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High-Throughput Reclassification of SCN5A Variants

American journal of human genetics, 2020-07, Vol.107 (1), p.111-123

2020

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Common genetic polymorphism at 4q25 locus predicts atrial fibrillation recurrence after successful cardioversion

Heart rhythm, 2013-06, Vol.10 (6), p.849-855

2013

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Genetic and Clinical Risk Prediction Model for Postoperative Atrial Fibrillation

Circulation. Arrhythmia and electrophysiology, 2015-02, Vol.8 (1), p.25-31

2015

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A Common Variant on Chromosome 4q25 is Associated With Prolonged PR Interval in Subjects With and Without Atrial Fibrillation

The American journal of cardiology, 2014-01, Vol.113 (2), p.309-313

2014

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A Genome-Wide Association Study to Identify Genomic Modulators of Rate Control Therapy in Patients With Atrial Fibrillation

The American journal of cardiology, 2014-08, Vol.114 (4), p.593-600

2014

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Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy

Epilepsy research, 2006-10, Vol.71 (2), p.129-134

2006

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Identification of a Novel Locus for Febrile Seizures and Epilepsy on Chromosome 21q22

Epilepsia (Copenhagen), 2006-10, Vol.47 (10), p.1622-1628

2006

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A KCNJ8 mutation associated with early repolarization and atrial fibrillation

Europace (London, England), 2012-10, Vol.14 (10), p.1428-1432

2012

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Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults

Pharmacogenetics and genomics, 2017-07, Vol.27 (7), p.247-254

2017

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Infantile Onset of Hereditary Spastic Paraplegia Poorly Predicts the Genotype

Pediatric neurology, 2007-06, Vol.36 (6), p.382-386

2007

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A new locus for autosomal dominant generalized epilepsy associated with mild mental retardation on chromosome 3p

Epilepsia (Copenhagen), 2011-05, Vol.52 (5), p.993-999

2011

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Familial essential tremor with apparent autosomal dominant inheritance: Should we also consider other inheritance modes?

Movement disorders, 2006-09, Vol.21 (9), p.1368-1374

2006

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Reappraisal of the role of the DRD3 gene in essential tremor

Parkinsonism & related disorders, 2008-08, Vol.14 (6), p.471-475

2008

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Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia

Neurogenetics, 2006-03, Vol.7 (1), p.47-50

2006

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Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures

Neuroscience letters, 2006-02, Vol.394 (1), p.74-78

2006

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Abstract 16849: Mortality Associated With Mitral Regurgitation and Impact of Intervention Among 76,402 Subjects Referred for Echocardiography Over 17 Years

Circulation (New York, N.Y.), 2018-11, Vol.138 (Suppl_1 Suppl 1), p.A16849-A16849

2018

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A new locus for autosomal dominant generalized epilepsy associated with mild mental retardation on chromosome 3p: Novel Epilepsy Locus on Chromosome 3

Epilepsia (Copenhagen), 2011-05, Vol.52 (5), p.993-999

2011

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A Combined Genetic and Clinical Risk Prediction Model for Postoperative Atrial Fibrillation

Circulation. Arrhythmia and electrophysiology, 2015-01, Vol.8 (1), p.25-31

2015

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Abstract 11840: A Common Genetic Variant of the Cardiac Sodium Channel Predisposes to Drug-induced QT Prolongation

Circulation (New York, N.Y.), 2019-11, Vol.140 (Suppl_1 Suppl 1), p.A11840-A11840

2019

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Abstract 19231: Transthyretin F64L Variant is Associated With Increased Risk of Heart Failure in a Large Clinical Cohort

Circulation (New York, N.Y.), 2016-11, Vol.134 (Suppl_1 Suppl 1), p.A19231-A19231

2016

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Original Research: Identification of a Novel Locus for Febrile Seizures and Epilepsy on Chromosome 21q22

Epilepsia (Copenhagen), 2006-10, Vol.47 (10), p.1622-1628

2006

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LPS- induced inflammation exacerbates phospho-tau pathology in rTg4510 mice

Journal of neuroinflammation, 2010-09, Vol.7 (1), p.56-56

2010

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The Antennae Galaxies (NGC 4038/4039) Revisited: Advanced Camera for Surveys and NICMOS Observations of a Prototypical Merger

The Astronomical journal, 2010-07, Vol.140 (1), p.75-109

2010

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FcγR-mediated SARS-CoV-2 infection of monocytes activates inflammation

Nature (London), 2022-06, Vol.606 (7914), p.576-584

2022

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High-Throughput Reclassification of SCN5A Variants

Common genetic polymorphism at 4q25 locus predicts atrial fibrillation recurrence after successful cardioversion

Genetic and Clinical Risk Prediction Model for Postoperative Atrial Fibrillation

A Common Variant on Chromosome 4q25 is Associated With Prolonged PR Interval in Subjects With and Without Atrial Fibrillation

A Genome-Wide Association Study to Identify Genomic Modulators of Rate Control Therapy in Patients With Atrial Fibrillation

Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy

Identification of a Novel Locus for Febrile Seizures and Epilepsy on Chromosome 21q22

A KCNJ8 mutation associated with early repolarization and atrial fibrillation

Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults

Infantile Onset of Hereditary Spastic Paraplegia Poorly Predicts the Genotype

A new locus for autosomal dominant generalized epilepsy associated with mild mental retardation on chromosome 3p

Familial essential tremor with apparent autosomal dominant inheritance: Should we also consider other inheritance modes?

Reappraisal of the role of the DRD3 gene in essential tremor

Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia

Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures

Abstract 16849: Mortality Associated With Mitral Regurgitation and Impact of Intervention Among 76,402 Subjects Referred for Echocardiography Over 17 Years

Transcriptional dysregulation underlies both a monogenic arrhythmia syndrome and common modifier of cardiac repolarization

A new locus for autosomal dominant generalized epilepsy associated with mild mental retardation on chromosome 3p: Novel Epilepsy Locus on Chromosome 3

A Combined Genetic and Clinical Risk Prediction Model for Postoperative Atrial Fibrillation

Abstract 11840: A Common Genetic Variant of the Cardiac Sodium Channel Predisposes to Drug-induced QT Prolongation

Abstract 19231: Transthyretin F64L Variant is Associated With Increased Risk of Heart Failure in a Large Clinical Cohort

Original Research: Identification of a Novel Locus for Febrile Seizures and Epilepsy on Chromosome 21q22

LPS- induced inflammation exacerbates phospho-tau pathology in rTg4510 mice

The Antennae Galaxies (NGC 4038/4039) Revisited: Advanced Camera for Surveys and NICMOS Observations of a Prototypical Merger

FcγR-mediated SARS-CoV-2 infection of monocytes activates inflammation

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