Rezultati - Leppig, Kathleen

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

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

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AB030. The evolving role of genetic counseling od 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 od 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 od Bowen, Deborah, Hyams, Travis, Laurino, Mercy, Woolley, Timothy, Cohen, Stacey, Leppig, Kathleen A., Jarvik, Gail

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The annual ASHG dinner od 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 od 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 od 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 od 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 od 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 od 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 od 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 od 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... od 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 od 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? od 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 od 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 od 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 od 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 od 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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