(Q28289535)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

title

An approach based on a genome-wide association study reveals candidate loci for narcolepsy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

genome-wide association study

9 February 2020

main subject

0 references

0 references

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

author name string

Mihoko Shimada

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

Taku Miyagawa

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

Minae Kawashima

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

Yutaka Honda

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

Makoto Honda

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

Katsushi Tokunaga

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

language of work or name

English

0 references

publication date

31 July 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

volume

128

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

page(s)

433-441

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20677014%20AND%20SRC:MED&resulttype=core&format=json

describes a project that uses

9 February 2020

genome-wide association study

1 reference

https://scigraph.springernature.com/pub.10.1007/s00439-010-0862-z

inferred from title

exact match

0 references

cites work

Genetic and familial aspects of narcolepsy

1 reference

https://api.crossref.org/works/10.1007%2FS00439-010-0862-Z

Polymorphisms in hypocretin/orexin pathway genes and narcolepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-010-0862-Z

Narcolepsy and low CSF orexin (hypocretin) concentration after a diencephalic stroke.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-010-0862-Z

21 January 2018

Sterol carrier protein-2

1 reference

https://api.crossref.org/works/10.1007%2FS00439-010-0862-Z

Statistical power of model selection strategies for genome-wide association studies

21 January 2018

1 reference

12 December 2020

Variant between CPT1B and CHKB associated with susceptibility to narcolepsy

1 reference

12 December 2020

Regulation of sterol carrier protein gene expression by the forkhead transcription factor FOXO3a

1 reference

12 December 2020

Hypocretin (orexin) deficiency in human narcolepsy.

1 reference

12 December 2020

Narcolepsy: clinical features, new pathophysiologic insights, and future perspectives

1 reference

12 December 2020

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

1 reference

12 December 2020

A haplotype map of the human genome

1 reference

12 December 2020

Genetic calcium signaling abnormalities in the central nervous system: seizures, migraine, and autism

1 reference

12 December 2020

TNFA promoter polymorphisms and narcolepsy.

1 reference

12 December 2020

The neurohormone orexin stimulates hypoxia-inducible factor-1 activity

1 reference

12 December 2020

The UCSC Genome Browser Database

1 reference

12 December 2020

Narcolepsy in orexin knockout mice: molecular genetics of sleep regulation

1 reference

12 December 2020

Further development of multiplex single nucleotide polymorphism typing method, the DigiTag2 assay

1 reference

12 December 2020

Allelic association studies of genome wide association data can reveal errors in marker position assignments

1 reference

12 December 2020

Integration of calcineurin and MEF2 signals by the coactivator p300 during T-cell apoptosis

1 reference

12 December 2020

Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk

1 reference

12 December 2020

Human histocompatibility leukocyte antigen (HLA) haplotype frequencies estimated from the data on HLA class I, II, and III antigens in 111 Japanese narcoleptics

1 reference

12 December 2020

Genomic structure of human L-type Ca2+ channel

1 reference

12 December 2020

A new multipoint method for genome-wide association studies by imputation of genotypes

1 reference

12 December 2020

The KEGG databases at GenomeNet

1 reference

12 December 2020

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

1 reference

12 December 2020

Linkage of human narcolepsy with HLA association to chromosome 4p13-q21

1 reference

12 December 2020

Genome-wide association studies: potential next steps on a genetic journey

1 reference

12 December 2020

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

1 reference

12 December 2020

Haploview: analysis and visualization of LD and haplotype maps

1 reference

12 December 2020

BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

The role of cerebrospinal fluid hypocretin measurement in the diagnosis of narcolepsy and other hypersomnias

1 reference

12 December 2020

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

1 reference

12 December 2020

Identification of a telomeric boundary of the HLA region with potential for predisposition to human narcolepsy

1 reference

12 December 2020

RTPrimerDB: the real-time PCR primer and probe database

1 reference

12 December 2020

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

1 reference

12 December 2020

A genome-wide association study identifies novel risk loci for type 2 diabetes

1 reference

12 December 2020

The structure of the human sterol carrier protein X/sterol carrier protein 2 gene (SCP2).

1 reference

12 December 2020

Genetic markers in narcolepsy

1 reference

12 December 2020

Narcolepsy: new understanding of irresistible sleep

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Aprepro-orexingene polymorphism is associated with narcolepsy: Table 1

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Whole-genome association study of bipolar disorder

1 reference

12 December 2020

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

1 reference

12 December 2020

Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations

1 reference

12 December 2020

Solution structure of the core NFATC1/DNA complex

1 reference

12 December 2020

Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance

1 reference

12 December 2020

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

1 reference

12 December 2020

Cloning, expression, and initial characterization of a novel cytokine-like gene family

1 reference

12 December 2020

Monozygotic twins concordant for narcolepsy-cataplexy without any detectable abnormality in the hypocretin (orexin) pathway.

1 reference

12 December 2020

Gene ontology: tool for the unification of biology

1 reference

12 December 2020

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

1 reference

12 December 2020

The International HapMap Project

1 reference

12 December 2020

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

1 reference

12 December 2020