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.

23 matches for Goate A, showing the first 20.

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
International Parkinson's Disease Genomics Consortium (IPDGC) · Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI) and 10 more consortia
Nature genetics · 2014 · PMID 25064009 · open access
12 pages+
rs1555399 rs2414739 rs14235 rs35749011 rs10797576 rs1474055
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use
CHD Exome+ Consortium · Consortium for Genetics of Smoking Behaviour
Biological psychiatry · 2019 · PMID 30679032
12 pages+
rs1727284 rs442467 rs11135030 rs11210887 rs12053870 rs1264322
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
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
rs6692219 rs11971186 rs1937455 rs6738833 rs13026471 rs6883351
Genome-wide association study for variants that modulate relationships between cerebrospinal fluid amyloid-beta 42, tau, and p-tau levels
Alzheimer’s Disease Neuroimaging Initiative
Alzheimer's research & therapy · 2018 · PMID 30153862 · open access
4 pages
rs15205 rs1036819 rs8027714 rs74025622
Proteo-genomics of soluble TREM2 in cerebrospinal fluid provides novel insights and identifies novel modulators for Alzheimer's disease
Molecular neurodegeneration · 2024 · PMID 38172904 · open access
4 pages
rs142232675 rs12664332 rs73823326 rs11827324
GWAS meta-analysis of cerebrospinal fluid Alzheimer's biomarkers reveals loci regulating lipids, brain volume and autophagy
Nature communications · 2026 · PMID 42014397 · open access
4 pages
rs4843552 rs798560 rs35327527 rs7928895
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Nature genetics · 2011 · PMID 21460841 · open access
3 pages
rs7561528 rs9349407 Alzheimer's Disease
Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers
Alzheimer’s Disease Neuroimaging Initiative (ADNI) · Alzheimer Disease Genetic Consortium (ADGC)
Acta neuropathologica · 2017 · PMID 28247064
2 pages
rs769449 rs9527039
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
P. S. P. genetics study group
Molecular neurodegeneration · 2024 · PMID 39152475 · open access
2 pages
rs11708828 rs62057121
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's disease
Alzheimer’s Disease Genetics Consortium (ADGC)
Genome biology · 2025 · PMID 40676597 · open access
2 pages
rs111486601 rs1898895
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Nature genetics · 2009 · PMID 19915575 · open access
1 page
rs393152
Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6
Genes, brain, and behavior · 2012 · PMID 22554406
1 page
rs2835872
Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans
Alzheimer Disease Genetics Consortium
JAMA · 2013 · PMID 23571587
1 page
rs115550680
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
European Alzheimer's Disease Initiative (EADI) · Genetic and Environmental Risk in Alzheimer's Disease and 2 more consortia
Nature genetics · 2013 · PMID 24162737
1 page
rs10498633
Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families
Drug and alcohol dependence · 2014 · PMID 24962325
1 page
rs2168784
Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation
Alzheimer's Disease Neuroimaging Initiative
PLoS genetics · 2014 · PMID 25340798 · open access
1 page
rs61812598
Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans
Alzheimer's Disease Genetics Consortium
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2017 · PMID 27770636
1 page
rs16961023
A genome wide association study of fast beta EEG in families of European ancestry
International journal of psychophysiology : official journal of the International Organization of Psychophysiology · 2017 · PMID 28040410
1 page
rs2252790
Transethnic genome-wide scan identifies novel Alzheimer's disease loci
Alzheimer's Disease Genetics Consortium
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2017 · PMID 28183528
1 page
rs11257238

Showing 20 of 23 · 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.