For researchers

Is your paper here?

2,677 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.

23 matches for Eisen T, showing the first 20.

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+
rs2744971 rs10843164 rs10182181 rs1412239 rs1421085 rs538656
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
CARe Consortium · COGENT Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24952745 · open access
12 pages+
rs1983546 rs12930096 rs12444261 rs1052536 rs1396515 rs1805128
New genetic loci link adipose and insulin biology to body fat distribution
ADIPOGen Consortium · CARDIOGRAMplusC4D Consortium and 11 more consortia
Nature · 2015 · PMID 25673412 · open access
12 pages+
rs6060717 rs11989744 rs4646404 rs319564 rs2179129 rs16996700
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+
rs62057070 rs10237280 rs78445564 rs17834032 rs75341124 rs4291964
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
HUNT All-In Psychiatry
Nature genetics · 2021 · PMID 34002096 · open access
12 pages+
rs2336147 rs10866641 rs67712855 rs748455 rs10917509 rs78308718
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 pages+
rs6916760 rs4506680 rs114427493 rs12274095 rs57551109 rs501842
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Wellcome Trust Case Control Consortium · Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) Investigators and 4 more consortia
Nature genetics · 2012 · PMID 22885922 · open access
10 pages
rs2075423 rs10203174 rs1496653 rs7955901 rs7177055 rs7640539
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
10 pages
rs3133370 rs2206656 rs4784256 rs196807 rs9505301 rs9818981
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 pages
rs6813195 rs17106184 rs849135 rs2261181 rs9936385 rs4458523
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Cardiogenics · CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21378990
7 pages
rs12526453 rs17114036 rs3798220 rs3825807 rs1231206 rs12936587
Genome-wide association study identifies multiple risk loci for renal cell carcinoma
Nature communications · 2017 · PMID 28598434 · open access
6 pages
rs4381241 rs67311347 rs11813268 rs74911261 rs4903064 Renal Cell Carcinoma
Genome-wide association study identifies 30 loci associated with bipolar disorder
eQTLGen Consortium · BIOS Consortium and 1 more consortia
Nature genetics · 2019 · PMID 31043756 · open access
6 pages
rs111444407 rs10950456 rs57957974 rs17183814 rs10896090 rs10035291
Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Nature genetics · 2009 · PMID 19305409
4 pages
rs17779747 rs10919071 rs2968863 rs11970286
Genome-wide association study reveals two new risk loci for bipolar disorder
Nature communications · 2014 · PMID 24618891
4 pages
rs12290811 rs17826816 rs12202969 rs6550435
Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups
PLoS genetics · 2010 · PMID 20421936 · open access
2 pages
rs17700144 rs17150703
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder
Bipolar Disorder Genome Study (BiGS) Consortium
American journal of human genetics · 2011 · PMID 21353194
2 pages
rs1064395 Bipolar Disorder
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
Nature genetics · 2013 · PMID 23955597 · open access
2 pages
rs877529 Multiple Myeloma
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder
Human molecular genetics · 2016 · PMID 27329760
2 pages
rs2517959 rs4236274
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma
American journal of human genetics · 2009 · PMID 19836008
1 page
rs31489
Common variation at 10p12.31 near MLLT10 influences meningioma risk
Nature genetics · 2011 · PMID 21804547 · open access
1 page
rs11012732

Showing 20 of 23 · 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.