For researchers

Is your paper here?

2,671 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.

14 matches for Ali M.

Association analysis in over 329,000 individuals identifies 116 independent variants influencing neuroticism
Nature genetics · 2018 · PMID 29255261
12 pages+
rs12802244 rs2298527 rs7696796 rs2214258 rs7634476 rs6986
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
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+
rs11135349 rs35553410 rs12967143 rs198457 rs7117514 rs57344483
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus
Communications biology · 2021 · PMID 33649486 · open access
12 pages+
rs2417930 rs3118518 rs1200108 rs6669560 rs116792882 rs12515400
Proteogenomic analysis of human cerebrospinal fluid identifies neurologically relevant regulation and implicates causal proteins for Alzheimer's disease
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528825
12 pages+
rs2365715 rs12983058 rs13060370 rs12921753 rs9391855 rs7214750
Genetic architecture of cerebrospinal fluid and brain metabolite levels and the genetic colocalization of metabolites with human traits
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528826
12 pages+
rs2298840 rs55647329 rs73060324 rs11986259 rs16825455 rs7073937
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma
Nature communications · 2016 · PMID 27363682 · open access
9 pages
rs6066835 rs34229995 rs7193541 rs7577599 rs6599192 rs34562254
Identification of sequence variants influencing immunoglobulin levels
Nature genetics · 2017 · PMID 28628107
6 pages
rs72704050 rs11651596 rs2133037 rs112763553 rs2239701 rs35043490
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
PRACTICAL consortium
Nature communications · 2018 · PMID 30213928 · open access
5 pages
rs4325816 rs6595443 rs17507636 rs58618031 Multiple Myeloma
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
rs12664332 rs73823326 rs11827324 rs142232675
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
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers
EADB consortium · GR@ACE study group
Acta neuropathologica · 2022 · PMID 36066633 · open access
3 pages
rs9877502 rs10937450 rs4686570
A study assessing the association of glycated hemoglobin A1C (HbA1C) associated variants with HbA1C, chronic kidney disease and diabetic retinopathy in populations of Asian ancestry
PloS one · 2013 · PMID 24244560 · open access
1 page
rs12602486
Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma
Nature communications · 2015 · PMID 26007630 · open access
1 page
rs57104699

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.