Educating physicians in the era of genomic medicine

por Murray, Michael F
Publicado 2014

Enabling Diagnostic Resulting as a New Category of Secondary Genomic Findings

por Murray, Michael F.
Publicado 2022

Addressing the routine failure to clinically identify monogenic cases of common disease

por Murray, Michael F., Khoury, Muin J., Abul-Husn, Noura S.
Publicado 2022

The intersection of genetics and COVID-19 in 2021: preview of the 2021 Rodney Howell Symposium

por Rasmussen, Sonja A., Abul-Husn, Noura S., Casanova, Jean-Laurent, Daly, Mark J., Rehm, Heidi L., Murray, Michael F.
Publicado 2021

Hereditary cancer genes are highly susceptible to splicing mutations

por Rhine, Christy L., Cygan, Kamil J., Soemedi, Rachel, Maguire, Samantha, Murray, Michael F., Monaghan, Sean F., Fairbrother, William G.
Publicado 2018

COVID-19 outcomes and the human genome

por Murray, Michael F., Kenny, Eimear E., Ritchie, Marylyn D., Rader, Daniel J., Bale, Allen E., Giovanni, Monica A., Abul-Husn, Noura S.
Publicado 2020

A loss of function variant in CASP7 protects against Alzheimer’s disease in homozygous APOE ε4 allele carriers

por Ayers, Kristin L., Mirshahi, Uyenlinh L., Wardeh, Amr H., Murray, Michael F., Hao, Ke, Glicksberg, Benjamin S., Li, Shuyu, Carey, David J., Chen, Rong
Publicado 2016

The Geisinger MyCode Community Health Initiative: an electronic health record-linked biobank for Precision Medicine research

por Carey, David J., Fetterolf, Samantha N., Davis, F. Daniel, Faucett, William A., Kirchner, H. Lester, Mirshahi, Uyenlinh, Murray, Michael F., Smelser, Diane T., Gerhard, Glenn S., Ledbetter, David H.
Publicado 2016

Healthcare Utilization and Costs after Receiving a Positive BRCA1/2 Result from a Genomic Screening Program

por Hao, Jing, Hassen, Dina, Manickam, Kandamurugu, Murray, Michael F., Hartzel, Dustin N., Hu, Yirui, Liu, Kunpeng, Rahm, Alanna Kulchak, Williams, Marc S., Lazzeri, Amanda, Buchanan, Adam, Sturm, Amy, Snyder, Susan R.
Publicado 2020

A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health

por Khoury, Muin J., Feero, W. Gregory, Chambers, David A., Brody, Lawrence E., Aziz, Nazneen, Green, Robert C., Janssens, A. Cecile J.W., Murray, Michael F., Rodriguez, Laura Lyman, Rutter, Joni L., Schully, Sheri D., Winn, Deborah M., Mensah, George A.
Publicado 2018

Correction: A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health

por Khoury, Muin J., Feero, W. Gregory, Chambers, David A., Brody, Lawrence C., Aziz, Nazneen, Green, Robert C., Janssens, A. Cecile J. W., Murray, Michael F., Rodriguez, Laura Lyman, Rutter, Joni L., Schully, Sheri D., Winn, Deborah M., Mensah, George A.
Publicado 2018

A systematic approach to the reporting of medically relevant findings from whole genome sequencing

por McLaughlin, Heather M, Ceyhan-Birsoy, Ozge, Christensen, Kurt D, Kohane, Isaac S, Krier, Joel, Lane, William J, Lautenbach, Denise, Lebo, Matthew S, Machini, Kalotina, MacRae, Calum A, Azzariti, Danielle R, Murray, Michael F, Seidman, Christine E, Vassy, Jason L, Green, Robert C, Rehm, Heidi L
Publicado 2014

Finding missed cases of familial hypercholesterolemia in health systems using machine learning

por Banda, Juan M., Sarraju, Ashish, Abbasi, Fahim, Parizo, Justin, Pariani, Mitchel, Ison, Hannah, Briskin, Elinor, Wand, Hannah, Dubois, Sebastien, Jung, Kenneth, Myers, Seth A., Rader, Daniel J., Leader, Joseph B., Murray, Michael F., Myers, Kelly D., Wilemon, Katherine, Shah, Nigam H., Knowles, Joshua W.
Publicado 2019

A Genome-First Approach to Characterize DICER1 Pathogenic Variant Prevalence, Penetrance, and Phenotype

por Mirshahi, Uyenlinh L., Kim, Jung, Best, Ana F., Chen, Zongming E., Hu, Ying, Haley, Jeremy S., Golden, Alicia, Stahl, Richard, Manickam, Kandamurugu, Carr, Ann G., Harney, Laura A., Field, Amanda, Hatton, Jessica, Schultz, Kris Ann P., Bauer, Andrew J., Hill, D. Ashley, Rosenberg, Philip S., Murray, Michael F., Carey, David J., Stewart, Douglas R.
Publicado 2021

