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Hereditary Cancer in Clinical Practice

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1. Content Type:Research

     |  28 July 2018

   CD36 – a plausible modifier of disease phenotype in familial adenomatous polyposis

   Authors:Merran Holmes, Toni Connor, Christopher Oldmeadow, Peter G. Pockney, Rodney J. Scott and Bente A. Talseth-Palmer
2. Content Type:Research

     |  4 July 2018

   A qualitative study of barriers to genetic counseling and potential for mobile technology education among women with ovarian cancer

   Authors:Rachel Isaksson Vogel, Kristin Niendorf, Heewon Lee, Sue Petzel, Hee Yun Lee and Melissa A. Geller
3. Content Type:Research

     |  5 June 2018

   High frequency of pathogenic non-founder germline mutations in BRCA1 and BRCA2 in families with breast and ovarian cancer in a founder population

   Authors:J. Maksimenko, A. Irmejs, G. Trofimovičs, D. Bērziņa, E. Skuja, G. Purkalne, E. Miklaševičs and J. Gardovskis
4. Content Type:Research

     |  10 May 2018

   Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviews

   Authors:Jennifer L. Schneider, Katrina A. B. Goddard, Kristin R. Muessig, James V. Davis, Alan F. Rope, Jessica E. Hunter, Susan K. Peterson, Louise S. Acheson, Sapna Syngal, Georgia L. Wiesner and Jacob A. Reiss
5. Content Type:Research

     |  27 April 2018

   Platinum-based neoadjuvant chemotherapy in BRCA1-positive breast cancer: a retrospective cohort analysis and literature review

   Authors:Nikolai Havn Sæther, Elina Skuja, Arvids Irmejs, Jelena Maksimenko, Edvins Miklasevics, Gunta Purkalne and Janis Gardovskis

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