Identification of six new genetic loci associated with atrial fibrillation in the Japanese population

The Tohoku Medical Megabank Project: Design and Mission

(2016) Shinichi Kuriyama et al.   JOURNAL OF EPIDEMIOLOGY

First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy

(2015) Katrien Smets et al.   BMC Medical Genetics

Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner

(2015) Anna Duarri et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Roles of Nebulin Family Members in the Heart

(2015) Marie-Louise Bang et al.   CIRCULATION JOURNAL

Regulation of ECM degradation and axon guidance by growth cone invadosomes

(2015) M. Santiago-Medina et al.   DEVELOPMENT

Integrating Genetic, Transcriptional, and Functional Analyses to Identify 5 Novel Genes for Atrial Fibrillation

(2014) Moritz F. Sinner et al.   CIRCULATION

Guidelines for Pharmacotherapy of Atrial Fibrillation (JCS 2013)

(2014)   CIRCULATION JOURNAL

A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation

(2013) Morten Salling Olesen et al.   CARDIOVASCULAR RESEARCH

Incident Atrial Fibrillation Among Asians, Hispanics, Blacks, and Whites

(2013) Thomas A. Dewland et al.   CIRCULATION

Altered regional cardiac wall mechanics are associated with differential cardiomyocyte calcium handling due to nebulette mutations in preclinical inherited dilated cardiomyopathy

(2013) K. Maiellaro-Rafferty et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

Identification of Xin-repeat proteins as novel ligands of the SH3 domains of nebulin and nebulette and analysis of their interaction during myofibril formation and remodeling

(2013) Stefan Eulitz et al.   MOLECULAR BIOLOGY OF THE CELL

The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together

(2013) Anna Duarri et al.   NEUROGENETICS

Mutations in potassium channelkcnd3cause spinocerebellar ataxia type 19

(2012) Anna Duarri et al.   ANNALS OF NEUROLOGY

Mutations inKCND3cause spinocerebellar ataxia type 22

(2012) Yi-Chung Lee et al.   ANNALS OF NEUROLOGY

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

(2012) Patrick T Ellinor et al.   NATURE GENETICS

Genomic inflation factors under polygenic inheritance

(2011) Jian Yang et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases

(2011) Hon-Cheong So et al.   GENETIC EPIDEMIOLOGY

Independent Susceptibility Markers for Atrial Fibrillation on Chromosome 4q25

(2010) Steven A. Lubitz et al.   CIRCULATION

Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis

(2010) Enkhsaikhan Purevjav et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Common variants in KCNN3 are associated with lone atrial fibrillation

(2010) Patrick T Ellinor et al.   NATURE GENETICS

Common Inherited Variation in Mitochondrial Genes Is Not Enriched for Associations with Type 2 Diabetes or Related Glycemic Traits

(2010) Ayellet V. Segrè et al.   PLoS Genetics

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry

(2009) Emelia J Benjamin et al.   NATURE GENETICS

Cardiac Neural Crest Expression of Hand2 Regulates Outflow and Second Heart Field Development

(2008) Yuka Morikawa et al.   CIRCULATION RESEARCH

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

(2008) Itsik Pe'er et al.   GENETIC EPIDEMIOLOGY

Prevalence of atrial fibrillation in the general population of Japan: An analysis based on periodic health examination

(2008) Hiroshi Inoue et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY