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Human Molecular Genetics|May 5, 2017
Recessive TAF1A mutations reveal ribosomopathy in siblings with end-stage pediatric dilated cardiomyopathyPamela A Long, Jeanne L Theis, Yu-Huan Shih, et al.Circulation. Genomic and Precision Medicine|December 16, 2020
Genetic Association Between Hypoplastic Left Heart Syndrome and CardiomyopathiesJeanne L Theis, Jessie J Hu, Rhianna S Sundsbak, et al.Human Molecular Genetics|November 26, 2015
Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cellsSaranya P Wyles, Xing Li, Sybil C Hrstka, et al.Circulation. Cardiovascular Genetics|June 19, 2015
Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection FractionJeanne L Theis, Michael T Zimmermann, Jared M Evans, et al.Journal of the American College of Cardiology|June 25, 2003
Familial atrial fibrillation is a genetically heterogeneous disorderDawood Darbar, Kathleen J Herron, Jeffrey D Ballew, et al.Human Genetics|July 13, 2015
Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndromeJeanne L Theis, Sybil C L Hrstka, Jared M Evans, et al.Human Molecular Genetics|June 15, 2006
Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillationTimothy M Olson, Alexey E Alekseev, Xiaoke K Liu, et al.Nature Clinical Practice. Cardiovascular Medicine|January 25, 2007
KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillationTimothy M Olson, Alexey E Alekseev, Christophe Moreau, et al.Circulation. Genomic and Precision Medicine|March 20, 2019
Rare Missense Variants in TLN1 Are Associated With Familial and Sporadic Spontaneous Coronary Artery DissectionTamiel N Turley, Jeanne L Theis, Rhianna S Sundsbak, et al.The Annals of Thoracic Surgery|February 4, 2021
From Safety to Benefit in Cell Delivery During Surgical Repair of Ebstein Anomaly: Initial ResultsKimberly A Holst, Joseph A Dearani, M Yasir Qureshi, et al.Pageof 8