Exome sequencing identifies ZNF644 mutations in high myopia (Q21092428)

2

Yingrui

Li

1 reference

15 August 2022

Dingding Zhang

3

Dingding

Zhang

1 reference

15 August 2022

Hao Zhang

4

Hao

Zhang

1 reference

15 August 2022

Yuanfeng Li

5

Yuanfeng

Li

1 reference

15 August 2022

Fang Lu

6

Fang

Lu

1 reference

15 August 2022

Xiaoqi Liu

7

Xiaoqi

Liu

1 reference

15 August 2022

Fei He

8

Fei

He

1 reference

15 August 2022

Bo Gong

9

Bo

Gong

1 reference

15 August 2022

Li Cai

10

Li

Cai

1 reference

15 August 2022

Shihuang Liao

12

Shihuang

Liao

1 reference

15 August 2022

Shi Ma

13

Shi

Ma

1 reference

15 August 2022

He Lin

14

He

Lin

1 reference

15 August 2022

Jing Cheng

15

Jing

Cheng

1 reference

15 August 2022

Hancheng Zheng

16

Hancheng

Zheng

1 reference

15 August 2022

Ying Shan

17

Ying

Shan

1 reference

15 August 2022

Bin Chen

18

Bin

Chen

1 reference

15 August 2022

Jianbin Hu

19

Jianbin

Hu

1 reference

15 August 2022

Xin Jin

20

Xin

Jin

1 reference

15 August 2022

Peiquan Zhao

21

Peiquan

Zhao

1 reference

15 August 2022

Yiye Chen

22

Yiye

Chen

1 reference

15 August 2022

Yong Zhang

23

Yong

Zhang

1 reference

15 August 2022

Ying Lin

24

Ying

Lin

1 reference

15 August 2022

Xi Li

25

Xi

Li

1 reference

15 August 2022

Yingchuan Fan

26

Yingchuan

Fan

1 reference

15 August 2022

Zhenglin Yang

29

Zhenglin

Creative Commons Attribution 4.0 International

Yang

1 reference

15 August 2022

language of work or name

English

0 references

publication date

June 2011

0 references

published in

PLOS Genetics

0 references

volume

7

0 references

issue

6

0 references

page(s)

e1002084

0 references

copyright license

start time

9 June 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene

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Exome sequencing identifies the cause of a mendelian disorder

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Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia

19 March 2017

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Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome

19 March 2017

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A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1

19 March 2017

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Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa

19 March 2017

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TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing

12 September 2017

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Mutations in SCARF2 are responsible for Van Den Ende-Gupta syndrome

12 September 2017

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Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome

12 September 2017

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Exome sequencing: the sweet spot before whole genomes

12 September 2017

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Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome

12 September 2017

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Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.

12 September 2017

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Mutations in the guanine nucleotide exchange factor gene IQSEC2 cause nonsyndromic intellectual disability

12 September 2017

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Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

12 September 2017

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12 September 2017

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Prevalence of myopia in urban and rural children in mainland China

12 September 2017

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Identification and replication of three novel myopia common susceptibility gene loci on chromosome 3q26 using linkage and linkage disequilibrium mapping

12 September 2017

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12 September 2017

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12 September 2017

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12 September 2017

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27 September 2017

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Impact of heredity in myopia

30 May 2018

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30 May 2018

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Prevalence and causes of visual impairment and blindness among 9980 Scandinavian adults: the Copenhagen City Eye Study.

21 January 2018

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21 January 2018

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De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

21 January 2018

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Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

21 January 2018

1 reference

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Prevalence and risk factors for refractive errors in adult Chinese in Singapore

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3111487

Genes and environment in refractive error: the twin eye study

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21695231

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1002084

1 reference

1377530

1377530

1 reference

1 reference

1 reference