The genetics of sleep disorders (Q35172453)

6 August 2017

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title

The genetics of sleep disorders. (English)

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6 August 2017

Emmanuel Mignot

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6 August 2017

Shahrad Taheri

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6 August 2017

publication date

1 August 2002

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6 August 2017

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6 August 2017

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6 August 2017

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6 August 2017

page(s)

242-250

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Mortality associated with sleep duration and insomnia

6 August 2017

cites work

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Functional consequences of sustained sleep deprivation in the rat.

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7 January 2021

Modulation of brain gene expression during sleep and wakefulness: a review of recent findings

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7 January 2021

Effect of SCN lesions on sleep in squirrel monkeys: evidence for opponent processes in sleep-wake regulation

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7 January 2021

Paradoxical timing of the circadian rhythm of sleep propensity serves to consolidate sleep and wakefulness in humans

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7 January 2021

Validation of the S and C components of the three-process model of alertness regulation.

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7 January 2021

Molecular analysis of mammalian circadian rhythms

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https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900103-5

7 January 2021

Circadian rhythm genetics: from flies to mice to humans

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7 January 2021

Stability, precision, and near-24-hour period of the human circadian pacemaker

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7 January 2021

Unihemispheric slow-wave sleep in the Amazonian dolphin, Inia geoffrensis

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7 January 2021

Corticothalamic resonance, states of vigilance and mentation

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7 January 2021

Activation of ventrolateral preoptic neurons during sleep

1 reference

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7 January 2021

Identification of sleep-promoting neurons in vitro.

1 reference

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7 January 2021

The role of hypocretins (orexins) in sleep regulation and narcolepsy.

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7 January 2021

Evidence for histaminergic arousal mechanisms in the hypothalamus of cat.

1 reference

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7 January 2021

The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene

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7 January 2021

Genetic and Environmental Determination of Human Sleep

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7 January 2021

Evidence for genetic influences on sleep disturbance and sleep pattern in twins

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7 January 2021

EEG sleep patterns in twins

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7 January 2021

Functional identification of the mouse circadian Clock gene by transgenic BAC rescue

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7 January 2021

Positional cloning of the mouse circadian clock gene

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7 January 2021

A CLOCK polymorphism associated with human diurnal preference

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7 January 2021

Familial advanced sleep-phase syndrome: A short-period circadian rhythm variant in humans

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7 January 2021

An hPer2 phosphorylation site mutation in familial advanced sleep phase syndrome

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7 January 2021

All's well that ends dead

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7 January 2021

Positional syntenic cloning and functional characterization of the mammalian circadian mutation tau.

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7 January 2021

Association of structural polymorphisms in the human period3 gene with delayed sleep phase syndrome

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7 January 2021

Genetic and familial aspects of narcolepsy

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7 January 2021

Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups

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7 January 2021

Narcolepsy in orexin knockout mice: molecular genetics of sleep regulation

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7 January 2021

Hypocretin (orexin) deficiency in human narcolepsy.

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7 January 2021

A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains

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7 January 2021

Reduced number of hypocretin neurons in human narcolepsy

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7 January 2021

Polymorphisms in the vicinity of the hypocretin/orexin are not associated with human narcolepsy

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7 January 2021

Polymorphisms in hypocretin/orexin pathway genes and narcolepsy

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7 January 2021

MAO-A and COMT polymorphisms and gene effects in narcolepsy

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7 January 2021

Significant association of the tumor necrosis factor receptor 2 (TNFR2) gene with human narcolepsy

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7 January 2021

Genetic factors in human sleep disorders with special reference to Norrie disease, Prader-Willi syndrome and Moebius syndrome

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7 January 2021

Narcolepsy in children

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7 January 2021

Cataplexy in variant forms of Niemann-Pick disease

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7 January 2021

Hypersomnia in the Prader Willi syndrome: clinical-electrophysiological features and underlying factors

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7 January 2021

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7 January 2021

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7 January 2021

Delayed emergence of a parkinsonian disorder in 38% of 29 older men initially diagnosed with idiopathic rapid eye movement sleep behaviour disorder

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7 January 2021

Restless legs syndrome: a review of clinical and pathophysiologic features

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7 January 2021

Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q.

