For researchers

Is your paper here?

2,662 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.

45 matches for Houlston 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
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+
rs2004038 rs34878803 rs13213986 rs7383287 rs11632038 rs116826541
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
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Nature genetics · 2023 · PMID 36539618
12 pages+
rs7859362 rs4675253 rs6434979 rs4236382 rs10751097 rs10978941
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 pages+
rs6574106 rs6916760 rs4506680 rs114427493 rs12274095 rs57551109
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
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors
GliomaScan Consortium
Nature genetics · 2017 · PMID 28346443
10 pages
rs12752552 rs3751667 rs11233250 rs2235573 rs4252707 rs12076373
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma
Nature communications · 2016 · PMID 27363682 · open access
9 pages
rs34229995 rs7193541 rs7577599 rs6599192 rs34562254 rs139402
Deciphering the genetics and mechanisms of predisposition to multiple myeloma
Nature communications · 2024 · PMID 39103364 · open access
9 pages
rs3731222 rs6090899 rs75712673 rs9386514 rs9856633 rs7621631
Identification of 19 new risk loci and potential regulatory mechanisms influencing susceptibility to testicular germ cell tumor
UK Testicular Cancer Collaboration · PRACTICAL Consortium
Nature genetics · 2017 · PMID 28604728
8 pages
rs6821144 rs17021463 rs17153755 rs7315956 rs1009647 rs11071896
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 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
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
PRACTICAL consortium
Nature communications · 2018 · PMID 30213928 · open access
5 pages
rs4325816 rs6595443 rs17507636 rs58618031 Multiple Myeloma
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
rs10901793 rs71467682 rs75031349 rs137884934 rs682888
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
COGENT Consortium · CORGI Consortium and 2 more consortia
Nature genetics · 2010 · PMID 20972440 · open access
4 pages
rs6687758 rs4925386 rs6691170 Colorectal Cancer
Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies
Clinical pharmacology and therapeutics · 2017 · PMID 27770449
4 pages
rs187976596 rs56249772 rs73726531 rs148222927
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
PRACTICAL consortium
Nature communications · 2017 · PMID 29196614 · open access
4 pages
rs9482849 rs3781093 Hodgkin Lymphoma Nodular Sclerosis Hodgkin Lymphoma
Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21
GliomaScan consortium
Scientific reports · 2018 · PMID 29743610 · open access
4 pages
rs55705857 rs2297440 rs634537 Glioma
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer
COGENT Study · Colorectal Cancer Association Study Consortium and 1 more consortia
Nature genetics · 2008 · PMID 19011631
3 pages
rs4444235 rs10411210 Colorectal Cancer
Genome-wide association study identifies five new breast cancer susceptibility loci
Breast Cancer Susceptibility Collaboration (UK)
Nature genetics · 2010 · PMID 20453838
3 pages
rs10995190 rs1011970 rs614367

Showing 20 of 45 · page 1 of 3

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.