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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.

67 matches for Dehghan A, showing the first 20.

Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Nature genetics · 2009 · PMID 19862010 · open access
12 pages+
rs10224002 rs16926246 rs628751 rs10495928 rs11085824 rs9374080
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Nature genetics · 2015 · PMID 26343387 · open access
12 pages+
rs1544935 rs1870634 rs2891168 rs56131196 rs72689147 rs2487928
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration
Human molecular genetics · 2016 · PMID 26561523
12 pages+
rs2731439 rs7439150 rs7916868 rs11780978 rs9808651 rs12913259
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
ICBP Consortium · AGEN Consortium and 3 more consortia
Nature communications · 2016 · PMID 26831199 · open access
12 pages+
rs6795744 rs228611 rs3750082 rs10491967 rs11666497 rs1800615
Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation
Inflammation Working Group of the CHARGE Consortium · PMI-WG-XCP and 1 more consortia
BMC genomics · 2016 · PMID 27286809 · open access
12 pages+
rs469772 rs4148191 rs4703642 rs6951245 rs1529711 rs4660808
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
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Nature genetics · 2018 · PMID 30297969
12 pages+
rs234853 rs184509201 rs3772071 rs11699802 rs231349 rs35913461
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
LifeLines Cohort Study · CHARGE Inflammation Working Group
American journal of human genetics · 2018 · PMID 30388399
12 pages+
rs56288844 rs149520992 rs6987444 rs2852151 rs9385532 rs12083537
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
rs4940525 rs2976178 rs1268176 rs3774726 rs9879531 rs62050038
GWAS for urinary sodium and potassium excretion highlights pathways shared with cardiovascular traits
Nature communications · 2019 · PMID 31409800 · open access
12 pages+
rs1513481 rs72704791 rs13163314 rs1957111 rs117287096 rs7140993
Urate, Blood Pressure, and Cardiovascular Disease: Evidence From Mendelian Randomization and Meta-Analysis of Clinical Trials
VA Million Veteran Program
Hypertension (Dallas, Tex. : 1979) · 2021 · PMID 33356394 · open access
12 pages+
rs1384291 rs11669336 rs9672635 rs7795876 rs195485 rs12214118
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes
Lifelines Cohort Study · VA Million Veteran Program
Nature communications · 2021 · PMID 33972514 · open access
12 pages+
rs71405688 rs17360994 rs1966384 rs8113963 rs144830380 rs61953500
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs118164457 rs7063597 rs3752435 rs4317621 rs4731113 rs4674280
Genetic analysis of over half a million people characterises C-reactive protein loci
Nature communications · 2022 · PMID 35459240 · open access
12 pages+
rs7127808 rs1338071 rs11790458 rs2596937 rs72730950 rs930035
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
12 pages+
rs4267865 rs57634870 rs11196296 rs3825801 rs79495865 rs1871045
Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities
Nature communications · 2022 · PMID 35922433 · open access
12 pages+
rs112350090 rs12863716 rs79051849 rs67846163 rs12771055 rs1583081
Pleiotropic genetic architecture and novel loci for C-reactive protein levels
Nature communications · 2022 · PMID 36376304 · open access
12 pages+
rs10925024 rs280322 rs1971318 rs2535907 rs2012927 rs7720409
Unravelling genetic architecture of circulatory amino acid levels, and their effect on risk of complex disorders
NAR genomics and bioinformatics · 2024 · PMID 38711861 · open access
12 pages+
rs138584093 rs11061610 rs895959 rs77440716 rs1165162 rs75661418
Multi-trait association analysis reveals shared genetic loci between Alzheimer's disease and cardiovascular traits
Nature communications · 2024 · PMID 39537608 · open access
12 pages+
rs28625968 rs2291434 rs6888113 rs2588917 rs3936052 rs4888388
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Genes & Health Research Team · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2025 · PMID 40038546 · open access
12 pages+
rs149780392 rs3794752 rs62233286 rs7095308 rs73048654 rs143445113

Showing 20 of 67 · page 1 of 4

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.