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.

17 matches for D'Amato M.

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
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
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
Genetic dissection of stool frequency implicates vitamin B1 metabolism and other actionable pathways in the modulation of gut motility
Gut · 2026 · PMID 41558814 · open access
6 pages
rs12407945 rs56074694 rs12700026 rs9460537 rs10079941 rs73142301
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
Cross-definition GWAS of IBS in 2.8 million individuals reveals cardiometabolic and triglyceride-linked mechanisms
Colorado Center for Personalized Medicine · Estonian Biobank Research Team and 3 more consortia
Gut · 2026 · PMID 42425734
5 pages
rs72700810 rs10184811 rs12221193 rs2195110 Irritable Bowel Syndrome
Genome-wide association identifies multiple ulcerative colitis susceptibility loci
NIDDK IBD Genetics Consortium
Nature genetics · 2010 · PMID 20228799
4 pages
rs13003464 rs11190140 rs2836878 rs2395185
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
Female-Specific Association Between Variants on Chromosome 9 and Self-Reported Diagnosis of Irritable Bowel Syndrome
Gastroenterology · 2018 · PMID 29626450
2 pages
rs10512344 Irritable Bowel Syndrome
Human Leukocyte Antigen Signatures as Pathophysiological Discriminants of Microscopic Colitis Subtypes
MC-Europe GETECCU GWAS group
Journal of Crohn's & colitis · 2024 · PMID 37768647
2 pages
rs9267445 rs2844531
HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants
International Serious Adverse Events Consortium · IBD Pharmacogenetics Study Group
Nature genetics · 2014 · PMID 25217962
1 page
rs6935723
Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms
Gut · 2019 · PMID 30661054
1 page
rs7077800
Genomewide Association Study of Severe Covid-19 with Respiratory Failure
Severe Covid-19 GWAS Group
The New England journal of medicine · 2020 · PMID 32558485 · open access
1 page
ABO Blood Group
GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome
Cell genomics · 2021 · PMID 34957435 · open access
1 page
rs2732706
Performance of the Use of Genetic Information to Assess the Risk of Colorectal Cancer in the Basque Population
Cancers · 2022 · PMID 36077729 · open access
1 page
rs541295

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.