCA1, BRCA2, PALB2, CHEK2 and TP53 in ductal carcinoma in situ diagnosed in women under the age of 50 years. Petridis C; Arora I; Shah V; Megalios A; Moss C; Mera A; Clifford A; Gillett C; Pinder SE; Tomlinson I; Roylance R; Simpson MA; Sawyer EJ Breast Cancer Res; 2019 May; 21(1):58. PubMed ID: 31060593 [TBL] [Abstract][Full Text] [Related]
6. Inherited breast cancer predisposition in Asians: multigene panel testing outcomes from Singapore. Wong ESY; Shekar S; Met-Domestici M; Chan C; Sze M; Yap YS; Rozen SG; Tan MH; Ang P; Ngeow J; Lee ASG NPJ Genom Med; 2016; 1():15003. PubMed ID: 29263802 [TBL] [Abstract][Full Text] [Related]
7. Germline Kwong A; Shin VY; Ho CYS; Khalid A; Au CH; Chan KKL; Ngan HYS; Chan TL; Ma ESK Cancers (Basel); 2021 Aug; 13(16):. PubMed ID: 34439348 [TBL] [Abstract][Full Text] [Related]
8. Under-ascertainment of breast cancer susceptibility gene carriers in a cohort of New Zealand female breast cancer patients. Lattimore V; Parsons MT; Spurdle AB; Pearson J; Lehnert K; Sullivan J; Lintott C; Bawden S; Morrin H; Robinson B; Walker L Breast Cancer Res Treat; 2021 Feb; 185(3):583-590. PubMed ID: 33113089 [TBL] [Abstract][Full Text] [Related]
9. Frequency of Pathogenic Germline Variants in Petridis C; Arora I; Shah V; Moss CL; Mera A; Clifford A; Gillett C; Pinder SE; Tomlinson I; Roylance R; Simpson MA; Sawyer EJ Cancer Epidemiol Biomarkers Prev; 2019 Jul; 28(7):1162-1168. PubMed ID: 31263054 [TBL] [Abstract][Full Text] [Related]
10. High frequency of pathogenic non-founder germline mutations in Maksimenko J; Irmejs A; Trofimovičs G; Bērziņa D; Skuja E; Purkalne G; Miklaševičs E; Gardovskis J Hered Cancer Clin Pract; 2018; 16():12. PubMed ID: 29928469 [TBL] [Abstract][Full Text] [Related]
11. Pathogenic and likely pathogenic variants in PALB2, CHEK2, and other known breast cancer susceptibility genes among 1054 BRCA-negative Hispanics with breast cancer. Weitzel JN; Neuhausen SL; Adamson A; Tao S; Ricker C; Maoz A; Rosenblatt M; Nehoray B; Sand S; Steele L; Unzeitig G; Feldman N; Blanco AM; Hu D; Huntsman S; Castillo D; Haiman C; Slavin T; Ziv E Cancer; 2019 Aug; 125(16):2829-2836. PubMed ID: 31206626 [TBL] [Abstract][Full Text] [Related]
12. Two Missense Variants Detected in Breast Cancer Probands Preventing BRCA2-PALB2 Protein Interaction. Caleca L; Catucci I; Figlioli G; De Cecco L; Pesaran T; Ward M; Volorio S; Falanga A; Marchetti M; Iascone M; Tondini C; Zambelli A; Azzollini J; Manoukian S; Radice P; Peterlongo P Front Oncol; 2018; 8():480. PubMed ID: 30410870 [TBL] [Abstract][Full Text] [Related]
13. Identification of germline pathogenic variants in DNA damage repair genes by a next-generation sequencing multigene panel in BRCAX patients. Rodríguez-Balada M; Roig B; Melé M; Albacar C; Serrano S; Salvat M; Querol M; Borràs J; Martorell L; Gumà J Clin Biochem; 2020 Feb; 76():17-23. PubMed ID: 31786208 [TBL] [Abstract][Full Text] [Related]
14. Characterization of genetic predisposition to molecular subtypes of breast cancer in Brazilian patients. Paixão D; Torrezan GT; Santiago KM; Formiga MN; Ahuno ST; Dias-Neto E; Tojal da Silva I; Foulkes WD; Polak P; Carraro DM Front Oncol; 2022; 12():976959. PubMed ID: 36119527 [TBL] [Abstract][Full Text] [Related]
15. Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer. Walsh T; Casadei S; Coats KH; Swisher E; Stray SM; Higgins J; Roach KC; Mandell J; Lee MK; Ciernikova S; Foretova L; Soucek P; King MC JAMA; 2006 Mar; 295(12):1379-88. PubMed ID: 16551709 [TBL] [Abstract][Full Text] [Related]
16. Association of Gene Variant Type and Location with Breast Cancer Risk in the General Population. Akamandisa MP; Boddicker NJ; Yadav S; Hu C; Hart SN; Ambrosone C; Anton-Culver H; Auer PL; Bodelon C; Burnside ES; Chen F; Eliassen HA; Goldgar DE; Haiman C; Hodge JM; Huang H; John EM; Karam R; Lacey JV; Lindstroem S; Martinez E; Na J; Neuhausen SL; O'Brien KM; Olson JE; Pal T; Palmer JR; Patel AV; Pesaran T; Polley EC; Richardson ME; Ruddy K; Sandler DP; Teras LR; Trentham-Dietz A; Vachon CM; Weinberg C; Winham SJ; Yao S; Zirpoli G; Kraft P; Weitzel JN; Domchek SM; Couch FJ; Nathanson KL medRxiv; 2024 Oct; ():. PubMed ID: 39417132 [TBL] [Abstract][Full Text] [Related]
17. Prevalence of germline BRCA mutations among women with carcinoma of the peritoneum or fallopian tube. Choi MC; Bae JS; Jung SG; Park H; Joo WD; Song SH; Lee C; Kim JH; Lee KC; Lee S; Lee JH J Gynecol Oncol; 2018 Jul; 29(4):e43. PubMed ID: 29770616 [TBL] [Abstract][Full Text] [Related]
18. Genetic Testing of Breast Cancer Patients with Very Early-Onset Breast Cancer (≤30 Years) Yields a High Rate of Germline Pathogenic Variants, Mainly in the BRCA1, TP53, and BRCA2 Genes. Apostolou P; Dellatola V; Papathanasiou A; Kalfakakou D; Fountzilas E; Tryfonopoulos D; Karageorgopoulou S; Yannoukakos D; Konstantopoulou I; Fostira F Cancers (Basel); 2024 Jun; 16(13):. PubMed ID: 39001430 [TBL] [Abstract][Full Text] [Related]
19. Gene panel sequencing in familial breast/ovarian cancer patients identifies multiple novel mutations also in genes others than BRCA1/2. Kraus C; Hoyer J; Vasileiou G; Wunderle M; Lux MP; Fasching PA; Krumbiegel M; Uebe S; Reuter M; Beckmann MW; Reis A Int J Cancer; 2017 Jan; 140(1):95-102. PubMed ID: 27616075 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]