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| Immune and viral correlates of “secondary viral control” after treatment interruption in chronically HIV-1 infected patients E Van Gulck, L Bracke, L Heyndrickx, S Coppens, D Atkinson, C Merlin, ... PLoS One 7 (5), e37792, 2012 | 53 | 2012 |
| Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach M Zimoń, E Battaloğlu, Y Parman, S Erdem, J Baets, E De Vriendt, ... neurogenetics 16, 33-42, 2015 | 46 | 2015 |
| Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole … D Kancheva, D Atkinson, P De Rijk, M Zimon, T Chamova, V Mitev, ... Genetics in Medicine 18 (6), 600-607, 2016 | 43 | 2016 |
| Human Rab7 mutation mimics features of Charcot–Marie–Tooth neuropathy type 2B in Drosophila K Janssens, S Goethals, D Atkinson, B Ermanoska, E Fransen, ... Neurobiology of disease 65, 211-219, 2014 | 41 | 2014 |
| MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability E Ylikallio, R Woldegebriel, M Tumiati, P Isohanni, MM Ryan, Z Stark, ... Brain 140 (8), 2093-2103, 2017 | 39 | 2017 |
| Efficient In Vitro Expansion of Human Immunodeficiency Virus (HIV)-Specific T-Cell Responses by gag mRNA-Electroporated Dendritic Cells from Treated and … ER Van Gulck, G Vanham, L Heyndrickx, S Coppens, K Vereecken, ... Journal of virology 82 (7), 3561-3573, 2008 | 35 | 2008 |
| Pontocerebellar hypoplasia type 1 for the neuropediatrician: Genotype–phenotype correlations and diagnostic guidelines based on new cases and overview of the literature I Ivanov, D Atkinson, I Litvinenko, L Angelova, S Andonova, H Mumdjiev, ... European Journal of Paediatric Neurology 22 (4), 674-681, 2018 | 30 | 2018 |
| Polyelectrolyte capsules-containing HIV-1 p24 and poly I: C modulate dendritic cells to stimulate HIV-1-specific immune responses W De Haes, S De Koker, C Pollard, D Atkinson, E Vlieghe, J Hoste, ... Molecular Therapy 18 (7), 1408-1416, 2010 | 26 | 2010 |
| Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity A Kurolap, F Kreuder, C Gonzaga-Jauregui, MP Duvdevani, T Harel, ... The American Journal of Human Genetics 109 (3), 518-532, 2022 | 12 | 2022 |
| Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family S Tey, N Shahrizaila, AP Drew, S Samulong, KJ Goh, E Battaloglu, ... neurogenetics 20, 117-127, 2019 | 12 | 2019 |
| Tyrosyl-tRNA synthetase has a noncanonical function in actin bundling B Ermanoska, B Asselbergh, L Morant, ML Petrovic-Erfurth, ... Nature communications 14 (1), 999, 2023 | 9 | 2023 |
| Interleukin‐12p70 Expression by Dendritic Cells of HIV‐1‐Infected Patients Fails to Stimulate gag‐Specific Immune Responses E Van Gulck, N Cools, D Atkinson, L Bracke, K Vereecken, M Vekemans, ... Journal of Immunology Research 2012 (1), 184979, 2012 | 8 | 2012 |
| Genetic survey of autosomal recessive peripheral neuropathy cases unravels high genetic heterogeneity in a Turkish cohort A Candayan, A Çakar, G Yunisova, AN Özdağ Acarlı, D Atkinson, ... Neurology: Genetics 7 (5), e621, 2021 | 4 | 2021 |
| Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole … D Kancheva, D Atkinson, P De Rijk, M Zimon, T Chamova, V Mitev, ... GENETICS IN MEDICINE 18 (1), 108-108, 2016 | 1 | 2016 |
| Stimulation of antiviral cellular immune responses by therapeutic vaccination of HIV-1-infected patients with dendritic cells transfected with gag, tat, rev and nef mRNA E Van Gulck, VF Van Tendeloo, E Vlieghe, M Vekemans, A Van de Velde, ... Retrovirology 8, 1-2, 2011 | 1 | 2011 |
| Alternative splicing expands the clinical spectrum of NDUFS6-related mitochondrial disorders C Armirola-Ricaurte, N Zonnekein, G Koutsis, S Amor-Barris, ... Genetics in Medicine 26 (6), 101117, 2024 | | 2024 |
| Bi-allelic variants in the neuronal cell adhesion molecule NRCAM lead to a novel neurodevelopmental disorder characterized by developmental delay, hypotonia, peripheral … A Kurolap, F Kreuder, C Gonzaga-Jauregui, MP Duvdevani, T Harel, ... Springer, 2023 | | 2023 |
| Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort (vol 7, e621, 2021) A Candayan, cakar, Arman, G Yunisova, ozdag Acarli, Ayse Nur, ... NEUROLOGY-GENETICS 8 (1), 2022 | | 2022 |
| Identification of novel causal genes for autosomal recessive Charcot-Marie-Tooth neuropathies D Atkinson University of Antwerp, 2018 | | 2018 |
