For researchers

Is your paper here?

2,647 papers hold this site up. Every variant and condition page names the research it was written from, and this is that list, gathered from the pages themselves. Search your name, your journal, or a PMID.

24 matches for Vithana E, showing the first 20.

New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics
NEIGHBORHOOD Consortium
Human molecular genetics · 2017 · PMID 28073927
12 pages+
rs6107845 rs2157719 rs114503346 rs10753787 rs72759609 rs8015152
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2018 · PMID 29760442 · open access
12 pages+
rs3808520 rs7026684 rs10980623 rs7040970 rs7308752 rs11553764
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
NEIGHBORHOOD consortium · ANZRAG consortium and 5 more consortia
Nature communications · 2021 · PMID 33627673 · open access
12 pages+
rs66819623 rs8141610 rs56233426 rs11710845 rs1412829 rs61870251
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
NEIGHBOR Consortium
Nature genetics · 2013 · PMID 23291589
10 pages
rs2307121 rs1007000 rs1536482 rs11145951 rs4938174 rs1564892
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
Consortium for Refractive Error and Myopia
Nature communications · 2016 · PMID 27020472 · open access
10 pages
rs10853531 rs11145488 rs12511037 rs1649081 rs16949788 rs10089517
Seven new loci associated with age-related macular degeneration
AMD Gene Consortium
Nature genetics · 2013 · PMID 23455636 · open access
7 pages
rs1864163 rs920915 rs8135665 rs8017304 rs9542236 rs13081855
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Consortium for Refractive Error and Myopia (CREAM) · Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Research Group and 2 more consortia
Nature genetics · 2013 · PMID 23396134
6 pages
rs1656404 rs4793501 rs10882165 rs17183295 rs11145465 Myopia
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology
NEIGHBORHOOD Consortium
Genetic epidemiology · 2015 · PMID 25631615
5 pages
rs11651885 rs301801 rs6671926 rs9546434 rs7972528
Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians
CHARGE Hematology Working Group
Diabetes · 2014 · PMID 24647736 · open access
4 pages
rs11667918 rs1046875 rs3755157 Type 2 Diabetes
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
BMES GWAS Group · NEIGHBORHOOD Consortium and 1 more consortia
Nature genetics · 2014 · PMID 25173106 · open access
4 pages
rs747782 rs10258482 rs12419342 Glaucoma
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia
LifeLines Cohort Study
American journal of human genetics · 2014 · PMID 24954895
3 pages
rs12416687 rs16833934 rs4842666
Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area
Human molecular genetics · 2011 · PMID 21307088
2 pages
rs6000762 Glaucoma
Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore
Human molecular genetics · 2011 · PMID 21665993
2 pages
rs17036350 rs2114039
Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism
PLoS genetics · 2011 · PMID 22144915 · open access
2 pages
rs7677751 Corneal Astigmatism
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Consortium for Refractive Error and Myopia · Fuchs' Genetics Multi-Center Study Group and 2 more consortia
American journal of human genetics · 2013 · PMID 24144296
2 pages
rs9811920 rs12193446
Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract
Human molecular genetics · 2014 · PMID 24951543
2 pages
rs11911275 Age-Related Nuclear Cataracts
CMPK1 and RBP3 are associated with corneal curvature in Asian populations
Human molecular genetics · 2014 · PMID 24963161
2 pages
rs17103186 rs1800813
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2014 · PMID 25241763 · open access
2 pages
rs17658229 rs17756712
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
rs9687065 rs1563788
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia
Nagahama Study Group
Human molecular genetics · 2013 · PMID 23933737
1 page
rs6469937

Showing 20 of 24 · page 1 of 2

Questions about this list

Why is my paper here? I never gave you permission.

Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page cites your work, and links to the paper on PubMed — which is what a citation is. Your title and author list come from Europe PMC, the same public record a library catalogue uses.

Why are all the authors listed instead of "et al."?

Because a study that needed 622 people is a different kind of study from one that needed four, and "et al." erases that. Twelve names show and the rest are one click away. Everyone is searchable, including the 187th name on a consortium paper — that person exists and may be looking for it.

My name is misspelt, or the paper is wrong.

Tell us and it is fixed. Names come from the public record and initials are inconsistent across databases; where two people share a form of a name we cannot separate them, and we would rather be corrected than guess.

My paper is not here. Does that mean you rejected it?

No. This catalogue is assembled from what a small team could read, and it is thinnest outside European-ancestry cohorts. A paper is absent because nobody has got to it, not because it was assessed and turned down.

Which pages rest on a paper?

Each row lists them, up to six, and links to each one. The count beside a row is how many pages cite it in total.

How often does this change?

It is rebuilt from the pages every hour. A paper appears the moment a page starts resting on it and disappears if that page stops — there is no separate list to keep in step, because the citation lives on the page that makes the claim.