检索结果 - Leppig, Kathleen

AB004. Genetic testing for individuals with developmental disabilities and congenital anomalies: choosing between chromosomes, DNA microarrays, and next generation sequencing platf... 由 Leppig, Kathleen

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Collaborations in medical genetics: 10‐Year history of an ongoing Vietnamese‐North American Collaboration 由 Leppig, Kathleen A.

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AB030. The evolving role of genetic counseling 由 Leppig, Kathleen, Sternen, Darci, Thompson, Jennifer, Laurino, Mercy

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Identifying opportunities for collaboration and growth of genetic counseling services in the Asia Region 由 Laurino, Mercy Y., Sternen, Darci L., Thompson, Jennifer K., Leppig, Kathleen A.

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Development of FamilyTalk: An intervention to support communication and educate families about colorectal cancer risk 由 Bowen, Deborah, Hyams, Travis, Laurino, Mercy, Woolley, Timothy, Cohen, Stacey, Leppig, Kathleen A., Jarvik, Gail

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The annual ASHG dinner 由 Leppig, Kathleen A., Plon, Sharon E., Milewicz, Dianna M., Levy-Lahad, Ephrat, Jarvik, Gail P.

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Trends in BRCA Test Utilization in an Integrated Health System, 2005–2015 由 Knerr, Sarah, Bowles, Erin J A, Leppig, Kathleen A, Buist, Diana S M, Gao, Hongyuan, Wernli, Karen J

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Preferences of biobank participants for receiving actionable genomic test results: results of a re-contacting study 由 Henrikson, Nora B., Scrol, Aaron, Leppig, Kathleen A., Ralston, James D., Larson, Eric B., Jarvik, Gail P.

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Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies 由 Stephens, Karen, Weaver, Molly, Leppig, Kathleen A., Maruyama, Kyoko, Emanuel, Peter D., Le Beau, Michelle M., Shannon, Kevin M.

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“It would be so much easier”: health system-led genetic risk notification—feasibility and acceptability of cascade screening in an integrated system 由 Henrikson, Nora B., Blasi, Paula R., Fullerton, Stephanie M., Grafton, Jane, Leppig, Kathleen A., Jarvik, Gail P., Larson, Eric B.

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Ethical conflicts in translational genetic research: lessons learned from the eMERGE-III experience 由 Halverson, Colin M. E., Bland, Harris T., Leppig, Kathleen A., Marasa, Maddalena, Myers, Melanie, Rasouly, Hila Milo, Wynn, Julia, Clayton, Ellen Wright

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Characteristics Associated with Participation in ENGAGED 2 – A Web-based Breast Cancer Risk Communication and Decision Support Trial 由 Wernli, Karen J, Bowles, Erin A, Knerr, Sarah, Leppig, Kathleen A, Ehrlich, Kelly, Gao, Hongyuan, Schwartz, Marc D, O’Neill, Suzanne C

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Motivating factors for physician ordering of Factor V Leiden genetic tests 由 Hindorff, Lucia A., Burke, Wylie, Laberge, Anne-Marie, Rice, Kenneth M., Lumley, Thomas, Leppig, Kathleen, Rosendaal, Frits R., Larson, Eric B., Psaty, Bruce M.

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A web-based personalized risk communication and decision-making tool for women with dense breasts: design and methods of a randomized controlled trial within an integrated health c... 由 Knerr, Sarah, Wernli, Karen J., Leppig, Kathleen, Ehrlich, Kelly, Graham, Amanda L., Farrell, David, Evans, Chalanda, Luta, George, Schwartz, Marc D., O’Neill, Suzanne C.

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Implementation matters: How patient experiences differ when genetic counseling accompanies the return of genetic variants of uncertain significance 由 Patel, Harsh V., Henrikson, Nora B., Ralston, James D, Leppig, Kathleen, Scrol, Aaron, Jarvik, Gail P., DeVange, Shannon, Larson, Eric B, Hartzler, Andrea L.

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What improves the likelihood of people receiving genetic test results communicating to their families about genetic risk? 由 Bowen, Deborah J, Makhnoon, Sukh, Shirts, Brian H., Fullerton, Stephanie M, Larson, Eric, Ralston, James D, Leppig, Kathleen, Crosslin, David R., Veenstra, David, Jarvik, Gail P.

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Patient and Family Preferences on Health System-Led Direct Contact for Cascade Screening 由 Henrikson, Nora B., Blasi, Paula, Figueroa Gray, Marlaine, Tiffany, Brooks T., Scrol, Aaron, Ralston, James D., Fullerton, Stephanie M., Lim, Catherine Y., Ewing, John, Leppig, Kathleen A.

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Genetic heterogeneity and core clinical features of NOG-related-symphalangism spectrum disorder 由 Carlson, Ryan J., Quesnel, Alicia, Wells, Dawson, Brownstein, Zippora, Gilony, Dror, Gulsuner, Suleyman, Leppig, Kathleen A., Avraham, Karen B., King, Mary-Claire, Walsh, Tom, Rubinstein, Jay

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Building a family network from genetic testing 由 Leppig, Kathleen A., Thiese, Heidi A., Carrel, David, Crosslin, David R., Dorschner, Michael O., Gordon, Adam S., Hartzler, Andrea, Ralston, James, Scrol, Aaron, Larson, Eric B., Jarvik, Gail P.

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Relationship between genetic knowledge and familial communication of CRC risk and intent to communicate CRCP genetic information: insights from FamilyTalk eMERGE III 由 Makhnoon, Sukh, Bowen, Deborah J, Shirts, Brian H, Fullerton, Stephanie M, Meischke, Hendrika W, Larson, Eric B, Ralston, James D, Leppig, Kathleen, Crosslin, David R, Veenstra, David, Jarvik, Gail P

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