T. Grimm
Karlsruhe Institute of Technology(DE)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Diverse Scientific and Economic Studies, Human auditory perception and evaluation, Retinal Diseases and Treatments, Mitochondrial Function and Pathology
Most-Cited Works
- → A Comprehensive Survey of Sequence Variation in the ABCA4 (ABCR) Gene in Stargardt Disease and Age-Related Macular Degeneration(2000)337 cited
- Genetic risks for children of women with myotonic dystrophy.(1991)
- → Sleep position classification from a depth camera using Bed Aligned Maps(2016)66 cited
- → A large german kindred with cold‐aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene(2007)22 cited
- → Identification of a novel mutation in the arginine vasopressin-neurophysin II gene in familial central diabetes insipidus(2002)20 cited
- → Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases.(1996)11 cited
- Mutations in severe hemophilia A: distribution within the factor VIII gene, origin and influence on inhibitor development.(1997)
- → Die X-chromosomal-rezessive Lymphoproliferative Erkrankung (XLP): Molekulargenetische Untersuchungen(1995)3 cited
- → Paramyotonia congenita and myotonic dystrophy are not allelic disorders(1989)1 cited
- → New Editors, Features and Procedures(1989)