Associated Papers
Structure-function analysis of enterovirus protease 2A in complex with its essential host factor SETD3.
Peters CE et al.
Nature Communications, 2022
The role of CDHR3 in susceptibility to otitis media.
Hirsch SD et al.
Journal of Molecular Medicine (berlin, Germany), 2021
Genetic determinants of host immunity against human rhinovirus infections.
Lamborn IT et al.
Human Genetics, 2020
Genetic susceptibility to severe childhood asthma and rhinovirus-C maintained by balancing selection in humans for 150 000 years.
O'Neill MB et al.
Human Molecular Genetics, 2020
Phenome-wide association studies across large population cohorts support drug target validation.
Diogo D et al.
Nature Communications, 2018
Mutation analysis of adenomas and carcinomas of the colon: Early and late drivers.
Wolff RK et al.
Genes, Chromosomes & Cancer, 2018
Cadherin-related Family Member 3 Genetics and Rhinovirus C Respiratory Illnesses.
Bønnelykke K et al.
American Journal of Respiratory and Critical Care Medicine, 2018
Reduced CDHR3 expression in children wheezing with rhinovirus.
Stenberg Hammar K et al.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology, 2018
An integrative functional genomics framework for effective identification of novel regulatory variants in genome-phenome studies.
Zhao J et al.
Genome Medicine, 2018
Genetic association of the functional CDHR3 genotype with early-onset adult asthma in Japanese populations.
Kanazawa J et al.
Allergology International : Official Journal of the Japanese Society of Allergology, 2017
Detection and interpretation of shared genetic influences on 42 human traits.
Pickrell JK et al.
Nature Genetics, 2016
Cadherin-related family member 3, a childhood asthma susceptibility gene product, mediates rhinovirus C binding and replication.
Bochkov YA et al.
Proceedings of the National Academy of Sciences of the United States of America, 2015
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
Nicotine and oxidative stress induced exomic variations are concordant and overrepresented in cancer-associated genes.
Bavarva JH et al.
Oncotarget, 2014
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations.
Bønnelykke K et al.
Nature Genetics, 2014
Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemia.
Sheehan VA et al.
Plos One, 2014