For researchers

Is your paper here?

2,660 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.

17 matches for Song Y.

Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma
UK Biobank Eye and Vision Consortium · NEIGHBORHOOD Consortium
Nature genetics · 2018 · PMID 29785010 · open access
12 pages+
rs6000889 rs17534001 rs73191218 rs4132172 rs62283814 rs12492846
Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates
Nature communications · 2019 · PMID 30846698 · open access
12 pages+
rs75458655 rs13088093 rs8038326 rs2863957 rs17388803 rs4585442
Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration
Human molecular genetics · 2023 · PMID 37384397
12 pages+
rs11242483 rs10814514 rs1057703 rs6737318 rs34731055 rs7115856
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+
rs12350099 rs1480637 rs2095140 rs13118508 rs2015110 rs509236
A genome-wide study on gene-nutrient interactions for hyperuricemia in a large Korean cohort (KoGES)
Scientific reports · 2025 · PMID 40835619 · open access
12 pages+
rs576114454 rs183195599 rs2725234 rs9999470 rs138409370 rs75786299
New insights into the genetic etiology of Alzheimer's disease and related dementias
EADB · GR@ACE and 7 more consortia
Nature genetics · 2022 · PMID 35379992 · open access
9 pages
rs3848143 rs62374257 rs3851179 rs6605556 rs7767350 rs6586028
Biological and clinical insights from genetics of insomnia symptoms
HUNT All In Sleep
Nature genetics · 2019 · PMID 30804566 · open access
6 pages
rs7711696 rs11184946 rs2062113 rs11651809 rs2296580 rs17669584
Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits
Nature human behaviour · 2022 · PMID 34426670
4 pages
rs199535 rs1971631 rs62132801 rs9964229
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease
Proceedings of the National Academy of Sciences of the United States of America · 2009 · PMID 19196962
2 pages
rs2742234 Hirschsprung Disease
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2
Human molecular genetics · 2010 · PMID 20460270
2 pages
rs17095355 Biliary Atresia
Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls
Nature communications · 2015 · PMID 26394188 · open access
2 pages
rs678741 rs13398147
Genome-wide association study of breakfast skipping links clock regulation with food timing
The American journal of clinical nutrition · 2019 · PMID 31190057
2 pages
rs8097544 rs6017427
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Alzheimer’s Disease Genetics Consortium (ADGC)
Genome biology · 2025 · PMID 40676597 · open access
2 pages
rs111486601 rs1898895
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
ANZRAG Consortium
Nature genetics · 2016 · PMID 26752265 · open access
1 page
rs1333037
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity
Nature communications · 2017 · PMID 28232668 · open access
1 page
rs12229892
Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease
Arthritis & rheumatology (Hoboken, N.J.) · 2021 · PMID 33393726
1 page
rs2087726
TMEM106B is a selective modulator of TDP-43 pathology in Alzheimer's disease
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026 · PMID 42720122
1 page
Research roundup — September 2026

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.