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.

8 matches for Tan L.

The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders
Translational psychiatry · 2023 · PMID 37236919 · open access
7 pages
rs1108048 rs10980625 rs11621425 rs12552125 rs1110339 rs7616662
Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study
Chinese Antipsychotics Pharmacogenomics Consortium
The lancet. Psychiatry · 2018 · PMID 29503163
4 pages
rs16921385 rs17022006 rs72790443 rs1471786
Genome-wide meta-analysis identifies ancestry-specific loci for Alzheimer's disease
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024 · PMID 39023044 · open access
4 pages
rs3804082 rs10806784 rs6140401 rs79872316
Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis
PLoS genetics · 2010 · PMID 20072603 · open access
2 pages
rs13182402 Osteoporosis
A Genome-Wide Association Study of α-Synuclein Levels in Cerebrospinal Fluid
Alzheimer’s Disease Neuroimaging Initiative
Neurotoxicity research · 2019 · PMID 29959729
2 pages
rs7072338 rs17794023
Genome-wide association and replication studies identified TRHR as an important gene for lean body mass
American journal of human genetics · 2009 · PMID 19268274
1 page
rs7832552
Genome-wide association study identifies <i>CBFA2T3</i> affecting the rate of CSF Aβ<sub>42</sub> decline in non-demented elders
Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Aging · 2019 · PMID 31370031 · open access
1 page
rs13333659
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study
JAMA neurology · 2020 · PMID 32310270
1 page
rs246814

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.