For researchers

Is your paper here?

2,655 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.

13 matches for Maier W.

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+
rs112481526 rs28455634 rs12672003 rs35306827 rs2336147 rs10866641
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs79210963 rs7933981 rs7900775 rs7575796 rs140365013 rs302317
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
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
rs62374257 rs3851179 rs6605556 rs7767350 rs6586028 rs7225151
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
rs17183814 rs10896090 rs10035291 rs111444407 rs10950456 rs57957974
Genome-wide association study reveals two new risk loci for bipolar disorder
Nature communications · 2014 · PMID 24618891
4 pages
rs12290811 rs17826816 rs12202969 rs6550435
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers
EADB consortium · GR@ACE study group
Acta neuropathologica · 2022 · PMID 36066633 · open access
3 pages
rs10937450 rs4686570 rs9877502
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder
Bipolar Disorder Genome Study (BiGS) Consortium
American journal of human genetics · 2011 · PMID 21353194
2 pages
rs1064395 Bipolar Disorder
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder
Human molecular genetics · 2016 · PMID 27329760
2 pages
rs2517959 rs4236274
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
European Alzheimer's Disease Initiative (EADI) · Genetic and Environmental Risk in Alzheimer's Disease and 2 more consortia
Nature genetics · 2013 · PMID 24162737
1 page
rs10498633
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
1 page
rs139967528
Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism
Nature communications · 2023 · PMID 37286573 · open access
1 page
rs10737681

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.