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Exome sequencing identifies ZNF644 mutations in high myopia
(Q21092428)
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From Wikidata
scientific article published in June 2011
Exome Sequencing Identifies ZNF644 Mutations in High Myopia
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English
Exome sequencing identifies ZNF644 mutations in high myopia
scientific article published in June 2011
Exome Sequencing Identifies ZNF644 Mutations in High Myopia
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instance of
scholarly article
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title
Exome sequencing identifies ZNF644 mutations in high myopia
(English)
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main subject
myopia
1 reference
based on heuristic
inferred from title
author
Jun Wang
series ordinal
28
object named as
Jun Wang
author given names
Jun
author last names
Wang
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Yang Huanming
series ordinal
27
object named as
Huanming Yang
author given names
Huanming
author last names
Yang
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Ruiqiang Li
series ordinal
11
author given names
Ruiqiang
author last names
Li
object named as
Ruiqiang Li
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
author name string
Yi Shi
series ordinal
1
author given names
Yi
author last names
Shi
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Yingrui Li
series ordinal
2
author given names
Yingrui
author last names
Li
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Dingding Zhang
series ordinal
3
author given names
Dingding
author last names
Zhang
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Hao Zhang
series ordinal
4
author given names
Hao
author last names
Zhang
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Yuanfeng Li
series ordinal
5
author given names
Yuanfeng
author last names
Li
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Fang Lu
series ordinal
6
author given names
Fang
author last names
Lu
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Xiaoqi Liu
series ordinal
7
author given names
Xiaoqi
author last names
Liu
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Fei He
series ordinal
8
author given names
Fei
author last names
He
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Bo Gong
series ordinal
9
author given names
Bo
author last names
Gong
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Li Cai
series ordinal
10
author given names
Li
author last names
Cai
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Shihuang Liao
series ordinal
12
author given names
Shihuang
author last names
Liao
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Shi Ma
series ordinal
13
author given names
Shi
author last names
Ma
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
He Lin
series ordinal
14
author given names
He
author last names
Lin
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Jing Cheng
series ordinal
15
author given names
Jing
author last names
Cheng
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Hancheng Zheng
series ordinal
16
author given names
Hancheng
author last names
Zheng
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Ying Shan
series ordinal
17
author given names
Ying
author last names
Shan
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Bin Chen
series ordinal
18
author given names
Bin
author last names
Chen
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Jianbin Hu
series ordinal
19
author given names
Jianbin
author last names
Hu
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Xin Jin
series ordinal
20
author given names
Xin
author last names
Jin
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Peiquan Zhao
series ordinal
21
author given names
Peiquan
author last names
Zhao
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Yiye Chen
series ordinal
22
author given names
Yiye
author last names
Chen
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Yong Zhang
series ordinal
23
author given names
Yong
author last names
Zhang
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Ying Lin
series ordinal
24
author given names
Ying
author last names
Lin
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Xi Li
series ordinal
25
author given names
Xi
author last names
Li
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Yingchuan Fan
series ordinal
26
author given names
Yingchuan
author last names
Fan
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
Zhenglin Yang
series ordinal
29
author given names
Zhenglin
author last names
Yang
1 reference
stated in
PubMed
PubMed publication ID
21695231
retrieved
15 August 2022
publication date
June 2011
0 references
language of work or name
English
0 references
published in
PLOS Genetics
0 references
volume
7
0 references
issue
6
0 references
page(s)
e1002084
0 references
copyright license
Creative Commons Attribution 4.0 International
start time
9 June 2011
1 reference
stated in
April 2022 Public Data File from Crossref
copyright status
copyrighted
0 references
cites work
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13
1 reference
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Exome sequencing reveals VCP mutations as a cause of familial ALS
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19 March 2017
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
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reference URL
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retrieved
19 March 2017
Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
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19 March 2017
Terminal osseous dysplasia is caused by a single recurrent mutation in the FLNA gene
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19 March 2017
Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
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19 March 2017
Analysis of genetic inheritance in a family quartet by whole-genome sequencing
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
retrieved
19 March 2017
Exome sequencing identifies the cause of a mendelian disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
retrieved
19 March 2017
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
retrieved
19 March 2017
Targeted capture and massively parallel sequencing of 12 human exomes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
retrieved
19 March 2017
Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
retrieved
19 March 2017
Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
retrieved
19 March 2017
A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
retrieved
19 March 2017
Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
retrieved
12 September 2017
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
retrieved
12 September 2017
Mutations in SCARF2 Are Responsible for Van Den Ende-Gupta Syndrome
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
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12 September 2017
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
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12 September 2017
Exome sequencing: the sweet spot before whole genomes
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PubMed Central
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12 September 2017
Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
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12 September 2017
Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
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12 September 2017
Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability
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12 September 2017
Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy
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An international collaborative family-based whole-genome linkage scan for high-grade myopia
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12 September 2017
Prevalence of myopia in urban and rural children in mainland China
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12 September 2017
Identification and replication of three novel myopia common susceptibility gene loci on chromosome 3q26 using linkage and linkage disequilibrium mapping
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Estimating heritability and shared environmental effects for refractive error in twin and family studies
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12 September 2017
Complex trait genetics of refractive error
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12 September 2017
Heritability of refractive error and ocular biometrics: the Genes in Myopia (GEM) twin study.
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12 September 2017
The prevalence of refractive errors among adults in the United States, Western Europe, and Australia
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12 September 2017
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).
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12 September 2017
Evidence That a Locus for Familial High Myopia Maps to Chromosome 18p
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12 September 2017
Prevalence and risk factors for refractive errors in an adult inner city population.
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12 September 2017
Prevalence of myopia in the United States
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12 September 2017
Causes of blindness and visual impairment in urban and rural areas in Beijing: the Beijing Eye Study
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27 September 2017
X-linked myopia: Bornholm eye disease. Linkage to DNA markers on the distal part of Xq.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
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30 May 2018
Impact of heredity in myopia
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
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30 May 2018
Refractive errors in an elderly Japanese population: the Tajimi study
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002084
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21 January 2018
Prevalence and causes of visual impairment and blindness among 9980 Scandinavian adults: the Copenhagen City Eye Study.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002084
retrieved
21 January 2018
The role of educational attainment in refraction: the Genes in Myopia (GEM) twin study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002084
retrieved
21 January 2018
De novo mutations of SETBP1 cause Schinzel-Giedion syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002084
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21 January 2018
Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002084
retrieved
21 January 2018
Prevalence and risk factors for refractive errors in adult Chinese in Singapore
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487
retrieved
29 November 2018
Genes and environment in refractive error: the twin eye study
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21695231
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1371/JOURNAL.PGEN.1002084
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1377530
OpenCitations bibliographic resource ID
1377530
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1377530
PMC publication ID
3111487
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1377530
PubMed publication ID
21695231
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1377530
ResearchGate publication ID
51240394
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Exome sequencing identifies ZNF644 mutations in high myopia
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