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There are 24580 results for: content related to: New data on BRCA mutations and prophylactic surgeries

  1. 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

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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

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    Secondary mutations of BRCA1/2 and drug resistance

    Cancer Science

    Volume 102, Issue 4, April 2011, Pages: 663–669, Kiranjit K. Dhillon, Elizabeth M. Swisher and Toshiyasu Taniguchi

    Version of Record online : 30 JAN 2011, DOI: 10.1111/j.1349-7006.2010.01840.x

  4. Impact of a paternal origin of germline BRCA1/2 mutations on the age at breast and ovarian cancer diagnosis in a Southern Swedish cohort

    Genes, Chromosomes and Cancer

    Volume 54, Issue 1, January 2015, Pages: 39–50, Carolina Ellberg, Helena Jernström, Per Broberg, Åke Borg and Håkan Olsson

    Version of Record online : 23 SEP 2014, DOI: 10.1002/gcc.22217

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    Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel

    Cancer

    Volume 121, Issue 1, January 1, 2015, Pages: 25–33, Nadine Tung, Chiara Battelli, Brian Allen, Rajesh Kaldate, Satish Bhatnagar, Karla Bowles, Kirsten Timms, Judy E. Garber, Christina Herold, Leif Ellisen, Jill Krejdovsky, Kim DeLeonardis, Kristin Sedgwick, Kathleen Soltis, Benjamin Roa, Richard J. Wenstrup and Anne-Renee Hartman

    Version of Record online : 3 SEP 2014, DOI: 10.1002/cncr.29010

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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

  7. All in the family: Evaluation of the process and content of sisters' communication about BRCA1 and BRCA2 genetic test results

    American Journal of Medical Genetics

    Volume 107, Issue 2, 15 January 2002, Pages: 143–150, Chanita Hughes, Caryn Lerman, Marc Schwartz, Beth N. Peshkin, Lari Wenzel, Steven Narod, Camille Corio, Kenneth P. Tercyak, Danielle Hanna, Claudine Isaacs and David Main

    Version of Record online : 28 NOV 2001, DOI: 10.1002/ajmg.10110

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    BRCA1 and BRCA2 germline mutations are frequently demonstrated in both high-risk pancreatic cancer screening and pancreatic cancer cohorts

    Cancer

    Volume 120, Issue 13, 1 July 2014, Pages: 1960–1967, Aimee L. Lucas, Laura E. Frado, Caroline Hwang, Sheila Kumar, Lauren G. Khanna, Elana J. Levinson, John A. Chabot, Wendy K. Chung and Harold Frucht

    Version of Record online : 15 APR 2014, DOI: 10.1002/cncr.28662

  9. Androgen receptor expression in breast cancer patients tested for BRCA1 and BRCA2 mutations

    Histopathology

    Volume 57, Issue 6, December 2010, Pages: 877–884, Gunda Pristauz, Edgar Petru, Elvira Stacher, Jochen B Geigl, Thomas Schwarzbraun, Oleksiy Tsybrovskyy, Raimund Winter and Farid Moinfar

    Version of Record online : 17 DEC 2010, DOI: 10.1111/j.1365-2559.2010.03724.x

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    Comparison of age at natural menopause in BRCA1/2 mutation carriers with a non–clinic-based sample of women in northern California

    Cancer

    Volume 119, Issue 9, 1 May 2013, Pages: 1652–1659, Wayne T. Lin, Mary Beattie, Lee-may Chen, Kutluk Oktay, Sybil L. Crawford, Ellen B. Gold, Marcelle Cedars and Mitchell Rosen

    Version of Record online : 29 JAN 2013, DOI: 10.1002/cncr.27952

  11. Single-nucleotide polymorphisms in the p53 pathway genes modify cancer risk in BRCA1 and BRCA2 carriers of Jewish-Ashkenazi descent

    Molecular Carcinogenesis

    Volume 49, Issue 6, June 2010, Pages: 545–555, Ronit I. Yarden, Eitan Friedman, Sally Metsuyanim, Tzvia Olender, Edna Ben-Asher and Moshe Z. Papa

    Version of Record online : 19 MAR 2010, DOI: 10.1002/mc.20618

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    Poly(ADP-Ribose) polymerase (PARP) inhibitors: Exploiting a synthetic lethal strategy in the clinic

    CA: A Cancer Journal for Clinicians

    Volume 61, Issue 1, January/February 2011, Pages: 31–49, Timothy A. Yap, Shahneen K. Sandhu, Craig P. Carden and Johann S. de Bono

