Duanxiang Li

发表

Identification of Novel Mutations in RBM20 in Patients with Dilated Cardiomyopathy

N. Norton, R. Hershberger, Duanxiang Li, 2010, Clinical and translational science.

Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy

R. Hershberger, P. Jakobs, D. Nauman, 2008, Clinical and translational science.

Coding Sequence Rare Variants Identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 From 312 Patients With Familial or Idiopathic Dilated Cardiomyopathy

N. Norton, R. Hershberger, Duanxiang Li, 2010, Circulation. Cardiovascular genetics.

Rare variant mutations identified in pediatric patients with dilated cardiomyopathy.

E. Martin, N. Norton, E. Rampersaud, 2011, Progress in pediatric cardiology.

Mutations of presenilin genes in dilated cardiomyopathy and heart failure.

Michael Litt, R. Hershberger, C. Allen, 2006, American journal of human genetics.

Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy.

E. Rampersaud, R. Hershberger, Duanxiang Li, 2013, Journal of cardiac failure.

Assessment of LMNA Copy Number Variation in 58 Probands with Dilated Cardiomyopathy

N. Norton, R. Hershberger, Duanxiang Li, 2011, Clinical and translational science.

Rare Variant Mutations in Pregnancy-Associated or Peripartum Cardiomyopathy

N. Norton, R. Hershberger, Duanxiang Li, 2010, Circulation.

Morphological Analysis of 13 LMNA Variants Identified in a Cohort of 324 Unrelated Patients With Idiopathic or Familial Dilated Cardiomyopathy

R. Hershberger, Duanxiang Li, A. Morales, 2010, Circulation. Cardiovascular genetics.

Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients With Dilated Cardiomyopathy

J. Potter, R. Hershberger, Duanxiang Li, 2009, Circulation. Cardiovascular genetics.

Functional Characterization of TNNC1 Rare Variants Identified in Dilated Cardiomyopathy*

N. Norton, J. Potter, R. Hershberger, 2011, The Journal of Biological Chemistry.

Late Onset Sporadic Dilated Cardiomyopathy Caused by a Cardiac Troponin T Mutation

J. Potter, Duanxiang Li, A. Morales, 2010, Clinical and translational science.

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.

Deborah A Nickerson, Stephan Züchner, Eden Martin, 2011, American journal of human genetics.

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.

P. Rahko, R. Hershberger, P. Jakobs, 2008, American heart journal.

Next-generation sequencing to identify genetic causes of cardiomyopathies

N. Norton, R. Hershberger, Duanxiang Li, 2012, Current opinion in cardiology.

Return of Genetic Results in the Familial Dilated Cardiomyopathy Research Project

N. Norton, Duanxiang Li, A. Morales, 2013, Journal of Genetic Counseling.

Exome Sequencing and Genome-Wide Linkage Analysis in 17 Families Illustrate the Complex Contribution of TTN Truncating Variants to Dilated Cardiomyopathy

Niklas Krumm, D. Nickerson, E. Martin, 2013, Circulation. Cardiovascular genetics.

Evaluating Pathogenicity of Rare Variants From Dilated Cardiomyopathy in the Exome Era

Deborah A Nickerson, Stephan Züchner, Eden Martin, 2012, Circulation. Cardiovascular genetics.

Novel Cardiac Troponin T Mutation as a Cause of Familial Dilated Cardiomyopathy

R. Brugada, M. Quiñones, J. Durand, 2001, Circulation.

The paper of the month : Identification of Novel Mutations in RBM 20 in Patients with Dilated Cardiomyopathy

N. Norton, Duanxiang Li, M. Hofmeyer, 2010 .

Cardiac magnetic resonance imaging of myocardial contrast uptake and blood flow in patients affected with idiopathic or familial dilated cardiomyopathy.

Michael Jerosch-Herold, Rami Alharethi, David C. Sheridan, 2008, American journal of physiology. Heart and circulatory physiology.

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

Ana Morales, Nadine Norton, N. Norton, 2010, Clinical and translational science.

Desmin mutation responsible for idiopathic dilated cardiomyopathy.

P. Burch, M. Quiñones, W. Zoghbi, 1999, Circulation.

Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23.

M. Gardner, R. Roberts, T. Tapscott, 1998, Circulation.

Rare Variant Mutations in Pregnancy-Associated or Peripartum Cardiomyopathy

N. Norton, R. Hershberger, Duanxiang Li, 2010, Circulation.

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.

M. Rieder, D. Nickerson, S. Züchner, 2011, American journal of human genetics.

Functional Characterization of TNNC1 Rare Variants Identified in Dilated Cardiomyopathy*

N. Norton, J. Potter, R. Hershberger, 2011, The Journal of Biological Chemistry.