For researchers

Is your paper here?

2,662 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.

16 matches for Ning C.

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
Developing an optimal stratification model for colorectal cancer screening and reducing racial disparities in multi-center population-based studies
Genome medicine · 2024 · PMID 38872215 · open access
12 pages+
rs4583925 rs4939824 rs34099011 rs7557709 rs1562871 rs11169484
Combining cross-sectional and longitudinal genomic approaches to identify determinants of cognitive and physical decline
Nature communications · 2025 · PMID 40374629 · open access
12 pages+
rs143479774 rs145177319 rs55993211 rs7309412 rs7613970 rs1026266
Genetic architecture of bone marrow fat fraction implies its involvement in osteoporosis risk
Nature communications · 2025 · PMID 40796918 · open access
12 pages+
rs2378715 rs79260952 rs12195627 rs117210562 rs11712037 rs10753536
Genome-wide association analysis of left ventricular imaging-derived phenotypes identifies 72 risk loci and yields genetic insights into hypertrophic cardiomyopathy
Nature communications · 2023 · PMID 38036550 · open access
8 pages
rs79548216 rs9428227 rs62253183 rs62250980 rs7928419 rs9462210
Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study
American journal of human genetics · 2021 · PMID 33308445
6 pages
rs4379175 rs28834970 rs7038415 rs9540128 rs2836883 Takayasu Arteritis
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
Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data
Nature communications · 2019 · PMID 31235808 · open access
5 pages
rs7852129 rs28822480 rs6495046 rs9831002 rs2046850
Identification of multiple genetic susceptibility loci in Takayasu arteritis
American journal of human genetics · 2013 · PMID 23830517
4 pages
rs12524487 rs113452171 rs10919543 Takayasu Arteritis
Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis
Vasculitis Clinical Research Consortium
Arthritis & rheumatology (Hoboken, N.J.) · 2017 · PMID 28029757 · open access
4 pages
rs62132293 rs7454108 rs35242582 ANCA-Associated Vasculitis
Identification of specific susceptibility loci for the early-onset colorectal cancer
Genome medicine · 2023 · PMID 36869385 · open access
2 pages
rs13197175 rs138234416
Identification of Susceptibility Loci in IL6, RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome-Wide Association Study
Arthritis & rheumatology (Hoboken, N.J.) · 2015 · PMID 25604533
1 page
rs4410768
Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk
GenPhenReSa Consortium
American journal of respiratory and critical care medicine · 2015 · PMID 26051272
1 page
rs6748088
Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
NEIGHBORHOOD consortium
Scientific reports · 2018 · PMID 29449654 · open access
1 page
rs72815193

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.