Pharmacogenomic (PGx) Counseling: Exploring Participant Questions about PGx Test Results

por Schmidlen, Tara, Sturm, Amy C., Scheinfeldt, Laura B.
Publicado 2020

Challenges in Translating GWAS Results to Clinical Care

por Scheinfeldt, Laura B., Schmidlen, Tara J., Gerry, Norman P., Christman, Michael F.
Publicado 2016

The Impact of Proband Indication for Genetic Testing on the Uptake of Cascade Testing Among Relatives

por Schmidlen, Tara J., Bristow, Sara L., Hatchell, Kathryn E., Esplin, Edward D., Nussbaum, Robert L., Haverfield, Eden V.
Publicado 2022

Validation of Pharmacogenomic Interaction Probability (PIP) Scores in Predicting Drug–Gene, Drug–Drug–Gene, and Drug–Gene–Gene Interaction Risks in a Large Patient Population...

por Ashcraft, Kristine, Grande, Kendra, Bristow, Sara L., Moyer, Nicolas, Schmidlen, Tara, Moretz, Chad, Wick, Jennifer A., Blaxall, Burns C.
Publicado 2022

Generation and Implementation of a Patient-Centered and Patient-Facing Genomic Test Report in the EHR

por Goehringer, Jessica M., Bonhag, Michele A., Jones, Laney K., Schmidlen, Tara, Schwartz, Marci, Rahm, Alanna Kulchak, Williams, Janet L., Williams, Marc S.
Publicado 2018

Early Outcome Data Assessing Utility of a Post-Test Genomic Counseling Framework for the Scalable Delivery of Precision Health

por Sturm, Amy C., Schmidlen, Tara, Scheinfeldt, Laura, Hovick, Shelly, McElroy, Joseph P., Toland, Amanda E., Roberts, J. Scott, Sweet, Kevin
Publicado 2018

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 2013

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 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 2015

Facilitating family communication of familial hypercholesterolemia genetic risk: Assessing engagement with innovative chatbot technology from the IMPACT-FH study

por Walters, Nicole L., Lindsey-Mills, Zoe T., Brangan, Andrew, Savage, Sarah K., Schmidlen, Tara J., Morgan, Kelly M., Tricou, Eric P., Betts, Megan M., Jones, Laney K., Sturm, Amy C., Campbell-Salome, Gemme
Publicado 2023

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 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 2014

Optimizing communication strategies and designing a comprehensive program to facilitate cascade testing for familial hypercholesterolemia

por Campbell-Salome, Gemme, Jones, Laney K., Walters, Nicole L., Morgan, Kelly M., Brangan, Andrew, Ladd, Ilene G., McGowan, Mary P., Wilemon, Katherine, Schmidlen, Tara J., Simmons, Emilie, Schwartz, Marci L. B., McMinn, Megan N., Tricou, Eric, Rahm, Alanna K., Ahmed, Catherine D., Sturm, Amy C.
Publicado 2023

Clinical outcomes of a genomic screening program for actionable genetic conditions

por Buchanan, Adam H., Lester Kirchner, H., Schwartz, Marci L. B., Kelly, Melissa A., Schmidlen, Tara, Jones, Laney K., Hallquist, Miranda L. G., Rocha, Heather, Betts, Megan, Schwiter, Rachel, Butry, Loren, Lazzeri, Amanda L., Frisbie, Lauren R., Rahm, Alanna Kulchak, Hao, Jing, Willard, Huntington F., Martin, Christa L., Ledbetter, David H., Williams, Marc S., Sturm, Amy C.
Publicado 2020

Developing and Optimizing Innovative Tools to Address Familial Hypercholesterolemia Underdiagnosis: Identification Methods, Patient Activation, and Cascade Testing for Familial Hyp...

por Campbell-Salome, Gemme, Jones, Laney K., Masnick, Max F., Walton, Nephi A., Ahmed, Catherine D., Buchanan, Adam H., Brangan, Andrew, Esplin, Edward D., Kann, David G., Ladd, Ilene G., Kelly, Melissa A., Kindt, Iris, Kirchner, H. Lester, McGowan, Mary P., McMinn, Megan N., Morales, Ana, Myers, Kelly D., Oetjens, Matthew T., Rahm, Alanna Kulchak, Schmidlen, Tara J., Sheldon, Amanda, Simmons, Emilie, Snir, Moran, Strande, Natasha T., Walters, Nicole L., Wilemon, Katherine, Williams, Marc S., Gidding, Samuel S., Sturm, Amy C.
Publicado 2021

Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations

por Lennon, Niall J, Kottyan, Leah C, Kachulis, Christopher, Abul-Husn, Noura, Arias, Josh, Belbin, Gillian, Below, Jennifer E, Berndt, Sonja, Chung, Wendy, Cimino, James J., Clayton, Ellen Wright, Connolly, John J., Crosslin, David, Dikilitas, Ozan, Velez Edwards, Digna R., Feng, QiPing, Fisher, Marissa, Freimuth, Robert, Ge, Tian, Glessner, Joseph T., Gordon, Adam, Guiducci, Candace, Hakonarson, Hakon, Harden, Maegan, Harr, Margaret, Hirschhorn, Joel, Hoggart, Clive, Hsu, Li, Irvin, Ryan, Jarvik, Gail P., Karlson, Elizabeth W., Khan, Atlas, Khera, Amit, Kiryluk, Krzysztof, Kullo, Iftikhar, Larkin, Katie, Limdi, Nita, Linder, Jodell E., Loos, Ruth, Luo, Yuan, Malolepsza, Edyta, Manolio, Teri, Martin, Lisa J., McCarthy, Li, Meigs, James B, Mersha, Tesfaye B., Mosley, Jonathan, Namjou, Bahram, Pai, Nihal, Pesce, Lorenzo L., Peters, Ulrike, Peterson, Josh, Prows, Cynthia A., Puckelwartz, Megan J., Rehm, Heidi, Roden, Dan, Rosenthal, Elisabeth A., Rowley, Robb, Sawicki, Konrad Teodor, Schaid, Dan, Schmidlen, Tara, Smit, Roelof, Smith, Johanna, Smoller, Jordan W., Thomas, Minta, Tiwari, Hemant, Toledo, Diana, Vaitinadin, Nataraja Sarma, Veenstra, David, Walunas, Theresa, Wang, Zhe, Wei, Wei-Qi, Weng, Chunhua, Wiesner, Georgia, Xianyong, Yin, Kenny, Eimear
Publicado 2023