For researchers

Is your paper here?

2,681 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.

81 matches for Hunter D, showing the first 20.

Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights
UROMOL Consortium
European urology · 2023 · PMID 37210288
4 pages
rs1414253 rs411482 rs4743687 rs17863783
Identification of ten loci associated with height highlights new biological pathways in human growth
Diabetes Genetics Initiative · FUSION and 4 more consortia
Nature genetics · 2008 · PMID 18391950
3 pages
rs4896582 rs1492820 rs10946808
A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation
PLoS genetics · 2008 · PMID 18483556 · open access
3 pages
rs8033165 rs12203592 Sun Sensitivity, Freckling and Skin Cancer Risk
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution
Wellcome Trust Case Control Consortium · Procardis Consortia and 1 more consortia
PLoS genetics · 2009 · PMID 19557161 · open access
3 pages
rs987237 rs7826222 rs2605100
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
Nature genetics · 2009 · PMID 19648918
3 pages
rs505922 ABO Blood Group Pancreatic Cancer
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
MAGIC
Nature genetics · 2010 · PMID 20935629
3 pages
rs1055144 rs6784615 rs6861681
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Nature communications · 2016 · PMID 26833246 · open access
3 pages
rs6738627 rs4788099 rs693839
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21
Oncotarget · 2016 · PMID 27579533 · open access
3 pages
rs10094872 rs35226131 Pancreatic Cancer
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Journal of the National Cancer Institute · 2019 · PMID 29917119
3 pages
rs10911251 rs3824999 rs17094983
Common variants of FUT2 are associated with plasma vitamin B12 levels
Nature genetics · 2008 · PMID 18776911
2 pages
FUT2 Secretor Status Vitamin B12
Genome-wide association study of tanning phenotype in a population of European ancestry
The Journal of investigative dermatology · 2009 · PMID 19340012
2 pages
rs35391 Eye Color and Pigmentation
Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels
Arteriosclerosis, thrombosis, and vascular biology · 2010 · PMID 20150558
2 pages
rs2115763 rs1834481
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
Nature genetics · 2010 · PMID 20972438 · open access
2 pages
rs8102137 rs798766
Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study
Journal of the National Cancer Institute · 2011 · PMID 21263130
2 pages
rs4973768 Breast Cancer
Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma
Human molecular genetics · 2011 · PMID 21700618
2 pages
rs12210050 rs7335046
Genome-wide association study identifies new prostate cancer susceptibility loci
Human molecular genetics · 2011 · PMID 21743057
2 pages
rs651164 rs902774
A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation
PLoS genetics · 2012 · PMID 22829776 · open access
2 pages
rs17496332 rs1573036
Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects
Annals of the rheumatic diseases · 2013 · PMID 22993228 · open access
2 pages
rs2187689 rs926849
A genome-wide association study of early menopause and the combined impact of identified variants
ReproGen Consortium
Human molecular genetics · 2013 · PMID 23307926 · open access
2 pages
rs1046089 Age at Menopause
Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohort
Circulation. Cardiovascular genetics · 2014 · PMID 24795349
2 pages
rs74019828 Telomere Length and Epigenetic Age Acceleration

Showing 20 of 81 · 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.