For researchers

Is your paper here?

2,677 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.

33 matches for He B, showing the first 13.

Variation in TAS2R receptor genes explains differential bitterness of two common antibiotics
Frontiers in genetics · 2022 · PMID 35967977 · open access
2 pages
Chronic Rhinosinusitis and the Bitter Taste Receptor One Gene, Three Answers: What TAS2R38 Decides
DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease
Proceedings of the National Academy of Sciences of the United States of America · 2008 · PMID 18667698
1 page
Blood Cell Counts
Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study
American journal of human genetics · 2009 · PMID 19185284
1 page
rs12272004
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness
PLoS genetics · 2010 · PMID 20485516 · open access
1 page
rs12447690
Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene
Psychiatric genetics · 2013 · PMID 23142968
1 page
rs7527939
Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials
BEYOND and BENEFIT Study Groups
Multiple sclerosis (Houndmills, Basingstoke, England) · 2019 · PMID 29521573
1 page
rs2454138
Meta-analysis of genome-wide association studies and functional assays decipher susceptibility genes for gastric cancer in Chinese populations
Gut · 2020 · PMID 31383772
1 page
rs10029005
Genetic variation in the body mass index of adult survivors of childhood acute lymphoblastic leukemia: A report from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort
Cancer · 2021 · PMID 33048379
1 page
rs62123082
Association of Variants Near the Bradykinin Receptor B<sub>2</sub> Gene With Angioedema in Patients Taking ACE Inhibitors
Journal of the American College of Cardiology · 2021 · PMID 34384552
1 page
rs34485356
Performance of the Use of Genetic Information to Assess the Risk of Colorectal Cancer in the Basque Population
Cancers · 2022 · PMID 36077729 · open access
1 page
rs541295
Identification of the BTN3A3 Gene as a Molecule Implicated in Generalized Pustular Psoriasis in a Chinese Population
The Journal of investigative dermatology · 2023 · PMID 36804966
1 page
rs148755083
Polygenic influences on the behavioral effects of alcohol withdrawal in a mixed-ancestry population from the collaborative study on the genetics of alcoholism (COGA)
Molecular and cellular neurosciences · 2023 · PMID 37031923
1 page
rs2093374
Genome-wide meta-analysis in lichen sclerosus identifies 14 genomic risk loci
The British journal of dermatology · 2026 · PMID 41850335 · open access
1 page
rs6887783

Showing 13 of 33 · page 2 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.