For researchers

Is your paper here?

2,676 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.

75 matches for Haiman CA, showing the first 15.

A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease
UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology · UK ProtecT Study Collaborators and 2 more consortia
Human molecular genetics · 2013 · PMID 23065704
1 page
rs11672691
Genome-wide association study of age at menarche in African-American women
Human molecular genetics · 2013 · PMID 23599027
1 page
rs10441737
Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A
Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO) · Colon Cancer Family Registry (CCFR) and 1 more consortia
Nature communications · 2014 · PMID 25105248 · open access
1 page
rs12241008
Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25
COLUMBUS Consortium
Nature communications · 2014 · PMID 25327703 · open access
1 page
rs140068132
Large-scale association analysis in Asians identifies new susceptibility loci for prostate cancer
Nature communications · 2015 · PMID 26443449 · open access
1 page
rs58262369
Benzene Uptake and Glutathione S-transferase T1 Status as Determinants of S-Phenylmercapturic Acid in Cigarette Smokers in the Multiethnic Cohort
PloS one · 2016 · PMID 26959369 · open access
1 page
rs6004031
Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer
Human molecular genetics · 2016 · PMID 28171663
1 page
rs12998806
Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans
Hispanic Colorectal Cancer Study
International journal of cancer · 2017 · PMID 28295283
1 page
rs7252505
A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 Diabetes
Diabetes Prevention Program Research Group · Broad Genomics Platform and 2 more consortia
Diabetes · 2017 · PMID 28838971 · open access
1 page
rs149483638
Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex
Blood advances · 2017 · PMID 29296818
1 page
rs11980379
Genetic analyses of diverse populations improves discovery for complex traits
Nature · 2019 · PMID 31217584
1 page
Obesity and Body Weight
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Leukemia · 2022 · PMID 36273105
1 page
rs9258807
Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry
European urology · 2023 · PMID 36872133
1 page
rs150947563
Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions
AOCS Group · OPAL Study Group and 1 more consortia
American journal of human genetics · 2024 · PMID 38723632
1 page
rs10810671
Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants That Confer Risk for Breast Cancer
Cancer research · 2024 · PMID 38832928
1 page
rs7580240

Showing 15 of 75 · page 4 of 4

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.