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The KATP channel is a molecular sensor of atrophy in skeletal muscle

The Journal of physiology, 2010-03, Vol.588 (5), p.773-784

2010

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Molecular and genetic basis of sudden cardiac death

The Journal of clinical investigation, 2013-01, Vol.123 (1), p.75-83

George, Jr, Alfred L

2013

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The genetic basis of variability in drug responses

Nature reviews. Drug discovery, 2002-01, Vol.1 (1), p.37-44

2002

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Susceptibility to innate immune activation in genetically-mediated myocarditis

The Journal of clinical investigation, 2024-07, Vol.134 (13)

2024

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Predicting the functional impact of KCNQ1 variants with artificial neural networks

PLoS computational biology, 2022-04, Vol.18 (4), p.e1010038-e1010038

2022

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Manipulating piggyBac Transposon Chromosomal Integration Site Selection in Human Cells

Molecular therapy, 2011-09, Vol.19 (9), p.1636-1644

2011

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Multiscale complexity analysis of the cardiac control identifies asymptomatic and symptomatic patients in long QT syndrome type 1

PloS one, 2014-04, Vol.9 (4), p.e93808-e93808

2014

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SCN1A splice variants exhibit divergent sensitivity to commonly used antiepileptic drugs

Epilepsia (Copenhagen), 2011-05, Vol.52 (5), p.1000-1009

2011

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Multiplexed transposon-mediated stable gene transfer in human cells

Proceedings of the National Academy of Sciences - PNAS, 2010-01, Vol.107 (4), p.1343-1348

2010

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KCNE4 domains required for inhibition of KCNQ1

The Journal of physiology, 2009-01, Vol.587 (2), p.303-314

2009

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Voltage-gated potassium channel KCNV2 (Kv8.2) contributes to epilepsy susceptibility

Proceedings of the National Academy of Sciences - PNAS, 2011-03, Vol.108 (13), p.5443-5448

2011

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Leaky channels make weak muscles

The Journal of clinical investigation, 2012-12, Vol.122 (12), p.4333-4336

George, Jr, Alfred L

2012

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Cholesterol-induced suppression of Kir2 channels is mediated by decoupling at the inter-subunit interfaces

iScience, 2022-05, Vol.25 (5), p.104329, Article 104329

2022

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Divergent sodium channel defects in familial hemiplegic migraine

Proceedings of the National Academy of Sciences - PNAS, 2008-07, Vol.105 (28), p.9799-9804

2008

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In Memoriam Arthur J. Atkinson, Jr. (1938–2024)

Clinical pharmacology and therapeutics, 2024-07, Vol.116 (1), p.20-21

2024

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Cardiac ion channels

Annual review of physiology, 2002-01, Vol.64 (1), p.431-475

2002

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Physiological genomics identifies genetic modifiers of long QT syndrome type 2 severity

The Journal of clinical investigation, 2018-03, Vol.128 (3), p.1043-1056

2018

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Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice

Neurobiology of disease, 2014-05, Vol.65, p.1-11

2014

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De novo KCNB1 mutations in epileptic encephalopathy

Annals of neurology, 2014-10, Vol.76 (4), p.529-540

2014

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RNA-based translation activators for targeted gene upregulation

Nature communications, 2023-10, Vol.14 (1), p.6827-6827, Article 6827

2023

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KCNQ2 - and KCNQ3 -Associated Epilepsy

2022

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Late Sodium Current Promotes Ventricular Arrhythmia in Epilepsy-Related Sudden Death

JACC. Clinical electrophysiology, 2024-05, Vol.10 (5), p.843-845

George, Alfred L.

2024

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Prevalence of long-QT syndrome gene variants in sudden infant death syndrome

Circulation (New York, N.Y.), 2007-01, Vol.115 (3), p.361-367

2007

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NOS1AP Is a Genetic Modifier of the Long-QT Syndrome

Circulation (New York, N.Y.), 2009-10, Vol.120 (17), p.1657-1663

2009

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Altered neurological and neurobehavioral phenotypes in a mouse model of the recurrent KCNB1-p.R306C voltage-sensor variant

Neurobiology of disease, 2024-05, Vol.194, p.106470-106470, Article 106470

2024

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The KATP channel is a molecular sensor of atrophy in skeletal muscle

Molecular and genetic basis of sudden cardiac death

The genetic basis of variability in drug responses

Susceptibility to innate immune activation in genetically-mediated myocarditis

Predicting the functional impact of KCNQ1 variants with artificial neural networks

Manipulating piggyBac Transposon Chromosomal Integration Site Selection in Human Cells

Multiscale complexity analysis of the cardiac control identifies asymptomatic and symptomatic patients in long QT syndrome type 1

SCN1A splice variants exhibit divergent sensitivity to commonly used antiepileptic drugs

Multiplexed transposon-mediated stable gene transfer in human cells

KCNE4 domains required for inhibition of KCNQ1

Voltage-gated potassium channel KCNV2 (Kv8.2) contributes to epilepsy susceptibility

Leaky channels make weak muscles

Cholesterol-induced suppression of Kir2 channels is mediated by decoupling at the inter-subunit interfaces

Divergent sodium channel defects in familial hemiplegic migraine

In Memoriam Arthur J. Atkinson, Jr. (1938–2024)

Cardiac ion channels

Physiological genomics identifies genetic modifiers of long QT syndrome type 2 severity

Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice

De novo KCNB1 mutations in epileptic encephalopathy

RNA-based translation activators for targeted gene upregulation

KCNQ2 - and KCNQ3 -Associated Epilepsy

Late Sodium Current Promotes Ventricular Arrhythmia in Epilepsy-Related Sudden Death

Prevalence of long-QT syndrome gene variants in sudden infant death syndrome

NOS1AP Is a Genetic Modifier of the Long-QT Syndrome

Altered neurological and neurobehavioral phenotypes in a mouse model of the recurrent KCNB1-p.R306C voltage-sensor variant

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