检索结果 - Rachel Nusbaum
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Disparities in uptake of BRCA1/2 genetic testing in a randomized trial of telephone counseling 由 Morgan Butrick, Scott P. Kelly, Beth N. Peshkin, George Luta, Rachel Nusbaum, Gillian W. Hooker, Kristi D. Graves, Lisa Feeley, Claudine Isaacs, Heiðdís Valdimarsdóttir, Lina Jandorf, Tiffani A. DeMarco, Marie Wood, Wendy McKinnon, Judy E. Garber, Shelley R. McCormick, Marc D. Schwartz
出版 2014Artigo -
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Patient Perceptions of Telephone vs. In-Person BRCA1/BRCA2 Genetic Counseling 由 Beth N. Peshkin, Scott P. Kelly, Rachel Nusbaum, Morgan Similuk, Tiffani A. DeMarco, Gillian W. Hooker, Heiðdís Valdimarsdóttir, Andrea Forman, Jessica Rispoli Joines, Claire Davis, Shelley R. McCormick, Wendy McKinnon, Kristi D. Graves, Claudine Isaacs, Judy E. Garber, Marie Wood, Lina Jandorf, Marc D. Schwartz
出版 2015Artigo -
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Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing 由 Lisa R. Susswein, Megan L. Marshall, Rachel Nusbaum, Kristen J. Vogel Postula, Scott M. Weissman, Lauren Yackowski, Erica Vaccari, Jeffrey Bissonnette, Jessica K. Booker, Mattia Cremona, Federica Gibellini, Patricia D. Murphy, Daniel Pineda‐Alvarez, Guido D. Pollevick, Zhixiong Xu, Gabi Richard, Sherri J. Bale, Rachel T. Klein, Kathleen S. Hruska, Wendy K. Chung
出版 2015Artigo -
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Randomized Noninferiority Trial of Telephone Versus In-Person Genetic Counseling for Hereditary Breast and Ovarian Cancer 由 Mark D. Schwartz, Heiðdís Valdimarsdóttir, Beth N. Peshkin, Jeanne S. Mandelblatt, Rachel Nusbaum, An-Tsun Huang, Yao-Jen Chang, Kristi D. Graves, Claudine Isaacs, Marie Wood, Wendy McKinnon, Judy E. Garber, Shelley R. McCormick, Anita Y. Kinney, George Luta, Sarah A. Kelleher, Kara-Grace Leventhal, Patti Vegella, Angie Tong, Lesley G. King
出版 2014Artigo
相关主题
Biology
Genetic counseling
Genetics
Internal medicine
Medicine
Family medicine
Genetic testing
Randomized controlled trial
Telephone counseling
Breast cancer
Cancer
Clinical psychology
Confidence interval
Oncology
Anthropology
CHEK2
Clinical endpoint
Colorectal cancer
DNA mismatch repair
Demography
Distress
Ethnic group
Family history
Gene
Germline mutation
Gynecology
Logistic regression
Lynch syndrome
MLH1
MSH2