For researchers

Is your paper here?

2,660 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.

69 matches for Ma M, showing the first 20.

Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels
Metabolites · 2022 · PMID 35050183 · open access
12 pages+
rs1653259 rs1934969 rs12678356 rs11689634 rs4149118 rs10509684
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs4267865 rs57634870 rs11196296 rs3825801 rs79495865 rs7819706
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+
rs2901260 rs5999721 rs112166402 rs11893881 rs116471547 rs151266052
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs1551728 rs16832694 rs16942312 rs17093810 rs6666757 rs2032289
Discerning asthma endotypes through comorbidity mapping
Nature communications · 2022 · PMID 36344522 · open access
12 pages+
rs1007027 rs11590405 rs17547610 rs7110818 rs78728108 rs1233493
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs2279292 rs2415339 rs34489326 rs3798461 rs4474826 rs67941002
Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases
Nature genetics · 2023 · PMID 36635386
12 pages+
rs10888445 rs3828671 rs9469582 rs10422369 rs174458 rs201393623
Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction
BioBank Japan Project
Nature genetics · 2023 · PMID 36653681 · open access
12 pages+
rs10500790 rs2629755 rs6902225 rs13387570 rs223449 rs9639575
Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci
23andMe Research Team · International Glaucoma Genetics Consortium
Nature genetics · 2023 · PMID 37386247 · open access
12 pages+
rs6697461 rs2811687 rs1782976 rs3125620 rs4749990 rs1392874
Translational genomics of osteoarthritis in 1,962,069 individuals
arcOGEN Consortium · ARGO Consortium and 7 more consortia
Nature · 2025 · PMID 40205036 · open access
12 pages+
rs12350099 rs1480637 rs2095140 rs13118508 rs2015110 rs509236
A genetic map of human metabolism across the allele frequency spectrum
Nature genetics · 2025 · PMID 41044249 · open access
12 pages+
rs625372 rs863944 rs112682793 rs116892712 rs6534655 rs7287003
Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population
BioBank Japan Project
Nature communications · 2025 · PMID 41184235 · open access
12 pages+
rs1541596 rs73193820 rs3764351 rs7188250 rs59788391 rs2261787
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population
Nature genetics · 2019 · PMID 30718926
9 pages
rs79407053 rs2908279 rs9505085 rs2844623 rs201597274 rs76550717
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs
PBC Consortia · Canadian PBC Consortium and 5 more consortia
Journal of hepatology · 2021 · PMID 34033851 · open access
9 pages
rs4709148 rs589446 rs11742270 rs859767 rs6550965 rs12419634
Unprocessed Red Meat and Processed Meat Consumption, Plasma Metabolome, and Risk of Ischemic Heart Disease: A Prospective Cohort Study of UK Biobank
Journal of the American Heart Association · 2023 · PMID 36974753 · open access
9 pages
rs3094621 rs3106165 rs6760497 rs71401819 rs55888687 rs178803
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Nature communications · 2024 · PMID 38233393 · open access
8 pages
rs12382607 rs4328011 rs139036121 rs5933079 rs181497961 rs111410539
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
HUNT All-In Stroke · China Kadoorie Biobank Collaborative Group and 5 more consortia
Nature genetics · 2020 · PMID 33199917
6 pages
rs4705938 rs3742321 rs55965782 rs2280543 rs6997005 rs7137731
Multi-Omics Integrative Analysis Identifies the NK Cell-STAT3 Axis as a Shared Immunogenetic Hub Underlying the Comorbidity of Primary Sclerosing Cholangitis and Ulcerative Colitis
Life (Basel, Switzerland) · 2026 · PMID 42355477 · open access
6 pages
rs9607629 rs11578418 rs368699386 rs10916666 rs6967184 rs148170789
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
International Parkinson Disease Genomics Consortium
Lancet (London, England) · 2011 · PMID 21292315
5 pages
rs6599388 rs1491942 rs11711441 rs356219 Parkinson's Disease

Showing 20 of 69 · page 2 of 4

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.