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There are 47683 results for: content related to: Genetic Testing for Breast and Ovarian Cancer Susceptibility: A Family Experience

  1. You have free access to this content
    Predictive factors for BRCA1/BRCA2 mutations in women with ductal carcinoma in situ

    Cancer

    Volume 118, Issue 6, 15 March 2012, Pages: 1515–1522, Soley Bayraktar, Nisreen Elsayegh, Angelica M. Gutierrez Barrera, Heather Lin, Henry Kuerer, Tunc Tasbas, Kimberly I. Muse, Kaylene Ready, Jennifer Litton, Funda Meric-Bernstam, Gabriel N. Hortobagyi, Constance T. Albarracin and Banu Arun

    Version of Record online : 25 AUG 2011, DOI: 10.1002/cncr.26428

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    BRCA1, a ‘complex’ protein involved in the maintenance of genomic stability

    The FEBS Journal

    Volume 282, Issue 4, February 2015, Pages: 630–646, Kienan I. Savage and D. Paul Harkin

    Version of Record online : 2 DEC 2014, DOI: 10.1111/febs.13150

  3. You have free access to this content
    BRCA1 gene in breast cancer

    Journal of Cellular Physiology

    Volume 196, Issue 1, July 2003, Pages: 19–41, Eliot M. Rosen, Saijun Fan, Richard G. Pestell and Itzhak D. Goldberg

    Version of Record online : 31 MAR 2003, DOI: 10.1002/jcp.10257

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    Significant clinical impact of recurrent BRCA1 and BRCA2 mutations in Mexico

    Cancer

    Volume 121, Issue 3, February 1, 2015, Pages: 372–378, Cynthia Villarreal-Garza, Rosa María Alvarez-Gómez, Carlos Pérez-Plasencia, Luis A. Herrera, Josef Herzog, Danielle Castillo, Alejandro Mohar, Clementina Castro, Lenny N. Gallardo, Dolores Gallardo, Miguel Santibáñez, Kathleen R. Blazer and Jeffrey N. Weitzel

    Version of Record online : 18 SEP 2014, DOI: 10.1002/cncr.29058

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    Prevalence of BRCA1 and BRCA2 mutations in Ashkenazi Jewish families with breast and pancreatic cancer

    Cancer

    Volume 118, Issue 2, 15 January 2012, Pages: 493–499, Zsofia K. Stadler, Erin Salo-Mullen, Sujata M. Patil, M. Catherine Pietanza, Joseph Vijai, Emmanouil Saloustros, Nichole A. L. Hansen, Noah D. Kauff, Robert C. Kurtz, David P. Kelsen, Kenneth Offit and Mark E. Robson

    Version of Record online : 19 MAY 2011, DOI: 10.1002/cncr.26191

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    Unravelling modifiers of breast and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers: update on genetic modifiers

    Journal of Internal Medicine

    Volume 271, Issue 4, April 2012, Pages: 331–343, D. R. Barnes and A. C. Antoniou

    Version of Record online : 23 MAR 2012, DOI: 10.1111/j.1365-2796.2011.02502.x

  7. A diagnostic genetic test for the physical mapping of germline rearrangements in the susceptibility breast cancer genes BRCA1 and BRCA2

    Human Mutation

    Volume 33, Issue 6, June 2012, Pages: 998–1009, Kevin Cheeseman, Etienne Rouleau, Anne Vannier, Aurélie Thomas, Adrien Briaux, Cedrick Lefol, Pierre Walrafen, Aaron Bensimon, Rosette Lidereau, Emmanuel Conseiller and Maurizio Ceppi

    Version of Record online : 4 APR 2012, DOI: 10.1002/humu.22060

  8. Germ-line mutations in BRCA1 or BRCA2 in the normal breast are associated with altered expression of estrogen-responsive proteins and the predominance of progesterone receptor A

    Genes, Chromosomes and Cancer

    Volume 39, Issue 3, March 2004, Pages: 236–248, Patricia A. Mote, Jennifer A. Leary, Kelly A. Avery, Kerstin Sandelin, Georgia Chenevix-Trench, Judy A. Kirk and Christine L. Clarke

    Version of Record online : 8 JAN 2004, DOI: 10.1002/gcc.10321

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    Improved survival for BRCA2-associated serous ovarian cancer compared with both BRCA-negative and BRCA1-associated serous ovarian cancer

    Cancer

    Volume 118, Issue 15, 1 August 2012, Pages: 3703–3709, David M. Hyman, Qin Zhou, Alexia Iasonos, Rachel N. Grisham, Angela G. Arnold, Mary F. Phillips, Jasmine Bhatia, Douglas A. Levine, Carol Aghajanian, Kenneth Offit, Richard R. Barakat, David R. Spriggs and Noah D. Kauff

    Version of Record online : 2 DEC 2011, DOI: 10.1002/cncr.26655

  10. Skin cancer risk in BRCA1/2 mutation carriers

    British Journal of Dermatology

    Volume 172, Issue 6, June 2015, Pages: 1498–1506, P.V. Gumaste, L.A. Penn, R.M. Cymerman, T. Kirchhoff, D. Polsky and B. McLellan

