For researchers

Is your paper here?

2,682 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.

15 matches for Liu W.

Whole exome sequencing analyses reveal novel genes in telomere length and their biomedical implications
GeroScience · 2024 · PMID 38837026
12 pages+
rs145943094 rs5748769 rs75010776 rs76382474 rs2009144 rs2396106
Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study
Stroke · 2018 · PMID 29273593
6 pages
rs9614159 rs74388387 rs9907978 rs10782008 rs117353193 Moyamoya Disease
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
5 pages
rs10806784 rs6140401 rs79872316 rs6682554 rs3804082
Novel Risk Loci Associated With Genetic Risk for Bipolar Disorder Among Han Chinese Individuals: A Genome-Wide Association Study and Meta-analysis
GeseDNA Research Team
JAMA psychiatry · 2021 · PMID 33263727
4 pages
rs11647445 rs3804640 rs6130764 rs11557713
Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome
Cell discovery · 2021 · PMID 34873157 · open access
3 pages
rs12453667 rs4794851 rs8064338
Genome-wide association study identifies multiple novel loci associated with disease progression in subjects with mild cognitive impairment
Translational psychiatry · 2011 · PMID 22833209 · open access
2 pages
rs7840202 rs12752888
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans
Arthritis & rheumatology (Hoboken, N.J.) · 2014 · PMID 24782177
2 pages
rs12525220 rs1854853
Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients
American journal of respiratory and critical care medicine · 2023 · PMID 36921087
2 pages
rs56108664 rs12009976
A genome-wide association study identifies two new risk loci for Graves' disease
China Consortium for Genetics of Autoimmune Thyroid Disease
Nature genetics · 2011 · PMID 21841780
1 page
rs12101261
Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4
Nature genetics · 2012 · PMID 23023329
1 page
rs103294
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23
Nature genetics · 2013 · PMID 24097066
1 page
rs4282438
Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations
China Consortium for Genetics of Autoimmune Thyroid Disease
Human molecular genetics · 2014 · PMID 24852370
1 page
rs2622590
Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study
China Consortium for the Genetics of Autoimmune Thyroid Disease
JAMA network open · 2019 · PMID 31050781 · open access
1 page
rs12451295
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population
Parkinson’s Disease & Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC)
NPJ Parkinson's disease · 2023 · PMID 36759515 · open access
1 page
rs34594498
Whole exome sequencing identified six novel genes for depressive symptoms
Molecular psychiatry · 2025 · PMID 39472661
1 page
rs7853605

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.