For researchers

Is your paper here?

2,663 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.

23 matches for Cho J, 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
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
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
International Multiple Sclerosis Genetics Consortium · International IBD Genetics Consortium
Nature genetics · 2015 · PMID 26192919
12 pages+
rs11641184 rs7657746 rs17736589 rs17771967 rs7134472 rs2816958
Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals
NHLBI Trans-Omics for Precision Medicine 1 Consortium
Nature communications · 2022 · PMID 35995766 · open access
12 pages+
rs114785138 rs57866552 rs73733867 rs10185736 rs11568525 rs76253609
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs9594366 rs16856530 rs62283809 rs10854002 rs2276133 rs7748159
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
GenOMICC Investigators · SCOURGE Consortium and 2 more consortia
Nature · 2023 · PMID 37198478 · open access
12 pages+
rs17713054 rs7949972 rs12046291 rs66833742 rs17078346 rs6775046
Novel risk loci for COVID-19 hospitalization among admixed American populations
SCOURGE Cohort Group
eLife · 2024 · PMID 39361370 · open access
12 pages+
rs17213127 rs7515509 rs34288077 rs7623460 rs34759782 rs12660421
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
NIDDK IBD Genetics Consortium · Belgian-French IBD Consortium and 1 more consortia
Nature genetics · 2008 · PMID 18587394
11 pages
rs3764147 rs2301436 rs9286879 rs1551398 rs7927894 rs11175593
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Nature genetics · 2012 · PMID 22504420 · open access
7 pages
rs1566045 rs7953528 rs163879 rs1864325 rs344081 rs3905706
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture
AOGC Consortium · UK10K Consortium
Nature · 2015 · PMID 26367794
7 pages
rs188303909 rs11024028 rs148771817 rs11692564 rs6542457 Spine Bone Mineral Density
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci
PLoS genetics · 2012 · PMID 22412388 · open access
6 pages
rs6545946 rs7705924 rs9258260 rs12677663 rs11229030 rs3091338
Genome-wide association study of intracranial aneurysm identifies three new risk loci
Nature genetics · 2010 · PMID 20364137 · open access
5 pages
rs11661542 rs9298506 rs12413409 rs9315204 Intracranial Aneurysm
Genome-wide association identifies multiple ulcerative colitis susceptibility loci
NIDDK IBD Genetics Consortium
Nature genetics · 2010 · PMID 20228799
4 pages
rs13003464 rs11190140 rs2836878 rs2395185
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium
Human molecular genetics · 2014 · PMID 24430505
4 pages
rs2982552 rs10416265 rs7902708 rs3020331
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Communications biology · 2022 · PMID 36352089 · open access
4 pages
rs6874700 rs80215221 rs1924557 Classic Bladder Exstrophy
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
arcOGEN Consortium
Annals of the rheumatic diseases · 2014 · PMID 23989986 · open access
3 pages
rs3757837 rs6094710 Hip Osteoarthritis
Genetic Variants Associated with Circulating Parathyroid Hormone
Journal of the American Society of Nephrology : JASN · 2017 · PMID 27927781
3 pages
rs4443100 rs35194449 rs4074995
Genomic Insights Into Inflammatory Bowel Disease in United States Hispanic Participants: An Ancestry-Focused Study
NIDDK IBD Genetics Consortium
Gastroenterology · 2026 · PMID 41661118
3 pages
rs188746689 rs144029176 rs115406035
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
Nature genetics · 2007 · PMID 17435756
1 page
rs2241880

Showing 20 of 23 · 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.