Tamara T. Koopmann

A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype

Dan Hu, Héctor Barajas-Martínez, Elena Burashnikov et al. · Circulation Cardiovascular Genetics · 2009 · 251 citations · Full text

A common genetic variant within SCN10A modulates cardiac SCN5A expression

Malou van den Boogaard, Scott Smemo, Ozanna Burnicka-Turek et al. · Journal of Clinical Investigation · 2014 · 186 citations · Full text

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

Heather J. Cordell, Jamie Bentham, Ana Töpf et al. · Nature Genetics · 2013 · 156 citations

Atrial Septal Defect, Genome-wide Association Study, Genetic Disorder +9

Genome-Wide Identification of Expression Quantitative Trait Loci (eQTLs) in Human Heart

Tamara T. Koopmann, Michiel Adriaens, Perry D. Moerland et al. · PLoS ONE · 2014 · 47 citations · Full text

Genetics, Human Heart, Genomics +19

Identification of known and unknown genes associated with mitral valve prolapse using an exome slice methodology

Aniek L. van Wijngaarden, Yasmine L. Hiemstra, Tamara T. Koopmann et al. · Journal of Medical Genetics · 2020 · 34 citations