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.

10 matches for Lee WJ.

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
CHARGE-EchoGen consortium · CHARGE-HF consortium and 1 more consortia
Nature genetics · 2016 · PMID 27618452 · open access
12 pages+
rs12247028 rs6779380 rs4691707 rs12705390 rs2898290 rs7076398
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
Human molecular genetics · 2017 · PMID 28334899
12 pages+
rs2188380 rs2144300 rs11984636 rs3786247 rs11208004 rs2244608
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
rs10494217 rs1051860 rs141845046 rs145878042 rs1715919 rs62266958
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+
rs145441283 rs187207161 rs767105335 rs77357563 rs2306899 rs2273171
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs11544336 rs11590766 rs11994760 rs12745732 rs13243849 rs1346482
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
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
EPIC-CVD Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS medicine · 2017 · PMID 28898252 · open access
10 pages
rs4745982 rs10823343 rs3824065 rs11154792 rs17509001 rs7040409
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
CHD Exome+ Consortium · ExomeBP Consortium and 4 more consortia
Nature genetics · 2016 · PMID 27618448
9 pages
rs2493292 rs11639856 rs1925153 rs3755652 rs11014166 rs11024074
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
CHARGE Neurology Working Group · COGENT-Kidney Consortium and 2 more consortia
American journal of human genetics · 2018 · PMID 29455858
7 pages
rs115234772 rs62319742 rs148772934 rs138973557 rs148753653 rs12135881
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index
Human molecular genetics · 2014 · PMID 24861553
4 pages
rs2535633 rs11030104 rs574367 rs591166

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.