Associated Papers
Genetic and Molecular Determinants of Familial Transmission of Skeletal Malocclusions.
Dehesa-Santos A et al.
Orthodontics & Craniofacial Research, 2025
Genetic architecture of non-syndromic skeletal class III malocclusion.
Zhou X et al.
Oral Diseases, 2023
Genetic screening in a Brazilian cohort with inborn errors of immunity.
Ferreira CS et al.
Bmc Genomic Data, 2023
The functional landscape of the human phosphoproteome.
Ochoa D et al.
Nature Biotechnology, 2020
Systematic analysis of the intersection of disease mutations with protein modifications.
Simpson CM et al.
Bmc Medical Genomics, 2019
OligoPVP: Phenotype-driven analysis of individual genomic information to prioritize oligogenic disease variants.
Boudellioua I et al.
Scientific Reports, 2018
Candidate gene analyses of 3-dimensional dentoalveolar phenotypes in subjects with malocclusion.
Weaver CA et al.
American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics, 2017
Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population.
Ostrowski J et al.
Scientific Reports, 2016
Patients with genetically heterogeneous synchronous colorectal cancer carry rare damaging germline mutations in immune-related genes.
Cereda M et al.
Nature Communications, 2016
Candidate Gene Analyses of Skeletal Variation in Malocclusion.
da Fontoura CS et al.
Journal of Dental Research, 2015
Identification of a Mutation in FGF23 Involved in Mandibular Prognathism.
Chen F et al.
Scientific Reports, 2015
Genetics of the dentofacial variation in human malocclusion.
Moreno Uribe LM et al.
Orthodontics & Craniofacial Research, 2015
A missense mutation in DUSP6 is associated with Class III malocclusion.
Nikopensius T et al.
Journal of Dental Research, 2013
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.
Miraoui H et al.
American Journal of Human Genetics, 2013