For researchers

Is your paper here?

2,676 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.

580 matches for An J, showing the first 20.

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
rs10494217 rs1051860 rs141845046 rs145878042 rs1715919 rs62266958
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Understanding Society Scientific Group
Nature genetics · 2019 · PMID 30804560 · open access
12 pages+
rs1215 rs34093919 rs1978968 rs79898473 rs1800888 rs7752448
Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct
23andMe Research Team · eQTLGen Consortium and 1 more consortia
American journal of human genetics · 2019 · PMID 30929738
12 pages+
rs17668708 rs67551275 rs3785356 rs34290285 rs12123821 rs45613035
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
EGG Consortium
Nature genetics · 2019 · PMID 31043758
12 pages+
rs9366778 rs10734564 rs10221267 rs1724889 rs2168443 rs4579095
Combined analysis of keratinocyte cancers identifies novel genome-wide loci
23andMe Research Team
Human molecular genetics · 2019 · PMID 31174203 · open access
12 pages+
rs9557210 rs138501911 rs6714430 rs35540156 rs7620634 rs1927729
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
23andMe Research Team · System Genomics of Parkinson's Disease Consortium and 1 more consortia
The Lancet. Neurology · 2019 · PMID 31701892
12 pages+
rs114138760 rs11578699 rs11557080 rs76116224 rs73038319 rs55961674
Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2
American journal of human genetics · 2019 · PMID 31761296
12 pages+
rs10841515 rs191305096 rs2067082 rs140676308 rs34616741 rs553470220
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+
rs34536594 rs6673575 rs11584075 rs6030 rs17734073 rs2149108
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+
rs13058527 rs150543164 rs4704780 rs72732974 rs74085345 rs62282070
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+
rs8176662 rs28761289 rs9521601 rs12821310 rs2761235 rs34010125
Genome-wide Association Study for Vitamin D Levels Reveals 69 Independent Loci
American journal of human genetics · 2020 · PMID 32059762
12 pages+
rs1858889 rs565277381 rs192785674 rs2762942 rs2585442 rs117576073
The genetic architecture of the human cerebral cortex
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
rs114489117 rs62399042 rs6554054 rs11070185 rs76470478 rs2301718
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+
rs7959830 rs4083463 rs13050142 rs7657200 rs4887113 rs7004112
Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma
Nature communications · 2020 · PMID 32296059 · open access
12 pages+
rs2016366 rs73012738 rs2007960 rs13383994 rs952579 rs411919
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
GenoMEL Consortium · Q-MEGA and QTWIN Investigators and 7 more consortia
Nature genetics · 2020 · PMID 32341527 · open access
12 pages+
rs16849932 rs548304 rs111595456 rs13283146 rs2857482 rs75818295
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+
rs893819 rs11790439 rs2195526 rs11899425 rs113543909 rs12919036
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs75990271 rs1328412 rs56687477 rs60573766 rs149265787 rs186568031
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
HPAP Consortium · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2020 · PMID 32541925 · open access
12 pages+
rs7026688 rs6438247 rs12918782 rs9913225 rs28712435 rs6714523
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts
Nature communications · 2020 · PMID 32887889 · open access
12 pages+
rs11957276 rs72951831 rs10866527 rs17190106 rs12354821 rs189268208
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
rs62037423 rs73101498 rs75865061 rs868868 rs991057 rs10998648

Showing 20 of 580 · page 4 of 29

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.