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.

38 matches for Weir D, showing the first 20.

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
PRACTICAL consortium · kConFab Investigators and 4 more consortia
Nature genetics · 2015 · PMID 26414677 · open access
12 pages+
rs12142240 rs2236918 rs704795 rs930036 rs6856693 rs11738223
Genome-wide association study identifies 74 loci associated with educational attainment
LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
12 pages+
rs56044892 rs12410444 rs12754946 rs1008078 rs17372140 rs78365243
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits
Nature communications · 2017 · PMID 28443625 · open access
12 pages+
rs6012558 rs4239436 rs6772896 rs765751 rs2645294 rs12679556
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults
CHARGE Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS genetics · 2017 · PMID 28448500 · open access
12 pages+
rs1406948 rs10923724 rs2371767 rs7766106 rs10101061 rs7973683
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Nature communications · 2018 · PMID 29844566 · open access
12 pages+
rs79582714 rs62037363 rs5758605 rs75477016 rs77418166 rs113714691
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
InterAct Consortium
PloS one · 2018 · PMID 29912962 · open access
12 pages+
rs4886640 rs7125196 rs259983 rs11725969 rs1894400 rs34063670
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
12 pages+
rs67455627 rs7956306 rs9896320 rs12202055 rs1403174 rs71427690
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity
Lifelines Cohort Study
Nature communications · 2019 · PMID 30670697 · open access
12 pages+
rs114846969 rs6029549 rs556107 rs117753190 rs6489786 rs217358
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use
CHD Exome+ Consortium · Consortium for Genetics of Smoking Behaviour
Biological psychiatry · 2019 · PMID 30679032
12 pages+
rs11135030 rs11210887 rs12053870 rs1264322 rs12770228 rs12783782
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
rs767105335 rs77357563 rs2306899 rs2273171 rs4846567 rs117874826
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
American journal of human genetics · 2021 · PMID 33713608
12 pages+
rs10071837 rs4899520 rs75823898 rs112226333 rs2553033 rs7905296
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
The power of genetic diversity in genome-wide association studies of lipids
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
12 pages+
rs7856817 rs11626768 rs180705493 rs2811468 rs532566544 rs5752963
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Lifelines Cohort Study
Nature genetics · 2022 · PMID 36071172 · open access
12 pages+
rs58541850 rs9867121 rs114590429 rs13235840 rs4518438 rs1160545
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs6139332 rs2014307 rs630839 rs6514424 rs6677770 rs505317
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs60966685 rs61857945 rs62376929 rs7105506 rs73249524 rs73581416
Translational genomics of osteoarthritis in 1,962,069 individuals
arcOGEN Consortium · ARGO Consortium and 7 more consortia
Nature · 2025 · PMID 40205036 · open access
12 pages+
rs7163797 rs7659054 rs60250748 rs79120566 rs8062183 rs13394110
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium
Bone Mineral Density in Childhood Study (BMDCS) Group
PLoS genetics · 2017 · PMID 28430825 · open access
11 pages
rs62105306 rs17057164 rs149352150 rs56330886 rs112778462 rs378854
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
LifeLines Cohort Study
Nature genetics · 2016 · PMID 27089181 · open access
10 pages
rs2075677 rs4958581 rs7554469 rs4938021 rs3756290 rs782212
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
CHD Exome+ Consortium · ExomeBP Consortium and 4 more consortia
Nature genetics · 2016 · PMID 27618448
9 pages
rs2493292 rs11639856 rs1925153 rs3755652 rs11014166 rs11024074

Showing 20 of 38 · 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.