For researchers

Is your paper here?

2,675 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.

78 matches for Ma S, showing the first 20.

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
CHARGE Consortium · DIAGRAM Consortium and 4 more consortia
PLoS genetics · 2015 · PMID 26426971 · open access
12 pages+
rs2820443 rs12955983 rs6737082 rs2821248 rs10840060 rs4727804
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits
Nature communications · 2017 · PMID 28443625 · open access
12 pages+
rs6012558 rs4239436 rs6772896 rs765751 rs2645294 rs12679556
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
23andMe Research Team · COGENT (Cognitive Genomics Consortium) and 1 more consortia
Nature genetics · 2018 · PMID 30038396
12 pages+
rs2043187 rs56085180 rs17020193 rs2053005 rs11660655 rs34031601
The genetic architecture of the human cerebral cortex
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
rs10237280 rs78445564 rs17834032 rs75341124 rs4291964 rs35391898
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
GenoMEL Consortium · Q-MEGA and QTWIN Investigators and 7 more consortia
Nature genetics · 2020 · PMID 32341527 · open access
12 pages+
rs75883022 rs79356439 rs72834823 rs12523094 rs593179 rs117648907
Transethnic Meta-Analysis of Genome-Wide Association Studies Identifies Three New Loci and Characterizes Population-Specific Differences for Coronary Artery Disease
Circulation. Genomic and precision medicine · 2020 · PMID 32469254
12 pages+
rs62010554 rs3008629 rs7214227 rs34914832 rs1058588 rs12469758
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
Nature genetics · 2020 · PMID 32514122
12 pages+
rs60984983 rs75024669 rs80202727 rs9921081 rs193457 rs2283159
Genetic and functional interaction network analysis reveals global enrichment of regulatory T cell genes influencing basal cell carcinoma susceptibility
Genome medicine · 2021 · PMID 33549134 · open access
12 pages+
rs41271951 rs801108 rs2882274 rs79522206 rs340797 rs6707137
A cross-population atlas of genetic associations for 220 human phenotypes
FinnGen
Nature genetics · 2021 · PMID 34594039
12 pages+
rs1788100 rs338593 rs619399 rs7310941 rs9688977 rs12010615
Leveraging deep phenotyping from health check-up cohort with 10,000 Korean individuals for phenome-wide association study of 136 traits
Scientific reports · 2022 · PMID 35121771 · open access
12 pages+
rs77162552 rs78857392 rs147803453 rs367872741 rs35729878 rs2523632
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
rs6632109 rs8049403 rs2048528 rs1518760 rs78475244 rs76668186
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+
rs13010821 rs13164873 rs16826031 rs16995249 rs17128737 rs17202814
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Biobank Japan · EPIC-CVD and 1 more consortia
Nature genetics · 2022 · PMID 36474045 · open access
12 pages+
rs192425087 rs2492304 rs66778572 rs8124182 rs2215614 rs72836800
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
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+
rs4515883 rs6743072 rs35073727 rs57631119 rs9380498 rs12187932
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
AURORA Study · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2024 · PMID 38637617
12 pages+
rs16948230 rs6801151 rs78201023 rs2214230 rs7243332 rs6032660
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
Multitrait analyses identify genetic variants associated with aortic valve function and aortic stenosis risk
FinnGen
Nature genetics · 2026 · PMID 41419685 · open access
12 pages+
rs4368668 rs73162770 rs1271934 rs1833126 rs330057 rs177990
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Colorado Center for Personalized Medicine · DBDS Genomic Consortium and 2 more consortia
Nature genetics · 2026 · PMID 41419686 · open access
12 pages+
rs5991029 rs35485101 rs2421650 rs77608177 rs2150026 rs11564336
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
CHD Exome+ Consortium · EPIC-CVD Consortium and 2 more consortia
Nature genetics · 2017 · PMID 28869590 · open access
11 pages
rs9505118 rs4689388 rs2706785 rs329122 rs2050188 rs12681990

Showing 20 of 78 · page 1 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.