BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 37153042)

  • 1. Germline multigene panel testing of patients with endometrial cancer.
    Kral J; Jelinkova S; Zemankova P; Vocka M; Borecka M; Cerna L; Cerna M; Dostalek L; Duskova P; Foretova L; Havranek O; Horackova K; Hovhannisyan M; Chvojka S; Kalousova M; Kosarova M; Koudova M; Krutilkova V; Machackova E; Nehasil P; Novotny J; Otahalova B; Puchmajerova A; Safarikova M; Slama J; Stranecky V; Subrt I; Tavandzis S; Zikan M; Zima T; Soukupova J; Kleiblova P; Kleibl Z; Janatova M
    Oncol Lett; 2023 Jun; 25(6):216. PubMed ID: 37153042
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prevalence of mutations in BRCA and MMR genes in patients affected with hereditary endometrial cancer.
    Vietri MT; D'Elia G; Caliendo G; Casamassimi A; Federico A; Passariello L; Cioffi M; Molinari AM
    Med Oncol; 2021 Jan; 38(2):13. PubMed ID: 33484353
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Increased incidence of pathogenic variants in ATM in the context of testing for breast and ovarian cancer predisposition.
    Macquere P; Orazio S; Bonnet F; Jones N; Bubien V; Chiron J; Lafon D; Barouk-Simonet E; Tinat J; Venat-Bouvet L; Gesta P; Longy M; Sevenet N
    J Hum Genet; 2022 Jun; 67(6):339-345. PubMed ID: 35017683
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population.
    da Costa E Silva Carvalho S; Cury NM; Brotto DB; de Araujo LF; Rosa RCA; Texeira LA; Plaça JR; Marques AA; Peronni KC; Ruy PC; Molfetta GA; Moriguti JC; Carraro DM; Palmero EI; Ashton-Prolla P; de Faria Ferraz VE; Silva WA
    BMC Med Genomics; 2020 Feb; 13(1):21. PubMed ID: 32039725
    [TBL] [Abstract][Full Text] [Related]  

  • 6. No Evidence of Increased Risk of Breast Cancer in Women With Lynch Syndrome Identified by Multigene Panel Testing.
    Stoll J; Rosenthal E; Cummings S; Willmott J; Bernhisel R; Kupfer SS
    JCO Precis Oncol; 2020 Nov; 4():51-60. PubMed ID: 35050728
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Increased Co-Occurrence of Pathogenic Variants in Hereditary Breast and Ovarian Cancer and Lynch Syndromes: A Consequence of Multigene Panel Genetic Testing?
    Infante M; Arranz-Ledo M; Lastra E; Abella LE; Ferreira R; Orozco M; Hernández L; Martínez N; Durán M
    Int J Mol Sci; 2022 Sep; 23(19):. PubMed ID: 36232793
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment.
    Desmond A; Kurian AW; Gabree M; Mills MA; Anderson MJ; Kobayashi Y; Horick N; Yang S; Shannon KM; Tung N; Ford JM; Lincoln SE; Ellisen LW
    JAMA Oncol; 2015 Oct; 1(7):943-51. PubMed ID: 26270727
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Utility of germline multi-gene panel testing in patients with endometrial cancer.
    Karpel HC; Chern JY; Smith J M; Smith A J; Pothuri B
    Gynecol Oncol; 2022 Jun; 165(3):546-551. PubMed ID: 35483985
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Increased Risk of Hereditary Prostate Cancer in Italian Families with Hereditary Breast and Ovarian Cancer Syndrome Harboring Mutations in
    D'Elia G; Caliendo G; Tzioni MM; Albanese L; Passariello L; Molinari AM; Vietri MT
    Genes (Basel); 2022 Sep; 13(10):. PubMed ID: 36292577
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Double heterozygotes of BRCA1/BRCA2 and mismatch repair gene pathogenic variants: case series and clinical implications.
