(Q36865910)

16 August 2017

KGVDB: a population-based genomic map of CNVs tagged by SNPs in Koreans (English)

1 reference

16 August 2017

Sanghoon Moon

1

1 reference

16 August 2017

Kwang Su Jung

2

1 reference

16 August 2017

Young Jin Kim

3

1 reference

16 August 2017

Mi Yeong Hwang

4

1 reference

16 August 2017

Kyungsook Han

5

1 reference

16 August 2017

Jong-Young Lee

6

1 reference

16 August 2017

Kiejung Park

7

1 reference

16 August 2017

Bong-Jo Kim

8

1 reference

16 August 2017

language of work or name

English

0 references

publication date

26 April 2013

1 reference

16 August 2017

1 reference

16 August 2017

29

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16 August 2017

11

1 reference

16 August 2017

1481-1483

1 reference

A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

Mapping copy number variation by population-scale genome sequencing

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

SCAN: SNP and copy number annotation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

Origins and functional impact of copy number variation in the human genome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

A robust statistical method for case-control association testing with copy number variation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

Sparse representation and Bayesian detection of genome copy number alterations from microarray data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

Detection of large-scale variation in the human genome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3661059

10.1093/BIOINFORMATICS/BTT173

4 September 2018

Identifiers

DOI

1 reference

journals/bioinformatics/MoonJKHHLPK13

16 August 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

16 August 2017

PubMed publication ID

23626002

1 reference