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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.

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+
rs4883201 rs11603023 rs11136341 rs4253772 rs13315871 rs2290159
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+
rs6556079 rs3805389 rs4081724 rs459193 rs7830933 rs9687846
Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia
Nature genetics · 2017 · PMID 28991256
12 pages+
rs13164092 rs867743 rs2073499 rs56775891 rs7438 rs17630293
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+
rs1724889 rs2168443 rs5030317 rs11641308 rs9912553 rs181451002
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+
rs118164457 rs7063597 rs3752435 rs4317621 rs4731113 rs4674280
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+
rs79495865 rs7819706 rs1473781 rs6876198 rs3743140 rs3806155
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+
rs60962207 rs7207973 rs10743288 rs1079660 rs12691682 rs1047981
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+
rs1861628 rs11728154 rs7203756 rs78499451 rs278941 rs59282311
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
12 pages+
rs62015803 rs6766511 rs74847755 rs12140915 rs11063029 rs321234
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+
rs10477399 rs9847595 rs6585252 rs75268076 rs62175706 rs67913572
The X chromosome's influences on the human brain
Science advances · 2025 · PMID 39854466 · open access
12 pages+
rs17281188 rs5934135 rs5935037 rs142344396 rs146210600 rs2743914
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 rs4881717
Genetic architecture of bone marrow fat fraction implies its involvement in osteoporosis risk
Nature communications · 2025 · PMID 40796918 · open access
12 pages+
rs79260952 rs117210562 rs11712037 rs10753536 rs10761756 rs6415470
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+
rs74401365 rs6085463 rs9531006 rs17242727 rs369835958 rs11221322
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
11 pages
rs16828537 rs73995038 rs801170 rs6696174 rs1482675 rs78732306
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
rs6040436 rs10486660 rs7783810 rs12529634 rs140691414 rs1434836
GWAS identifies genetic loci, lifestyle factors and circulating biomarkers that are risk factors for sarcoidosis
Nature communications · 2025 · PMID 40075078 · open access
7 pages
rs11202051 rs546039326 rs77029323 rs1140310 rs17041517 rs1152002
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
Genome-wide meta-analysis across East Asian and European populations provides insights into the molecular basis of lung cancer
Genome medicine · 2026 · PMID 42152146 · open access
6 pages
rs4887067 rs13167280 rs4291686 rs36108040 rs1039766 rs12822733

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.