Daniel Quiat
6PUBLICATIONS
35CO-AUTHORS
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Publications (6)
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|Sep 28, 2023
Genetic Contribution to End-Stage Cardiomyopathy Requiring Heart Transplantation.Yuri Kim, Oddný Brattberg Gunnarsdóttir, Anissa Viveiros
|May 18, 2022
An ancient founder mutation located between <i>ROBO1</i> and <i>ROBO2</i> is responsible for increased microtia risk in Amerindigenous populations.Daniel Quiat, Seong Won Kim, Qi Zhang
|May 10, 2022
Population Prevalence of Premature Truncating Variants in Plakophilin-2 and Association With Arrhythmogenic Right Ventricular Cardiomyopathy: A UK Biobank Analysis.Robyn J Hylind, Alexandre C Pereira, Daniel Quiat
|Feb 07, 2022
Genome-Wide De Novo Variants in Congenital Heart Disease Are Not Associated With Maternal Diabetes or Obesity.Sarah U Morton, Alexandre C Pereira, Daniel Quiat
|Jul 17, 2021
Genomic frontiers in congenital heart disease.Sarah U Morton, Daniel Quiat, Jonathan G Seidman
|Mar 04, 2021
Discordant clinical features of identical hypertrophic cardiomyopathy twins.Giuliana G Repetti, Yuri Kim, Alexandre C Pereira
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Frequent Collaborators
6 joint publications
Christine E Seidman
5 joint publications
Jonathan G Seidman
4 joint publications
Alexandre C Pereira
3 joint publications
Sarah U Morton
3 joint publications
Barbara McDonough
3 joint publications
Steven R DePalma
2 joint publications
Yuri Kim
1 joint publications
Giuliana G Repetti
1 joint publications
Gavin Y Oudit
1 joint publications
Mark W Russell
