For researchers

Is your paper here?

2,660 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 Bryois J.

Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways
23andMe Research Team
Nature genetics · 2018 · PMID 29942085
12 pages+
rs1431181 rs480330 rs11022718 rs12484971 rs7175083 rs1330745
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Nature genetics · 2018 · PMID 29942086
12 pages+
rs11932971 rs13381096 rs2450333 rs11123816 rs113795690 rs176217
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Nature genetics · 2019 · PMID 30617256
12 pages+
rs183321458 rs539159088 rs11763230 rs28399637 rs35349669 rs983392
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways
23andMe Research Team
Nature genetics · 2019 · PMID 30804565
12 pages+
rs4483990 rs56382918 rs7297799 rs77598468 rs10761240 rs35748596
Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income
Nature communications · 2019 · PMID 31844048 · open access
12 pages+
rs12614880 rs13402908 rs240702 rs62166490 rs27565 rs2068428
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
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs12541 rs61833239 rs13016542 rs11711948 rs9674103 rs11619756
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
eQTLGen · 23andMe and 1 more consortia
Nature genetics · 2018 · PMID 29700475 · open access
10 pages
rs10950398 rs11643192 rs7430565 rs116755193 rs4904738 rs62099069
The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls
Bipolar Disorder Working Group of the Psychiatric Genomics Consortium · Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Biological psychiatry · 2020 · PMID 31926635
3 pages
rs58235352 rs113872034 rs61533748
Biological annotation of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals
Molecular psychiatry · 2019 · PMID 29520040
1 page
rs11794152
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.