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.

69 matches for Franke A, showing the first 20.

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Nature genetics · 2010 · PMID 21102463
12 pages+
rs4902642 rs3810936 rs2062305 rs10495903 rs7423615 rs12521868
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
Nature genetics · 2011 · PMID 21297633 · open access
12 pages+
rs907611 rs7608910 rs11739663 rs7134599 rs267939 rs3024505
New gene functions in megakaryopoiesis and platelet formation
Nature · 2011 · PMID 22139419
12 pages+
rs3811444 rs625132 rs17030845 rs7616006 rs1354034 rs399604
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
International IBD Genetics Consortium (IIBDGC)
Nature · 2012 · PMID 23128233 · open access
12 pages+
rs10486483 rs16967103 rs2945412 rs10065637 rs483905 rs28374715
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
Collaborative Association Study of Psoriasis (CASP) · Genetic Analysis of Psoriasis Consortium and 2 more consortia
Nature genetics · 2012 · PMID 23143594 · open access
12 pages+
rs2910686 rs892085 rs13437088 rs2066819 rs12445568 rs11121129
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
International Multiple Sclerosis Genetics Consortium (IMSGC) · Wellcome Trust Case Control Consortium 2 (WTCCC2) and 1 more consortia
Nature genetics · 2013 · PMID 24076602 · open access
12 pages+
rs35967351 rs2726518 rs1843938 rs7120737 rs12296430 rs4772201
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
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
ICBP Consortium · AGEN Consortium and 3 more consortia
Nature communications · 2016 · PMID 26831199 · open access
12 pages+
rs6795744 rs228611 rs3750082 rs10491967 rs11666497 rs1800615
Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota
Nature genetics · 2016 · PMID 27723756
12 pages+
rs7113056 rs79387448 rs56006724 rs148330122 rs2071199 rs62295801
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
CHD Exome+ Consortium · EPIC-CVD Consortium and 9 more consortia
Nature genetics · 2018 · PMID 29273807 · open access
12 pages+
rs9891146 rs13447324 rs5758651 rs34149579 rs12236219 rs284860
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
rs679843 rs10964603 rs924981 rs35636653 rs1078442 rs4918943
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Nature communications · 2019 · PMID 31511532 · open access
12 pages+
rs7597336 rs12790943 rs74375025 rs6998967 rs73065147 rs147215801
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs2003892 rs56299595 rs7212325 rs11183212 rs577703186 rs184980867
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs17599910 rs2116498 rs2288183 rs2306376 rs2393595 rs6934083
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
23andMe Research Team · D.E.S.I.R. study group
Nature genetics · 2024 · PMID 38839884 · open access
12 pages+
rs72804595 rs1424470 rs2116829 rs395961 rs61875279 rs57325344
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Colorado Center for Personalized Medicine · DBDS Genomic Consortium and 2 more consortia
Nature genetics · 2026 · PMID 41419686 · open access
12 pages+
rs6791877 rs10066455 rs6606660 rs8137366 rs5991029 rs35485101
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
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Australian Asthma Genetics Consortium (AAGC)
Nature genetics · 2015 · PMID 26482879 · open access
11 pages
rs112111458 rs10214237 rs6473227 rs6602364 rs7127307 rs2143950
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
23andMe Research Team · DESIR study group
The Lancet. Neurology · 2017 · PMID 29029846 · open access
10 pages
rs10208712 rs35987657 rs17636328 rs61192259 rs62535767 rs340561
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
23andMe Research Team · AAGC collaborators and 2 more consortia
Nature genetics · 2017 · PMID 29083406 · open access
10 pages
rs11204896 rs35469349 rs16922576 rs10865050 rs1814576 rs3091307

Showing 20 of 69 · page 1 of 4

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.