For researchers

Is your paper here?

2,657 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.

27 matches for Ellinghaus D, 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
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+
rs148330122 rs2071199 rs62295801 rs7656342 rs17421787 rs9291879
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+
rs5758651 rs34149579 rs12236219 rs284860 rs1131877 rs2277598
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
GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets
BSTOP study group · Estonian Biobank research team
Nature communications · 2025 · PMID 40021644 · open access
9 pages
rs75826800 rs7108441 rs74688172 rs4728141 rs7171410 rs8107351
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease
UK-PSC Consortium · International IBD Genetics Consortium and 1 more consortia
Nature genetics · 2017 · PMID 27992413 · open access
8 pages
rs13140464 rs56258221 rs60652743 rs72837826 rs80060485 rs36023390
Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms
Psoriasis Association Genetics Extension
American journal of human genetics · 2015 · PMID 25574825 · open access
5 pages
rs17716942 rs465969 rs11795343 rs41268896 Atopic Dermatitis
Detailed stratified GWAS analysis for severe COVID-19 in four European populations
COVICAT study group, Aachen Study (COVAS) · Norwegian SARS-CoV-2 Study group and 2 more consortia
Human molecular genetics · 2022 · PMID 35848942 · open access
5 pages
rs77534576 rs143334143 rs35731912 rs2269899 COVID-19 with Respiratory Failure Requiring Mechanical Ventilation
New loci associated with kidney function and chronic kidney disease
Nature genetics · 2010 · PMID 20383146
4 pages
rs267734 rs10774021 rs7805747 rs6465825
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
DBDS Consortium · 23andMe Research Team
Gut · 2021 · PMID 33888516 · open access
4 pages
rs11585073 rs11176001 rs722587 Haemorrhoidal Disease
Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL)
IBSEN study group
Nature genetics · 2010 · PMID 20228798
3 pages
rs5771069 rs9268923 Ulcerative Colitis
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis
International PSC Study Group
Nature communications · 2023 · PMID 36828809 · open access
3 pages
rs2523593 rs3094210 rs6905775
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
EPICURE Consortium · EMINet Consortium
Human molecular genetics · 2012 · PMID 22949513
2 pages
rs13026414 Epilepsy
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis
Nature genetics · 2015 · PMID 26482880
2 pages
rs626283 Alcohol-Related Cirrhosis
Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci
Scientific reports · 2017 · PMID 28374850 · open access
2 pages
rs727139 Chronic Venous Disease

Showing 20 of 27 · 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.