For researchers

Is your paper here?

2,652 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.

12 matches for Giegling I.

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
rs7633520 rs11716820 rs7646366 rs28433345 rs10798879 rs71324996
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Nature genetics · 2018 · PMID 29942086
12 pages+
rs28888764 rs28522849 rs4687625 rs56306491 rs1115535 rs11646221
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
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
rs7767350 rs6586028 rs7225151 rs74685827 rs60755019 rs3848143
Genome-wide association study identifies 48 common genetic variants associated with handedness
Nature human behaviour · 2021 · PMID 32989287
6 pages
rs62036618 rs35551703 rs66479618 rs1422070 rs11168884 rs3132584
GWAS meta-analysis of cerebrospinal fluid Alzheimer's biomarkers reveals loci regulating lipids, brain volume and autophagy
Nature communications · 2026 · PMID 42014397 · open access
4 pages
rs4843552 rs798560 rs35327527 rs7928895
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
rs4686570 rs9877502 rs10937450
Common variants conferring risk of schizophrenia
Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
2 pages
rs12807809 Schizophrenia
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders
Schizophrenia Working Group of the Psychiatric Genomics Consortium · Bipolar Disorder Working Group of the Psychiatric Genomics Consortium and 3 more consortia
Biological psychiatry · 2022 · PMID 34099189
2 pages
rs793571 rs28473013
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
1 page
rs4105144
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
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
Anorexia Nervosa Genetics Initiative · Eating Disorders Working Group of the Psychiatric Genomics Consortium
Nature genetics · 2019 · PMID 31308545
1 page
rs9821797

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.