T Strachan
Comenius University Bratislava(SK)
Publications by Year
Research Areas
Neurofibromatosis and Schwannoma Cases, Meningioma and schwannoma management, Sexual Differentiation and Disorders, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Pluripotent Stem Cells Research
Most-Cited Works
- → Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family(1997)925 cited
- → A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity.(1992)466 cited
- → Keratin 16 and keratin 17 mutations cause pachyonychia congenita(1995)353 cited
- → SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development(2000)330 cited
- → Genotype/phenotype correlations in type 2 neurofibromatosis (NF2): evidence for more severe disease associated with truncating mutations.(1998)222 cited
- → A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p(1994)194 cited
- → Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determination(1999)176 cited
- → A genetic study of type 2 neurofibromatosis in the United Kingdom. II. Guidelines for genetic counselling.(1992)167 cited
- → Complete nucleotide sequence of a gene encoding a functional human class I histocompatibility antigen (HLA-CW3).(1984)158 cited
- → ATP2A2 Mutations in Darier's Disease: Variant Cutaneous Phenotypes Are Associated with Missense Mutations, But Neuropsychiatry Features Are Independent of Mutation Class(1999)142 cited