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An inwardly rectifying K+ channel is required for patterning

Development (Cambridge), 2012-10, Vol.139 (19), p.3653-3664

2012

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A PERIOD3 variant causes a circadian phenotype and is associated with a seasonal mood trait

Proceedings of the National Academy of Sciences - PNAS, 2016-03, Vol.113 (11), p.E1536-E1544

2016

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DEC2 modulates orexin expression and regulates sleep

Proceedings of the National Academy of Sciences - PNAS, 2018-03, Vol.115 (13), p.3434-3439

2018

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Lamin B1 duplications cause autosomal dominant leukodystrophy

Nature genetics, 2006-10, Vol.38 (10), p.1114-1123

2006

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Protein mutated in paroxysmal dyskinesia interacts with the active zone protein RIM and suppresses synaptic vesicle exocytosis

Proceedings of the National Academy of Sciences - PNAS, 2015-03, Vol.112 (10), p.2935-2941

2015

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MicroRNA-23a promotes myelination in the central nervous system

Proceedings of the National Academy of Sciences - PNAS, 2013-10, Vol.110 (43), p.17468-17473

2013

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Dicer ablation in oligodendrocytes provokes neuronal impairment in mice

Annals of neurology, 2009-12, Vol.66 (6), p.843-857

2009

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Very large G protein-coupled receptor 1 regulates myelin-associated glycoprotein via Gαs/Gαq-mediated protein kinases A/C

Proceedings of the National Academy of Sciences - PNAS, 2013-11, Vol.110 (47), p.19101-19106

2013

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Lamin B1 mediates cell-autonomous neuropathology in a leukodystrophy mouse model

The Journal of clinical investigation, 2013-06, Vol.123 (6), p.2719-2729

2013

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Episodic Neurological Channelopathies

Neuron (Cambridge, Mass.), 2010-10, Vol.68 (2), p.282-292

2010

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Mutations in Potassium Channel Kir2.6 Cause Susceptibility to Thyrotoxic Hypokalemic Periodic Paralysis

Cell, 2010-01, Vol.140 (1), p.88-98

2010

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Episodic neurologic disorders: syndromes, genes, and mechanisms

Annual review of neuroscience, 2013-07, Vol.36 (1), p.25-50

2013

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Mutations in PNKD causing paroxysmal dyskinesia alters protein cleavage and stability

Human molecular genetics, 2011-06, Vol.20 (12), p.2322-2332

2011

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Dopamine dysregulation in a mouse model of paroxysmal nonkinesigenic dyskinesia

The Journal of clinical investigation, 2012-02, Vol.122 (2), p.507-518

2012

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PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine

Neurology, 2012-11, Vol.79 (21), p.2097

2012

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Dual roles of FBXL3 in the mammalian circadian feedback loops are important for period determination and robustness of the clock

Proceedings of the National Academy of Sciences - PNAS, 2013-03, Vol.110 (12), p.4750-4755

2013

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The intricate dance of post-translational modifications in the rhythm of life

Nature structural & molecular biology, 2016-12, Vol.23 (12), p.1053

2016

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Episodic and Electrical Nervous System Disorders Caused by Nonchannel Genes

Annual review of physiology, 2015-01, Vol.77 (1), p.525-541

2015

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p75 neurotrophin receptor is a clock gene that regulates oscillatory components of circadian and metabolic networks

The Journal of neuroscience, 2013-06, Vol.33 (25), p.10221-10234

2013

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Casein kinase 1 proteomics reveal prohibitin 2 function in molecular clock

PloS one, 2012-02, Vol.7 (2), p.e31987-e31987

2012

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Adult-onset autosomal dominant leukodystrophy: linking nuclear envelope to myelin

The Journal of neuroscience, 2011-01, Vol.31 (4), p.1163-1166

2011

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Human circadian variations

The Journal of clinical investigation, 2021-08, Vol.131 (16)

2021

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Regulation of Myelination in the Central Nervous System by Nuclear Lamin B1 and Non-coding RNAs

Translational neurodegeneration, 2014-02, Vol.3 (1), p.4-4, Article 4

2014

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COL25A1 triggers and promotes Alzheimer’s disease-like pathology in vivo

Neurogenetics, 2010-02, Vol.11 (1), p.41-52

2010

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The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway

Human molecular genetics, 2004-12, Vol.13 (24), p.3161-3170

2004

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An inwardly rectifying K+ channel is required for patterning

A PERIOD3 variant causes a circadian phenotype and is associated with a seasonal mood trait

DEC2 modulates orexin expression and regulates sleep

Lamin B1 duplications cause autosomal dominant leukodystrophy

Protein mutated in paroxysmal dyskinesia interacts with the active zone protein RIM and suppresses synaptic vesicle exocytosis

MicroRNA-23a promotes myelination in the central nervous system

Dicer ablation in oligodendrocytes provokes neuronal impairment in mice

Very large G protein-coupled receptor 1 regulates myelin-associated glycoprotein via Gαs/Gαq-mediated protein kinases A/C

Lamin B1 mediates cell-autonomous neuropathology in a leukodystrophy mouse model

Episodic Neurological Channelopathies

Mutations in Potassium Channel Kir2.6 Cause Susceptibility to Thyrotoxic Hypokalemic Periodic Paralysis

Episodic neurologic disorders: syndromes, genes, and mechanisms

Mutations in PNKD causing paroxysmal dyskinesia alters protein cleavage and stability

Dopamine dysregulation in a mouse model of paroxysmal nonkinesigenic dyskinesia

PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine

Dual roles of FBXL3 in the mammalian circadian feedback loops are important for period determination and robustness of the clock

The intricate dance of post-translational modifications in the rhythm of life

Episodic and Electrical Nervous System Disorders Caused by Nonchannel Genes

p75 neurotrophin receptor is a clock gene that regulates oscillatory components of circadian and metabolic networks

Casein kinase 1 proteomics reveal prohibitin 2 function in molecular clock

Adult-onset autosomal dominant leukodystrophy: linking nuclear envelope to myelin

Human circadian variations

Regulation of Myelination in the Central Nervous System by Nuclear Lamin B1 and Non-coding RNAs

COL25A1 triggers and promotes Alzheimer’s disease-like pathology in vivo

The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway

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