For researchers

Is your paper here?

2,676 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.

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
10 pages
rs3825765 rs75826800 rs13029175 rs7108441 rs74688172 rs4728141
High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences
American journal of respiratory and critical care medicine · 2016 · PMID 26651848
9 pages
rs13213152 rs3129788 rs1233491 rs8321 rs389884 rs11244
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
Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants
Nature communications · 2017 · PMID 28537254 · open access
8 pages
rs12118303 rs118086960 rs559406 rs34517439 rs2944542 rs61871342
Single- and Multimarker Genome-Wide Scans Evidence Novel Genetic Risk Modifiers for Venous Thromboembolism
Thrombosis and haemostasis · 2021 · PMID 33592630
8 pages
rs1649936 rs72983636 rs16861990 rs6825454 rs145241704 rs59559305
Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility
Nature communications · 2015 · PMID 25903422 · open access
7 pages
rs34394770 rs8128234 rs7709212 rs3747517 rs842625 rs12564022
A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis
American journal of human genetics · 2017 · PMID 28886342 · open access
7 pages
rs16879765 rs629535 rs7838717 rs1509406 rs2306022 rs6016142
A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies
German Network for Research on Autoimmune Encephalitis (GENERATE)
Brain : a journal of neurology · 2023 · PMID 35348614 · open access
7 pages
rs62231498 rs7749544 rs3130545 rs378956 rs3094633 rs314304
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
Genome-wide meta-analysis reveals shared new <i>loci</i> in systemic seropositive rheumatic diseases
Myositis Genetics Consortium · Scleroderma Genetics Consortium
Annals of the rheumatic diseases · 2019 · PMID 30573655
6 pages
rs2422345 rs13389408 rs112846137 rs13101828 rs193107685 rs10954214
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4
Australian Asthma Genetics Consortium (AAGC)
Nature communications · 2021 · PMID 34785669 · open access
6 pages
rs2844594 rs3848669 rs13208697 rs4372325 rs12334935 rs2918299
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
Large-scale association analyses identify host factors influencing human gut microbiome composition
Nature genetics · 2021 · PMID 33462485
5 pages
rs7605229 rs7322849 rs11110281 rs61841503 rs71348714
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
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis
UK NIHR BioResource Rare Diseases Consortium · UK PAH Cohort Study Consortium and 1 more consortia
The Lancet. Respiratory medicine · 2019 · PMID 30527956 · open access
4 pages
rs2856830 rs13266183 rs10103692 Pulmonary Arterial Hypertension
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
Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus
Experimental dermatology · 2015 · PMID 25827949
3 pages
rs9267531 rs3131060 Cutaneous Lupus Erythematosus
Meta-analysis identifies seven susceptibility loci involved in the atopic march
Nature communications · 2015 · PMID 26542096 · open access
3 pages
rs993226 rs9357733 rs17690965

Showing 20 of 69 · page 2 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.