For researchers

Is your paper here?

2,673 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.

113 matches for Evans D, showing the first 20.

Genome-wide association study identifies five loci associated with lung function
Wellcome Trust Case Control Consortium · NSHD Respiratory Study Team
Nature genetics · 2010 · PMID 20010834
3 pages
rs12899618 rs10516526 rs12504628
Genome-wide association study identifies five new breast cancer susceptibility loci
Breast Cancer Susceptibility Collaboration (UK)
Nature genetics · 2010 · PMID 20453838
3 pages
rs10995190 rs1011970 rs614367
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Nature genetics · 2011 · PMID 21460841 · open access
3 pages
rs7561528 rs9349407 Alzheimer's Disease
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility
Spondyloarthritis Research Consortium of Canada (SPARCC) · Australo-Anglo-American Spondyloarthritis Consortium (TASC) and 1 more consortia
Nature genetics · 2011 · PMID 21743469
3 pages
rs11616188 rs11249215 Ankylosing Spondylitis
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 pages
rs4851266 rs9320913 rs1056667
Genome-wide meta-analysis identifies new susceptibility loci for migraine
North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
3 pages
rs11759769 rs12134493 rs4379368
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
arcOGEN Consortium
Annals of the rheumatic diseases · 2014 · PMID 23989986 · open access
3 pages
rs3757837 rs6094710 Hip Osteoarthritis
Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants
EArly Genetics & Lifecourse Epidemiology (EAGLE) Consortium
The Journal of allergy and clinical immunology · 2014 · PMID 24315451
3 pages
rs3751972 rs2016444 rs12500579
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Nature communications · 2016 · PMID 26833246 · open access
3 pages
rs6738627 rs4788099 rs693839
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways
Human molecular genetics · 2016 · PMID 27559109
3 pages
rs8111874 rs35106244 Diarrhoeal Disease in Infancy
A genome-wide association study reveals variants in ARL15 that influence adiponectin levels
GIANT Consortium
PLoS genetics · 2009 · PMID 20011104 · open access
2 pages
rs1648707 Adiponectin Levels
Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals
Atherosclerosis · 2010 · PMID 20018283
2 pages
rs17366568 Adiponectin Levels
Genome-wide association study reveals multiple loci associated with primary tooth development during infancy
PLoS genetics · 2010 · PMID 20195514 · open access
2 pages
rs8079702 Tooth Eruption Timing
Genome-wide association studies of the PR interval in African Americans
Candidate-gene Association Resource (CARe) Consortium
PLoS genetics · 2011 · PMID 21347284 · open access
2 pages
rs6798015 rs10865355
Genome-wide association study identifies four loci associated with eruption of permanent teeth
PLoS genetics · 2011 · PMID 21931568 · open access
2 pages
rs12424086 Tooth Eruption Timing
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
Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control selection on genetic association studies
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2014 · PMID 24753544
2 pages
rs4793529 rs12682344
A novel common variant in DCST2 is associated with length in early life and height in adulthood
Early Genetics and Lifecourse Epidemiology (EAGLE) Consortium · Genetic Investigation of ANthropometric Traits (GIANT) Consortium and 1 more consortia
Human molecular genetics · 2015 · PMID 25281659 · open access
2 pages
rs1380294 rs905938
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium
Aging cell · 2016 · PMID 27325353 · open access
2 pages
rs752045 Hand Grip Strength
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins
Journal of medical genetics · 2016 · PMID 27587472
2 pages
rs247616 Cholesterol (LDL, HDL and Total)

Showing 20 of 113 · page 4 of 6

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.