For researchers

Is your paper here?

2,675 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.

16 matches for Han N.

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
rs954734 rs62170823 rs926300 rs9836970 rs9597254 rs640177
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function
Nature communications · 2018 · PMID 30061609 · open access
12 pages+
rs252746 rs143246821 rs916888 rs963406 rs79294353 rs111898810
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data
arcOGEN Consortium
Nature genetics · 2019 · PMID 30664745 · open access
12 pages+
rs11059094 rs17659798 rs10218792 rs1149620 rs1913707 rs3771501
Cerebral small vessel disease genomics and its implications across the lifespan
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 pages+
rs17205972 rs7596872 rs55940034 rs2303655 rs55897749 rs72934583
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+
rs10248717 rs11672003 rs149590572 rs113920320 rs111589301 rs12992267
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+
rs13010821 rs13164873 rs16826031 rs16995249 rs17128737 rs17202814
A genome-wide association study of mass spectrometry proteomics using a nanoparticle enrichment platform
Nature genetics · 2025 · PMID 41310232 · open access
12 pages+
rs7948204 rs6665824 rs288296 rs73143813 rs7604812 rs9442970
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
A systematic analysis of protein-altering exonic variants in chronic obstructive pulmonary disease
American journal of physiology. Lung cellular and molecular physiology · 2021 · PMID 33909500
4 pages
rs13195509 rs11155242 rs2523989 rs11938093
Genome-wide association study of Tourette's syndrome
North American Brain Expression Consortium · UK Human Brain Expression Database
Molecular psychiatry · 2013 · PMID 22889924 · open access
2 pages
rs7868992 Tourette Syndrome
Genetic Associations and Architecture of Asthma-COPD Overlap
Chest · 2022 · PMID 35104449 · open access
2 pages
rs9273410 rs7312770
Heritability and genome-wide association study of diffusing capacity of the lung
The European respiratory journal · 2018 · PMID 30049742
1 page
rs17280293
Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia
Nature communications · 2018 · PMID 30305637 · open access
1 page
rs117410836
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes
Genetic epidemiology · 2019 · PMID 31407831
1 page
rs16947122
Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning
Molecular psychiatry · 2022 · PMID 35974141 · open access
1 page
rs11711421
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes
PSP Genetics Study Group
Nature communications · 2024 · PMID 39251599 · open access
1 page
rs12197948

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.