Megan J. Puckelwartz

Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice

Megan J. Puckelwartz, Elizabeth R. Kessler, Yuan Zhang et al. · Human Molecular Genetics · 2008 · 191 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

Niall J. Lennon, Leah C. Kottyan, Christopher Kachulis et al. · Nature Medicine · 2024 · 189 citations · Full text

Life Sciences, Genetics, Health Informatics +17

Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis

Ruben Attali, Nasim Warwar, Alain Israël et al. · Human Molecular Genetics · 2009 · 172 citations

Life Sciences, Genetics, Molecular Genetics +17

Population-Based Variation in Cardiomyopathy Genes

Jessica R. Golbus, Megan J. Puckelwartz, John Fahrenbach et al. · Circulation Cardiovascular Genetics · 2012 · 157 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Nesprin-1 mutations in human and murine cardiomyopathy

Megan J. Puckelwartz, Eric Kessler, Gene Kim et al. · Journal of Molecular and Cellular Cardiology · 2009 · 143 citations

Medicine, Genetics, Molecular Genetics +13