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine

por Vassy, Jason L, Lautenbach, Denise M, McLaughlin, Heather M, Kong, Sek Won, Christensen, Kurt D, Krier, Joel, Kohane, Isaac S, Feuerman, Lindsay Z, Blumenthal-Barby, Jennifer, Roberts, J Scott, Lehmann, Lisa Soleymani, Ho, Carolyn Y, Ubel, Peter A, MacRae, Calum A, Seidman, Christine E, Murray, Michael F, McGuire, Amy L, Rehm, Heidi L, Green, Robert C
Publicado 2014

Implementing genomic medicine in the clinic: the future is here

por Manolio, Teri A., Chisholm, Rex L., Ozenberger, Brad, Roden, Dan M., Williams, Marc S., Wilson, Richard, Bick, David, Bottinger, Erwin P., Brilliant, Murray H., Eng, Charis, Frazer, Kelly A., Korf, Bruce, Ledbetter, David H., Lupski, James R., Marsh, Clay, Mrazek, David, Murray, Michael F., O'Donnell, Peter H., Rader, Daniel J., Relling, Mary V., Shuldiner, Alan R., Valle, David, Weinshilboum, Richard, Green, Eric D., Ginsburg, Geoffrey S.
Publicado 2013

Electronic Health Record Phenotype in Subjects with Genetic Variants Associated with Arrhythmogenic Right Ventricular Cardiomyopathy: A Study in 30,716 Subjects with Exome Sequenci...

por Haggerty, Christopher M., James, Cynthia A., Calkins, Hugh, Tichnell, Crystal, Leader, Joseph B., Hartzel, Dustin N., Nevius, Christopher D., Pendergrass, Sarah A., Person, Thomas N., Schwartz, Marci, Ritchie, Marylyn D., Carey, David J., Ledbetter, David H., Williams, Marc S., Dewey, Frederick E., Lopez, Alexander, Penn, John, Overton, John D., Reid, Jeffrey G., Lebo, Matthew, Mason-Suares, Heather, Austin-Tse, Christina, Rehm, Heidi L., Delisle, Brian P., Makowski, Daniel J., Mehra, Vishal C., Murray, Michael F., Fornwalt, Brandon K.
Publicado 2017

Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

por Buchanan, Adam H, Manickam, Kandamurugu, Meyer, Michelle N, Wagner, Jennifer K, Hallquist, Miranda L G, Williams, Janet L, Rahm, Alanna Kulchak, Williams, Marc S, Chen, Zong-Ming E, Shah, Chaitali K, Garg, Tullika K, Lazzeri, Amanda L, Schwartz, Marci L B, Lindbuchler, D'Andra M, Fan, Audrey L, Leeming, Rosemary, Servano, Pedro O, Smith, Ashlee L, Vogel, Victor G, Abul-Husn, Noura S, Dewey, Frederick E, Lebo, Matthew S, Mason-Suares, Heather M, Ritchie, Marylyn D, Davis, F Daniel, Carey, David J, Feinberg, David T, Faucett, W Andrew, Ledbetter, David H, Murray, Michael F
Publicado 2017

Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

por Buchanan, Adam H., Manickam, Kandamurugu, Meyer, Michelle N., Wagner, Jennifer K., Hallquist, Miranda L. G., Williams, Janet L., Rahm, Alanna Kulchak, Williams, Marc S., Chen, Zong-Ming E., Shah, Chaitali K., Garg, Tullika K., Lazzeri, Amanda L., Schwartz, Marci L. B., Lindbuchler, D’ Andra M., Fan, Audrey L., Leeming, Rosemary, Servano, Pedro O., Smith, Ashlee L., Vogel, Victor G., Abul-Husn, Noura S., Dewey, Frederick E., Lebo, Matthew S., Mason-Suares, Heather M., Ritchie, Marylyn D., Davis, F. Daniel, Carey, David J., Feinberg, David T., Faucett, W. Andrew, Ledbetter, David H., Murray, Michael F.
Publicado 2021

Exome Sequencing–Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants

por Manickam, Kandamurugu, Buchanan, Adam H., Schwartz, Marci L. B., Hallquist, Miranda L. G., Williams, Janet L., Rahm, Alanna Kulchak, Rocha, Heather, Savatt, Juliann M., Evans, Alyson E., Butry, Loren M., Lazzeri, Amanda L., Lindbuchler, D’Andra M., Flansburg, Carroll N., Leeming, Rosemary, Vogel, Victor G., Lebo, Matthew S., Mason-Suares, Heather M., Hoskinson, Derick C., Abul-Husn, Noura S., Dewey, Frederick E., Overton, John D., Reid, Jeffrey G., Baras, Aris, Willard, Huntington F., McCormick, Cara Z., Krishnamurthy, Sarath B., Hartzel, Dustin N., Kost, Korey A., Lavage, Daniel R., Sturm, Amy C., Frisbie, Lauren R., Person, T. Nate, Metpally, Raghu P., Giovanni, Monica A., Lowry, Lacy E., Leader, Joseph B., Ritchie, Marylyn D., Carey, David J., Justice, Anne E., Kirchner, H. Lester, Faucett, W. Andrew, Williams, Marc S., Ledbetter, David H., Murray, Michael F.
Publicado 2018