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.

52 matches for Franke L, showing the first 20.

Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Nature metabolism · 2020 · PMID 33067605
12 pages+
rs4865884 rs60515336 rs78716942 rs11569334 rs150106684 rs4134826
Genetic insights into biological mechanisms governing human ovarian ageing
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
rs2844466 rs140353819 rs540836853 rs2736609 rs9438982 rs117146677
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs147660927 rs7209222 rs9272456 rs4515883 rs6743072 rs35073727
Genome-wide characterization of circulating metabolic biomarkers
China Kadoorie Biobank Collaborative Group · Estonian Biobank Research Team and 1 more consortia
Nature · 2024 · PMID 38448586 · open access
12 pages+
rs12037485 rs111705570 rs79683221 rs4649085 rs9469905 rs7350906
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
LifeLines Cohort Study
Nature genetics · 2016 · PMID 27089181 · open access
10 pages
rs782212 rs12903563 rs12961969 rs35688236 rs2075677 rs4958581
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
International Headache Genetics Consortium
Nature genetics · 2016 · PMID 27322543
9 pages
rs2506142 rs4081947 rs6791480 rs6693567 rs10155855 rs10218452
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
Global BPgen Consortium · CARDIoGRAM Consortium and 4 more consortia
Nature genetics · 2013 · PMID 23583979
8 pages
rs17287293 rs11118555 rs13030174 rs826838 rs11578508 rs4140885
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index
Bone Mineral Density in Childhood Study (BMDCS) · Early Genetics and Lifecourse Epidemiology (EAGLE) consortium and 2 more consortia
Human molecular genetics · 2016 · PMID 26604143
8 pages
rs12041852 rs13253111 rs13387838 rs17024393 rs3829849 rs7550711
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
Spanish Consortium on the Genetics of Coeliac Disease (CEGEC) · PreventCD Study Group and 1 more consortia
Nature genetics · 2011 · PMID 22057235 · open access
7 pages
rs10800746 rs61579022 rs2030519 rs13132308 rs55743914 rs11875687
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)
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function
The Journal of clinical investigation · 2017 · PMID 28394258
5 pages
rs6702619 rs17696696 rs7127129 rs2649 rs11207426
Large-scale association analyses identify host factors influencing human gut microbiome composition
Nature genetics · 2021 · PMID 33462485
5 pages
rs71348714 rs7605229 rs7322849 rs11110281 rs61841503
Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci
PLoS genetics · 2011 · PMID 21383967 · open access
4 pages
rs1953126 rs2298428 rs11984075 Celiac Disease
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis
Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate · Wellcome Trust Case Control Consortium
Nature genetics · 2012 · PMID 23143596 · open access
4 pages
rs13397 rs13426947 rs59466457 rs2834512
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
Proceedings of the National Academy of Sciences of the United States of America · 2014 · PMID 25201988
4 pages
rs1487441 rs9858213 rs13401104 rs3789044
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
4 pages
rs10908557 rs6885307 rs2347867 rs2721195
Multiple common variants for celiac disease influencing immune gene expression
Nature genetics · 2010 · PMID 20190752 · open access
3 pages
rs2327832 rs10806425 Celiac Disease
Discovery and fine mapping of serum protein loci through transethnic meta-analysis
LifeLines Cohort Study
American journal of human genetics · 2012 · PMID 23022100
3 pages
rs204999 rs11078597 rs4561508
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 association study identifies novel genetic variants contributing to variation in blood metabolite levels
Nature communications · 2015 · PMID 26068415
3 pages
rs12297049 rs2540641 rs16844839

Showing 20 of 52 · 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.