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.
150 related articles for article (PubMed ID: 37169825)
1. PALB2 germline mutations in a large cohort of Middle Eastern breast-ovarian cancer patients. Siraj AK; Bu R; Parvathareddy SK; Iqbal K; Azam S; Qadri Z; Al-Rasheed M; Haqawi W; Diaz M; Victoria IG; Al-Badawi IA; Tulbah A; Al-Dayel F; Ajarim D; Al-Kuraya KS Sci Rep; 2023 May; 13(1):7666. PubMed ID: 37169825 [TBL] [Abstract][Full Text] [Related]
2. PALB2 germline mutations in a multi-gene panel testing cohort of 1905 breast-ovarian cancer patients in Argentina. Gonzalez A; Del Greco F; Vargas-Roig L; Brun B; Tabares G; Mampel A; Montes C; Martin C; Lopez M; Rossi N; Bruno L; Ponce C; Quaglio P; Yanzi A; Acevedo S; Lugo L; Lopez Breccia P; Avila S; Sisterna S; Del Castillo MS; Vazquez M; Nuñez LM Breast Cancer Res Treat; 2022 Jul; 194(2):403-412. PubMed ID: 35610400 [TBL] [Abstract][Full Text] [Related]
3. Identification and characterization of ATM founder mutation in BRCA-negative breast cancer patients of Arab ethnicity. Bu R; Siraj AK; Al-Rasheed M; Iqbal K; Azam S; Qadri Z; Haqawi W; Tulbah A; Al-Dayel F; Almalik O; Al-Kuraya KS Sci Rep; 2023 Nov; 13(1):20924. PubMed ID: 38017116 [TBL] [Abstract][Full Text] [Related]
4. Spectrum and clinical relevance of PALB2 germline mutations in 7657 Chinese BRCA1/2-negative breast cancer patients. Wu Y; Ouyang T; Li J; Wang T; Fan Z; Fan T; Lin B; Xu Y; Xie Y Breast Cancer Res Treat; 2020 Feb; 179(3):605-614. PubMed ID: 31768816 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. Frequency and molecular characteristics of PALB2-associated cancers in Russian patients. Preobrazhenskaya EV; Shleykina AU; Gorustovich OA; Martianov AS; Bizin IV; Anisimova EI; Sokolova TN; Chuinyshena SA; Kuligina ES; Togo AV; Belyaev AM; Ivantsov AO; Sokolenko AP; Imyanitov EN Int J Cancer; 2021 Jan; 148(1):203-210. PubMed ID: 32997802 [TBL] [Abstract][Full Text] [Related]
7. PALB2 mutations in BRCA1/2-mutation negative breast and ovarian cancer patients from Poland. Kluska A; Balabas A; Piatkowska M; Czarny K; Paczkowska K; Nowakowska D; Mikula M; Ostrowski J BMC Med Genomics; 2017 Mar; 10(1):14. PubMed ID: 28279176 [TBL] [Abstract][Full Text] [Related]
8. Spectrum and characteristics of germline PALB2 pathogenic variants in 1556 early-onset breast cancer patients in China. Li J; He P; Cai Q; Chen L; Wang Y; Cai W; Qiu Y; Liu S; Guo W; Chen M; Lin Y; Wang C; Fu F J Cancer Res Clin Oncol; 2024 Jun; 150(6):322. PubMed ID: 38914840 [TBL] [Abstract][Full Text] [Related]
9. Prevalence of PALB2 Germline Mutations in Early-onset and Familial Breast/Ovarian Cancer Patients from Pakistan. Rashid MU; Khan FA; Muhammad N; Loya A; Hamann U Cancer Res Treat; 2019 Jul; 51(3):992-1000. PubMed ID: 30309218 [TBL] [Abstract][Full Text] [Related]
10. Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and Ukraine. Myszka A; Nguyen-Dumont T; Karpinski P; Sasiadek MM; Akopyan H; Hammet F; Tsimiklis H; Park DJ; Pope BJ; Slezak R; Kitsera N; Siekierzynska A; Southey MC Fam Cancer; 2018 Jul; 17(3):345-349. PubMed ID: 29052111 [TBL] [Abstract][Full Text] [Related]
11. Germline mutations of PALB2 gene in a sequential series of Chinese patients with breast cancer. Zhang K; Zhou J; Zhu X; Luo M; Xu C; Yu J; Deng M; Zheng S; Chen Y Breast Cancer Res Treat; 2017 Dec; 166(3):865-873. PubMed ID: 28825143 [TBL] [Abstract][Full Text] [Related]
13. A systematic review of predicted pathogenic PALB2 variants: an analysis of mutational overlap between epithelial cancers. Janssen B; Bellis S; Koller T; Tischkowitz M; Liau SS J Hum Genet; 2020 Jan; 65(2):199-205. PubMed ID: 31619740 [TBL] [Abstract][Full Text] [Related]
14. Frequency of germline pathogenic variants in breast cancer predisposition genes among young Turkish breast cancer patients. Isiklar AD; Aliyeva L; Yesilyurt A; Soyder A; Basaran G Breast Cancer Res Treat; 2023 Nov; 202(2):297-304. PubMed ID: 37615792 [TBL] [Abstract][Full Text] [Related]
15. Frequency of heterozygous germline pathogenic variants in genes for Fanconi anemia in patients with non-BRCA1/BRCA2 breast cancer: a meta-analysis. Alter BP; Best AF Breast Cancer Res Treat; 2020 Jul; 182(2):465-476. PubMed ID: 32488392 [TBL] [Abstract][Full Text] [Related]
16. Profiling of the genetic features of patients with breast, ovarian, colorectal and extracolonic cancers: Association to CHEK2 and PALB2 germline mutations. Infante M; Arranz-Ledo M; Lastra E; Olaverri A; Ferreira R; Orozco M; Hernández L; Martínez N; Durán M Clin Chim Acta; 2024 Jan; 552():117695. PubMed ID: 38061684 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Contribution of the PALB2 c.2323C>T [p.Q775X] founder mutation in well-defined breast and/or ovarian cancer families and unselected ovarian cancer cases of French Canadian descent. Tischkowitz M; Sabbaghian N; Hamel N; Pouchet C; Foulkes WD; Mes-Masson AM; Provencher DM; Tonin PN BMC Med Genet; 2013 Jan; 14():5. PubMed ID: 23302520 [TBL] [Abstract][Full Text] [Related]
19. Pathologic findings in breast, fallopian tube, and ovary specimens in non-BRCA hereditary breast and/or ovarian cancer syndromes: a study of 18 patients with deleterious germline mutations in RAD51C, BARD1, BRIP1, PALB2, MUTYH, or CHEK2. Schoolmeester JK; Moyer AM; Goodenberger ML; Keeney GL; Carter JM; Bakkum-Gamez JN Hum Pathol; 2017 Dec; 70():14-26. PubMed ID: 28709830 [TBL] [Abstract][Full Text] [Related]
20. Spectrum of PALB2 germline mutations and characteristics of PALB2-related breast cancer: Screening of 16,501 unselected patients with breast cancer and 5890 controls by next-generation sequencing. Zhou J; Wang H; Fu F; Li Z; Feng Q; Wu W; Liu Y; Wang C; Chen Y Cancer; 2020 Jul; 126(14):3202-3208. PubMed ID: 32339256 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]