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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 26157685)

  • 21. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
    Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
    Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
    [TBL] [Abstract][Full Text] [Related]  

  • 22. BRCA1 and BRCA2 mutations in ethnic Lebanese Arab women with high hereditary risk breast cancer.
    El Saghir NS; Zgheib NK; Assi HA; Khoury KE; Bidet Y; Jaber SM; Charara RN; Farhat RA; Kreidieh FY; Decousus S; Romero P; Nemer GM; Salem Z; Shamseddine A; Tfayli A; Abbas J; Jamali F; Seoud M; Armstrong DK; Bignon YJ; Uhrhammer N
    Oncologist; 2015 Apr; 20(4):357-64. PubMed ID: 25777348
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Bilateral breast carcinoma and local recurrence: prevalence of BRCA-1 and BRCA-2 gene mutations in an unselected patient sample].
    Bremer M; Steinmann D; Dörk T; Börger J; Rades D; Karstens JH
    Strahlenther Onkol; 2001 Jul; 177(7):325-9. PubMed ID: 11505617
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Exome sequencing in one family with gastric- and rectal cancer.
    Thutkawkorapin J; Picelli S; Kontham V; Liu T; Nilsson D; Lindblom A
    BMC Genet; 2016 Feb; 17():41. PubMed ID: 26872740
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Novel germline mutations in breast cancer susceptibility genes BRCA1, BRCA2 and p53 gene in breast cancer patients from India.
    Hedau S; Jain N; Husain SA; Mandal AK; Ray G; Shahid M; Kant R; Gupta V; Shukla NK; Deo SS; Das BC
    Breast Cancer Res Treat; 2004 Nov; 88(2):177-86. PubMed ID: 15564800
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cumulative BRCA mutation analysis in the Greek population confirms that homogenous ethnic background facilitates genetic testing.
    Tsigginou A; Vlachopoulos F; Arzimanoglou I; Zagouri F; Dimitrakakis C
    Hered Cancer Clin Pract; 2015; 13(1):17. PubMed ID: 26300996
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Multiplex exome sequencing reveals genome-wide frequency and distribution of mutations in the 'Micro-Tom' Targeting Induced Local Lesions in Genomes (TILLING) mutant library.
    Yano R; Hoshikawa K; Okabe Y; Wang N; Dung PT; Imriani PS; Shiba H; Ariizumi T; Ezura H
    Plant Biotechnol (Tokyo); 2019 Dec; 36(4):223-231. PubMed ID: 31983876
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Limited family structure and triple-negative breast cancer (TNBC) subtype as predictors of BRCA mutations in a genetic counseling cohort of early-onset sporadic breast cancers.
    Zugazagoitia J; Pérez-Segura P; Manzano A; Blanco I; Vega A; Custodio A; Teulé A; Fachal L; Martínez B; González-Sarmiento R; Cruz-Hernández JJ; Chirivella I; Garcés V; Garre P; Romero A; Caldés T; Díaz-Rubio E; de la Hoya M
    Breast Cancer Res Treat; 2014 Nov; 148(2):415-21. PubMed ID: 25342642
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Whole-exome sequencing and targeted gene sequencing provide insights into the role of PALB2 as a male breast cancer susceptibility gene.
    Silvestri V; Zelli V; Valentini V; Rizzolo P; Navazio AS; Coppa A; Agata S; Oliani C; Barana D; Castrignanò T; Viel A; Russo A; Tibiletti MG; Zanna I; Masala G; Cortesi L; Manoukian S; Azzollini J; Peissel B; Bonanni B; Peterlongo P; Radice P; Palli D; Giannini G; Chillemi G; Montagna M; Ottini L
    Cancer; 2017 Jan; 123(2):210-218. PubMed ID: 27648926
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The susceptibility gene screening in a Chinese high-altitude pulmonary edema family by whole-exome sequencing.
    Yang YZ; Wang YP; Xu J; Ge RL
    Yi Chuan; 2017 Feb; 39(2):135-142. PubMed ID: 28242600
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinicopathologic characteristics and BRCA-1/BRCA-2 mutations of Turkish patients with breast cancer.
    Aydin F; Akagun T; Yildiz B; Fidan E; Ozdemir F; Kavgaci H
    Bratisl Lek Listy; 2011; 112(9):521-3. PubMed ID: 21954532
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Rapid detection of copy number variations and point mutations in
    Germani A; Libi F; Maggi S; Stanzani G; Lombardi A; Pellegrini P; Mattei M; De Marchis L; Amanti C; Pizzuti A; Torrisi MR; Piane M
    Oncotarget; 2018 Sep; 9(72):33648-33655. PubMed ID: 30263092
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Risk assessment, genetic counseling, and genetic testing for BRCA-related cancer in women: U.S. Preventive Services Task Force recommendation statement.
    Moyer VA;
    Ann Intern Med; 2014 Feb; 160(4):271-81. PubMed ID: 24366376
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A portrait of germline mutation in Brazilian at-risk for hereditary breast cancer.
    de Souza Timoteo AR; Gonçalves AÉMM; Sales LAP; Albuquerque BM; de Souza JES; de Moura PCP; de Aquino MAA; Agnez-Lima LF; Lajus TBP
    Breast Cancer Res Treat; 2018 Dec; 172(3):637-646. PubMed ID: 30159786
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Exome sequencing reveals three novel candidate predisposition genes for diffuse gastric cancer.
    Donner I; Kiviluoto T; Ristimäki A; Aaltonen LA; Vahteristo P
    Fam Cancer; 2015 Jun; 14(2):241-6. PubMed ID: 25576241
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Can unknown predisposition in familial breast cancer be family-specific?
    Lynch H; Wen H; Kim YC; Snyder C; Kinarsky Y; Chen PX; Xiao F; Goldgar D; Cowan KH; Wang SM
    Breast J; 2013; 19(5):520-8. PubMed ID: 23800003
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Characterization of familial breast cancer in Saudi Arabia.
    Merdad A; Gari MA; Hussein S; Al-Khayat S; Tashkandi H; Al-Maghrabi J; Al-Thubaiti F; Hussein IR; Koumosani T; Shaer N; Chaudhary AG; Abuzenadah AM; Al-Qahtani MH; Dallol A
    BMC Genomics; 2015; 16 Suppl 1(Suppl 1):S3. PubMed ID: 25923920
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes.
    Spinella JF; Healy J; Saillour V; Richer C; Cassart P; Ouimet M; Sinnett D
    BMC Cancer; 2015 Jul; 15():539. PubMed ID: 26201965
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer.
    Lin PH; Kuo WH; Huang AC; Lu YS; Lin CH; Kuo SH; Wang MY; Liu CY; Cheng FT; Yeh MH; Li HY; Yang YH; Hsu YH; Fan SC; Li LY; Yu SL; Chang KJ; Chen PL; Ni YH; Huang CS
    Oncotarget; 2016 Feb; 7(7):8310-20. PubMed ID: 26824983
    [TBL] [Abstract][Full Text] [Related]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.