For researchers

Is your paper here?

2,663 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.

14 matches for Campbell P.

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
CHD Exome+ Consortium · EPIC-CVD Consortium and 9 more consortia
Nature genetics · 2018 · PMID 29273807 · open access
12 pages+
rs5758651 rs34149579 rs12236219 rs284860 rs1131877 rs2277598
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
Lifelines Cohort Study
Nature communications · 2018 · PMID 30367059 · open access
12 pages+
rs4445669 rs9298749 rs10957494 rs77819282 rs1045476 rs28502438
Discovery of common and rare genetic risk variants for colorectal cancer
Nature genetics · 2019 · PMID 30510241 · open access
12 pages+
rs116353863 rs117079142 rs11884596 rs12708491 rs4901473 rs6469654
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+
rs117042741 rs35564340 rs1919364 rs11108175 rs78341008 rs9983528
Whole-genome sequence-based analysis of thyroid function
UK0K Consortium
Nature communications · 2015 · PMID 25743335 · open access
7 pages
rs12410532 rs310763 rs6923866 rs3008034 rs112817873 rs11103377
Large-Scale Genome-Wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer
Gastroenterology · 2019 · PMID 30529582
6 pages
rs7542665 rs201395236 rs113569514 rs3830041 rs77969132 rs1886450
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Gut · 2021 · PMID 33632709 · open access
5 pages
rs73161913 rs62131228 rs6014965 rs61975764 rs80158569
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 with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes
European journal of human genetics : EJHG · 2016 · PMID 26014426 · open access
3 pages
rs117145500 rs11031005 rs1641549
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Journal of the National Cancer Institute · 2019 · PMID 29917119
3 pages
rs10911251 rs3824999 rs17094983
Genome-wide association studies and Mendelian randomization analyses provide insights into the causes of early-onset colorectal cancer
Colorectal Transdisciplinary (CORECT) Study, the Colon Cancer Family Registry (CCFR), Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO)
Annals of oncology : official journal of the European Society for Medical Oncology · 2024 · PMID 38408508 · open access
3 pages
rs2427291 rs10808556 rs12427378
Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms
Nature communications · 2015 · PMID 25849990 · open access
2 pages
rs12339666 Myeloproliferative Neoplasms
Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis
Colon Cancer Family Registry and the Genetics and Epidemiology of Colorectal Cancer Consortium
Gastroenterology · 2013 · PMID 23266556
1 page
rs11903757
Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3
European journal of endocrinology · 2021 · PMID 34524976
1 page
rs12687280

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.