Cardiovascular Nursing on Human Genomics: What do cardiovascular nurses need to know about congestive heart failure?

nork Frazier, Lorraine, Wung, Shu-Fen, Sparks, Elizabeth, Eastwood, Cathy
Argitaratua 2009

Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy

nork Arad, Michael, Benson, D. Woodrow, Perez-Atayde, Antonio R., McKenna, William J., Sparks, Elizabeth A., Kanter, Ronald J., McGarry, Kate, Seidman, J.G., Seidman, Christine E.
Argitaratua 2002

Subtle Abnormalities in Contractile Function Are an Early Manifestation of Sarcomere Mutations in Dilated Cardiomyopathy

nork Lakdawala, Neal K., Thune, Jens J., Colan, Steven D., Cirino, Allison L., Farrohi, Faranak, Rivero, Jose, McDonough, Barbara, Sparks, Elizabeth, Orav, E. J., Seidman, J. G., Seidman, Christine E., Ho, Carolyn Y.
Argitaratua 2012

Familial Dilated Cardiomyopathy caused by an Alpha-Tropomyosin Mutation: The Distinctive Natural History of Sarcomeric DCM

nork Lakdawala, Neal, Dellefave, Lisa, Redwood, Charles S., Sparks, Elizabeth, Cirino, Allison L., Depalma, Steve, Colan, Steven D., Funke, Birgit, Zimmerman, Rebekah S., Robinson, Paul, Watkins, Hugh, Seidman, Christine E., Seidman, J. G., McNally, Elizabeth M., Ho, Carolyn Y.
Argitaratua 2010

Diltiazem Treatment for Preclinical Hypertrophic Cardiomyopathy Mutation Carriers: A Pilot Randomized Trial to Modify Disease Expression

nork Ho, Carolyn Y., Lakdawala, Neal K., Cirino, Allison L., Lipshultz, Steven E., Sparks, Elizabeth, Abbasi, Siddique A., Kwong, Raymond Y., Antman, Elliott M., Semsarian, Christopher, González, Arantxa, López, Begoña, Diez, Javier, Orav, E. John, Colan, Steven D., Seidman, Christine E.
Argitaratua izan da JACC Heart Fail (2014)

The Cardiac Myosin Binding Protein C Arg502Trp Mutation: A Common Cause of Hypertrophic Cardiomyopathy

nork Saltzman, Adam J., Mancini-DiNardo, Debora, Li, Chumei, Chung, Wendy K., Ho, Carolyn Y., Hurst, Stephanie, Wynn, Julia, Care, Melanie, Hamilton, Robert M., Seidman, Gregor W., Gorham, Joshua, McDonough, Barbara, Sparks, Elizabeth, Seidman, Jonathan G., Seidman, Christine E., Rehm, Heidi L.
Argitaratua 2010

The SMAD-binding domain of SKI: a hotspot for de novo mutations causing Shprintzen–Goldberg syndrome

nork Schepers, Dorien, Doyle, Alexander J, Oswald, Gretchen, Sparks, Elizabeth, Myers, Loretha, Willems, Patrick J, Mansour, Sahar, Simpson, Michael A, Frysira, Helena, Maat-Kievit, Anneke, Van Minkelen, Rick, Hoogeboom, Jeanette M, Mortier, Geert R, Titheradge, Hannah, Brueton, Louise, Starr, Lois, Stark, Zornitza, Ockeloen, Charlotte, Lourenco, Charles Marques, Blair, Ed, Hobson, Emma, Hurst, Jane, Maystadt, Isabelle, Destrée, Anne, Girisha, Katta M, Miller, Michelle, Dietz, Harry C, Loeys, Bart, Van Laer, Lut
Argitaratua izan da Eur J Hum Genet (2015)

Truncations of Titin Causing Dilated Cardiomyopathy

nork Herman, Daniel S., Lam, Lien, Taylor, Matthew R.G., Wang, Libin, Teekakirikul, Polakit, Christodoulou, Danos, Conner, Lauren, DePalma, Steven R., McDonough, Barbara, Sparks, Elizabeth, Teodorescu, Debbie Lin, Cirino, Allison L., Banner, Nicholas R., Pennell, Dudley J., Graw, Sharon, Merlo, Marco, Di Lenarda, Andrea, Sinagra, Gianfranco, Bos, J. Martijn, Ackerman, Michael J., Mitchell, Richard N., Murry, Charles E., Lakdawala, Neal K., Ho, Carolyn Y., Barton, Paul J.R., Cook, Stuart A., Mestroni, Luisa, Seidman, J.G., Seidman, Christine E.
Argitaratua 2012

Mutations in Smooth Muscle Alpha-Actin (ACTA2) Cause Coronary Artery Disease, Stroke, and Moyamoya Disease, Along with Thoracic Aortic Disease

nork Guo, Dong-Chuan, Papke, Christina L., Tran-Fadulu, Van, Regalado, Ellen S., Avidan, Nili, Johnson, Ralph Jay, Kim, Dong H., Pannu, Hariyadarshi, Willing, Marcia C., Sparks, Elizabeth, Pyeritz, Reed E., Singh, Michael N., Dalman, Ronald L., Grotta, James C., Marian, Ali J., Boerwinkle, Eric A., Frazier, Lorraine Q., LeMaire, Scott A., Coselli, Joseph S., Estrera, Anthony L., Safi, Hazim J., Veeraraghavan, Sudha, Muzny, Donna M., Wheeler, David A., Willerson, James T., Yu, Robert K., Shete, Sanjay S., Scherer, Steven E., Raman, C.S., Buja, L. Maximilian, Milewicz, Dianna M.
Argitaratua 2009

ROBO4 Variants Predispose Individuals to Bicuspid Aortic Valve and Thoracic Aortic Aneurysm

nork Gould, Russell A, Aziz, Hamza, Woods, Courtney E, Seman-Senderos, Manuel Alejandro, Sparks, Elizabeth, Preuss, Christoph, Wünnemann, Florian, Bedja, Djahida, Moats, Cassandra R, McClymont, Sarah A, Rose, Rebecca, Sobeira, Nara, Ling, Hua, MacCarrick, Gretchen, Anand Kumar, Ajay, Luyckx, Ilse, Cannaerts, Elyssa, Verstraeten, Aline, Björk, Hanna M, Lehsau, Ann-Cathrin, Jaskula-Ranga, Vinod, Lauridsen, Henrik, Shah, Asad A, Bennett, Christopher L, Ellinor, Patrick T, Lin, Honghuang, Isselbacher, Eric M, Cardenas, Christian Lacks Lino, Butcher, Jonathan T, Hughes, G. Chad, Lindsay, Mark E., Mertens, Luc, Franco-Cereceda, Anders, Verhagen, Judith MA, Wessels, Marja, Mohamed, Salah A, Per, Eriksson, Mital, Seema, Laer, Lut Van, Loeys, Bart L, Andelfinger, Gregor, McCallion, Andrew S, Dietz, Harry C
Argitaratua izan da Nat Genet (2018)