A C-terminal skeletal muscle sodium channel mutation associated with myotonia disrupts fast inactivation

Por Wu, Fen-fen, Gordon, Erynn, Hoffman, Eric P, Cannon, Stephen C
Publicado em 2005

“It’s not like judgment day”: Public understanding of and reactions to personalized genomic risk information

Por Gordon, Erynn S., Griffin, Georgia, Wawak, Lisa, Pang, Hauchie, Gollust, Sarah E., Bernhardt, Barbara A.
Publicado em 2011

Incorporating direct-to-consumer genomic information into patient care: attitudes and experiences of primary care physicians

Por Bernhardt, Barbara A, Zayac, Cara, Gordon, Erynn S, Wawak, Lisa, Pyeritz, Reed E, Gollust, Sarah E
Publicado em 2012

Genetic Testing of Children for Predisposition to Mood Disorders: Anticipating the Clinical Issues

Por Erickson, Jessica A., Kuzmich, Lili, Ormond, Kelly E., Gordon, Erynn, Christman, Michael F., Cho, Mildred K., Levinson, Douglas F.
Publicado em 2014

The Coriell personalized medicine collaborative pharmacogenomics appraisal, evidence scoring and interpretation system

Por Gharani, Neda, Keller, Margaret A, Stack, Catharine B, Hodges, Laura M, Schmidlen, Tara J, Lynch, Daniel E, Gordon, Erynn S, Christman, Michael F
Publicado em 2013

Huntington disease reduced penetrance alleles occur at high frequency in the general population

Por Kay, Chris, Collins, Jennifer A., Miedzybrodzka, Zosia, Madore, Steven J., Gordon, Erynn S., Gerry, Norman, Davidson, Mark, Slama, Ramy A., Hayden, Michael R.
Publicado no Neurology (2016)

A randomized trial of the clinical utility of genetic testing for obesity: Design and implementation considerations

Por Wang, Catharine, Gordon, Erynn S., Stack, Catharine B., Liu, Ching-Ti, Norkunas, Tricia, Wawak, Lisa, Christman, Michael F., Green, Robert C., Bowen, Deborah J.
Publicado em 2013

A randomized trial examining the impact of communicating genetic and lifestyle risks for obesity

Por Wang, Catharine, Gordon, Erynn S., Norkunas, Tricia, Wawak, Lisa, Liu, Ching-Ti, Winter, Michael, Kasper, Rachel S., Christman, Michael F., Green, Robert C., Bowen, Deborah J.
Publicado no Obesity (Silver Spring) (2016)

Using the Coriell Personalized Medicine Collaborative Data to conduct a genome‐wide association study of sleep duration

Por Scheinfeldt, Laura B., Gharani, Neda, Kasper, Rachel S., Schmidlen, Tara J., Gordon, Erynn S., Jarvis, Joseph P., Delaney, Susan, Kronenthal, Courtney J., Gerry, Norman P., Christman, Michael F.
Publicado no Am J Med Genet B Neuropsychiatr Genet (2015)

Outcomes of a randomized controlled trial of genomic counseling for patients receiving personalized and actionable complex disease reports

Por Sweet, Kevin, Sturm, Amy C., Schmidlen, Tara, McElroy, Joseph, Scheinfeldt, Laura, Manickam, Kandamurugu, Gordon, Erynn S., Hovick, Shelly, Roberts, J. Scott, Toland, Amanda Ewart, Christman, Michael
Publicado no J Genet Couns (2017)

Genetic Knowledge Among Participants in the Coriell Personalized Medicine Collaborative

Por Schmidlen, Tara J., Scheinfeldt, Laura, Zhaoyang, Ruixue, Kasper, Rachel, Sweet, Kevin, Gordon, Erynn S., Keller, Margaret, Stack, Cathy, Gharani, Neda, Daly, Mary B., Jarvis, Joseph, Christman, Michael F.
Publicado no J Genet Couns (2015)

Common Genetic Risk for Melanoma Encourages Preventive Behavior Change

Por Diseati, Lori, Scheinfeldt, Laura B., Kasper, Rachel S., Zhaoyang, Ruixue, Gharani, Neda, Schmidlen, Tara J., Gordon, Erynn S., Sessions, Cecili K., Delaney, Susan K., Jarvis, Joseph P., Gerry, Norman, Christman, Michael
Publicado no J Pers Med (2015)

Counselees’ Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: A Qualitative Research Study

Por Sweet, Kevin, Hovick, Shelly, Sturm, Amy C., Schmidlen, Tara, Gordon, Erynn, Bernhardt, Barbara, Wawak, Lisa, Wernke, Karen, McElroy, Joseph, Scheinfeldt, Laura, Toland, Amanda Ewart, Roberts, J. Scott, Christman, Michael
Publicado no J Genet Couns (2016)

Precision Military Medicine: Conducting a multi-site clinical utility study of genomic and lifestyle risk factors in the United States Air Force

Por Delaney, Susan K., Brenner, Ruth, Schmidlen, Tara J., Dempsey, Michael P., London, Kim E., Gordon, Erynn S., Bellafante, Mark, Nasuti, Ashley, Scheinfeldt, Laura B., Rajula, Kaveri D., Jose, Leo, Jarvis, Joseph P., Gerry, Norman P., Christman, Michael F.
Publicado no NPJ Genom Med (2017)

Design and Implementation of a Randomized Controlled Trial of Genomic Counseling for Patients with Chronic Disease

Por Sweet, Kevin, Gordon, Erynn S., Sturm, Amy C., Schmidlen, Tara J., Manickam, Kandamurugu, Toland, Amanda Ewart, Keller, Margaret A., Stack, Catharine B., García-España, J. Felipe, Bellafante, Mark, Tayal, Neeraj, Embi, Peter, Binkley, Philip, Hershberger, Ray E., Sadee, Wolfgang, Christman, Michael, Marsh, Clay
Publicado em 2014

Characterizing Genetic Variants for Clinical Action

Por Ramos, Erin M., Din-Lovinescu, Corina, Berg, Jonathan S., Brooks, Lisa D., Duncanson, Audrey, Dunn, Michael, Good, Peter, Hubbard, Tim, Jarvik, Gail P., O'Donnell, Christopher, Sherry, Stephen T., Aronson, Naomi, Biesecker, Leslie G., Blumberg, Bruce, Calonge, Ned, Colhoun, Helen M., Epstein, Robert S., Flicek, Paul, Gordon, Erynn S., Green, Eric D., Green, Robert C., Hurles, Matthew, Kawamoto, Kensaku, Knaus, William, Ledbetter, David H., Levy, Howard P., Lyon, Elaine, Maglott, Donna, McLeod, Howard L., Rahman, Nazneen, Randhawa, Gurvaneet, Wicklund, Catherine, Manolio, Teri A., Chisholm, Rex L., Williams, Marc S.
Publicado em 2014