Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

Por Cowan, Jason, Li, Duanxiang, Gonzalez-Quintana, Jorge, Morales, Ana, Hershberger, Ray E.
Publicado em 2009

Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1 and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy

Por Hershberger, Ray E., Norton, Nadine, Morales, Ana, Li, Duanxiang, Siegfried, Jill D., Gonzalez-Quintana, Jorge
Publicado em 2010

Identification of Novel Mutations in RBM20 in Patients with Dilated Cardiomyopathy

Por Li, Duanxiang, Morales, Ana, Gonzalez‐Quintana, Jorge, Norton, Nadine, Siegfried, Jill D., Hofmeyer, Mark, Hershberger, Ray E.
Publicado em 2010

SCN5A Rare Variants in Familial Dilated Cardiomyopathy Decrease Peak Sodium Current Depending on the Common Polymorphism H558R and Common Splice Variant Q1077del

Por Cheng, Jianding, Morales, Ana, Siegfried, Jill D., Li, Duanxiang, Norton, Nadine, Song, Junyao, Gonzalez‐Quintana, Jorge, Makielski, Jonathan C., Hershberger, Ray E.
Publicado em 2010

Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy

Por Norton, Nadine, Li, Duanxiang, Rieder, Mark J., Siegfried, Jill D., Rampersaud, Evadnie, Züchner, Stephan, Mangos, Steve, Gonzalez-Quintana, Jorge, Wang, Libin, McGee, Sean, Reiser, Jochen, Martin, Eden, Nickerson, Deborah A., Hershberger, Ray E.
Publicado em 2011