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7 January 2021

Restless legs syndrome in monozygotic twins: clinical correlates

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7 January 2021

Dopaminergic neurotransmission and restless legs syndrome: a genetic association analysis

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7 January 2021

The Sleep Apnea Syndromes

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7 January 2021

Prospective study of the association between sleep-disordered breathing and hypertension

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7 January 2021

Relation of sleep-disordered breathing to cardiovascular disease risk factors: the Sleep Heart Health Study

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7 January 2021

The occurrence of sleep-disordered breathing among middle-aged adults

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7 January 2021

Snoring, sleep disturbance, and behaviour in 4-5 year olds

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900103-5

7 January 2021

Genetic factors in self-reported snoring and excessive daytime sleepiness: a twin study

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7 January 2021

Obstructive Sleep Apnea in Family Members

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7 January 2021

Familial lethal sleep apnea

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7 January 2021

A family study of sleep apnea. Anatomic and physiologic interactions

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7 January 2021

Familial aggregates in obstructive sleep apnea syndrome.

1 reference

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7 January 2021

Family studies in patients with the sleep apnea-hypopnea syndrome

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7 January 2021

Ventilatory-control Abnormalities in Familial Sleep Apnea

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7 January 2021

Genetic and environmental factors in relative body weight and human adiposity

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7 January 2021

Genetic determinants of regional fat distribution

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7 January 2021

Sleep-disordered breathing and glucose metabolism in hypertensive men: a population-based study

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7 January 2021

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900103-5

1 reference

7 January 2021

Impact of sleep debt on metabolic and endocrine function

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7 January 2021

The association of sudden unexpected infant death with obstructive sleep apnea

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900103-5

7 January 2021

Sleep-disordered breathing and upper-airway anomalies in first-degree relatives of ALTE children

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https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900103-5

7 January 2021

Comparison of peripheral chemoreceptor responses in monozygotic and dizygotic twin infants

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7 January 2021

Chemical and behavioral control of breathing in adult twins.

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7 January 2021

Genetics and obstructive sleep apnea syndrome: a study of human leukocyte antigen (HLA) typing.

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7 January 2021

Reduction of REM sleep latency associated with HLA-DQB1*0602 in normal adults

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7 January 2021

Snoring, family history, and genetic markers in men. The Copenhagen Male Study

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7 January 2021

Angiotensin-converting enzyme gene insertion/deletion (I/D) polymorphism in hypertensive patients with different degrees of obstructive sleep apnea

1 reference

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7 January 2021

Effects of three candidate genes on prevalence and incidence of hypertension in a Caucasian population.

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7 January 2021

Genetics of lipoprotein abnormalities associated with coronary artery disease susceptibility

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7 January 2021

The effects of APOE genotype on age at onset and progression of neurodegenerative diseases

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7 January 2021

No relation between apolipoprotein E alleles and obstructive sleep apnea.

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7 January 2021

Association between apolipoprotein E epsilon4 and sleep-disordered breathing in adults

1 reference

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7 January 2021

Insomnia and its treatment. Prevalence and correlates

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7 January 2021

Familial incidence of insomnia

1 reference

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7 January 2021

Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei

1 reference

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7 January 2021

Molecular pathology of fatal familial insomnia

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7 January 2021

The pathophysiology of fatal familial insomnia.

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7 January 2021

Current clinical diagnosis in Creutzfeldt-Jakob disease: Identification of uncommon variants

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7 January 2021

Altered circadian activity rhythms and sleep in mice devoid of prion protein

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7 January 2021

Molecular biology of prion diseases

1 reference

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7 January 2021

Effect of the D178N Mutation and the Codon 129 Polymorphism on the Metabolism of the Prion Protein

1 reference

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7 January 2021

Changes in sleep--waking cycle induced by lesions of medialis dorsalis thalamic nuclei in the cat.

1 reference

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7 January 2021

Sleep disorders: disorders of arousal? Enuresis, somnambulism, and nightmares occur in confusional states of arousal, not in "dreaming sleep".

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7 January 2021

Night terror in adults through three generations

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7 January 2021

Hereditary factors in sleepwalking and night terrors

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7 January 2021

Prevalence and Genetics of Sleepwalking: A Population-based Twin Study

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https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900103-5

7 January 2021

Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900103-5

7 January 2021

Autosomal dominant nocturnal frontal lobe epilepsy: demonstration of focal frontal onset and intrafamilial variation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900103-5

7 January 2021

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900103-5

7 January 2021

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900103-5

7 January 2021

An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kinetics

1 reference

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7 January 2021

An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy

1 reference

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7 January 2021

Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24

1 reference

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7 January 2021

The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900103-5

7 January 2021

CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2802%2900103-5

7 January 2021

Circadian rhythms from flies to human

1 reference

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7 January 2021

10.1016/S1474-4422(02)00103-5

Identifiers

DOI

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6 August 2017

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