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Paper Details

Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease.
Genome Med
90
2018
-catenin, CHD, HMG-box, Notch, PAH, PAH-CHD, Pulmonary arterial hypertension, SOX17, Wnt, association, candidate risk gene, congenital heart disease, gnomAD, idiopathic and familial PAH, idiopathic/familial PAH, patients, protein, pulmonary, pulmonary arterial hypertension, right-sided heart failure, risk gene, risk genes
Author NameAffiliation
Dunbar IvyChildren's Hospital Colorado
Eric D AustinVanderbilt University School of Medicine
Rizwan HamidVanderbilt University School of Medicine
Rizwan HamidVanderbilt University School of Medicine
Jeffrey G ReidRegeneron Pharmaceuticals
Jeffrey G ReidRegeneron Pharmaceuticals
John D OvertonRegeneron Pharmaceuticals
John D OvertonRegeneron Pharmaceuticals
Aris BarasRegeneron Pharmaceuticals
Frederick E DeweyRegeneron Pharmaceuticals
Yufeng ShenColumbia University Medical Center
Yufeng ShenColumbia University
Wendy K ChungColumbia University Medical Center
Wendy K ChungColumbia University Medical Center
Wendy K ChungHerbert Irving Comprehensive Cancer Center, Columbia University Medical Center
Wendy K Chung
Wendy K ChungColumbia University Medical Center
Wendy K ChungColumbia University Medical Center
Wendy K ChungHerbert Irving Comprehensive Cancer Center, Columbia University Medical Center
Wendy K Chung
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