For researchers

Is your paper here?

2,676 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.

35 matches for Day F, showing the first 20.

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Nature genetics · 2013 · PMID 23563607 · open access
12 pages+
rs10182181 rs1412239 rs1421085 rs538656 rs1514177 rs3101336
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Australian Ovarian Cancer Study · GENICA Network and 4 more consortia
Nature · 2014 · PMID 25231870 · open access
12 pages+
rs2274465 rs6747380 rs6758290 rs4369815 rs17236969 rs17233066
Defining the role of common variation in the genomic and biological architecture of adult human height
Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25282103 · open access
12 pages+
rs6137287 rs9993613 rs3020418 rs3767627 rs7692995 rs17556750
New genetic loci link adipose and insulin biology to body fat distribution
ADIPOGen Consortium · CARDIOGRAMplusC4D Consortium and 11 more consortia
Nature · 2015 · PMID 25673412 · open access
12 pages+
rs6556079 rs2377058 rs3805389 rs4081724 rs459193 rs7830933
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 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
Elucidating the genetic architecture of reproductive ageing in the Japanese population
Nature communications · 2018 · PMID 29773799 · open access
12 pages+
rs9393800 rs707938 rs1799949 rs291269 rs1516883 rs144048300
Elucidating the genetic basis of social interaction and isolation
Nature communications · 2018 · PMID 29970889 · open access
12 pages+
rs74338595 rs10992800 rs12472555 rs111610257 rs36030660 rs139920
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
23andMe Research Team · COGENT (Cognitive Genomics Consortium) and 1 more consortia
Nature genetics · 2018 · PMID 30038396
12 pages+
rs76077165 rs76241163 rs10800624 rs11201507 rs12772959 rs16846735
Genome-wide association study for risk taking propensity indicates shared pathways with body mass index
Communications biology · 2018 · PMID 30271922 · open access
12 pages+
rs62519827 rs9841382 rs6923811 rs7817124 rs4653015 rs283914
Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors
JAMA · 2018 · PMID 30575882
12 pages+
rs13154197 rs1876829 rs7122422 rs10512606 rs4849294 rs1316979
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+
rs9366778 rs10734564 rs10221267 rs1724889 rs2168443 rs4579095
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
23andMe Research Team
Nature communications · 2019 · PMID 31649266 · open access
12 pages+
rs11246003 rs7412010 rs149934734 rs35417544 rs62323682 rs4821939
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+
rs73212896 rs59194935 rs750062 rs77432559 rs10738700 rs78087596
Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan
PRACTICAL Consortium · 23andMe Research Team
Nature communications · 2020 · PMID 32210231 · open access
12 pages+
rs10164550 rs1598656 rs142058842 rs7402990 rs2222746 rs6589961
Genetic analyses identify widespread sex-differential participation bias
FinnGen Study · 23andMe Research Team and 1 more consortia
Nature genetics · 2021 · PMID 33888908
12 pages+
rs35883430 rs1175109 rs10894757 rs10468986 rs6968125 rs114328297
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour
eQTLGen Consortium · BIOS Consortium and 1 more consortia
Nature human behaviour · 2021 · PMID 34211149 · open access
12 pages+
rs7987501 rs10445366 rs7785195 rs11887646 rs10955084 rs7516843
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
Physical and neurobehavioral determinants of reproductive onset and success
Nature genetics · 2016 · PMID 27089180
10 pages
rs1040124 rs12522910 rs4840367 rs658385 rs2248699 rs538498277
Assessing the causal association of glycine with risk of cardio-metabolic diseases
Nature communications · 2019 · PMID 30837465 · open access
8 pages
rs62051533 rs13299380 rs62202111 rs9923732 rs9862438 rs12297321

Showing 20 of 35 · 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.