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.

33 matches for Wheeler E, showing the first 20.

Hundreds of variants clustered in genomic loci and biological pathways affect human height
Nature · 2010 · PMID 20881960 · open access
12 pages+
rs822552 rs12694997 rs7853377 rs7532866 rs4605213 rs4640244
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Nature genetics · 2013 · PMID 23563607 · open access
12 pages+
rs10182181 rs1412239 rs1421085 rs538656 rs1514177 rs3101336
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
Cell · 2016 · PMID 27863252 · open access
12 pages+
rs111527163 rs1887639 rs7716229 rs2078064 rs11671005 rs35304300
A cross-platform approach identifies genetic regulators of human metabolism and health
MacTel Consortium
Nature genetics · 2021 · PMID 33414548
12 pages+
rs2608920 rs4253272 rs731165 rs74095612 rs2306386 rs4143279
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs118164457 rs182859029 rs7063597 rs3752435 rs4317621 rs4731113
Mapping the proteo-genomic convergence of human diseases
Science (New York, N.Y.) · 2021 · PMID 34648354
12 pages+
rs74161804 rs115458416 rs11103042 rs1882325 rs563610140 rs73185617
Mapping the serum proteome to neurological diseases using whole genome sequencing
Nature communications · 2021 · PMID 34857772 · open access
12 pages+
rs227439 rs35984397 rs67924081 rs28483039 rs11004802 rs217053
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs11196296 rs3825801 rs79495865 rs1871045 rs80102379 rs7819706
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs60128210 rs244080 rs2534653 rs4932747 rs6073369 rs11576244
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
MAGIC · Procardis Consortium
Nature genetics · 2010 · PMID 20935630 · open access
11 pages
rs543874 rs10150332 rs2241423 rs2287019 rs12444979 rs206936
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
EPIC-CVD Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS medicine · 2017 · PMID 28898252 · open access
10 pages
rs4745982 rs10823343 rs3824065 rs11154792 rs17509001 rs7040409
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Multiple Tissue Human Expression Resource (MUTHER) Consortium
Nature genetics · 2012 · PMID 22581228
8 pages
rs35747 rs4691380 rs2785980 rs1371614 rs13179048 rs6048205
Lowering of Circulating Sclerostin May Increase Risk of Atherosclerosis and Its Risk Factors: Evidence From a Genome-Wide Association Meta-Analysis Followed by Mendelian Randomization
Arthritis & rheumatology (Hoboken, N.J.) · 2023 · PMID 37096546
7 pages
rs13042961 rs11960484 rs17138656 rs7143806 rs34136735 rs34498262
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
rs182052 rs2980879 rs6488898 rs2590838 rs4805885 Adiponectin Levels
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa
Cell · 2019 · PMID 31675503
6 pages
rs1088639 rs151330263 rs115231893 rs569795903 rs7564935 rs148228241
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
6 pages
rs3784634 rs5400 rs17853166 rs75619922 rs7225887 rs56381411
Genome-wide association analysis identifies 20 loci that influence adult height
Diabetes Genetics Initiative · Wellcome Trust Case Control Consortium and 1 more consortia
Nature genetics · 2008 · PMID 18391952
5 pages
rs6060373 rs1390401 rs6724465 rs2814993 rs2282978
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways
WTCCC
Diabetes · 2010 · PMID 20858683 · open access
5 pages
rs1799884 rs1046896 rs6474359 rs7998202 Type 2 Diabetes
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
DIAGRAM Consortium · GIANT Consortium and 3 more consortia
Nature genetics · 2010 · PMID 20081858 · open access
4 pages
rs11920090 rs7944584 rs11605924 Fasting Blood Glucose
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

Showing 20 of 33 · 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.