For researchers

Is your paper here?

2,673 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.

15 matches for Satizabal CL.

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
The genetic architecture of the human cerebral cortex
Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium and 5 more consortia
Science (New York, N.Y.) · 2020 · PMID 32193296
12 pages+
rs78155705 rs62005276 rs639016 rs34322452 rs11070172 rs9881533
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 meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Estonian Biobank Research Team
American journal of human genetics · 2022 · PMID 35580588 · open access
12 pages+
rs72622585 rs13148153 rs4660885 rs61734651 rs11881070 rs11152089
Genetic architecture of subcortical brain structures in 38,851 individuals
Nature genetics · 2019 · PMID 31636452
9 pages
rs3133370 rs2206656 rs4784256 rs196807 rs9505301 rs2410767
New insights into the genetic etiology of Alzheimer's disease and related dementias
EADB · GR@ACE and 7 more consortia
Nature genetics · 2022 · PMID 35379992 · open access
9 pages
rs3848143 rs62374257 rs3851179 rs6605556 rs7767350 rs6586028
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate
Brain : a journal of neurology · 2022 · PMID 35511193 · open access
6 pages
rs3744027 rs6503417 rs12149643 rs73191849 rs13403122 Cerebral Small Vessel Disease
Stroke genetics informs drug discovery and risk prediction across ancestries
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
rs72934589 rs76110445 rs12415501 rs60401382 Cardioembolic Stroke
The genetics of circulating BDNF: towards understanding the role of BDNF in brain structure and function in middle and old ages
Brain communications · 2020 · PMID 33345186 · open access
3 pages
rs75945125 rs71329093 rs2242882
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
CHARGE consortium
Nature medicine · 2023 · PMID 37069360 · open access
3 pages
rs112407396 rs72485816 rs6011998
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
Stroke · 2020 · PMID 32517579
2 pages
rs2598420 rs3758575
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
1 page
rs139967528
Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
Nature communications · 2018 · PMID 30258056 · open access
1 page
rs34113929
Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels
Communications biology · 2022 · PMID 35396452 · open access
1 page
rs7502280
Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning
Molecular psychiatry · 2022 · PMID 35974141 · open access
1 page
rs11711421

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.