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There are 18183 results for: content related to: Are physician recommendations for BRCA1/2 testing in patients with breast cancer appropriate? A population-based study

  1. You have free access to this content
    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

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    Psychiatric implications of cancer genetic testing

    Cancer

    Volume 121, Issue 3, February 1, 2015, Pages: 341–360, April Malia Hirschberg, Gayun Chan-Smutko and William F. Pirl

    Version of Record online : 18 SEP 2014, DOI: 10.1002/cncr.28879

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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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    Comprehensive sequencing of PALB2 in patients with breast cancer suggests PALB2 mutations explain a subset of hereditary breast cancer

    Cancer

    Volume 120, Issue 7, 1 April 2014, Pages: 963–967, Priscilla H. Fernandes, Jennifer Saam, Jenny Peterson, Elisha Hughes, Rajesh Kaldate, Shelly Cummings, Aaron Theisen, Sonia Chen, Jeffrey Trost and Benjamin B. Roa

    Version of Record online : 10 JAN 2014, DOI: 10.1002/cncr.28504

  5. 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

  6. Early use of clinical BRCA1/2 testing: Associations with race and breast cancer risk

    American Journal of Medical Genetics Part A

    Volume 117A, Issue 2, 1 March 2003, Pages: 154–160, Katrina Armstrong, Barbara Weber, Jill Stopfer, Kathleen Calzone, Mary Putt, James Coyne and J. Sanford Schwartz

    Version of Record online : 7 OCT 2002, DOI: 10.1002/ajmg.a.10928

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    When parents disclose BRCA1/2 test results: Their communication and perceptions of offspring response

    Cancer

    Volume 118, Issue 13, 1 July 2012, Pages: 3417–3425, Angela R. Bradbury, Linda Patrick-Miller, Brian L. Egleston, Olufunmilayo I. Olopade, Mary B. Daly, Cynthia W. Moore, Colleen B. Sands, Helen Schmidheiser, Preethi K. Kondamudi, Maia Feigon, Comfort N. Ibe and Christopher K. Daugherty

    Version of Record online : 9 JAN 2012, DOI: 10.1002/cncr.26471

  8. Cost Effectiveness Analysis of Genetic Testing for Breast and Ovarian Cancer Susceptibility Genes: BRCA1 and BRCA2

    The Breast Journal

    Volume 20, Issue 3, May/June 2014, Pages: 325–326, Rajesh Kaldate, Alissa Huston, Heidi McCoy, Dawn Cardeiro and Katia Noyes

    Version of Record online : 7 APR 2014, DOI: 10.1111/tbj.12269

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    Long-term outcomes of BRCA1/BRCA2 testing: risk reduction and surveillance

    Cancer

    Volume 118, Issue 2, 15 January 2012, Pages: 510–517, Marc D. Schwartz, Claudine Isaacs, Kristi D. Graves, Elizabeth Poggi, Beth N. Peshkin, Christy Gell, Clinton Finch, Scott Kelly, Kathryn L. Taylor and Lauren Perley

    Version of Record online : 29 JUN 2011, DOI: 10.1002/cncr.26294

  10. 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

  11. 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

  12. Commercialization of BRCA1/2 testing: Practitioner awareness and use of a new genetic test

    American Journal of Medical Genetics

    Volume 83, Issue 3, 19 March 1999, Pages: 157–163, M.K. Cho, P. Sankar, P.R. Wolpe and L. Godmilow

    Version of Record online : 4 MAR 1999, DOI: 10.1002/(SICI)1096-8628(19990319)83:3<157::AID-AJMG4>3.0.CO;2-G

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    Utilization of BRCA1/2 genetic testing in the clinical setting

    Cancer

    Volume 94, Issue 6, 15 March 2002, Pages: 1876–1885, Soo-Chin Lee, Barbara A. Bernhardt and Kathy J. Helzlsouer

    Version of Record online : 15 MAR 2002, DOI: 10.1002/cncr.10420

  14. Development of a culturally tailored genetic counseling booklet about hereditary breast and ovarian cancer for Black women

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 4, April 2010, Pages: 836–845, Jennifer Permuth-Wey, Susan Vadaparampil, Alnecia Rumphs, Anita Yeomans Kinney and Tuya Pal

    Version of Record online : 26 MAR 2010, DOI: 10.1002/ajmg.a.33187

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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

  16. Life insurance and breast cancer risk assessment: Adverse selection, genetic testing decisions, and discrimination

    American Journal of Medical Genetics Part A

    Volume 120A, Issue 3, 30 July 2003, Pages: 359–364, Katrina Armstrong, Barbara Weber, Genevieve FitzGerald, John C. Hershey, Mark V. Pauly, Jean Lemaire, Krupa Subramanian and David A. Asch

    Version of Record online : 11 APR 2003, DOI: 10.1002/ajmg.a.20025

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    Development and validation of risk models and molecular diagnostics to permit personalized management of cancer

    Cancer

    Volume 120, Issue 1, 1 January 2014, Pages: 11–19, Xia Pu, Yuanqing Ye and Xifeng Wu

    Version of Record online : 2 OCT 2013, DOI: 10.1002/cncr.28393

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    Population-based cancer registries for quality-of-life research

    Cancer

    Volume 119, Issue S11, 1 June 2013, Pages: 2109–2123, Melissa S. Y. Thong, Floortje Mols, Kevin D. Stein, Tenbroeck Smith, Jan-Willem W. Coebergh and Lonneke V. van de Poll-Franse

    Version of Record online : 20 MAY 2013, DOI: 10.1002/cncr.28056

  19. 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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    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