BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Colorectal cancer AND PALB2, ENSG00000083093, 79728
45 results:

  • 1. Direct letters to relatives at risk of hereditary cancer-study protocol for a multi-center randomized controlled trial of healthcare-assisted versus family-mediated risk disclosure at Swedish cancer genetics clinics (DIRECT-study).
    Hawranek C; Ehrencrona H; Öfverholm A; Hellquist BN; Rosén A
    Trials; 2023 Dec; 24(1):810. PubMed ID: 38105176
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. 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]  

  • 3. Report on the Effect of the Implementation of an Early Detection and Prevention of cancer Program on Families at High Hereditary Risk-Concentrating on Patients Undergoing Genetic Diagnostics and Counseling in Central Poland.
    Kałużewski T; Kubiak I; Bednarek M; Sałamunia J; Kucharska D; Kępczyński Ł; Stempień M; Kubicki T; Trzciński R; Gordon-Sönmez Z; Bartosińska-Dyc A; Gach A; Kałużewski B
    Int J Mol Sci; 2023 Aug; 24(17):. PubMed ID: 37685988
    [TBL] [Abstract] [Full Text] [Related]  

  • 4. Screening Practices for Breast and Nonbreast cancers in High-Risk Mutation Carriers.
    Coogan AC; Lunt LG; Keshwani SS; Sandhu O; Zhang Y; O'Donoghue C; Madrigrano A
    J Surg Res; 2023 Nov; 291():388-395. PubMed ID: 37516046
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. 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]  

  • 6. Personalized Systemic Therapies in Hereditary cancer Syndromes.
    Mastrodomenico L; Piombino C; Riccò B; Barbieri E; Venturelli M; Piacentini F; Dominici M; Cortesi L; Toss A
    Genes (Basel); 2023 Mar; 14(3):. PubMed ID: 36980956
    [TBL] [Abstract] [Full Text] [Related]  

  • 7. Characteristics of familial pancreatic cancer families with additional colorectal carcinoma.
    Lehman B; Matthäi E; Gercke N; Denzer UW; Figiel J; Hess T; Slater EP; Bartsch DK
    Fam Cancer; 2023 Jul; 22(3):323-330. PubMed ID: 36717525
    [TBL] [Abstract] [Full Text] [Related]  

  • 8. Hereditary cancer variants and homologous recombination deficiency in biliary tract cancer.
    Okawa Y; Iwasaki Y; Johnson TA; Ebata N; Inai C; Endo M; Maejima K; Sasagawa S; Fujita M; Matsuda K; Murakami Y; Nakamura T; Hirano S; Momozawa Y; Nakagawa H
    J Hepatol; 2023 Feb; 78(2):333-342. PubMed ID: 36243179
    [TBL] [Abstract] [Full Text] [Related]  

  • 9. Concurrent BRAFV600E and BRCA Mutations in MSS Metastatic colorectal cancer: Prevalence and Case Series of mCRC patients with prolonged OS.
    Cannon TL; Randall JN; Sokol ES; Alexander SM; Wadlow RC; Winer AA; Barnett DM; Rayes DL; Nimeiri HS; McGregor KA
    Cancer Treat Res Commun; 2022; 32():100569. PubMed ID: 35567913
    [TBL] [Abstract] [Full Text] [Related]  

  • 10. Identification and Management of Pathogenic Variants in BRCA1, BRCA2, and palb2 in a Tumor-Only Genomic Testing Program.
    Bychkovsky BL; Li T; Sotelo J; Tayob N; Mercado J; Gomy I; Chittenden A; Kane S; Stokes S; Hughes ME; Kim JS; Umeton R; Awad MM; Konstantinopoulos PA; Yurgelun MB; Wolpin BM; Taplin ME; Newmark RE; Johnson BE; Lindeman NI; MacConaill LE; Garber JE; Lin NU
    Clin Cancer Res; 2022 Jun; 28(11):2349-2360. PubMed ID: 35363308
    [TBL] [Abstract] [Full Text] [Related]  

  • 11. Core Homologous Recombination Mutations and Improved Survival in Nonpancreatic GI cancers.
    Tan E; Whiting J; Knepper T; Xie H; Imanirad I; Carballido E; Felder S; Frakes J; Mo Q; Permuth JB; Somerer K; Kim R; Anaya DA; Fleming JB; Walko C; Sahin IH
    Am J Clin Oncol; 2022 Apr; 45(4):137-141. PubMed ID: 35320814
    [TBL] [Abstract] [Full Text] [Related]  

