BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 28695303)

  • 1. A comparison of cosegregation analysis methods for the clinical setting.
    Rañola JMO; Liu Q; Rosenthal EA; Shirts BH
    Fam Cancer; 2018 Apr; 17(2):295-302. PubMed ID: 28695303
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Considerations in assessing germline variant pathogenicity using cosegregation analysis.
    Belman S; Parsons MT; Spurdle AB; Goldgar DE; Feng BJ
    Genet Med; 2020 Dec; 22(12):2052-2059. PubMed ID: 32773770
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.
    Caputo SM; Golmard L; Léone M; Damiola F; Guillaud-Bataille M; Revillion F; Rouleau E; Derive N; Buisson A; Basset N; Schwartz M; Vilquin P; Garrec C; Privat M; Gay-Bellile M; Abadie C; Abidallah K; Airaud F; Allary AS; Barouk-Simonet E; Belotti M; Benigni C; Benusiglio PR; Berthemin C; Berthet P; Bertrand O; Bézieau S; Bidart M; Bignon YJ; Birot AM; Blanluet M; Bloucard A; Bombled J; Bonadona V; Bonnet F; Bonnet-Dupeyron MN; Boulaire M; Boulouard F; Bouras A; Bourdon V; Brahimi A; Brayotel F; Bressac de Paillerets B; Bronnec N; Bubien V; Buecher B; Cabaret O; Carriere J; Chiesa J; Chieze-Valéro S; Cohen C; Cohen-Haguenauer O; Colas C; Collonge-Rame MA; Conoy AL; Coulet F; Coupier I; Crivelli L; Cusin V; De Pauw A; Dehainault C; Delhomelle H; Delnatte C; Demontety S; Denizeau P; Devulder P; Dreyfus H; d'Enghein CD; Dupré A; Durlach A; Dussart S; Fajac A; Fekairi S; Fert-Ferrer S; Fiévet A; Fouillet R; Mouret-Fourme E; Gauthier-Villars M; Gesta P; Giraud S; Gladieff L; Goldbarg V; Goussot V; Guibert V; Guillerm E; Guy C; Hardouin A; Heude C; Houdayer C; Ingster O; Jacquot-Sawka C; Jones N; Krieger S; Lacoste S; Lallaoui H; Larbre H; Laugé A; Le Guyadec G; Le Mentec M; Lecerf C; Le Gall J; Legendre B; Legrand C; Legros A; Lejeune S; Lidereau R; Lignon N; Limacher JM; Doriane Livon ; Lizard S; Longy M; Lortholary A; Macquere P; Mailliez A; Malsa S; Margot H; Mari V; Maugard C; Meira C; Menjard J; Molière D; Moncoutier V; Moretta-Serra J; Muller E; Nevière Z; Nguyen Minh Tuan TV; Noguchi T; Noguès C; Oca F; Popovici C; Prieur F; Raad S; Rey JM; Ricou A; Salle L; Saule C; Sevenet N; Simaga F; Sobol H; Suybeng V; Tennevet I; Tenreiro H; Tinat J; Toulas C; Turbiez I; Uhrhammer N; Vande Perre P; Vaur D; Venat L; Viellard N; Villy MC; Warcoin M; Yvard A; Zattara H; Caron O; Lasset C; Remenieras A; Boutry-Kryza N; Castéra L; Stoppa-Lyonnet D
    Am J Hum Genet; 2021 Oct; 108(10):1907-1923. PubMed ID: 34597585
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Classification of genetic variants in genes associated with Lynch syndrome using a clinical history weighting algorithm.
    Morris B; Hughes E; Rosenthal E; Gutin A; Bowles KR
    BMC Genet; 2016 Jul; 17(1):99. PubMed ID: 27363726
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An algorithm for optimal testing in co-segregation analysis.
    Buie RW; Rañola JMO; Chen AT; Shirts BH
    Hum Mutat; 2022 May; 43(5):547-556. PubMed ID: 35225377
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Statewide Retrospective Review of Familial Pancreatic Cancer in Delaware, and Frequency of Genetic Mutations in Pancreatic Cancer Kindreds.
    Catts ZA; Baig MK; Milewski B; Keywan C; Guarino M; Petrelli N
    Ann Surg Oncol; 2016 May; 23(5):1729-35. PubMed ID: 26727920
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2.
    Goldgar DE; Easton DF; Deffenbaugh AM; Monteiro AN; Tavtigian SV; Couch FJ;
    Am J Hum Genet; 2004 Oct; 75(4):535-44. PubMed ID: 15290653
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Penetrance estimates for
    Evans DG; Woodward E; Harkness EF; Howell A; Plaskocinska I; Maher ER; Tischkowitz MD; Lalloo F
    J Med Genet; 2018 Jul; 55(7):442-448. PubMed ID: 29483236
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of BRCA1 and BRCA2 splicing variants: a collaborative report by ENIGMA consortium members.
