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.

40 matches for Lin K, showing the first 20.

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+
rs7629654 rs10477399 rs9847595 rs6585252 rs75268076 rs62175706
Identification of 16 novel Alzheimer's disease loci using multi-ancestry meta-analyses
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025 · PMID 39998322 · open access
12 pages+
rs1179689749 rs1587397386 rs166907 rs1023546743 rs1269322417 rs1412811394
Translational genomics of osteoarthritis in 1,962,069 individuals
arcOGEN Consortium · ARGO Consortium and 7 more consortia
Nature · 2025 · PMID 40205036 · open access
12 pages+
rs11911487 rs1152620 rs2738292 rs11726937 rs55658362 rs2279864
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Multicenter Genetic Studies of Schizophrenia Consortium · Psychosis Endophenotypes International Consortium and 1 more consortia
Nature genetics · 2013 · PMID 23974872 · open access
10 pages
rs114002140 rs7085104 rs6461049 rs1006737 rs17691888 rs17504622
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
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
ExomeBP Consortium · MAGIC Consortium and 1 more consortia
Nature genetics · 2018 · PMID 29632382 · open access
6 pages
rs16826069 rs1127787 rs7572857 rs2233580 rs56200889 rs35658696
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
HUNT All-In Stroke · China Kadoorie Biobank Collaborative Group and 5 more consortia
Nature genetics · 2020 · PMID 33199917
6 pages
rs6997005 rs7137731 rs4705938 rs3742321 rs55965782 rs2280543
Stroke genetics informs drug discovery and risk prediction across ancestries
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
rs72934589 rs76110445 rs12415501 rs60401382 Cardioembolic Stroke
Matching heterogeneous cohorts by projected principal components reveals two novel Alzheimer's disease-associated genes in the Hispanic population
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026 · PMID 41755704 · open access
5 pages
rs182804071 rs192423465 rs2120001636 rs985256115 rs374043832
Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair
Human molecular genetics · 2018 · PMID 29220522 · open access
4 pages
rs11585357 rs11170678 rs143290289 rs310642
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study
23andMe Research Team, China Kadoorie Biobank Collaborative Group, and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
JAMA psychiatry · 2021 · PMID 34586374 · open access
4 pages
rs1950829 rs4936272 rs17410557 rs112176860
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Nature communications · 2016 · PMID 26833246 · open access
3 pages
rs6738627 rs4788099 rs693839
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
SLAGEN Consortium and Collaborators
Human molecular genetics · 2014 · PMID 24256812
2 pages
rs34517613 Amyotrophic Lateral Sclerosis
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects
23andMe Research Team
Nature communications · 2022 · PMID 36470867 · open access
2 pages
rs12752133 rs3756059
Risk Variants Associated With Normal Pressure Hydrocephalus: Genome-Wide Association Study in the FinnGen Cohort
for FinnGen
Neurology · 2024 · PMID 39141892 · open access
2 pages
rs7962263 rs62434144
Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci
International journal of cancer · 2018 · PMID 28960316
1 page
rs6589219
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · open access
1 page
rs492571
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information
Biological psychiatry · 2022 · PMID 34865855 · open access
1 page
rs10821140
Genotyping and population characteristics of the China Kadoorie Biobank
China Kadoorie Biobank Collaborative Group
Cell genomics · 2023 · PMID 37601966 · open access
1 page
rs2903657

Showing 20 of 40 · page 2 of 2

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.