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.

11 matches for Smeland O.

Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Nature genetics · 2018 · PMID 29942086
12 pages+
rs6668048 rs17836155 rs2485371 rs11932971 rs13381096 rs2450333
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+
rs58499557 rs6675690 rs1861979 rs57246240 rs12218858 rs1419859
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+
rs2336147 rs10866641 rs67712855 rs748455 rs78308718 rs6875495
The genetic architecture of the human thalamus and its overlap with ten common brain disorders
Nature communications · 2021 · PMID 34006833 · open access
12 pages+
rs34316881 rs1316356 rs58333527 rs6869935 rs4649098 rs6062262
Vertex-wise multivariate genome-wide association study identifies 780 unique genetic loci associated with cortical morphology
NeuroImage · 2021 · PMID 34560273
12 pages+
rs1949350 rs7092736 rs4714854 rs62125949 rs6681821 rs1995804
The genetic architecture of human cerebellar morphology supports a key role for the cerebellum in human evolution and psychopathology
Communications biology · 2026 · PMID 41703085 · open access
12 pages+
rs9301159 rs17577153 rs78235713 rs56023569 rs1957792 rs28571213
The genetic landscape of basal ganglia and implications for common brain disorders
Nature communications · 2024 · PMID 39353893 · open access
7 pages
rs6138937 rs10414860 rs9393688 rs2817145 rs56000151 rs1953352
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
rs3145 rs793571 rs28473013
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders
Nature genetics · 2017 · PMID 27918536
1 page
rs6481128

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.