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.

63 matches for Easton D, showing the first 20.

Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Breast and Ovarian Cancer Susceptibility Collaboration · Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON) and 3 more consortia
Nature genetics · 2013 · PMID 23535729
12 pages+
rs204247 rs720475 rs11780156 rs11199914 rs1436904 rs3903072
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
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
BOCS · kConFab Investigators and 3 more consortia
Nature genetics · 2015 · PMID 25751625 · open access
12 pages+
rs2012709 rs12048493 rs72755295 rs4593472 rs13267382 rs745570
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
Association analysis identifies 65 new breast cancer risk loci
NBCS Collaborators · ABCTB Investigators and 1 more consortia
Nature · 2017 · PMID 29059683 · open access
12 pages+
rs72814839 rs72765759 rs111605422 rs185004002 rs970821 rs3821902
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+
rs9891146 rs13447324 rs5758651 rs34149579 rs12236219 rs284860
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Profile Study · Australian Prostate Cancer BioResource (APCB) and 7 more consortia
Nature genetics · 2018 · PMID 29892016
12 pages+
rs4962416 rs684232 rs182314334 rs2121875 rs17021918 rs11859370
Discovery of common and rare genetic risk variants for colorectal cancer
Nature genetics · 2019 · PMID 30510241 · open access
12 pages+
rs12144319 rs116353863 rs117079142 rs11884596 rs12708491 rs4901473
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium and 8 more consortia
Nature genetics · 2019 · PMID 30778226 · open access
12 pages+
rs10494217 rs1051860 rs141845046 rs145878042 rs1715919 rs62266958
Association analyses identify 31 new risk loci for colorectal cancer susceptibility
PRACTICAL consortium
Nature communications · 2019 · PMID 31089142 · open access
12 pages+
rs61336918 rs77776598 rs16969681 rs75686861 rs10849438 rs12143541
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
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+
rs6925777 rs7136086 rs10164550 rs1598656 rs142058842 rs7402990
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
GenoMEL Consortium · Q-MEGA and QTWIN Investigators and 7 more consortia
Nature genetics · 2020 · PMID 32341527 · open access
12 pages+
rs75883022 rs79356439 rs72834823 rs12523094 rs593179 rs117648907
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
Nature genetics · 2021 · PMID 33398198 · open access
12 pages+
rs2018336 rs2038542 rs10412482 rs7618603 rs2074840 rs2672843
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
Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci
NBCS Investigators
Breast cancer research : BCR · 2022 · PMID 35414113 · open access
12 pages+
rs4980383 rs10995187 rs10087804 rs9397436 rs3819405 rs34066050
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+
rs1551728 rs16832694 rs16942312 rs17093810 rs6666757 rs2032289
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
12 pages+
rs10886810 rs1037137 rs11892008 rs6151589 rs4713343 rs78416326
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
GIANT Consortium
Nature genetics · 2010 · PMID 21102462
11 pages
rs1364063 rs4840086 rs9939609 rs10980926 rs7642134 rs17188434
A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer
Breast and Prostate Cancer Cohort Consortium (BPC3) · PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25217961 · open access
10 pages
rs1041449 rs17599629 rs9287719 rs56232506 rs17694493 rs76934034

Showing 20 of 63 · page 1 of 4

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.