Cardiac-specific inactivation of Prdm16 effects cardiac conduction abnormalities and cardiomyopathy-associated phenotypes

Mutations in voltage-gated L-type calcium channel: Implications in cardiac arrhythmia

(2018) Qing Zhang et al.   Channels

iPSC-derived cardiomyocytes reveal abnormal TGF-β signalling in left ventricular non-compaction cardiomyopathy

(2016) Kazuki Kodo et al.   NATURE CELL BIOLOGY

Overexpression of SCN5A in mouse heart mimics human syndrome of enhanced atrioventricular nodal conduction

(2015) Gong Xin Liu et al.   HEART RHYTHM

Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians

(2014) Kyung-Won Hong et al.   HUMAN MOLECULAR GENETICS

Mice Carrying a Hypomorphic Evi1 Allele Are Embryonic Viable but Exhibit Severe Congenital Heart Defects

(2014) Emilie A. Bard-Chapeau et al.   PLoS One

Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy

(2013) Anne-Karin Arndt et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The Prdm family: expanding roles in stem cells and development

(2012) T. Hohenauer et al.   DEVELOPMENT

RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome

(2011) Bo Li et al.   BMC BIOINFORMATICS

Prdm16 is required for normal palatogenesis in mice

(2009) Bryan C. Bjork et al.   HUMAN MOLECULAR GENETICS

A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits

(2009) Yoon Shin Cho et al.   NATURE GENETICS