Genetic Knowledge and Attitudes of Parents of Children with Congenital Heart Defects

nork Fitzgerald-Butt, Sara M., Klima, Jennifer, Kelleher, Kelly, Chisolm, Deena, McBride, Kim L.
Argitaratua izan da Am J Med Genet A (2014)

Lifetime Prevalence of Sexual Intercourse and Contraception Use at Last Sex Among Adolescents and Young Adults With Congenital Heart Disease

nork Fry, Kevin M., Gerhardt, Cynthia A., Ash, Jerry, Zaidi, Ali N., Garg, Vidu, McBride, Kim L., Fitzgerald-Butt, Sara M.
Argitaratua izan da J Adolesc Health (2015)

NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling

nork McBride, Kim L., Riley, Maurisa F., Zender, Gloria A., Fitzgerald-Butt, Sara M., Towbin, Jeffrey A., Belmont, John W., Cole, Susan E.
Argitaratua 2008

Measuring Genetic Knowledge: A Brief Survey Instrument for Adolescents and Adults

nork Fitzgerald-Butt, Sara M., Bodine, Andrew, Fry, Kevin M., Ash, Jerry, Zaidi, Ali N., Garg, Vidu, Gerhardt, Cynthia A., McBride, Kim L.
Argitaratua izan da Clin Genet (2015)

Association of Common Variants in ERBB4 with Congenital Left Ventricular Outflow Tract Obstruction Defects

nork McBride, Kim L., Zender, Gloria A., Fitzgerald–Butt, Sara M., Seagraves, Nikki J., Fernbach, Susan D., Zapata, Gladys, Lewin, Mark, Towbin, Jeffrey A., Belmont, John W.
Argitaratua 2011

Novel Familial Dilated Cardiomyopathy Mutation in MYL2 Affects the Structure and Function of Myosin Regulatory Light Chain

nork Huang, Wenrui, Liang, Jingsheng, Yuan, Chen-Ching, Kazmierczak, Katarzyna, Zhou, Zhiqun, Morales, Ana, McBride, Kim L., Fitzgerald-Butt, Sara M., Hershberger, Ray E., Szczesna-Cordary, Danuta
Argitaratua izan da FEBS J (2015)

Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome)

nork McBride, Kim L, Zender, Gloria A, Fitzgerald-Butt, Sara M, Koehler, Daniel, Menesses-Diaz, Andres, Fernbach, Susan, Lee, Kwanghyuk, Towbin, Jeffrey A, Leal, Suzanne, Belmont, John W
Argitaratua 2009

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20

nork Hanchard, Neil A., Swaminathan, Shanker, Bucasas, Kristine, Furthner, Dieter, Fernbach, Susan, Azamian, Mahshid S., Wang, Xueqing, Lewin, Mark, Towbin, Jeffrey A., D'Alessandro, Lisa C.A., Morris, Shaine A., Dreyer, William, Denfield, Susan, Ayres, Nancy A., Franklin, Wayne J., Justino, Henri, Lantin-Hermoso, M. Regina, Ocampo, Elena C., Santos, Alexia B., Parekh, Dhaval, Moodie, Douglas, Jeewa, Aamir, Lawrence, Emily, Allen, Hugh D., Penny, Daniel J., Fraser, Charles D., Lupski, James R., Popoola, Mojisola, Wadhwa, Lalita, Brook, J. David, Bu'Lock, Frances A., Bhattacharya, Shoumo, Lalani, Seema R., Zender, Gloria A., Fitzgerald-Butt, Sara M., Bowman, Jessica, Corsmeier, Don, White, Peter, Lecerf, Kelsey, Zapata, Gladys, Hernandez, Patricia, Goodship, Judith A., Garg, Vidu, Keavney, Bernard D., Leal, Suzanne M., Cordell, Heather J., Belmont, John W., McBride, Kim L.
Argitaratua izan da Hum Mol Genet (2016)