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.

43 matches for Ma P, showing the first 20.

Connecting genetic risk to disease end points through the human blood plasma proteome
Nature communications · 2017 · PMID 28240269 · open access
12 pages+
rs135150 rs7184253 rs12997015 rs16935432 rs2193873 rs1005776
Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease
IMPROVE study group
PLoS genetics · 2017 · PMID 28369058 · open access
12 pages+
rs116661163 rs140000161 rs3195944 rs1580006 rs2271025 rs9323280
Association analysis identifies 65 new breast cancer risk loci
NBCS Collaborators · ABCTB Investigators and 1 more consortia
Nature · 2017 · PMID 29059683 · open access
12 pages+
rs13183434 rs12250948 rs11822830 rs1744947 rs17838698 rs9361840
Genomic atlas of the human plasma proteome
Nature · 2018 · PMID 29875488
12 pages+
rs574174001 rs117059302 rs185253449 rs9851301 rs11160165 rs192170963
Genetic determinants of plasma protein levels in the Estonian population
Estonian Biobank Research Team
Scientific reports · 2024 · PMID 38565889 · open access
12 pages+
rs2569488 rs4235826 rs4656601 rs6543113 rs4778890 rs2908201
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
Penn Medicine Biobank
Nature genetics · 2025 · PMID 40195560
12 pages+
rs72801029 rs6539283 rs6885658 rs12906348 rs12724121 rs2904129
Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits
DIAMANTE Hispanic/Latino Consortium · Global Hispanic Lipids Consortium
Nature communications · 2025 · PMID 40210677 · open access
12 pages+
rs557199842 rs6910047 rs17206182 rs16989540 rs536240710 rs181676594
Ischemic stroke is associated with the ABO locus: the EuroCLOT study
EuroCLOT Investigators · Wellcome Trust Case Control Consortium 2 and 3 more consortia
Annals of neurology · 2013 · PMID 23381943 · open access
11 pages
rs2022309 rs10922162 rs3211770 rs1318606 rs555212 rs10982156
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
AOCS study group · EMBRACE Study and 4 more consortia
Nature genetics · 2017 · PMID 28346442
9 pages
rs1879586 rs7207826 rs11651755 rs688187 rs7902587 rs9886651
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
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis
Nature communications · 2020 · PMID 31959851 · open access
6 pages
rs2180769 rs2228079 rs2230624 rs12700186 rs3853750 rs60156285
Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes
Milieu Intérieur Consortium
Genome medicine · 2022 · PMID 35264221 · open access
6 pages
rs11553092 rs8006968 rs9534309 rs7541061 rs2235503 rs8318
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs6015450 rs11191548 rs7129220 rs1173771 rs13139571
Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns
COPDGene Investigators
American journal of respiratory and critical care medicine · 2014 · PMID 25006744
5 pages
rs17486278 rs17368659 rs56113850 rs379123 rs11852372
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
ABCTB Investigators · EMBRACE and 4 more consortia
Nature genetics · 2017 · PMID 29058716
5 pages
rs10995201 rs9397437 rs6562760 rs6678914 rs67397200
Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study
International Consortium on Lithium Genetics (ConLi+Gen)
JAMA psychiatry · 2018 · PMID 29121268
5 pages
rs66486766 rs324899 rs6942227 rs209474 rs6728642
Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study
JAMA psychiatry · 2019 · PMID 31596458
5 pages
rs77038697 rs117302528 rs11200733 rs73076581 rs45543740
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
GEMO Study Collaborators · EMBRACE Collaborators and 3 more consortia
Nature communications · 2021 · PMID 33597508 · open access
5 pages
rs7222250 rs60882887 rs12470785 rs79183898 rs736596
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
KORA-Study Group · Nantes Referral Center for inherited cardiac arrhythmia
Nature genetics · 2022 · PMID 35210625
5 pages
rs41310232 rs11645463 rs7433206 rs34760424 Brugada Syndrome
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
4 pages
rs2107595 rs879324 rs13407662 Ischaemic Stroke

Showing 20 of 43 · page 1 of 3

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.