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.

26 matches for Wray N, showing the first 20.

Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
Nature communications · 2018 · PMID 30573740 · open access
12 pages+
rs17739590 rs2146959 rs10917958 rs10032922 rs10905359 rs1475417
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
23andMe Research Team · Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Nature neuroscience · 2019 · PMID 30718901
12 pages+
rs35553410 rs12967143 rs198457 rs7117514 rs57344483 rs3213572
Genome-wide association study of medication-use and associated disease in the UK Biobank
Nature communications · 2019 · PMID 31015401 · open access
12 pages+
rs7596240 rs1723022 rs59180873 rs80257854 rs7655751 rs111820018
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration
Nature communications · 2020 · PMID 32242144 · open access
12 pages+
rs35408430 rs2618515 rs11826529 rs10908465 rs72856836 rs10085881
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
HUNT All-In Psychiatry
Nature genetics · 2021 · PMID 34002096 · open access
12 pages+
rs28455634 rs12672003 rs35306827 rs2336147 rs10866641 rs67712855
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs140365013 rs302317 rs77622099 rs619091 rs12652777 rs12476312
Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease
Nature communications · 2022 · PMID 35668104 · open access
12 pages+
rs78018648 rs72721018 rs28765985 rs79142397 rs72794293 rs9611886
150 risk variants for diverticular disease of intestine prioritize cell types and enable polygenic prediction of disease susceptibility
Cell genomics · 2023 · PMID 37492107 · open access
12 pages+
rs9514637 rs9983489 rs2276068 rs352143 rs10179961 rs71350022
The correlates of neonatal complement component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders
Cell genomics · 2023 · PMID 38116117 · open access
12 pages+
rs7769158 rs3130321 rs9469058 rs2535300 rs11751198 rs61229539
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
rs6461049 rs1006737 rs17691888 rs17504622 rs778371 rs11995572
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
eQTLGen · 23andMe and 1 more consortia
Nature genetics · 2018 · PMID 29700475 · open access
10 pages
rs4261101 rs10950398 rs11643192 rs7430565 rs116755193 rs4904738
Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes
Nature genetics · 2025 · PMID 40962958
9 pages
rs4749820 rs7708883 rs4462678 rs9959583 rs4131786 rs1435746
GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression
Nature communications · 2021 · PMID 33608531 · open access
8 pages
rs200964 rs967823 rs73370726 rs35788599 rs10500661 rs34074411
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults
Genome medicine · 2020 · PMID 32641083 · open access
7 pages
rs6897260 rs112545364 rs2227543 rs2843700 rs62059801 rs4269772
GWAS of epigenetic aging rates in blood reveals a critical role for TERT
Nature communications · 2018 · PMID 29374233 · open access
6 pages
rs2736099 rs143093668 rs6915893 rs78781855 rs1005277 Telomere Length and Epigenetic Age Acceleration
Genome-wide association study identifies 30 loci associated with bipolar disorder
eQTLGen Consortium · BIOS Consortium and 1 more consortia
Nature genetics · 2019 · PMID 31043756 · open access
6 pages
rs10896090 rs10035291 rs111444407 rs10950456 rs57957974 rs17183814
Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness
GEFOS Any-Type of Fracture Consortium
Nature communications · 2017 · PMID 29313844 · open access
5 pages
rs72979233 rs4926611 rs11614333 rs2110927 rs80103986
Genetic signatures of high-altitude adaptation in Tibetans
Proceedings of the National Academy of Sciences of the United States of America · 2017 · PMID 28373541
3 pages
rs71673426 rs78720557 rs2584462
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
SLALOM Consortium · PARALS Consortium and 2 more consortia
Nature genetics · 2021 · PMID 34873335 · open access
3 pages
rs2453555 rs9275477 rs75087725
Meta-analysis of genome-wide association studies of anxiety disorders
Molecular psychiatry · 2016 · PMID 26754954 · open access
2 pages
rs1709393 Anxiety Disorder

Showing 20 of 26 · page 1 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.