For researchers

Is your paper here?

2,657 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.

8 matches for Demontis D.

Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs72974238 rs6538539 rs708228 rs17571951 rs79210963 rs7933981
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Nature medicine · 2023 · PMID 37464041
12 pages+
rs7017108 rs34269011 rs12517438 rs1931388 rs12530388 rs2418449
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
Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality
ADHD Group of the Psychiatric Genomics Consortium, International Cannabis Consortium
Molecular psychiatry · 2020 · PMID 30610198
5 pages
rs113551349 rs797267 rs56319043 rs2782639 ADHD (Attention Deficit Hyperactivity Disorder)
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
ADHD Working Group of the Psychiatric Genomics Consortium · iPSYCH-Broad Consortium
Nature genetics · 2023 · PMID 36702997
4 pages
rs76857496 rs6537401 rs114142727 rs2311059
Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications
Veterans Affairs Million Veteran Program
Nature genetics · 2023 · PMID 37985822 · open access
3 pages
rs12497569 rs11570190 rs10835372
A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder
23andMe Research Team · Psychiatric Genomics Consortium: ADHD Subgroup and 1 more consortia
Biological psychiatry · 2018 · PMID 29325848 · open access
1 page
rs8039398
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder
ADHD Working Group of the Psychiatric Genomics Consortium (PGC)
Nature communications · 2021 · PMID 33495439 · open access
1 page
rs7118422

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.