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.

32 matches for Jackson R, showing the first 20.

Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia
Nature communications · 2017 · PMID 28165464 · open access
12 pages+
rs58055674 rs34004493 rs3755397 rs7690934 rs9392504 rs2267708
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects
American journal of human genetics · 2018 · PMID 29304378
12 pages+
rs71569047 rs10450586 rs34406563 rs7112229 rs11606709 rs4647728
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
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Nature communications · 2020 · PMID 32439900 · open access
12 pages+
rs17099893 rs7803297 rs11214037 rs922000 rs3784192 rs3794809
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+
rs114876144 rs145437104 rs3134988 rs7575245 rs269781 rs4741016
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Nature communications · 2022 · PMID 36050321 · open access
12 pages+
rs17060733 rs13226149 rs1811677 rs55756479 rs1061056 rs12109259
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
rs6632109 rs8049403 rs2048528 rs1518760 rs78475244 rs76668186
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+
rs11570441 rs11656344 rs11030613 rs11769128 rs11955611 rs11991223
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
Nature communications · 2023 · PMID 36918541 · open access
12 pages+
rs72825047 rs11195260 rs10793848 rs2066626 rs2762049 rs55824920
Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations
PLoS genetics · 2017 · PMID 28498854 · open access
8 pages
rs115795127 rs7651190 rs11563582 rs62434120 rs113866309 rs76987554
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Nature genetics · 2012 · PMID 22504420 · open access
7 pages
rs163879 rs1864325 rs344081 rs3905706 rs1566045 rs7953528
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture
AOGC Consortium · UK10K Consortium
Nature · 2015 · PMID 26367794
7 pages
rs188303909 rs11024028 rs148771817 rs11692564 rs6542457 Spine Bone Mineral Density
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs12012576 rs139120857 rs5942972 rs7063103 rs62603531 rs151113194
Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma
Nature genetics · 2014 · PMID 25261932 · open access
5 pages
rs79480871 rs116446171 rs13255292 rs4733601 Diffuse Large B Cell Lymphoma
Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region
American journal of human genetics · 2014 · PMID 25279986
5 pages
rs12195582 rs4937362 rs17749561 rs13254990 Follicular Lymphoma
Genome-wide association study of colorectal cancer identifies six new susceptibility loci
Nature communications · 2015 · PMID 26151821
4 pages
rs11190164 rs35360328 rs812481 rs73208120
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
Nature genetics · 2009 · PMID 19648918
3 pages
rs505922 ABO Blood Group Pancreatic Cancer
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia
Nature genetics · 2013 · PMID 23770605 · open access
3 pages
rs13401811 rs17483466 rs11636802
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Journal of the National Cancer Institute · 2019 · PMID 29917119
3 pages
rs10911251 rs3824999 rs17094983

Showing 20 of 32 · 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.