For researchers

Is your paper here?

2,663 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.

37 matches for Hewitt A, 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+
rs2487048 rs6107845 rs2157719 rs114503346 rs10753787 rs72759609
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
CHD Exome+ Consortium · EPIC-CVD Consortium and 9 more consortia
Nature genetics · 2018 · PMID 29273807 · open access
12 pages+
rs284860 rs1131877 rs2277598 rs295322 rs62623713 rs11555762
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 association meta-analysis highlights light-induced signaling as a driver for refractive error
CREAM Consortium · 23andMe Research Team and 1 more consortia
Nature genetics · 2018 · PMID 29808027 · open access
12 pages+
rs2162488 rs4332760 rs41393947 rs10879211 rs1346720 rs55684140
Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology
Human molecular genetics · 2019 · PMID 31809533
12 pages+
rs2092524 rs6999835 rs10862708 rs77587000 rs4839470 rs73173591
Using Mendelian randomization to evaluate the causal relationship between serum C-reactive protein levels and age-related macular degeneration
European journal of epidemiology · 2020 · PMID 31900758
12 pages+
rs6698653 rs728538 rs150852956 rs28399607 rs146342974 rs9366639
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression
NEIGHBORHOOD consortium · UK Biobank Eye and Vision Consortium
Nature genetics · 2020 · PMID 31959993
12 pages+
rs756481 rs984586 rs2188836 rs62172701 rs73153655 rs62038917
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error
Consortium for Refractive Error and Myopia (CREAM) · UK Biobank Eye and Vision Consortium
Communications biology · 2020 · PMID 32193507 · open access
12 pages+
rs485554 rs13180294 rs10786330 rs9806595 rs1548942 rs11740254
Association of Myopia and Intraocular Pressure With Retinal Detachment in European Descent Participants of the UK Biobank Cohort: A Mendelian Randomization Study
JAMA ophthalmology · 2020 · PMID 32352494
12 pages+
rs4145443 rs9911460 rs35638197 rs1367023 rs3007364 rs1896539
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+
rs1412829 rs61870251 rs34175429 rs938604 rs1893261 rs62521288
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus
Communications biology · 2021 · PMID 33649486 · open access
12 pages+
rs2417930 rs3118518 rs1200108 rs6669560 rs116792882 rs12515400
Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images
UK Biobank Eye and Vision Consortium · International Glaucoma Genetics Consortium
PLoS genetics · 2021 · PMID 33979322 · open access
12 pages+
rs62252355 rs2008905 rs73348111 rs13215351 rs79833181 rs2787394
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs11207980 rs598253 rs57825321 rs12603290 rs186793936 rs9844432
Association of Novel Loci With Keratoconus Susceptibility in a Multitrait Genome-Wide Association Study of the UK Biobank Database and Canadian Longitudinal Study on Aging
International Glaucoma Genetics Consortium
JAMA ophthalmology · 2022 · PMID 35446358
12 pages+
rs1828671 rs943423 rs2645775 rs7327928 rs10780724 rs11786528
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs9344003 rs12974635 rs10519014 rs11691472 rs2679184 rs2854915
Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci
23andMe Research Team · International Glaucoma Genetics Consortium
Nature genetics · 2023 · PMID 37386247 · open access
12 pages+
rs10257125 rs1658436 rs4414666 rs17254069 rs280875 rs2218471
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
rs10089517 rs6495367 rs6500957 rs72483203 rs929474 rs10853531
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
International Visible Trait Genetics Consortium
Nature genetics · 2018 · PMID 29662168 · open access
10 pages
rs6440008 rs10960765 rs58979150 rs11041426 rs72917317 rs10899501
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
Nature genetics · 2018 · PMID 30054594
10 pages
rs12699251 rs10505100 rs61861119 rs73174345 rs11710139 rs9284802

Showing 20 of 37 · 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.