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Prof.dr. D. Lindhout

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Expertise Clinical genetics; Teratology; Epilepsy; Congenital anomaly; Congenital malformation; Antiepileptic drug; Seizures; Neurogenetics
Expertise (NL) Klinische genetica; Teratologie; Epilepsie; Congenitale anomalieën; Congenitale misvormingen; Anti-epileptica; Neurogenetica
Digital Author ID info:eu-repo/dai/nl/074039210
Addition Emeritus

Active as

Professor emeritus
Organisation Department of Medical Genetics (UU)
Chair (EN) Medical genetics
Chair (NL) Medische genetica

Publications

(the most recent at the top)
Genetic risk estimation by healthcare professionals
Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree
High rate of mosaicism in tuberous sclerosis complex
Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation
Maternal use of antiepileptic drugs and the risk of major congenital malformations: a joint European prospective study of human teratogenesis associated with maternal epilepsy.
All publications..

Completed research projects

(the most recent research is at the top)
Supervisor Molecular characterization of epilepsy by microarray analysis of gene expression in the human and rat hippocampus
Supervisor Preparing for breast cancer genetic counselling: Web-based education for counselees
Supervisor Clinical and genetic complexities of the generalized myoclonus epilepsies

Classification

D21400 Genetics
D21700 Physiology

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