For researchers

Is your paper here?

2,661 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.

97 matches for Deloukas P, showing the first 17.

Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) and 2 more consortia
Molecular psychiatry · 2015 · PMID 25288136
2 pages
rs9902453 rs7800944
Genetic studies of body mass index yield new insights for obesity biology
LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
2 pages
rs16851483 rs2121279
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
rs9687065 rs1563788
Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study
Lancet (London, England) · 2008 · PMID 18455228 · open access
1 page
rs3736228
Variants in MTNR1B influence fasting glucose levels
Nature genetics · 2009 · PMID 19060907
1 page
rs560887
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Wellcome Trust Case Control Consortium · Genetic Investigation of ANthropometric Traits Consortium
Nature genetics · 2009 · PMID 19079261
1 page
rs10838738
Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies
Wellcome Trust Case Control Consortium · DCCT/EDIC Research Group and 2 more consortia
PloS one · 2009 · PMID 19587794 · open access
1 page
rs11153730
Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone
PLoS genetics · 2010 · PMID 21124946 · open access
1 page
rs1021188
A variant in MCF2L is associated with osteoarthritis
arcOGEN Consortium
American journal of human genetics · 2011 · PMID 21871595
1 page
rs11842874
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci
DIAGRAM · MuTHER
Nature genetics · 2011 · PMID 21874001
1 page
rs4812829
A genome-wide association search for type 2 diabetes genes in African Americans
DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
1 page
rs7560163
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
arcOGEN Consortium · arcOGEN Collaborators
Lancet (London, England) · 2012 · PMID 22763110 · open access
1 page
rs11177
Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis
LeishGEN Consortium · Wellcome Trust Case Control Consortium 2
Nature genetics · 2013 · PMID 23291585 · open access
1 page
rs9271858
Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease
WTCCC+
PloS one · 2013 · PMID 23593153 · open access
1 page
rs6730157
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
1 page
rs60780116
Genome-wide association study of circulating interleukin 6 levels identifies novel loci
CHARGE Inflammation Working Group
Human molecular genetics · 2021 · PMID 33517400 · open access
1 page
rs11265618
Genome-Wide association between EYA1 and Aspirin-induced peptic ulceration
EBioMedicine · 2021 · PMID 34864618 · open access
1 page
rs12678747

Showing 17 of 97 · page 5 of 5

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.