(Q34474283)

2 August 2017

1 reference

title

Genes for normal sleep and sleep disorders (English)

1 reference

2 August 2017

Mehdi Tafti

1

0 references

Yves Dauvilliers

series ordinal

3

object named as

Yves Dauvilliers

1 reference

2 August 2017

Stéphanie Maret

2

1 reference

2 August 2017

language of work or name

English

0 references

publication date

1 January 2005

1 reference

2 August 2017

1 reference

2 August 2017

volume

37

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2 August 2017

issue

8

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2 August 2017

page(s)

580-589

1 reference

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

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Relationships in sleep characteristics of identical and fraternal twins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

EEG sleep patterns in twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Individual 'fingerprints' in human sleep EEG topography.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

An electroencephalographic fingerprint of human sleep.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

A CLOCK polymorphism associated with human diurnal preference

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

The 3111T/C polymorphism of hClock is associated with evening preference and delayed sleep timing in a Japanese population sample.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

The 3111 Clock gene polymorphism is not associated with sleep and circadian rhythmicity in phenotypically characterized human subjects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

A single-nucleotide polymorphism in the 5'-untranslated region of the hPER2 gene is associated with diurnal preference.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Sleep-wake cycle abnormalities in fatal familial insomnia. Evidence of the role of the thalamus in sleep regulation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Familial and sporadic fatal insomnia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Dissociation in circadian rhythms in a pseudohypersomnia form of fatal familial insomnia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

An hPer2 phosphorylation site mutation in familial advanced sleep phase syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Interacting molecular loops in the mammalian circadian clock

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Functional consequences of a CKIdelta mutation causing familial advanced sleep phase syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Genetic and familial aspects of narcolepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Reduced number of hypocretin neurons in human narcolepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Hypocretin (orexin) deficiency in human narcolepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

CSF hypocretin-1 levels in narcolepsy, Kleine-Levin syndrome, and other hypersomnias and neurological conditions

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Narcolepsy in orexin knockout mice: molecular genetics of sleep regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Genetic ablation of orexin neurons in mice results in narcolepsy, hypophagia, and obesity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Familial incidence of insomnia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Family studies in insomnia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Functional characterization of the new human GABA(A) receptor mutation beta3(R192H).

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

REM sleep behavior disorder and degenerative dementia: an association likely reflecting Lewy body disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Development of parasomnias from childhood to early adolescence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Hereditary factors in sleepwalking and night terrors

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

HLA and genetic susceptibility to sleepwalking.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Kleine-Levin syndrome: an autoimmune hypothesis based on clinical and genetic analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Hypothalamic astrocytoma. Syndrome of hyperphagia, obesity, and disturbances of behavior and endocrine and autonomic function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Familial Kleine-Levin syndrome: two siblings with unusually long hypersomnic spells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Melatonin rhythms in delayed sleep phase syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Delayed sleep phase syndrome. A chronobiological disorder with sleep-onset insomnia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Etiology and treatment of intrinsic circadian rhythm sleep disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Altered phase relation between sleep timing and core body temperature rhythm in delayed sleep phase syndrome and non-24-hour sleep-wake syndrome in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Possible association of human leucocyte antigen DR1 with delayed sleep phase syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Hypersomnia in dystrophia myotonica: a neurophysiological and immunogenetic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

A monozygotic twin pair discordant for narcolepsy and CSF hypocretin-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

MAO-A and COMT polymorphisms and gene effects in narcolepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Sexual dimorphism of the catechol-O-methyltransferase gene in narcolepsy is associated with response to modafinil

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Significant association of a single nucleotide polymorphism in the tumor necrosis factor-alpha (TNF-alpha) gene promoter with human narcolepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

A narcolepsy susceptibility locus maps to a 5 Mb region of chromosome 21q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

mCRY1 and mCRY2 are essential components of the negative limb of the circadian clock feedback loop

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

A whole-genome scan for obstructive sleep apnea and obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Charcot-Marie-Tooth disease and sleep apnoea syndrome: a family study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Haptoglobin polymorphism is a risk factor for cardiovascular disease in patients with obstructive sleep apnea syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Restless legs syndrome: a review of clinical and pathophysiologic features

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Familial restless legs with periodic movements in sleep: electrophysiologic, biochemical, and pharmacologic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Evidence for a genetic association between monoamine oxidase A and restless legs syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Restless legs syndrome: diagnostic criteria, special considerations, and epidemiology. A report from the restless legs syndrome diagnosis and epidemiology workshop at the National Institutes of Health

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Mutational analysis of neurotensin in familial restless legs syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Autosomal dominant restless legs syndrome maps on chromosome 14q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Nocturnal enuresis in a nationwide twin cohort.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Total genome scan analysis in a single extended family for primary nocturnal enuresis: evidence for a new locus (ENUR3) for primary nocturnal enuresis on chromosome 22q11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Pharmacogenomics in the treatment of narcolepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset families

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F07853890500372047

10.1080/07853890500372047

21 January 2018

Identifiers

DOI

1 reference

release_dzgueap7bzey5cztxucwidjboa

2 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/dzgueap7bzey5cztxucwidjboa

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference