(Q33604802)

28 July 2017

0 references

A genome-wide association study of optic disc parameters (English)

1 reference

genome-wide association study

28 July 2017

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author

Yurii S. Aulchenko

9

1 reference

28 July 2017

12

1 reference

28 July 2017

14

Andre G Uitterlinden

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Cornelia M. van Duijn

20

Cornelia M van Duijn

0 references

Christopher J. Hammond

Christopher J Hammond

16

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Najaf Amin

Najaf Amin

8

0 references

Albert Hofman

11

Albert Hofman

1 reference

28 July 2017

Mohammad Kamran Ikram

3

M Kamran Ikram

2 references

ORCID Public Data File 2021

28 July 2017

13

Ben A Oostra

1 reference

28 July 2017

19

Caroline C W Klaver

1 reference

28 July 2017

15

Pirro Hysi

1 reference

28 July 2017

7

Aaron Isaacs

1 reference

28 July 2017

Johannes R. Vingerling

18

Johannes R Vingerling

1 reference

28 July 2017

5

Paulus T V M de Jong

1 reference

28 July 2017

1

Wishal D Ramdas

1 reference

Leonieke M E van Koolwijk

28 July 2017

2

Leonieke M E van Koolwijk

1 reference

28 July 2017

10

Roger C W Wolfs

1 reference

28 July 2017

17

Hans G Lemij

1 reference

28 July 2017

4

Nomdo M Jansonius

1 reference

28 July 2017

Arthur A B Bergen

6

1 reference

28 July 2017

10 June 2010

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28 July 2017

1 reference

28 July 2017

6

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28 July 2017

e1000978

1 reference

28 July 2017

6

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Creative Commons Attribution 4.0 International

28 July 2017

start time

10 June 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

genome-wide association study

1 reference

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

inferred from title

cites work

1 reference

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21 June 2018

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Null mutations in LTBP2 cause primary congenital glaucoma

21 June 2018

1 reference

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A comprehensive negative regulatory program controlled by Brn3b to ensure ganglion cell specification from multipotential retinal precursors

21 June 2018

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Zeb1 links epithelial-mesenchymal transition and cellular senescence

21 June 2018

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The Rotterdam Study: objectives and design update

21 June 2018

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21 June 2018

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Optic disc size in a population-based study in central India: the Central India Eye and Medical Study (CIEMS).

21 June 2018

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Genetic contributions to glaucoma: heritability of intraocular pressure, retinal nerve fiber layer thickness, and optic disc morphology

21 June 2018

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Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration

21 June 2018

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Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

21 June 2018

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21 June 2018

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Optic disk size and glaucoma

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

Predictive factors for open-angle glaucoma among patients with ocular hypertension in the European Glaucoma Prevention Study

21 June 2018

1 reference

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Transcriptional activation of the SALL1 by the human SIX1 homeodomain during kidney development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

Optic disc size in a population based study in northern China: the Beijing Eye Study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

GDF11 controls the timing of progenitor cell competence in developing retina

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

Digital imaging of the optic nerve head: monoscopic and stereoscopic analysis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

Determinants and heritability of intraocular pressure and cup-to-disc ratio in a defined older population

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

A role of ath5 in inducing neuroD and the photoreceptor pathway

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

Tissue-specific regulation of retinal and pituitary precursor cell proliferation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

21 June 2018

1 reference

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Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

Math5 is required for retinal ganglion cell and optic nerve formation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

The optic nerve head as a biomechanical structure: initial finite element modeling

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

A SALL1 mutation causes a branchio-oto-renal syndrome-like phenotype

21 June 2018

1 reference

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Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

Six6 (Optx2) is a novel murine Six3-related homeobox gene that demarcates the presumptive pituitary/hypothalamic axis and the ventral optic stalk

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

Comparison between laser scanning tomography and computerised image analysis of the optic disc.

21 June 2018

1 reference

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Math5 encodes a murine basic helix-loop-helix transcription factor expressed during early stages of retinal neurogenesis.

21 June 2018

1 reference

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Review of alterations of the cyclin-dependent kinase inhibitor INK4 family genes p15, p16, p18 and p19 in human leukemia-lymphoma cells

21 June 2018

1 reference

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Reproducibility of optic disk topographic measurements with the Topcon ImageNet and the Heidelberg Retina Tomograph

21 June 2018

1 reference

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p15INK4B is a potential effector of TGF-beta-induced cell cycle arrest

21 June 2018

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Measurement variability in digital analysis of optic discs

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

Size of the physiologic cup of the optic nerve head. hereditary and environmental factors

21 June 2018

1 reference

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Optic disk size in open-angle glaucoma: the Blue Mountains Eye Study.

21 June 2018

1 reference

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The association between glaucomatous visual fields and optic nerve head features in the Ocular Hypertension Treatment Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

Heritability of risk factors for primary open-angle glaucoma: the Beaver Dam Eye Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

Discrete gene sets depend on POU domain transcription factor Brn3b/Brn-3.2/POU4f2 for their expression in the mouse embryonic retina

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

Mutations of p16 and p15 tumor suppressor genes and replication errors contribute independently to the pathogenesis of sporadic malignant melanoma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

Stickler and branchio-oto-renal syndromes in a patient with mutations in EYA1 and COL2A1 genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomalies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

Expression of the optx2 homeobox gene during mouse development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

Expression of doublecortin (DCX) and doublecortin-like kinase (DCLK) within the developing chick brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

A third locus for dominant optic atrophy on chromosome 22q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

Swollen optic discs in a patient with the chromosome 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

Causes of incident visual field loss in a general elderly population: the Rotterdam study

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

Primary open-angle glaucoma

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

Changing views on open-angle glaucoma: definitions and prevalences--The Rotterdam Study

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

Linkage disequilibrium in young genetically isolated Dutch population

30 October 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

The Effect of Genetic Drift in a Young Genetically Isolated Population

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000978

The Effect of Genetic Drift in a Young Genetically Isolated Population

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2883590

Comparing ophthalmoscopy, slide viewing, and semiautomated systems in optic disc morphometry

30 October 2018

1 reference

PubMed

12 December 2020

1 reference

12 December 2020

The heritability of optic disc parameters: a classic twin study

1 reference

PubMed

12 December 2020

Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma

1 reference

PubMed

12 December 2020

10.1371/JOURNAL.PGEN.1000978

Identifiers

DOI

1 reference

28 July 2017

1 reference

28 July 2017

1 reference