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 Beaumont R, showing the first 20.

Genome-wide associations for birth weight and correlations with adult disease
CHARGE Consortium Hematology Working Group · Early Growth Genetics (EGG) Consortium
Nature · 2016 · PMID 27680694
12 pages+
rs35261542 rs28510415 rs700059 rs3753639 rs62466330 rs6016377
Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers
PloS one · 2017 · PMID 28957414 · open access
12 pages+
rs67183237 rs7735282 rs143845082 rs10479001 rs149535568 rs174559
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry
GIANT Consortium
Human molecular genetics · 2019 · PMID 30239722 · open access
12 pages+
rs17783165 rs7119797 rs1468602 rs8024806 rs11760290 rs12369214
Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms
Nature communications · 2019 · PMID 30696823 · open access
12 pages+
rs1931814 rs62124718 rs11165655 rs12051 rs1449403 rs12871550
Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates
Nature communications · 2019 · PMID 30846698 · open access
12 pages+
rs75458655 rs13088093 rs8038326 rs2863957 rs17388803 rs4585442
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
EGG Consortium
Nature genetics · 2019 · PMID 31043758
12 pages+
rs4719648 rs61885091 rs11055030 rs2306547 rs2647873 rs6575803
Using human genetics to understand the disease impacts of testosterone in men and women
Endometrial Cancer Association Consortium
Nature medicine · 2020 · PMID 32042192 · open access
12 pages+
rs204995 rs11155076 rs4919686 rs168189 rs4828043 rs6997799
Genetic Evidence for Different Adiposity Phenotypes and Their Opposing Influences on Ectopic Fat and Risk of Cardiometabolic Disease
Diabetes · 2021 · PMID 33980691
12 pages+
rs12130231 rs441792 rs987469 rs7258937 rs9764678 rs10172678
Genetic insights into biological mechanisms governing human ovarian ageing
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
rs2844466 rs140353819 rs540836853 rs2736609 rs9438982 rs117146677
Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion, after accounting for BMI in adulthood
Diabetologia · 2023 · PMID 37280435 · open access
12 pages+
rs4523214 rs2072858 rs72711335 rs13100148 rs55927253 rs80022979
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
Early Growth Genetics (EGG) Consortium
Nature genetics · 2023 · PMID 37798380 · open access
10 pages
rs6040436 rs10486660 rs7783810 rs12529634 rs140691414 rs1434836
Genetic predictors of participation in optional components of UK Biobank
Nature communications · 2021 · PMID 33563987 · open access
7 pages
rs12189679 rs2622102 rs11134465 rs1565440 rs1261078 rs2049604
Biological and clinical insights from genetics of insomnia symptoms
HUNT All In Sleep
Nature genetics · 2019 · PMID 30804566 · open access
6 pages
rs7711696 rs11184946 rs2062113 rs11651809 rs2296580 rs17669584
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci
PLoS genetics · 2016 · PMID 27494321 · open access
5 pages
rs77641763 rs9961653 rs75804782 rs11162296 rs17190618
Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects
Estonian Biobank Research Team · Genes & Health Research Team
Nature communications · 2026 · PMID 42225636 · open access
5 pages
rs72964564 rs77864822 rs7933420 rs10036439 rs613937
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development
American journal of human genetics · 2018 · PMID 29290336
4 pages
rs12614435 rs77831929 rs4404097 rs56202902
Genetic effects on the timing of parturition and links to fetal birth weight
Early Growth Genetics Consortium · Estonian Biobank Research Team and 1 more consortia
Nature genetics · 2023 · PMID 37012456 · open access
4 pages
rs28654158 rs113828443 rs34555419 rs6472846
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics
Early Growth Genetics (EGG) Consortium
Human molecular genetics · 2018 · PMID 29309628 · open access
1 page
rs2971669
Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms
Gut · 2019 · PMID 30661054
1 page
rs7077800
Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour
Nature communications · 2019 · PMID 30952852 · open access
1 page
rs8045740

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.