For researchers

Is your paper here?

2,677 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.

25 matches for Marioni R, showing the first 20.

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
Genome-wide association study identifies 74 loci associated with educational attainment
LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
12 pages+
rs12142680 rs56044892 rs12410444 rs12754946 rs1008078 rs17372140
Genetic prediction of male pattern baldness
PLoS genetics · 2017 · PMID 28196072 · open access
12 pages+
rs79284724 rs17752365 rs1842202 rs73209413 rs113222435 rs73212804
Association analysis in over 329,000 individuals identifies 116 independent variants influencing neuroticism
Nature genetics · 2018 · PMID 29255261
12 pages+
rs1901013 rs11072662 rs2283079 rs6476086 rs17102884 rs34220720
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+
rs71324996 rs8070135 rs151231 rs954734 rs62170823 rs926300
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+
rs149520992 rs6987444 rs2852151 rs9385532 rs12083537 rs67129560
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
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
Genetics of DNA Methylation Consortium · NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Genome biology · 2021 · PMID 34187551 · open access
12 pages+
rs7550821 rs76344745 rs10508861 rs4832646 rs7744326 rs75243280
Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids
Biological psychiatry · 2023 · PMID 36764567
12 pages+
rs7095996 rs2064454 rs11557064 rs200837054 rs2722698 rs59125977
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs4515883 rs6743072 rs35073727 rs57631119 rs9380498 rs12187932
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · open access
11 pages
rs16982520 rs7406910 rs34591516 rs1126930 rs10407022 rs470113
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
Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults
Genome medicine · 2020 · PMID 32641083 · open access
7 pages
rs62059801 rs4269772 rs62378712 rs6897260 rs112545364 rs2227543
GWAS of epigenetic aging rates in blood reveals a critical role for TERT
Nature communications · 2018 · PMID 29374233 · open access
6 pages
rs2736099 rs143093668 rs6915893 rs78781855 rs1005277 Telomere Length and Epigenetic Age Acceleration
Multivariate genome-wide analysis of aging-related traits identifies novel loci and new drug targets for healthy aging
Nature aging · 2023 · PMID 37550455 · open access
5 pages
rs16843603 rs34891485 rs12705966 rs13141210 rs28455998
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
Proceedings of the National Academy of Sciences of the United States of America · 2014 · PMID 25201988
4 pages
rs1487441 rs9858213 rs13401104 rs3789044
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
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

Showing 20 of 25 · 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.