Copy number variation in Thai population (Q34041126)

30 July 2017

title

Copy number variation in Thai population (English)

1 reference

Surakameth Mahasirimongkol

30 July 2017

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9

object named as

Surakameth Mahasirimongkol

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Bhoom Suktitipat

1

object named as

Bhoom Suktitipat

1 reference

30 July 2017

Varodom Charoensawan

12

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author name string

Chaiwat Naktang

2

1 reference

30 July 2017

Wuttichai Mhuantong

3

1 reference

30 July 2017

Thitima Tularak

4

1 reference

30 July 2017

Paramita Artiwet

5

1 reference

30 July 2017

Ekawat Pasomsap

6

1 reference

30 July 2017

Wallaya Jongjaroenprasert

7

1 reference

30 July 2017

Suthat Fuchareon

8

1 reference

30 July 2017

Surakameth Mahasirimongkol

9

1 reference

30 July 2017

Wasan Chantratita

10

1 reference

30 July 2017

Boonsit Yimwadsana

11

1 reference

30 July 2017

Natini Jinawath

13

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30 July 2017

language of work or name

English

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publication date

13 August 2014

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30 July 2017

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30 July 2017

volume

9

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30 July 2017

issue

8

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30 July 2017

page(s)

e104355

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Creative Commons Attribution 4.0 International

30 July 2017

copyright license

start time

13 August 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

The Database of Genomic Variants: a curated collection of structural variation in the human genome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

Copy number variations in neurodevelopmental disorders

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

A map of copy number variations in Chinese populations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

Copy number variation across European populations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

Genome-wide association study identifies variations in 6p21.3 associated with nevirapine-induced rash

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

PanSNPdb: the Pan-Asian SNP genotyping database

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

Association between HLA-B*4001 and lipodystrophy among HIV-infected patients from Thailand who received a stavudine-containing antiretroviral regimen

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

Structural variation in the human genome and its role in disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

Copy number variations in East-Asian population and their evolutionary and functional implications

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4131886

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants

28 July 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0104355

Integrating common and rare genetic variation in diverse human populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0104355

Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0104355

A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0104355

The effect of algorithms on copy number variant detection

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0104355

21 January 2018

1 reference

https://api.crossref.org/works/10.1371/JOURNAL.PONE.0104355

A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25118596

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0104355

1 reference

30 July 2017

0 references

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30 July 2017

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