Christine E. Seidman

发表

Jyoti Rao, Arun Sharma, Marcelo Cicconet, 2019, Circulation research.

SARS-CoV-2 entry factors are highly expressed in nasal epithelial cells together with innate immune genes

Masahiro Yoshida, Fabian J. Theis, Oliver Eickelberg, 2020, Nature Medicine.

A One-Page Summary Report of Genome Sequencing for the Healthy Adult

Robert C. Green, Isaac S. Kohane, Heidi L. Rehm, 2015, Public Health Genomics.

Hypertrophic cardiomyopathy: Translating cellular cross talk into therapeutics

Christine E. Seidman, J. Seidman, C. Seidman, 2012, The Journal of cell biology.

Dynamic Cellular Integration Drives Functional Assembly of the Heart’s Pacemaker Complex

Christine E. Seidman, Trevor Henley, Michael Bressan, 2018, Cell reports.

Clinical and Mechanistic Insights Into the Genetics of Cardiomyopathy.

Stuart A. Cook, Jonathan G. Seidman, Christine E. Seidman, 2016, Journal of the American College of Cardiology.

Genome-Wide Assessment for Genetic Variants Associated with Ventricular Dysfunction after Primary Coronary Artery Bypass Graft Surgery

Dan M. Roden, Christine E. Seidman, Kuang-Yu Liu, 2011, PloS one.

Expert consensus document American College of Cardiology / European Society of Cardiology Clinical Expert Consensus Document on Hypertrophic Cardiomyopathy

E. D. Wigle, Judith S. Hochman, Mark A. Hlatky, 2003 .

Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy

George Church, Wolfgang A. Linke, Stuart A. Cook, 2015, Science.

A Mouse Model of Familial Hypertrophic Cardiomyopathy

Frederick J. Schoen, Christine E. Seidman, David A. Conner, 1996, Science.

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

Christine E. Seidman, Stefan Heller, Saumil N. Merchant, 1998, Nature Genetics.

A small-molecule inhibitor of sarcomere contractility suppresses hypertrophic cardiomyopathy in mice

Christine E. Seidman, James A. Spudich, Robert S. McDowell, 2016, Science.

Allele-Specific Silencing of Mutant Myh6 Transcripts in Mice Suppresses Hypertrophic Cardiomyopathy

Christine E. Seidman, J. Seidman, C. Seidman, 2013, Science.

FAMILIAL HYPERTROPHIC CARDIOMYOPATHY IS A DISEASE OF THE SARCOMERE

Wj McKenna, Christine E. Seidman, Calum A. MacRae, 1994 .

Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011))

Sara Chandros Hull, Robert C. Green, Sean D. Mooney, 2016 .

De novo mutations in histone modifying genes in congenital heart disease

Murim Choi, Hongyu Zhao, Alexander E. Lopez, 2013, Nature.

α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere

Christine E. Seidman, Calum MacRae, Ludwig Thierfelder, 1994, Cell.