Impact of integrated translational research on clinical exome sequencing
Klee, Eric W., Cousin, Margot A., Pinto e Vairo, Filippo, Morales-Rosado, Joel A., Macke, Erica L., Jenkinson, W. Garrett, Ferrer, Alejandro, Schultz-Rogers, Laura E., Olson, Rory J., Oliver, Gavin R., Sigafoos, Ashley N., Schwab, Tanya L., Zimmermann, Michael T., Urrutia, Raul A., Kaiwar, Charu, Gupta, Aditi, Blackburn, Patrick R., Boczek, Nicole J., Prochnow, Carri A., Lowy, Rebecca J., Mulvihill, Lindsay A., McAllister, Tammy M., Aoudia, Stacy L., Kruisselbrink, Teresa M., Gunderson, Lauren B., Kemppainen, Jennifer L., Fisher, Laura J., Tarnowski, Jessica M., Hager, Megan M., Kroc, Sarah A., Bertsch, Nicole L., Agre, Katherine E., Jackson, Jessica L., Macklin-Mantia, Sarah K., Murphree, Marine I., Rust, Laura M., Summer Bolster, Jolene M., Beck, Scott A., Atwal, Paldeep S., Ellingson, Marissa S., Barnett, Sarah S., Rasmussen, Kristen J., Lahner, Carrie A., Niu, Zhiyv, Hasadsri, Linda, Ferber, Matthew J., Marcou, Cherisse A., Clark, Karl J., Pichurin, Pavel N., Deyle, David R., Morava-Kozicz, Eva, Gavrilova, Ralitza H., Dhamija, Radhika, Wierenga, Klaas J., Lanpher, Brendan C., Babovic-Vuksanovic, Dusica, Farrugia, Gianrico, Schimmenti, Lisa A., Stewart, A. Keith, Lazaridis, Konstantinos N.
Published in Genetics in medicine (01.03.2021)
Published in Genetics in medicine (01.03.2021)
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Journal Article
Correction: Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)
Pinto E Vairo, Filippo, Kemppainen, Jennifer L, Vitek, Carolyn R Rohrer, Whalen, Denise A, Kolbert, Kayla J, Sikkink, Kaitlin J, Kroc, Sarah A, Kruisselbrink, Teresa, Shupe, Gabrielle F, Knudson, Alyssa K, Burke, Elizabeth M, Loftus, Elle C, Bandel, Lorelei A, Prochnow, Carri A, Mulvihill, Lindsay A, Thomas, Brittany, Gable, Dale M, Graddy, Courtney B, Garzon, Giovanna G Moreno, Ekpoh, Idara U, Porquera, Eva M Carmona, Fervenza, Fernando C, Hogan, Marie C, El Ters, Mireille, Warrington, Kenneth J, Davis, 3rd, John M, Koster, Matthew J, Orandi, Amir B, Basiaga, Matthew L, Vella, Adrian, Kumar, Seema, Creo, Ana L, Lteif, Aida N, Pittock, Siobhan T, Tebben, Peter J, Abate, Ejigayehu G, Joshi, Avni Y, Ristagno, Elizabeth H, Patnaik, Mrinal S, Schimmenti, Lisa A, Dhamija, Radhika, Sabrowsky, Sonia M, Wierenga, Klaas J, Keddis, Mira T, Samadder, Niloy Jewel J, Presutti, Richard J, Robinson, Steven I, Stephens, Michael C, Roberts, Lewis R, Faubion, Jr, William A, Driscoll, Sherilyn W, Wong-Kisiel, Lily C, Selcen, Duygu, Flanagan, Eoin P, Ramanan, Vijay K, Jackson, Lauren M, Mauermann, Michelle L, Ortega, Victor E, Anderson, Sarah A, Aoudia, Stacy L, Klee, Eric W, McAllister, Tammy M, Lazaridis, Konstantinos N
Published in Journal of translational medicine (30.04.2024)
Published in Journal of translational medicine (30.04.2024)
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Journal Article
Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)
