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.

46 matches for Andreassen OA, showing the first 20.

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
rs11591402 rs1427829 rs3001723 rs1592757 rs4275621 rs2243517
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
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis
Estonian Biobank · DBDS Genomic Consortium
Communications biology · 2024 · PMID 38671141 · open access
7 pages
rs9980363 rs1945016 rs17649684 rs13128363 rs11749692 rs955007
The genetic landscape of basal ganglia and implications for common brain disorders
Nature communications · 2024 · PMID 39353893 · open access
7 pages
rs2817145 rs56000151 rs1953352 rs4938400 rs6138937 rs10414860
Large-scale brainstem neuroimaging and genetic analyses provide new insights into the neuronal mechanisms of hypertension
HGG advances · 2025 · PMID 39663699 · open access
7 pages
rs13140033 rs783622 rs76344126 rs1863244 rs11243203 rs12030641
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
Characterization of the genetic architecture of infant and early childhood body mass index
Nature metabolism · 2022 · PMID 35315439
5 pages
rs78412508 rs12672489 rs2767486 rs1820721 rs2816985
Genetic effects on the timing of parturition and links to fetal birth weight
Early Growth Genetics Consortium · Estonian Biobank Research Team and 1 more consortia
Nature genetics · 2023 · PMID 37012456 · open access
4 pages
rs113828443 rs34555419 rs6472846 rs28654158
Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth
iPSYCH-BROAD
PLoS genetics · 2020 · PMID 33227023 · open access
3 pages
rs1404792 rs4935984 rs13081151
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
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset
Members of the DBDS Genomic Consortium · Danish RA Genetics Working Group and 1 more consortia
Annals of the rheumatic diseases · 2022 · PMID 35470158 · open access
3 pages
rs7320598 rs10261758 rs1538981
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
Genome-wide association analyses using machine learning-based phenotyping reveal genetic architecture of occupational creativity and overlap with psychiatric disorders
Psychiatry research · 2024 · PMID 38335777
3 pages
rs34427167 rs35800293 rs73079014
Common variants conferring risk of schizophrenia
Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
2 pages
rs12807809 Schizophrenia
Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism
Nature communications · 2024 · PMID 39214992 · open access
2 pages
rs149247216 rs5942980
Genome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestry
Nature human behaviour · 2025 · PMID 40335706 · open access
2 pages
rs10010217 rs4785475
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
Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis
PGC ADHD Working Group · PGC Bipolar Disorder Working Group
Biological psychiatry · 2017 · PMID 27890468
1 page
rs7089973

Showing 20 of 46 · page 2 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.