For researchers

Is your paper here?

2,673 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.

51 matches for Chen J, 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+
rs7248104 rs4883201 rs11603023 rs11136341 rs4253772 rs13315871
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Australian Ovarian Cancer Study · GENICA Network and 4 more consortia
Nature · 2014 · PMID 25231870 · open access
12 pages+
rs2274465 rs6747380 rs6758290 rs4369815 rs17236969 rs17233066
New genetic loci link adipose and insulin biology to body fat distribution
ADIPOGen Consortium · CARDIOGRAMplusC4D Consortium and 11 more consortia
Nature · 2015 · PMID 25673412 · open access
12 pages+
rs12143789 rs798528 rs6060717 rs11989744 rs4646404 rs319564
Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia
Nature genetics · 2017 · PMID 28991256
12 pages+
rs13261217 rs2381759 rs61041384 rs6846161 rs10510653 rs2383377
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
EGG Consortium
Nature genetics · 2019 · PMID 31043758
12 pages+
rs754868 rs3746448 rs4809731 rs62023486 rs75034466 rs7285579
A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic aetiology with obesity
The European respiratory journal · 2021 · PMID 33766948
12 pages+
rs6696174 rs1482675 rs78732306 rs117331805 rs2425059 rs6730783
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+
rs17256082 rs12784552 rs142484519 rs118164457 rs7063597 rs3752435
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+
rs9899520 rs75307421 rs3780012 rs4267865 rs57634870 rs11196296
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
12 pages+
rs62454414 rs6541092 rs661857 rs2967516 rs17160476 rs6667222
Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease
Estonian Biobank Research Team · Genes & Health Research Team
Nature communications · 2023 · PMID 37872160 · open access
12 pages+
rs2983518 rs71430783 rs10139757 rs12409301 rs1108990 rs1398868
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs1683935 rs71474196 rs72798545 rs1523539 rs7307263 rs11716527
Causal relevance of different blood pressure traits on risk of cardiovascular diseases: GWAS and Mendelian randomisation in 100,000 Chinese adults
China Kadoorie Biobank Collaborative Group
Nature communications · 2024 · PMID 39048560 · open access
12 pages+
rs9322356 rs78236399 rs13116214 rs2853795 rs835445 rs11191454
The X chromosome's influences on the human brain
Science advances · 2025 · PMID 39854466 · open access
12 pages+
rs142344396 rs146210600 rs2743914 rs3105280 rs5924922 rs781792327
Cross-population GWAS and proteomics improve risk prediction and reveal mechanisms in atrial fibrillation
Nature communications · 2025 · PMID 40645996 · open access
12 pages+
rs17782520 rs10146690 rs147245721 rs186553022 rs188502675 rs59661877
Genetic architecture of bone marrow fat fraction implies its involvement in osteoporosis risk
Nature communications · 2025 · PMID 40796918 · open access
12 pages+
rs2378715 rs79260952 rs12195627 rs117210562 rs11712037 rs10753536
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium and 4 more consortia
Nature genetics · 2026 · PMID 41644669 · open access
12 pages+
rs9864554 rs9672082 rs7321973 rs12133184 rs2758605 rs35397235
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
Early Growth Genetics (EGG) Consortium
Nature genetics · 2023 · PMID 37798380 · open access
10 pages
rs7722058 rs10925945 rs3822394 rs6557677 rs6040436 rs10486660
GWAS identifies genetic loci, lifestyle factors and circulating biomarkers that are risk factors for sarcoidosis
Nature communications · 2025 · PMID 40075078 · open access
8 pages
rs17041517 rs1152002 rs72695390 rs6761132 rs11202051 rs546039326
Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese
Circulation. Cardiovascular genetics · 2013 · PMID 24165912
6 pages
rs10930597 rs2030114 rs16890334 rs17135875 rs1330225 rs8002688
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
6 pages
rs75619922 rs7225887 rs56381411 rs3784634 rs5400 rs17853166

Showing 20 of 51 · 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.