    Laish I; Friedman E; Levi-Reznick G; Kedar I; Katz L; Levi Z; Halpern N; Parnasa S; Abu-Shatya A; Half E; Goldberg Y
    Breast Cancer Res Treat; 2021 Aug; 188(3):685-694. PubMed ID: 34086170
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome.
    Rashid MU; Naeemi H; Muhammad N; Loya A; Yusuf MA; Lubiński J; Jakubowska A; Hamann U
    Hered Cancer Clin Pract; 2016; 14():14. PubMed ID: 27413415
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Real-World Data on Detection of Germline and Somatic Pathogenic/Likely Pathogenic Variants in
    Stegel V; Blatnik A; Škof E; Dragoš VŠ; Krajc M; Gregorič B; Škerl P; Strojnik K; Klančar G; Banjac M; Žgajnar J; Ravnik M; Novaković S
    Cancers (Basel); 2022 Mar; 14(6):. PubMed ID: 35326583
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The results of multigene panel sequencing in Slovak HBOC families.
    Konecny M; Kosova K; Tilandyova P; Wachsmannova L; Baldovic M; Krajcovic J; Patlevicova A; Markus J; Ciernikova S
    Neoplasma; 2021 May; 68(3):652-664. PubMed ID: 33724863
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
    Yurgelun MB; Allen B; Kaldate RR; Bowles KR; Judkins T; Kaushik P; Roa BB; Wenstrup RJ; Hartman AR; Syngal S
    Gastroenterology; 2015 Sep; 149(3):604-13.e20. PubMed ID: 25980754
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Screening for hereditary cancers in patients with endometrial cancer reveals a high frequency of germline mutations in cancer predisposition genes.
    Tian W; Bi R; Ren Y; He H; Shi S; Shan B; Yang W; Wang Q; Wang H
    Int J Cancer; 2019 Sep; 145(5):1290-1298. PubMed ID: 31054147
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Up-Front Multigene Panel Testing for Cancer Susceptibility in Patients With Newly Diagnosed Endometrial Cancer: A Multicenter Prospective Study.
    Levine MD; Pearlman R; Hampel H; Cosgrove C; Cohn D; Chassen A; Suarez A; Barrington DA; McElroy JP; Waggoner S; Nakayama J; Billingsley C; Resnick K; Andrews S; Singh S; Jenison E; Clements A; Neff R; Goodfellow PJ;
    JCO Precis Oncol; 2021 Nov; 5():1588-1602. PubMed ID: 34994648
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prevalence of Germline Pathogenic Variants in Cancer Predisposing Genes in Czech and Belgian Pancreatic Cancer Patients.
    Wieme G; Kral J; Rosseel T; Zemankova P; Parton B; Vocka M; Van Heetvelde M; Kleiblova P; Blaumeiser B; Soukupova J; van den Ende J; Nehasil P; Tejpar S; Borecka M; Gómez García EB; Blok MJ; Safarikova M; Kalousova M; Geboes K; De Putter R; Poppe B; De Leeneer K; Kleibl Z; Janatova M; Claes KBM
    Cancers (Basel); 2021 Sep; 13(17):. PubMed ID: 34503238
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Landscape of pathogenic variations in a panel of 34 genes and cancer risk estimation from 5131 HBOC families.
    Castéra L; Harter V; Muller E; Krieger S; Goardon N; Ricou A; Rousselin A; Paimparay G; Legros A; Bruet O; Quesnelle C; Domin F; San C; Brault B; Fouillet R; Abadie C; Béra O; Berthet P; ; Frébourg T; Vaur D
    Genet Med; 2018 Dec; 20(12):1677-1686. PubMed ID: 29988077
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The frequency of cancer predisposition gene mutations in hereditary breast and ovarian cancer patients in Taiwan: From BRCA1/2 to multi-gene panels.
    Sung PL; Wen KC; Chen YJ; Chao TC; Tsai YF; Tseng LM; Qiu JT; Chao KC; Wu HH; Chuang CM; Wang PH; Huang CF
    PLoS One; 2017; 12(9):e0185615. PubMed ID: 28961279
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.