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.

18 matches for Ma C.

Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
Understanding Society Scientific Group · Geisinger-Regeneron DiscovEHR Collaboration
Nature genetics · 2017 · PMID 28166213 · open access
12 pages+
rs7872188 rs10515750 rs113745635 rs11658500 rs1458979 rs1551943
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Understanding Society Scientific Group
Nature genetics · 2019 · PMID 30804560 · open access
12 pages+
rs11205354 rs1215 rs34093919 rs1978968 rs79898473 rs1800888
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
HUNT All-In Psychiatry
Nature genetics · 2021 · PMID 34002096 · open access
12 pages+
rs10866641 rs67712855 rs748455 rs78308718 rs6875495 rs55706012
Population-based genome-wide association study of plasma complex lipid species
Nature communications · 2026 · PMID 42069741 · open access
12 pages+
rs11777348 rs183959498 rs376624295 rs6134729 rs10443218 rs11040367
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation
UK BiLEVE
Nature communications · 2015 · PMID 26635082 · open access
8 pages
rs6681426 rs61067109 rs6441207 rs6856422 rs148274477 rs12149828
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation
International HIV Controllers Study
Science (New York, N.Y.) · 2010 · PMID 21051598
6 pages
rs4418214 rs2523590 rs2255221 rs2395029 rs9262632 HIV-1 Viral Control
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
A large-scale, consortium-based genomewide association study of asthma
GABRIEL Consortium
The New England journal of medicine · 2010 · PMID 20860503
3 pages
rs1342326 rs3894194 Asthma
Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population
Nature genetics · 2012 · PMID 23042114
3 pages
rs9368677 rs10995251 Atopic Dermatitis
Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations
BMC genetics · 2019 · PMID 31315583 · open access
3 pages
rs10160510 rs112332856 rs35395
Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne
Nature communications · 2014 · PMID 24399259
2 pages
rs7531806 Severe Acne
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
rs72760500 rs2687197
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
1 page
rs60780116
Genome-wide association analysis identifies common variants influencing infant brain volumes
ENIGMA Consortium
Translational psychiatry · 2017 · PMID 28763065 · open access
1 page
rs114518130
Comparison of the loci associated with HbA1c and blood glucose levels identified by a genome-wide association study in the Japanese population
Diabetology international · 2023 · PMID 37090135
1 page
rs2299620
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy
FINNPEC Study Group, FinnGen Project, and the Estonian Biobank Research Team
JAMA cardiology · 2023 · PMID 37285119 · open access
1 page
rs117928258
Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism
Nature communications · 2023 · PMID 37286573 · open access
1 page
rs10737681
Cardiovascular Significance and Genetics of Epicardial and Pericardial Adiposity
FinnGen
JAMA cardiology · 2024 · PMID 38477908
1 page
rs748510

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.