    Version of Record online : 29 APR 2015, DOI: 10.1111/bjd.13626

  11. Hereditary Breast Cancer Syndromes: Molecular Pathogenesis and Diagnostics

    Standard Article

    eLS

    S Vos, P Groep, E Wall and Paul J Diest

    Published Online : 10 SEP 2015, DOI: 10.1002/9780470015902.a0005375

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    Genome-wide analysis reveals a role for BRCA1 and PALB2 in transcriptional co-activation

    The EMBO Journal

    Volume 33, Issue 8, 16 April 2014, Pages: 890–905, Alessandro Gardini, David Baillat, Matteo Cesaroni and Ramin Shiekhattar

    Version of Record online : 3 MAR 2014, DOI: 10.1002/embj.201385567

    Corrected by:

    Corrigendum: Genome-wide analysis reveals a role for BRCA1 and PALB2 in transcriptional co-activation

    Vol. 33, Issue 18, 2134, Version of Record online: 17 SEP 2014

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    MicroRNA expression signatures for the prediction of BRCA1/2 mutation-associated hereditary breast cancer in paraffin-embedded formalin-fixed breast tumors

    International Journal of Cancer

    Volume 136, Issue 3, 1 February 2015, Pages: 593–602, Miljana Tanic, Kira Yanowski, Gonzalo Gómez-López, María Socorro Rodriguez-Pinilla, Iván Marquez-Rodas, Ana Osorio, David G. Pisano, Beatriz Martinez-Delgado and Javier Benítez

    Version of Record online : 19 JUN 2014, DOI: 10.1002/ijc.29021

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    Familial Breast Cancer

    Clinical Genetics

    Volume 82, Issue 2, August 2012, Pages: 105–114, F Lalloo and D G Evans

    Version of Record online : 13 APR 2012, DOI: 10.1111/j.1399-0004.2012.01859.x

  15. An Overview of Hereditary Breast and Ovarian Cancer Syndrome

    Journal of Midwifery & Women’s Health

    Volume 57, Issue 6, November/December 2012, Pages: 577–584, Edith Caroline Smith

    Version of Record online : 10 OCT 2012, DOI: 10.1111/j.1542-2011.2012.00199.x

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    The histologic phenotypes of breast carcinoma occurring before age 40 years in women with and without BRCA1 or BRCA2 germline mutations

    Cancer

    Volume 83, Issue 11, 1 December 1998, Pages: 2335–2345, Jane E. Armes, A. J. Matthew Egan, Melissa C. Southey, Gillian S. Dite, Margaret R. E. McCredie, Graham G. Giles, John L. Hopper and Deon J. Venter

    Version of Record online : 9 NOV 2000, DOI: 10.1002/(SICI)1097-0142(19981201)83:11<2335::AID-CNCR13>3.0.CO;2-N

  17. Multiple copies of mutant BRCA1 and BRCA2 alleles in breast tumors from germ-line mutation carriers

    Genes, Chromosomes and Cancer

    Volume 28, Issue 4, August 2000, Pages: 432–442, Synnöve Staff, Nina N. Nupponen, Åke Borg, Jorma J. Isola and Minna M. Tanner

    Version of Record online : 14 JUN 2000, DOI: 10.1002/1098-2264(200008)28:4<432::AID-GCC9>3.0.CO;2-J

  18. Identification of BRCA1-deficient ovarian cancers

    Acta Obstetricia et Gynecologica Scandinavica

    Volume 90, Issue 6, June 2011, Pages: 593–599, ANNE-BINE SKYTTE, MARIANNE WALDSTRØM, ANDERS AAMANN RASMUSSEN, DORTHE CRÜGER, EMMA R. WOODWARD and STEEN KØLVRAA

    Version of Record online : 15 APR 2011, DOI: 10.1111/j.1600-0412.2011.01121.x

  19. A guide for functional analysis of BRCA1 variants of uncertain significance

    Human Mutation

    Volume 33, Issue 11, November 2012, Pages: 1526–1537, Gaël A. Millot, Marcelo A. Carvalho, Sandrine M. Caputo, Maaike P.G. Vreeswijk, Melissa A. Brown, Michelle Webb, Etienne Rouleau, Susan L. Neuhausen, Thomas v. O. Hansen, Alvaro Galli, Rita D. Brandão, Marinus J. Blok, Aneliya Velkova, Fergus J. Couch, Alvaro N.A. Monteiro and on behalf of the ENIGMA (Evidence-based Network for the Interpretation of Germline Mutant Alleles) Consortium Functional Assay Working Group

    Version of Record online : 16 JUL 2012, DOI: 10.1002/humu.22150

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    The molecular pathogenesis of hereditary ovarian carcinoma

    Cancer

    Volume 116, Issue 22, 15 November 2010, Pages: 5261–5271, Barbara M. Norquist, Rochelle L. Garcia, Kimberly H. Allison, Chris H. Jokinen, Lauren E. Kernochan, Catherine C. Pizzi, Bethany J. Barrow, Barbara A. Goff and Elizabeth M. Swisher

    Version of Record online : 3 NOV 2010, DOI: 10.1002/cncr.25439