For researchers

Is your paper here?

2,661 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.

50 matches for Mitchell B, showing the first 20.

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
Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness
GEFOS Any-Type of Fracture Consortium
Nature communications · 2017 · PMID 29313844 · open access
5 pages
rs72979233 rs4926611 rs11614333 rs2110927 rs80103986
Stroke genetics informs drug discovery and risk prediction across ancestries
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
rs72934589 rs76110445 rs12415501 rs60401382 Cardioembolic Stroke
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
New loci associated with kidney function and chronic kidney disease
Nature genetics · 2010 · PMID 20383146
4 pages
rs267734 rs10774021 rs7805747 rs6465825
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
4 pages
rs2107595 rs879324 rs13407662 Ischaemic Stroke
Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis
PLoS genetics · 2016 · PMID 27701424 · open access
4 pages
rs11880992 rs10948155 rs12206662 rs10471753
Genetic Variants Associated with Circulating Parathyroid Hormone
Journal of the American Society of Nephrology : JASN · 2017 · PMID 27927781
3 pages
rs4443100 rs35194449 rs4074995
Genome-wide analysis of clopidogrel active metabolite levels identifies novel variants that influence antiplatelet response
Pharmacogenetics and genomics · 2017 · PMID 28207573
3 pages
rs7915414 rs187941554 rs149772317
Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels
Circulation. Cardiovascular genetics · 2009 · PMID 20031604
2 pages
rs11225434 rs495366
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque
CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21909108 · open access
2 pages
rs11781551 rs17398575
Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans
COMPASS and METASTROKE Consortia
Stroke · 2015 · PMID 26089329
2 pages
rs4471613 rs9899375
An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels
Circulation · 2018 · PMID 29593015
2 pages
rs17573010 Cholesterol (LDL, HDL and Total)
Genome-wide association analysis of common genetic variants of resistant hypertension
eMERGE network
The pharmacogenomics journal · 2019 · PMID 30237584
2 pages
rs11749255 Resistant Hypertension
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium
PLoS genetics · 2009 · PMID 19557197 · open access
1 page
rs10146997
CUBN is a gene locus for albuminuria
CKDGen Consortium
Journal of the American Society of Nephrology : JASN · 2011 · PMID 21355061
1 page
Kidney Function
A genome-wide association search for type 2 diabetes genes in African Americans
DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
1 page
rs7560163
Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm
Journal of medical genetics · 2013 · PMID 23572186
1 page
rs11951031
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants
METASTROKE Consortium · CARDIoGRAM Consortium and 2 more consortia
Stroke · 2014 · PMID 24262325
1 page
rs12646447
Genetic variation at 16q24.2 is associated with small vessel stroke
METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
Annals of neurology · 2017 · PMID 27997041 · open access
1 page
rs12445022

Showing 20 of 50 · page 2 of 3

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.