Kris Van Den Bogaert, Dr.
Affiliations: | 2004 | Universiteit Antwerpen (Belgium) |
Area:
Genetics, AudiologyGoogle:
"Kris Van Den Bogaert"Parents
Sign in to add mentor| Paul Govaerts | grad student | 2004 | Universiteit Antwerpen (Belgium) | |
| (Genetic research on monogenic and complex forms of otosclerosis.) | ||||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Veyt N, Van Buggenhout G, Devriendt K, et al. (2024) Expanding the phenotype of copy number variations involving NR0B1 (DAX1). European Journal of Human Genetics : Ejhg |
| Parijs I, Brison N, Vancoillie L, et al. (2023) Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles. European Journal of Human Genetics : Ejhg |
| Hardcastle A, Berry AM, Campbell IM, et al. (2022) Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data. American Journal of Medical Genetics. Part A |
| Aerden M, Bauters M, Van Den Bogaert K, et al. (2020) Genotype-phenotype correlations of UBA2 mutations in patients with ectrodactyly. European Journal of Medical Genetics. 104009 |
| Muys J, Jacquemyn Y, Blaumeiser B, et al. (2020) Prenatally detected copy number variants in a national cohort: a postnatal follow-up study. Prenatal Diagnosis |
| Muys J, Blaumeiser B, Jacquemyn Y, et al. (2018) The BElgian PREnatal MicroArray (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations. Prenatal Diagnosis |
| Brady PD, Delle Chiaie B, Christenhusz G, et al. (2014) A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 469-76 |
| Declau F, Van den Bogaert K, Van De Heyning P, et al. (2007) Phenotype-genotype correlations in otosclerosis: clinical features of OTSC2. Advances in Oto-Rhino-Laryngology. 65: 114-8 |
| Thys M, Van Den Bogaert K, Iliadou V, et al. (2007) A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13-16.1. European Journal of Human Genetics : Ejhg. 15: 362-8 |
| Pauw RJ, De Leenheer EM, Van Den Bogaert K, et al. (2006) The phenotype of the first otosclerosis family linked to OTSC5. Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 27: 308-15 |