For researchers

Is your paper here?

2,673 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.

44 matches for Ge T, showing the first 20.

The genetic architecture of the human cerebral cortex
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
rs170239 rs2358483 rs149142 rs78155705 rs62005276 rs639016
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Nature metabolism · 2020 · PMID 33067605
12 pages+
rs7178801 rs76480089 rs1634517 rs62193063 rs9807908 rs3742564
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+
rs77622099 rs619091 rs12652777 rs12476312 rs79445414 rs10860960
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+
rs1887200 rs11904581 rs6139109 rs1442883 rs973730 rs6020177
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs2276133 rs7748159 rs9266669 rs7636138 rs11880613 rs2728099
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Nature medicine · 2023 · PMID 37464041
12 pages+
rs4478545 rs9627391 rs12898464 rs35883476 rs4571923 rs7230285
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+
rs3130321 rs9469058 rs2535300 rs11751198 rs61229539 rs379464
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
AURORA Study · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2024 · PMID 38637617
12 pages+
rs2470937 rs10132977 rs896686 rs1541903 rs61702433 rs2107448
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium and 4 more consortia
Nature genetics · 2026 · PMID 41644669 · open access
12 pages+
rs9864554 rs9672082 rs7321973 rs12133184 rs2758605 rs35397235
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 study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
Early Growth Genetics (EGG) Consortium
Nature genetics · 2023 · PMID 37798380 · open access
10 pages
rs7722058 rs10925945 rs3822394 rs6557677 rs6040436 rs10486660
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
International Headache Genetics Consortium
Nature genetics · 2016 · PMID 27322543
9 pages
rs2506142 rs4081947 rs6791480 rs6693567 rs10155855 rs10218452
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
DBDS Genetic Consortium · GO Consortium
Nature communications · 2022 · PMID 35110524 · open access
9 pages
rs751450 rs3135842 rs4757353 rs28487989 rs16934882 rs3010044
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
ADHD Working Group of the Psychiatric Genomics Consortium (PGC) · Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium and 1 more consortia
Nature genetics · 2019 · PMID 30478444
8 pages
rs56135409 rs11591402 rs1427829 rs3001723 rs1592757 rs4275621
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
COGS–Cancer Research UK GWAS–ELLIPSE (part of GAME-ON) Initiative · Australian Prostate Cancer Bioresource and 3 more consortia
Nature genetics · 2013 · PMID 23535732
7 pages
rs3850699 rs1894292 rs2273669 rs1270884 rs11650494 rs1218582
Genome-wide association study identifies 48 common genetic variants associated with handedness
Nature human behaviour · 2021 · PMID 32989287
7 pages
rs62036618 rs35551703 rs66479618 rs1422070 rs11168884 rs2040498
A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies
German Network for Research on Autoimmune Encephalitis (GENERATE)
Brain : a journal of neurology · 2023 · PMID 35348614 · open access
7 pages
rs7749544 rs3130545 rs378956 rs3094633 rs314304 rs62231498
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
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes
Brain : a journal of neurology · 2022 · PMID 35022648 · open access
5 pages
rs4974130 rs3001038 rs244620 rs62023078 rs1518111

Showing 20 of 44 · page 1 of 3

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.