For researchers

Is your paper here?

2,682 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.

17 matches for Burgess S.

Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality
Nature genetics · 2016 · PMID 27798624
12 pages+
rs11920570 rs12501032 rs12576326 rs12721051 rs12889267 rs12941356
Genomic atlas of the human plasma proteome
Nature · 2018 · PMID 29875488
12 pages+
rs55636108 rs61985370 rs112206797 rs71426155 rs72732234 rs28383228
Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors
JAMA · 2018 · PMID 30575882
12 pages+
rs13154197 rs1876829 rs7122422 rs10512606 rs4849294 rs1316979
Using human genetics to understand the disease impacts of testosterone in men and women
Endometrial Cancer Association Consortium
Nature medicine · 2020 · PMID 32042192 · open access
12 pages+
rs10202148 rs11054861 rs11919691 rs12690320 rs2954111 rs388430
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
rs77357563 rs2306899 rs2273171 rs4846567 rs117874826 rs2785990
Urate, Blood Pressure, and Cardiovascular Disease: Evidence From Mendelian Randomization and Meta-Analysis of Clinical Trials
VA Million Veteran Program
Hypertension (Dallas, Tex. : 1979) · 2021 · PMID 33356394 · open access
12 pages+
rs10077826 rs4915419 rs17828856 rs1925258 rs11128603 rs3769005
A cross-platform approach identifies genetic regulators of human metabolism and health
MacTel Consortium
Nature genetics · 2021 · PMID 33414548
12 pages+
rs2306386 rs4143279 rs12223234 rs77010315 rs12610250 rs10466245
Genetic insights into biological mechanisms governing human ovarian ageing
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
rs2844466 rs140353819 rs540836853 rs2736609 rs9438982 rs117146677
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology
Nature communications · 2023 · PMID 37596262 · open access
12 pages+
rs9411463 rs998727 rs1445292 rs2708628 rs557661075 rs1863870
Novel loci and biomedical consequences of iron homoeostasis variation
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
12 pages+
rs143437464 rs186044114 rs113000093 rs485073 rs55925547 rs996347
Cross-population GWAS and proteomics improve risk prediction and reveal mechanisms in atrial fibrillation
Nature communications · 2025 · PMID 40645996 · open access
12 pages+
rs878340 rs11719535 rs62266924 rs28572114 rs6849689 rs11714244
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · open access
11 pages
rs16982520 rs7406910 rs34591516 rs1126930 rs10407022 rs470113
Genome-Wide Association and Two-Sample Mendelian Randomization Analyses of Plasma Ghrelin and Gastrointestinal Cancer Risk
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2023 · PMID 37791980 · open access
9 pages
rs143729751 rs56284847 rs17032621 rs715827 rs55821288 rs73026596
Assessing the causal association of glycine with risk of cardio-metabolic diseases
Nature communications · 2019 · PMID 30837465 · open access
8 pages
rs62202111 rs9923732 rs9862438 rs12297321 rs11647428 rs2276724
GWAS identifies genetic loci, lifestyle factors and circulating biomarkers that are risk factors for sarcoidosis
Nature communications · 2025 · PMID 40075078 · open access
8 pages
rs6761132 rs11202051 rs546039326 rs77029323 rs1140310 rs17041517
Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation Analysis
PLoS medicine · 2016 · PMID 27898682 · open access
2 pages
rs7678928 rs75950518
Genome-wide analyses of 200,453 individuals yield new insights into the causes and consequences of clonal hematopoiesis
Nature genetics · 2022 · PMID 35835912 · open access
1 page
rs12524502

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.