(Q40341088)

19 September 2017

Genome-wide association study of HLA-DQB1*06:02 negative essential hypersomnia (English)

1 reference

genome-wide association study

19 September 2017

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author

Seik-Soon Khor

1

1 reference

19 September 2017

14

Emmanuel Mignot

1 reference

19 September 2017

10

Juliette Faraco

1 reference

19 September 2017

11

Tom Rico

1 reference

19 September 2017

2

Taku Miyagawa

1 reference

19 September 2017

15

Katsushi Tokunaga

1 reference

19 September 2017

Hiromi Toyoda

3

1 reference

19 September 2017

Maria Yamasaki

4

1 reference

19 September 2017

Yoshiya Kawamura

5

1 reference

19 September 2017

Hisashi Tanii

6

1 reference

19 September 2017

Yuji Okazaki

7

1 reference

19 September 2017

Tsukasa Sasaki

8

1 reference

19 September 2017

Ling Lin

9

1 reference

19 September 2017

Yutaka Honda

12

1 reference

19 September 2017

Makoto Honda

13

1 reference

19 September 2017

16 April 2013

1 reference

19 September 2017

1 reference

19 September 2017

1

1 reference

19 September 2017

e66

1 reference

describes a project that uses

19 September 2017

genome-wide association study

1 reference

Effects of oral L-carnitine administration in narcolepsy patients: a randomized, double-blind, cross-over and placebo-controlled trial

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Abnormally low serum acylcarnitine levels in narcolepsy patients

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Genevar: a database and Java application for the analysis and visualization of SNP-gene associations in eQTL studies

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

LocusZoom: regional visualization of genome-wide association scan results

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Common regulatory variation impacts gene expression in a cell type-dependent manner

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Genome-wide association study of bipolar disorder in European American and African American individuals

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Narcolepsy is strongly associated with the T-cell receptor alpha locus

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Polymorphism located between CPT1B and CHKB, and HLA-DRB1*1501-DQB1*0602 haplotype confer susceptibility to CNS hypersomnias (essential hypersomnia)

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Tissue-specific genetic control of splicing: implications for the study of complex traits

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Variant between CPT1B and CHKB associated with susceptibility to narcolepsy

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

CSF hypocretin-1 assessment in sleep and neurological disorders

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Sprouty proteins, masterminds of receptor tyrosine kinase signaling

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

PLINK: a tool set for whole-genome association and population-based linkage analyses

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

A haplotype map of the human genome

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Haploview: analysis and visualization of LD and haplotype maps

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Sleep, consciousness and the spontaneous and evoked electrical activity of the brain. Is there a cortical integrating mechanism?

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Bioenergetic approaches for neuroprotection in Parkinson's disease

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Direct and indirect excitation of laterodorsal tegmental neurons by Hypocretin/Orexin peptides: implications for wakefulness and narcolepsy

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

HLA-DR2 and Dw2 in narcolepsy and in other disorders of excessive somnolence without cataplexy.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Narcolepsy and hypersomnia: review and classification of 642 personally observed cases

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Difference in the characteristics of subjective and objective sleepiness between narcolepsy and essential hypersomnia.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Deficiency in short-chain fatty acid beta-oxidation affects theta oscillations during sleep.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

Meta-analysis of double blind randomized controlled clinical trials of acetyl-L-carnitine versus placebo in the treatment of mild cognitive impairment and mild Alzheimer's disease

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

A circadian output in Drosophila mediated by neurofibromatosis-1 and Ras/MAPK.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3642778

HLA antigens in Japanese patients with narcolepsy. All the patients were DR2 positive

20 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23646285

12 December 2020

inferred from PubMed ID database lookup

Polymorphism located in TCRA locus confers susceptibility to essential hypersomnia with HLA-DRB1*1501-DQB1*0602 haplotype

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23646285

12 December 2020

inferred from PubMed ID database lookup

DNA polymorphism related to HLA-DR2 Dw2 in patients with narcolepsy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23646285

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.7717/PEERJ.66

1 reference

19 September 2017

1 reference

19 September 2017

1 reference