    Thomassen M; Blanco A; Montagna M; Hansen TV; Pedersen IS; Gutiérrez-Enríquez S; Menéndez M; Fachal L; Santamariña M; Steffensen AY; Jønson L; Agata S; Whiley P; Tognazzo S; Tornero E; Jensen UB; Balmaña J; Kruse TA; Goldgar DE; Lázaro C; Diez O; Spurdle AB; Vega A
    Breast Cancer Res Treat; 2012 Apr; 132(3):1009-23. PubMed ID: 21769658
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Power of pedigree likelihood analysis in extended pedigrees to classify rare variants of uncertain significance in cancer risk genes.
    Rosenthal EA; Ranola JMO; Shirts BH
    Fam Cancer; 2017 Oct; 16(4):611-620. PubMed ID: 28534081
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pathogenicity evaluation of BRCA1 and BRCA2 unclassified variants identified in Portuguese breast/ovarian cancer families.
    Santos C; Peixoto A; Rocha P; Pinto P; Bizarro S; Pinheiro M; Pinto C; Henrique R; Teixeira MR
    J Mol Diagn; 2014 May; 16(3):324-34. PubMed ID: 24607278
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exceptions to the rule: case studies in the prediction of pathogenicity for genetic variants in hereditary cancer genes.
    Rosenthal ET; Bowles KR; Pruss D; van Kan A; Vail PJ; McElroy H; Wenstrup RJ
    Clin Genet; 2015 Dec; 88(6):533-41. PubMed ID: 25639900
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Germline genetic variants in men with prostate cancer and one or more additional cancers.
    Pilié PG; Johnson AM; Hanson KL; Dayno ME; Kapron AL; Stoffel EM; Cooney KA
    Cancer; 2017 Oct; 123(20):3925-3932. PubMed ID: 28657667
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Assessment of the InSiGHT Interpretation Criteria for the Clinical Classification of 24 MLH1 and MSH2 Gene Variants.
    Tricarico R; Kasela M; Mareni C; Thompson BA; Drouet A; Staderini L; Gorelli G; Crucianelli F; Ingrosso V; Kantelinen J; Papi L; De Angioletti M; Berardi M; Gaildrat P; Soukarieh O; Turchetti D; Martins A; Spurdle AB; Nyström M; Genuardi M;
    Hum Mutat; 2017 Jan; 38(1):64-77. PubMed ID: 27629256
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary cancer syndromes.
    Fostira F; Thodi G; Konstantopoulou I; Sandaltzopoulos R; Yannoukakos D
    J BUON; 2007 Sep; 12 Suppl 1():S13-22. PubMed ID: 17935271
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dealing With BRCA1/2 Unclassified Variants in a Cancer Genetics Clinic: Does Cosegregation Analysis Help?
    Zuntini R; Ferrari S; Bonora E; Buscherini F; Bertonazzi B; Grippa M; Godino L; Miccoli S; Turchetti D
    Front Genet; 2018; 9():378. PubMed ID: 30254663
    [No Abstract]   [Full Text] [Related]  

  • 17. Genetic evidence and integration of various data sources for classifying uncertain variants into a single model.
    Goldgar DE; Easton DF; Byrnes GB; Spurdle AB; Iversen ES; Greenblatt MS;
    Hum Mutat; 2008 Nov; 29(11):1265-72. PubMed ID: 18951437
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Methylation Tolerance-Based Functional Assay to Assess Variants of Unknown Significance in the MLH1 and MSH2 Genes and Identify Patients With Lynch Syndrome.
    Bouvet D; Bodo S; Munier A; Guillerm E; Bertrand R; Colas C; Duval A; Coulet F; Muleris M
    Gastroenterology; 2019 Aug; 157(2):421-431. PubMed ID: 30998989
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Muir-Torre Syndrome and founder mismatch repair gene mutations: A long gone historical genetic challenge.
    Ponti G; Manfredini M; Tomasi A; Pellacani G
    Gene; 2016 Sep; 589(2):127-32. PubMed ID: 26143115
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic testing and prevention of hereditary cancer at the MMCI--over 10 years of experience.
    Foretova L; Petrakova K; Palacova M; Kalabova R; Svoboda M; Navratilova M; Schneiderova M; Bolcak K; Krejci E; Drazan L; Mikova M; Hazova J; Vasickova P; Machackova E
    Klin Onkol; 2010; 23(6):388-400. PubMed ID: 21348412
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.