For researchers

Is your paper here?

2,683 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.

20 matches for Djurovic S.

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
rs62037363 rs5758605 rs75477016 rs77418166 rs113714691 rs77482156
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Nature genetics · 2018 · PMID 29942086
12 pages+
rs11117646 rs2058898 rs2067783 rs7423572 rs2284871 rs7203132
Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes
Alzheimer’s Disease Neuroimaging Initiative · Pediatric Imaging, Neurocognition and Genetics Study
Molecular psychiatry · 2020 · PMID 30279459 · open access
12 pages+
rs1861979 rs57246240 rs12218858 rs1419859 rs17178139 rs77956314
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Nature genetics · 2019 · PMID 30617256
12 pages+
rs28399637 rs35349669 rs983392 rs114360492 rs184384746 rs187370608
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+
rs1080066 rs73313052 rs9375477 rs117461235 rs68175985 rs71471500
Genome-wide Association Analysis of Parkinson's Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk Loci
Biological psychiatry · 2021 · PMID 32201043
12 pages+
rs8005172 rs140278703 rs34884217 rs12651314 rs10516839 rs28624974
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+
rs78308718 rs6875495 rs55706012 rs6993953 rs11137399 rs4748468
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
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
10 pages
rs2410767 rs10439607 rs10217651 rs35200015 rs3133370 rs2206656
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
10 pages
rs62374257 rs3851179 rs6605556 rs7767350 rs6586028 rs7225151
The genetic landscape of basal ganglia and implications for common brain disorders
Nature communications · 2024 · PMID 39353893 · open access
8 pages
rs9393688 rs2817145 rs56000151 rs1953352 rs4938400 rs6138937
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
rs111444407 rs10950456 rs57957974 rs17183814 rs10896090 rs10035291
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
3 pages
rs793571 rs28473013 rs3145
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
rs9877502 rs10937450 rs4686570
Common variants conferring risk of schizophrenia
Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
2 pages
rs12807809 Schizophrenia
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
Identification of common variants associated with human hippocampal and intracranial volumes
Alzheimer's Disease Neuroimaging Initiative · EPIGEN Consortium and 4 more consortia
Nature genetics · 2012 · PMID 22504417
1 page
rs10784502
A comprehensive family-based replication study of schizophrenia genes
JAMA psychiatry · 2013 · PMID 23894747
1 page
rs1261117
Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs
Journal of psychopharmacology (Oxford, England) · 2015 · PMID 25944848
1 page
rs16935279
Identification of a novel polymorphism associated with reduced clozapine concentration in schizophrenia patients-a genome-wide association study adjusting for smoking habits
Translational psychiatry · 2020 · PMID 32555152 · open access
1 page
rs10023464

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.