| Huntington disease in the South African population occurs on diverse and ethnically distinct genetic haplotypes FK Baine, C Kay, ME Ketelaar, JA Collins, A Semaka, CN Doty, A Krause, ... European Journal of Human Genetics 21 (10), 1120-1127, 2013 | 73 | 2013 |
| The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population C Kay, JA Collins, GEB Wright, F Baine, Z Miedzybrodzka, F Aminkeng, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 …, 2018 | 69 | 2018 |
| The frequency of Huntington disease and Huntington disease-like 2 in the South African population FK Baine, A Krause, LJ Greenberg Neuroepidemiology 46 (3), 198-202, 2016 | 34 | 2016 |
| A comprehensive haplotype-targeting strategy for allele-specific HTT suppression in Huntington disease C Kay, JA Collins, NS Caron, L de Andrade Agostinho, H Findlay-Black, ... The American Journal of Human Genetics 105 (6), 1112-1125, 2019 | 26 | 2019 |
| Duplication of the Asymmetric Leaves1/Rough Sheath 2/Phantastica (ARP) gene precedes the explosive radiation of the Ruschioideae N Illing, C Klak, C Johnson, D Brito, N Negrao, F Baine, V van Kets, ... Development Genes and Evolution 219, 331-338, 2009 | 13 | 2009 |
| A study of Huntington disease-like syndromes in black South African patients reveals a single SCA2 mutation and a unique distribution of normal alleles across five repeat loci FK Baine, N Peerbhai, A Krause Journal of the neurological sciences 390, 200-204, 2018 | 11 | 2018 |
| Tracing the mutated HTT and haplotype of the African ancestor who spread Huntington disease into the Middle East F Squitieri, T Mazza, S Maffi, A De Luca, Q AlSalmi, S AlHarasi, JA Collins, ... Genetics in Medicine 22 (11), 1903-1908, 2020 | 8 | 2020 |
| A probable cis-acting genetic modifier of Huntington disease frequent in individuals with African ancestry J Dawson, FK Baine-Savanhu, M Ciosi, A Maxwell, DG Monckton, ... Human Genetics and Genomics Advances 3 (4), 2022 | 5 | 2022 |
| Implications of direct-to-consumer whole-exome sequencing in South Africa Z Lombard, F Baine, A Krause, A Lochan, S Macaulay, C Spencer, ... SAMJ: South African Medical Journal 106 (2), 139-140, 2016 | 2 | 2016 |
| Identification of a suitable SNP for allele-specific silencing of the disease-causing gene in SCA1 patients in South Africa FK Baine | 1 | 2010 |
| and Amanda Krause J Dawson, FK Baine-Savanhu, M Ciosi, A Maxwell, DG Monckton | | 2022 |
| C03 A CIS-acting modifier of age at diagnosis of huntington disease in black south african patients J Levesley, F Baine, M Ciosi, A Maxwell, DG Monckton, A Krause Journal of Neurology, Neurosurgery & Psychiatry 89 (Suppl 1), A27-A28, 2018 | | 2018 |
| J11 Investigating phenocopies in a cohort of south african patients with a huntington’s disease-like phenotype FK Baine, A Krause Journal of Neurology, Neurosurgery & Psychiatry 87 (Suppl 1), A79-A79, 2016 | | 2016 |
| Huntington disease phenocopies or misdiagnosis: A black South African cohort FK Baine, A Krause MOVEMENT DISORDERS 31, S353-S353, 2016 | | 2016 |
| J38 Disease-associated Htt Haplotypes In The South African Population FK Baine, C Kay, M Ketelaar, J Collins, A Krause, LJ Greenberg, ... Journal of Neurology, Neurosurgery & Psychiatry 85 (Suppl 1), A77-A78, 2014 | | 2014 |
