For researchers

Is your paper here?

2,660 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.

22 matches for Klopp N, showing the first 20.

Discovery and refinement of loci associated with lipid levels
Global Lipids Genetics Consortium
Nature genetics · 2013 · PMID 24097068 · open access
12 pages+
rs4883201 rs11603023 rs11136341 rs4253772 rs13315871 rs2290159
Defining the role of common variation in the genomic and biological architecture of adult human height
Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25282103 · open access
12 pages+
rs17807185 rs12120956 rs3739707 rs6137287 rs9993613 rs3020418
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
CHARGE-EchoGen consortium · CHARGE-HF consortium and 1 more consortia
Nature genetics · 2016 · PMID 27618452 · open access
12 pages+
rs12247028 rs6779380 rs4691707 rs12705390 rs2898290 rs7076398
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
International Multiple Sclerosis Genetics Consortium · Wellcome Trust Case Control Consortium 2
Nature · 2011 · PMID 21833088 · open access
11 pages
rs11154801 rs12212193 rs7522462 rs9282641 rs10466829 rs2119704
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
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
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
MAGIC investigators · GIANT Consortium
Nature genetics · 2010 · PMID 20581827
8 pages
rs1552224 rs5945326 rs11634397 rs231362 rs7957197 rs1470579
Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk
American journal of human genetics · 2011 · PMID 21565293
6 pages
rs12138950 rs4338740 rs12045440 rs17767419 rs10917468 Thyroid Volume
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
Genome-wide association study identifies 48 common genetic variants associated with handedness
Nature human behaviour · 2021 · PMID 32989287
6 pages
rs35551703 rs66479618 rs1422070 rs11168884 rs3132584 rs62036618
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Nature genetics · 2010 · PMID 21076409 · open access
5 pages
rs17391905 rs1886512 rs17608766 rs1733724 Cardiac Conduction Intervals (PR Interval and QRS Duration)
New loci associated with kidney function and chronic kidney disease
Nature genetics · 2010 · PMID 20383146
4 pages
rs267734 rs10774021 rs7805747 rs6465825
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
International Lung Cancer Consortium · GIANT consortium
Nature genetics · 2011 · PMID 21946350 · open access
4 pages
rs1036429 rs2798641 rs12447804 rs6903823
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
LifeLines Cohort Study · CARDIoGRAM Consortium and 3 more consortia
Nature genetics · 2013 · PMID 23263486
3 pages
rs1481012 rs4475146 Gout
Wnt signaling and Dupuytren's disease
Dutch Dupuytren Study Group · German Dupuytren Study Group and 2 more consortia
The New England journal of medicine · 2011 · PMID 21732829
2 pages
rs11672517 Dupuytren's Disease
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
Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus
PLoS genetics · 2008 · PMID 18846228 · open access
1 page
rs2251746
A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3
Human molecular genetics · 2011 · PMID 21216879
1 page
rs700752
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
Common variants at 12q15 and 12q24 are associated with infant head circumference
Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium and 1 more consortia
Nature genetics · 2012 · PMID 22504419
1 page
rs1042725

Showing 20 of 22 · 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.