    Version of Record online : 4 JAN 2011, DOI: 10.3322/caac.20095

  13. Microarray analysis of differentially expressed genes in ovarian and fallopian tube epithelium from risk-reducing salpingo-oophorectomies

    Genes, Chromosomes and Cancer

    Volume 54, Issue 5, May 2015, Pages: 276–287, Kristina Veskimäe, Synnöve Staff, Francesco Tabaro, Matti Nykter, Jorma Isola and Johanna Mäenpää

    Version of Record online : 23 FEB 2015, DOI: 10.1002/gcc.22241

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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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    Prevalence of BRCA1 and BRCA2 mutations in Pakistani breast and ovarian cancer patients

    International Journal of Cancer

    Volume 119, Issue 12, 15 December 2006, Pages: 2832–2839, Muhammad U. Rashid, Anbreen Zaidi, Diana Torres, Faisal Sultan, Axel Benner, Bilal Naqvi, Abdul R. Shakoori, Antje Seidel-Renkert, Humirah Farooq, Steven Narod, Asim Amin and Ute Hamann

    Version of Record online : 22 SEP 2006, DOI: 10.1002/ijc.22269

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    Relevance and efficacy of breast cancer screening in BRCA1 and BRCA2 mutation carriers above 60 years: A national cohort study

    International Journal of Cancer

    Volume 135, Issue 12, 15 December 2014, Pages: 2940–2949, Sepideh Saadatmand, Janet R. Vos, Maartje J. Hooning, Jan C. Oosterwijk, Linetta B. Koppert, Geertruida H. de Bock, Margreet G. Ausems, Christi J. van Asperen, Cora M. Aalfs, Encarna B. Gómez Garcia, Hanne Meijers-Heijboer, Nicoline Hoogerbrugge, Marianne Piek, Caroline Seynaeve, Cornelis Verhoef, Matti Rookus, Madeleine M. Tilanus-Linthorst and the Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON)

    Version of Record online : 20 MAY 2014, DOI: 10.1002/ijc.28941

  17. Young adult daughters of BRCA1/2 positive mothers: What do they know about hereditary cancer and how much do they worry?

    Psycho-Oncology

    Volume 22, Issue 9, September 2013, Pages: 2024–2031, Andrea F. Patenaude, Nadine Tung, Paula D. Ryan, Leif W. Ellisen, Larissa Hewitt, Katherine A. Schneider, Kenneth P. Tercyak, Julie Aldridge and Judy E. Garber

    Version of Record online : 18 FEB 2013, DOI: 10.1002/pon.3257

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    Prognostic impact of BRCA1 pathogenic and BRCA1/BRCA2 unclassified variant mutations in patients with ovarian carcinoma

    Cancer

    Volume 104, Issue 5, 1 September 2005, Pages: 1004–1012, Ewa Joanna Majdak, Jaroslaw Debniak, Tomasz Milczek, Cees J. Cornelisse, Peter Devilee, Janusz Emerich, Jacek Jassem and Geertruida Hendrika De Bock

    Version of Record online : 26 JUL 2005, DOI: 10.1002/cncr.21276

  19. BRCA1/2 testing: uptake, phenocopies, and strategies to improve detection rates in initially negative families

    Clinical Genetics

    Volume 82, Issue 5, November 2012, Pages: 478–483, C Fischer, C Engel, C Sutter, S Zachariae, R Schmutzler, A Meindl, S Heidemann, T Grimm, TO Goecke, I Debatin, D Horn, P Wieacker, D Gadzicki, K Becker, D Schäfer, F Stock, T Voigtländer and on behalf of the German Consortium for Hereditary Breast and Ovarian Cancer

    Version of Record online : 19 OCT 2011, DOI: 10.1111/j.1399-0004.2011.01788.x

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    Association between BRCA1 and BRCA2 mutations and cancer phenotype in Spanish breast/ovarian cancer families: Implications for genetic testing

    International Journal of Cancer

    Volume 97, Issue 4, 1 February 2002, Pages: 466–471, Miguel de la Hoya, Ana Osorio, Javier Godino, Sara Sulleiro, Alicia Tosar, Pedro Perez-Segura, Cristina Fernandez, Raquel Rodríguez, Eduardo Díaz-Rubio, Javier Benítez, Peter Devilee and Trinidad Caldés

    Version of Record online : 18 OCT 2001, DOI: 10.1002/ijc.1627