For researchers

Is your paper here?

2,663 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.

49 matches for Chen YI, showing the first 20.

Discovery and refinement of loci associated with lipid levels
Global Lipids Genetics Consortium
Nature genetics · 2013 · PMID 24097068 · open access
12 pages+
rs702485 rs11563251 rs7248104 rs4883201 rs11603023 rs11136341
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
PRACTICAL consortium · kConFab Investigators and 4 more consortia
Nature genetics · 2015 · PMID 26414677 · open access
12 pages+
rs12142240 rs2236918 rs704795 rs930036 rs6856693 rs11738223
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+
rs6026748 rs11128722 rs6891344 rs6271 rs2493134 rs12940887
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
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
METASTROKE Consortium of the ISGC · Neurology Working Group of the CHARGE Consortium and 1 more consortia
Nature genetics · 2017 · PMID 28416818
12 pages+
rs60848348 rs1454934 rs36004974 rs577676 rs11598047 rs10800507
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
CHD Exome+ Consortium · EPIC-CVD Consortium and 9 more consortia
Nature genetics · 2018 · PMID 29273807 · open access
12 pages+
rs284860 rs1131877 rs2277598 rs295322 rs62623713 rs11555762
Multi-ethnic genome-wide association study for atrial fibrillation
Nature genetics · 2018 · PMID 29892015
12 pages+
rs10027347 rs10165883 rs1044258 rs10479177 rs10760361 rs10842383
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
LifeLines Cohort Study · CHARGE Inflammation Working Group
American journal of human genetics · 2018 · PMID 30388399
12 pages+
rs12749227 rs4845623 rs9271608 rs72698571 rs2246469 rs56288844
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies
Nature communications · 2019 · PMID 30604766 · open access
12 pages+
rs35255404 rs231889 rs10066990 rs10851885 rs11039221 rs111449836
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Lifelines Cohort Study
Nature communications · 2019 · PMID 30670697 · open access
12 pages+
rs72834327 rs116376114 rs114846969 rs6029549 rs556107 rs117753190
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
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Nature · 2020 · PMID 32499647 · open access
12 pages+
rs61342118 rs7656416 rs12907887 rs73085586 rs13086331 rs117737118
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+
rs11718848 rs11537816 rs16859180 rs1449592 rs13196885 rs576629818
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus
Communications biology · 2021 · PMID 33649486 · open access
12 pages+
rs2417930 rs3118518 rs1200108 rs6669560 rs116792882 rs12515400
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
American journal of human genetics · 2021 · PMID 33713608
12 pages+
rs12332985 rs146576224 rs10180829 rs672769 rs10071837 rs4899520
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs146474788 rs17256082 rs12784552 rs142484519 rs118164457 rs7063597
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs11207980 rs598253 rs57825321 rs12603290 rs186793936 rs9844432
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+
rs12669223 rs3768301 rs72830009 rs7100404 rs7076754 rs835576
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+
rs114785138 rs57866552 rs73733867 rs10185736 rs11568525 rs76253609
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+
rs9344003 rs12974635 rs10519014 rs11691472 rs2679184 rs2854915

Showing 20 of 49 · 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.