(Q84725622)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20703242%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

title

Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage (English)

1 reference

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9 February 2020

author name string

Joon Seol Bae

1

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9 February 2020

Hyun Sub Cheong

2

1 reference

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9 February 2020

Byung Lae Park

3

1 reference

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9 February 2020

Lyoung Hyo Kim

4

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9 February 2020

Tae Joon Park

5

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9 February 2020

Jason Yongha Kim

6

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9 February 2020

Charisse Flerida A Pasaje

7

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9 February 2020

Jin Sol Lee

8

1 reference

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9 February 2020

Tailin Cui

9

1 reference

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9 February 2020

Ituro Inoue

10

1 reference

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9 February 2020

Hyoung Doo Shin

11

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9 February 2020

publication date

12 August 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20703242%20AND%20SRC:MED&resulttype=core&format=json

Journal of Human Genetics

9 February 2020

published in

1 reference

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9 February 2020

volume

55

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9 February 2020

issue

11

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9 February 2020

page(s)

726-730

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https://scigraph.springernature.com/pub.10.1038/jhg.2010.97

9 February 2020

exact match

0 references

cites work

Case-fatality rates and functional outcome after subarachnoid hemorrhage: a systematic review

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Pathogenesis and histopathology of saccular aneurysms: review of the literature

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Subarachnoid haemorrhage in first and second degree relatives of patients with subarachnoid haemorrhage

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Attributable risk of common and rare determinants of subarachnoid hemorrhage

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Copy-number variations associated with neuropsychiatric conditions

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Copy number variation: new insights in genome diversity

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Segmental copy number variation shapes tissue transcriptomes.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Strong association of de novo copy number mutations with autism

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Epidermal growth factor receptor gene and protein and gefitinib sensitivity in non-small-cell lung cancer

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Copy number variation and schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Subtle chromosomal rearrangements in children with unexplained mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Identification of SNP markers for common CNV regions and association analysis of risk of subarachnoid aneurysmal hemorrhage in Japanese population

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Common variants at 30 loci contribute to polygenic dyslipidemia

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

The highly conserved DAD1 protein involved in apoptosis is required for N-linked glycosylation

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Modeling genetic inheritance of copy number variations.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Interpreting experimental results using gene ontologies

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

GOstat: find statistically overrepresented Gene Ontologies within a group of genes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Common genetic variants on 5p14.1 associate with autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Copy number variation at 1q21.1 associated with neuroblastoma

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Genotype, haplotype and copy-number variation in worldwide human populations

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Recurrent CNVs disrupt three candidate genes in schizophrenia patients

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Mutational and selective effects on copy-number variants in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Hotspots for copy number variation in chimpanzees and humans

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Identification and characterization of human cDNAs specific to BCS1, PET112, SCO1, COX15, and COX11, five genes involved in the formation and function of the mitochondrial respiratory chain

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

FBXW7 targets mTOR for degradation and cooperates with PTEN in tumor suppression

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.97

7 January 2021

Identifiers

DOI

10.1038/JHG.2010.97

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20703242%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

1 reference