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.

21 matches for Toft M, showing the first 20.

Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
23andMe Research Team · System Genomics of Parkinson's Disease Consortium and 1 more consortia
The Lancet. Neurology · 2019 · PMID 31701892
12 pages+
rs114138760 rs11578699 rs11557080 rs76116224 rs73038319 rs55961674
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
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
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Nature medicine · 2023 · PMID 37464041
12 pages+
rs2389015 rs8030745 rs2274794 rs72724899 rs79714693 rs6471757
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+
rs72850156 rs10414623 rs7769158 rs3130321 rs9469058 rs2535300
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+
rs16948230 rs6801151 rs78201023 rs7243332 rs6032660 rs10487459
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
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
The genetic landscape of basal ganglia and implications for common brain disorders
Nature communications · 2024 · PMID 39353893 · open access
7 pages
rs10414860 rs9393688 rs2817145 rs56000151 rs1953352 rs4938400
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
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
rs3001038 rs244620 rs1518111 rs4974130
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
FUT2-ABO epistasis increases the risk of early childhood asthma and Streptococcus pneumoniae respiratory illnesses
Nature communications · 2020 · PMID 33328473 · open access
3 pages
rs11465702 rs907091 rs340933
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
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
rs381218 rs115884658
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
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information
Biological psychiatry · 2022 · PMID 34865855 · open access
1 page
rs10821140

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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.