For researchers

Is your paper here?

2,665 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.

12 matches for Palles C.

Association analyses identify 31 new risk loci for colorectal cancer susceptibility
PRACTICAL consortium
Nature communications · 2019 · PMID 31089142 · open access
12 pages+
rs61336918 rs77776598 rs16969681 rs75686861 rs10849438 rs12143541
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Nature genetics · 2023 · PMID 36539618
12 pages+
rs6434979 rs4236382 rs10751097 rs10978941 rs62042090 rs17686932
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis
23andMe Research team · Esophageal cancer consortium
Gut · 2022 · PMID 34187846 · open access
8 pages
rs2145318 rs2597301 rs1431196 rs2106353 rs761777 rs9372625
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis
Barrett's and Esophageal Adenocarcinoma Consortium (BEACON) · Esophageal Adenocarcinoma GenEtics Consortium (EAGLE) and 1 more consortia
The Lancet. Oncology · 2016 · PMID 27527254 · open access
6 pages
rs2464469 rs17451754 rs9918259 rs1979654 rs75783973 Oesophageal Cancer
Identification of nine new susceptibility loci for endometrial cancer
Nature communications · 2018 · PMID 30093612 · open access
6 pages
rs113998067 rs1740828 rs9668337 rs10850382 rs7981863 Endometrial Cancer
Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases
BEACON · 23andMe Research Team
Nature communications · 2019 · PMID 31527586 · open access
4 pages
rs10940767 rs4676893 rs7282609 Gastroesophageal Reflux Disease
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis
Swedish Low-Risk Colorectal Cancer Study Group
Human molecular genetics · 2014 · PMID 24737748
3 pages
rs1035209 rs34245511 rs2427308
Five endometrial cancer risk loci identified through genome-wide association analysis
National Study of Endometrial Cancer Genetics Group (NSECG) · Australian National Endometrial Cancer Study Group (ANECS) and 2 more consortia
Nature genetics · 2016 · PMID 27135401 · open access
3 pages
rs11841589 rs2498796 Endometrial Cancer
Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study
Journal of the National Cancer Institute · 2011 · PMID 21263130
2 pages
rs4973768 Breast Cancer
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer
Scientific reports · 2015 · PMID 25990418 · open access
2 pages
rs11255841 rs2293582
GWAS meta-analysis of 16 790 patients with Barrett's oesophagus and oesophageal adenocarcinoma identifies 16 novel genetic risk loci and provides insights into disease aetiology beyond the single marker level
Wellcome Trust Case Control Consortium 2 (WTCCC2) · Esophageal Adenocarcinoma Genetics Consortium (EAGLE) and 1 more consortia
Gut · 2023 · PMID 35882562
2 pages
rs2687197 rs72760500
Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci
International journal of cancer · 2018 · PMID 28960316
1 page
rs6589219

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.