For researchers

Is your paper here?

2,655 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.

24 matches for Børglum AD, showing the first 20.

Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits
Nature neuroscience · 2020 · PMID 32451486 · open access
12 pages+
rs148382129 rs9926289 rs9937709 rs73403005 rs7073987 rs1724429
Genetic analyses identify widespread sex-differential participation bias
FinnGen Study · 23andMe Research Team and 1 more consortia
Nature genetics · 2021 · PMID 33888908
12 pages+
rs6968125 rs114328297 rs2814162 rs28575268 rs67624109 rs1368546
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+
rs112481526 rs28455634 rs12672003 rs35306827 rs2336147 rs10866641
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
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs1779454 rs3135363 rs2038760 rs7928827 rs7146217 rs518295
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Nature medicine · 2023 · PMID 37464041
12 pages+
rs1931388 rs12530388 rs2418449 rs11612312 rs11157241 rs4753209
The correlates of neonatal complement component 3 and 4 protein concentrations with a focus on psychiatric and autoimmune disorders
Cell genomics · 2023 · PMID 38116117 · open access
12 pages+
rs7769158 rs3130321 rs9469058 rs2535300 rs11751198 rs61229539
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
AURORA Study · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2024 · PMID 38637617
12 pages+
rs6032660 rs10487459 rs175086 rs13037326 rs10992779 rs13161130
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
rs4261101 rs10950398 rs11643192 rs7430565 rs116755193 rs4904738
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 30 loci associated with bipolar disorder
eQTLGen Consortium · BIOS Consortium and 1 more consortia
Nature genetics · 2019 · PMID 31043756 · open access
6 pages
rs17183814 rs10896090 rs10035291 rs111444407 rs10950456 rs57957974
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 association study of febrile seizures implicates fever response and neuronal excitability genes
Brain : a journal of neurology · 2022 · PMID 35022648 · open access
4 pages
rs1518111 rs4974130 rs3001038 rs244620
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
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
Nature communications · 2017 · PMID 29030599 · open access
3 pages
rs34831921 rs55730499 Human Lifespan and Longevity
FUT2-ABO epistasis increases the risk of early childhood asthma and Streptococcus pneumoniae respiratory illnesses
Nature communications · 2020 · PMID 33328473 · open access
3 pages
rs907091 rs340933 rs11465702
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
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
Common variants conferring risk of schizophrenia
Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
2 pages
rs12807809 Schizophrenia
Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - Findings from a Danish population-based study
Brain, behavior, and immunity · 2021 · PMID 32534018
2 pages
rs115884658 rs381218

Showing 20 of 24 · page 1 of 2

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.