Pinto E Vairo, Filippo, Kemppainen, Jennifer L, Vitek, Carolyn R Rohrer, Whalen, Denise A, Kolbert, Kayla J, Sikkink, Kaitlin J, Kroc, Sarah A, Kruisselbrink, Teresa, Shupe, Gabrielle F, Knudson, Alyssa K, Burke, Elizabeth M, Loftus, Elle C, Bandel, Lorelei A, Prochnow, Carri A, Mulvihill, Lindsay A, Thomas, Brittany, Gable, Dale M, Graddy, Courtney B, Garzon, Giovanna G Moreno, Ekpoh, Idara U, Porquera, Eva M Carmona, Fervenza, Fernando C, Hogan, Marie C, El Ters, Mireille, Warrington, Kenneth J, Davis, 3rd, John M, Koster, Matthew J, Orandi, Amir B, Basiaga, Matthew L, Vella, Adrian, Kumar, Seema, Creo, Ana L, Lteif, Aida N, Pittock, Siobhan T, Tebben, Peter J, Abate, Ejigayehu G, Joshi, Avni Y, Ristagno, Elizabeth H, Patnaik, Mrinal S, Schimmenti, Lisa A, Dhamija, Radhika, Sabrowsky, Sonia M, Wierenga, Klaas J, Keddis, Mira T, Samadder, Niloy Jewel J, Presutti, Richard J, Robinson, Steven I, Stephens, Michael C, Roberts, Lewis R, Faubion, Jr, William A, Driscoll, Sherilyn W, Wong-Kisiel, Lily C, Selcen, Duygu, Flanagan, Eoin P, Ramanan, Vijay K, Jackson, Lauren M, Mauermann, Michelle L, Ortega, Victor E, Anderson, Sarah A, Aoudia, Stacy L, Klee, Eric W, McAllister, Tammy M, Lazaridis, Konstantinos N
Published in Journal of translational medicine (23.06.2023)
Published in Journal of translational medicine (23.06.2023)
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Journal Article
Abstract 13770: Systemic Intervention to Increase the Frequency of Genetic Counseling and Testing in Eligible Dilated Cardiomyopathy Patients
Mohananey, Akanksha, Rosenbaum, Andrew, Kruisselbrink, Teresa M, Prochnow, Carri A, Lin, Grace, Redfield, Margaret M, Pereira, Naveen L
Published in Circulation (New York, N.Y.) (16.11.2021)
Published in Circulation (New York, N.Y.) (16.11.2021)
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Journal Article
Impact of integrated translational research on clinical exome sequencing
Klee, Eric W., Cousin, Margot A., Pinto e Vairo, Filippo, Morales-Rosado, Joel A., Macke, Erica L., Jenkinson, W. Garrett, Ferrer, Alejandro, Schultz-Rogers, Laura E., Olson, Rory J., Oliver, Gavin R., Sigafoos, Ashley N., Schwab, Tanya L., Zimmermann, Michael T., Urrutia, Raul A., Kaiwar, Charu, Gupta, Aditi, Blackburn, Patrick R., Boczek, Nicole J., Prochnow, Carri A., Lowy, Rebecca J., Mulvihill, Lindsay A., McAllister, Tammy M., Aoudia, Stacy L., Kruisselbrink, Teresa M., Gunderson, Lauren B., Kemppainen, Jennifer L., Fisher, Laura J., Tarnowski, Jessica M., Hager, Megan M., Kroc, Sarah A., Bertsch, Nicole L., Agre, Katherine E., Jackson, Jessica L., Macklin-Mantia, Sarah K., Murphree, Marine I., Rust, Laura M., Summer Bolster, Jolene M., Beck, Scott A., Atwal, Paldeep S., Ellingson, Marissa S., Barnett, Sarah S., Rasmussen, Kristen J., Lahner, Carrie A., Niu, Zhiyv, Hasadsri, Linda, Ferber, Matthew J., Marcou, Cherisse A., Clark, Karl J., Pichurin, Pavel N., Deyle, David R., Morava-Kozicz, Eva, Gavrilova, Ralitza H., Dhamija, Radhika, Wierenga, Klaas J., Lanpher, Brendan C., Babovic-Vuksanovic, Dusica, Farrugia, Gianrico, Schimmenti, Lisa A., Stewart, A. Keith, Lazaridis, Konstantinos N.
Published in Genetics in medicine (01.02.2023)
Published in Genetics in medicine (01.02.2023)
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