  • 12. Pancreatic cancer with Mutation in BRCA1/2, MLH1, and APC Genes: Phenotype Correlation and Detection of a Novel Germline BRCA2 Mutation.
    Vietri MT; D'Elia G; Caliendo G; Albanese L; Signoriello G; Napoli C; Molinari AM
    Genes (Basel); 2022 Feb; 13(2):. PubMed ID: 35205366
    [TBL] [Abstract] [Full Text] [Related]  

  • 13. New Perspectives on the Recurrent Monoallelic Germline Mutations of DNA Repair and Checkpoint Genes and Clinical Variability.
    Sahin I; Saat H
    Genet Test Mol Biomarkers; 2022 Jan; 26(1):17-25. PubMed ID: 35089076
    [No Abstract]    [Full Text] [Related]  

  • 14. The Effect of Gene Mutations on Metastasis and Overall Survival in Metastatic and Nonmetastatic Colon cancers.
    Ozdemir Y; Cag M; Colak E; Coskun N; Basgoz N; Sarici H; Kaan D; Dogan M; Deniz K; Inanc M; Ozkul Y
    Asian Pac J Cancer Prev; 2021 Dec; 22(12):3839-3846. PubMed ID: 34967562
    [TBL] [Abstract] [Full Text] [Related]  

  • 15. 30 year experience of index case identification and outcomes of cascade testing in high-risk breast and colorectal cancer predisposition genes.
    Woodward ER; Green K; Burghel GJ; Bulman M; Clancy T; Lalloo F; Schlecht H; Wallace AJ; Evans DG
    Eur J Hum Genet; 2022 Apr; 30(4):413-419. PubMed ID: 34866136
    [TBL] [Abstract] [Full Text] [Related]  

  • 16. Germline mutations in a DNA repair pathway are associated with familial colorectal cancer.
    Xu P; Sun D; Gao Y; Jiang Y; Zhong M; Zhao G; Chen J; Wang Z; Liu Q; Hong J; Chen H; Chen YX; Fang JY
    JCI Insight; 2021 Sep; 6(18):. PubMed ID: 34549727
    [TBL] [Abstract] [Full Text] [Related]  

  • 17. Case-case analysis addressing ascertainment bias for multigene panel testing implicates BRCA1 and palb2 in endometrial cancer.
    Johnatty SE; Pesaran T; Dolinsky J; Yussuf A; LaDuca H; James PA; O'Mara TA; Spurdle AB
    Hum Mutat; 2021 Oct; 42(10):1265-1278. PubMed ID: 34245638
    [TBL] [Abstract] [Full Text] [Related]  

  • 18. Optimization of prediction methods for risk assessment of pathogenic germline variants in the Japanese population.
    Senda N; Kawaguchi-Sakita N; Kawashima M; Inagaki-Kawata Y; Yoshida K; Takada M; Kataoka M; Torii M; Nishimura T; Kawaguchi K; Suzuki E; Kataoka Y; Matsumoto Y; Yoshibayashi H; Yamagami K; Tsuyuki S; Takahara S; Yamauchi A; Shinkura N; Kato H; Moriguchi Y; Okamura R; Kan N; Suwa H; Sakata S; Mashima S; Yotsumoto F; Tachibana T; Tanaka M; Togashi K; Haga H; Yamada T; Kosugi S; Inamoto T; Sugimoto M; Ogawa S; Toi M
    Cancer Sci; 2021 Aug; 112(8):3338-3348. PubMed ID: 34036661
    [TBL] [Abstract] [Full Text] [Related]  

  • 19. Disease spectrum of gastric cancer susceptibility genes.
    McKinley SK; Singh P; Yin K; Wang J; Zhou J; Bao Y; Wu M; Pathak K; Mullen JT; Braun D; Hughes KS
    Med Oncol; 2021 Mar; 38(5):46. PubMed ID: 33760988
    [TBL] [Abstract] [Full Text] [Related]  

  • 20. Predicted Chemotherapy Benefit for Breast cancer Patients With Germline Pathogenic Variants in cancer Susceptibility Genes.
    Kurian AW; Ward KC; Abrahamse P; Hamilton AS; Katz SJ
    JNCI Cancer Spectr; 2021 Feb; 5(1):. PubMed ID: 33426465
    [TBL] [Abstract] [Full Text] [Related]  


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