For researchers

Is your paper here?

2,671 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.

37 matches for Brennan P, 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+
rs16857609 rs6762644 rs9790517 rs6828523 rs204247 rs720475
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
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
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
SpiroMeta Consortium
Nature genetics · 2017 · PMID 28604730 · open access
12 pages+
rs13218875 rs34662244 rs67340775 rs2004038 rs34878803 rs13213986
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+
rs6904031 rs56387622 rs11624333 rs1895062 rs13294895 rs2223621
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 pages+
rs12113633 rs62169409 rs4140952 rs7629500 rs61758556 rs240471
Novel Association of Genetic Markers Affecting CYP2A6 Activity and Lung Cancer Risk
Cancer research · 2016 · PMID 27488534
10 pages
rs113029345 rs76935404 rs10425738 rs11878604 rs7247903 rs2316205
Genetic Analysis of Lung Cancer and the Germline Impact on Somatic Mutation Burden
ILCCO consortium
Journal of the National Cancer Institute · 2022 · PMID 35511172 · open access
7 pages
rs11571815 rs72905558 rs3129813 rs78062588 rs9258381 rs6457312
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations
Ovarian Cancer Association Consortium (OCAC) · PRACTICAL Consortium and 3 more consortia
Cancer research · 2016 · PMID 27197191
6 pages
rs11844632 rs4808075 rs56084662 rs11571833 rs186507655 rs148883465
Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
ABCTB Investigators · AOCS Study Group & Australian Cancer Study (Ovarian Cancer) and 5 more consortia
Cancer discovery · 2016 · PMID 27432226
6 pages
rs2628317 rs17762342 rs739704 rs3802173 rs1469713 rs9657608
Genome-wide association study identifies multiple risk loci for renal cell carcinoma
Nature communications · 2017 · PMID 28598434 · open access
6 pages
rs4381241 rs67311347 rs11813268 rs74911261 rs4903064 Renal Cell Carcinoma
Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma
Frontiers of medicine · 2021 · PMID 32889700
6 pages
rs465498 rs1200399 rs2517873 rs4573350 rs1264308 rs17038564
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 lung adenocarcinoma in East Asia and comparison with a European population
Nature communications · 2023 · PMID 37236969 · open access
5 pages
rs75031349 rs137884934 rs682888 rs10901793 rs71467682
Genome-wide association study reveals two new risk loci for bipolar disorder
Nature communications · 2014 · PMID 24618891
4 pages
rs12290811 rs17826816 rs12202969 rs6550435
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
Nature communications · 2018 · PMID 29422604 · open access
4 pages
rs13303010 rs1517037 rs4795218 rs2941471
Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights
UROMOL Consortium
European urology · 2023 · PMID 37210288
4 pages
rs4743687 rs17863783 rs1414253 rs411482
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia
Nature genetics · 2013 · PMID 23770605 · open access
3 pages
rs13401811 rs17483466 rs11636802
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer
Nature genetics · 2015 · PMID 26098869 · open access
3 pages
rs17688601 rs9854771 Pancreatic Cancer

Showing 20 of 37 · 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.