For researchers

Is your paper here?

2,673 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 20.

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Multiple Tissue Human Expression Resource (MUTHER) Consortium
Nature genetics · 2012 · PMID 22581228
8 pages
rs35747 rs4691380 rs2785980 rs1371614 rs13179048 rs6048205
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Cardiogenics · CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21378990
7 pages
rs12526453 rs17114036 rs3798220 rs3825807 rs1231206 rs12936587
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
Spanish Consortium on the Genetics of Coeliac Disease (CEGEC) · PreventCD Study Group and 1 more consortia
Nature genetics · 2011 · PMID 22057235 · open access
7 pages
rs10800746 rs61579022 rs2030519 rs13132308 rs55743914 rs11875687
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
rs6692219 rs11971186 rs1937455 rs6738833 rs13026471 rs6883351
Genome-wide association study identifies 48 common genetic variants associated with handedness
Nature human behaviour · 2021 · PMID 32989287
7 pages
rs62036618 rs35551703 rs66479618 rs1422070 rs11168884 rs2040498
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
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
rs182052 rs2980879 rs6488898 rs2590838 rs4805885 Adiponectin Levels
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
UK Brain Expression Consortium (UKBEC) · OxGSK Consortium
The Lancet. Respiratory medicine · 2015 · PMID 26423011 · open access
6 pages
rs4372354 rs2047409 rs9274600 rs2532349 rs61784651 rs11729080
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
ExomeBP Consortium · MAGIC Consortium and 1 more consortia
Nature genetics · 2018 · PMID 29632382 · open access
6 pages
rs16826069 rs1127787 rs7572857 rs2233580 rs56200889 rs35658696
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
6 pages
rs56381411 rs3784634 rs5400 rs17853166 rs75619922 rs7225887
Genome-wide association analysis identifies 20 loci that influence adult height
Diabetes Genetics Initiative · Wellcome Trust Case Control Consortium and 1 more consortia
Nature genetics · 2008 · PMID 18391952
5 pages
rs6060373 rs1390401 rs6724465 rs2814993 rs2282978
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways
WTCCC
Diabetes · 2010 · PMID 20858683 · open access
5 pages
rs1799884 rs1046896 rs6474359 rs7998202 Type 2 Diabetes
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs6015450 rs11191548 rs7129220 rs1173771 rs13139571
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Myocardial Infarction Genetics Consortium · Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19198609
4 pages
rs1746048 rs6725887 rs1122608 Coronary Artery Disease
Genome-wide association study identifies eight loci associated with blood pressure
Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19430483 · open access
4 pages
rs12946454 rs1530440 rs16948048 rs17367504
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
Genetic Factors for Osteoporosis (GEFOS) Consortium
Nature genetics · 2009 · PMID 19801982 · open access
4 pages
rs7524102 rs7932354 rs11898505 Spine Bone Mineral Density
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
DIAGRAM Consortium · GIANT Consortium and 3 more consortia
Nature genetics · 2010 · PMID 20081858 · open access
4 pages
rs11920090 rs7944584 rs11605924 Fasting Blood Glucose
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis
Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate · Wellcome Trust Case Control Consortium
Nature genetics · 2012 · PMID 23143596 · open access
4 pages
rs13397 rs13426947 rs59466457 rs2834512
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci
International Genetics of Ankylosing Spondylitis Consortium (IGAS) · Australo-Anglo-American Spondyloarthritis Consortium (TASC) and 4 more consortia
Nature genetics · 2013 · PMID 23749187
4 pages
rs10045403 rs17765610 rs35164067 Ankylosing Spondylitis
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
4 pages
rs10908557 rs6885307 rs2347867 rs2721195

Showing 20 of 97 · page 3 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.