For researchers

Is your paper here?

2,657 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.

16 matches for Roberts D.

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
Cell · 2016 · PMID 27863252 · open access
12 pages+
rs2038700 rs72699818 rs138692864 rs11555542 rs2033784 rs2115536
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
CHD Exome+ Consortium · EPIC-CVD Consortium and 9 more consortia
Nature genetics · 2018 · PMID 29273807 · open access
12 pages+
rs5758651 rs34149579 rs12236219 rs284860 rs1131877 rs2277598
Genomic atlas of the human plasma proteome
Nature · 2018 · PMID 29875488
12 pages+
rs55636108 rs61985370 rs112206797 rs71426155 rs72732234 rs28383228
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+
rs75267082 rs62432759 rs1051447 rs948493 rs9397738 rs13157326
Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income
Nature communications · 2019 · PMID 31844048 · open access
12 pages+
rs6028090 rs11808748 rs1440277 rs2332719 rs1352890 rs12119149
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
rs5762879 rs62100531 rs62250976 rs62308111 rs6546232 rs7081113
The Polygenic and Monogenic Basis of Blood Traits and Diseases
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
rs576668364 rs59521405 rs6058638 rs6072078 rs6912255 rs6922558
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology
Nature communications · 2023 · PMID 37596262 · open access
12 pages+
rs9411463 rs998727 rs1445292 rs2708628 rs557661075 rs1863870
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
23andMe Research Team · D.E.S.I.R. study group
Nature genetics · 2024 · PMID 38839884 · open access
12 pages+
rs62262150 rs6527594 rs72665066 rs28842577 rs3738555 rs4886357
Novel loci and biomedical consequences of iron homoeostasis variation
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
12 pages+
rs143437464 rs186044114 rs485073 rs55925547 rs996347 rs112856048
Genome-wide analyses of variance in blood cell phenotypes provide new insights into complex trait biology and prediction
Nature communications · 2025 · PMID 40335489 · open access
12 pages+
rs550563462 rs544555124 rs546497406 rs141494605 rs79490353 rs12192635
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
EPIC-CVD Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS medicine · 2017 · PMID 28898252 · open access
10 pages
rs4745982 rs10823343 rs3824065 rs11154792 rs17509001 rs7040409
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
23andMe Research Team · DESIR study group
The Lancet. Neurology · 2017 · PMID 29029846 · open access
10 pages
rs10208712 rs35987657 rs17636328 rs61192259 rs62535767 rs340561
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease
UK-PSC Consortium · International IBD Genetics Consortium and 1 more consortia
Nature genetics · 2017 · PMID 27992413 · open access
8 pages
rs13140464 rs56258221 rs60652743 rs72837826 rs80060485 rs36023390
The influence of rare variants in circulating metabolic biomarkers
INTERVAL Study
PLoS genetics · 2020 · PMID 32150548 · open access
1 page
rs12191266
Large genome-wide association study identifies three novel risk variants for restless legs syndrome
Communications biology · 2020 · PMID 33239738 · open access
1 page
rs10188680

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.