For researchers

Is your paper here?

2,661 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.

13 matches for Hagenaars SP.

Genetic prediction of male pattern baldness
PLoS genetics · 2017 · PMID 28196072 · open access
12 pages+
rs117769774 rs17186024 rs9801466 rs79032435 rs78448052 rs6457977
Association analysis in over 329,000 individuals identifies 116 independent variants influencing neuroticism
Nature genetics · 2018 · PMID 29255261
12 pages+
rs13224947 rs1901013 rs11072662 rs2283079 rs6476086 rs17102884
A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence
Molecular psychiatry · 2019 · PMID 29326435 · open access
12 pages+
rs12137231 rs62034318 rs55692411 rs2878628 rs2647261 rs26949
Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways
23andMe Research Team
Nature communications · 2018 · PMID 29662059 · open access
12 pages+
rs6483414 rs9530139 rs6679379 rs7548151 rs66975207 rs35715914
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
rs28433345 rs10798879 rs71324996 rs8070135 rs151231 rs954734
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
InterAct Consortium
PloS one · 2018 · PMID 29912962 · open access
12 pages+
rs4886640 rs7125196 rs259983 rs11725969 rs1894400 rs34063670
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
23andMe Research Team · Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Nature neuroscience · 2019 · PMID 30718901
12 pages+
rs12967143 rs198457 rs7117514 rs57344483 rs3213572 rs1343605
Cerebral small vessel disease genomics and its implications across the lifespan
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
12 pages+
rs73923006 rs6797002 rs7603972 rs17205972 rs7596872 rs55940034
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
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
9 pages
rs3133370 rs2206656 rs4784256 rs196807 rs9505301 rs2410767
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
CHARGE Neurology Working Group · COGENT-Kidney Consortium and 2 more consortia
American journal of human genetics · 2018 · PMID 29455858
7 pages
rs115234772 rs62319742 rs148772934 rs138973557 rs148753653 rs12135881
Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci
Molecular psychiatry · 2016 · PMID 27067015 · open access
4 pages
rs62353264 rs12378446 rs1187264 rs1187256
Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Translational psychiatry · 2018 · PMID 29317602 · open access
1 page
rs4478037

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.