Thomas Geuens

Molecular Defects in the Motor Adaptor BICD2 Cause Proximal Spinal Muscular Atrophy with Autosomal-Dominant Inheritance

Ivan Litvinenko, Bob Asselbergh, Leonardo Almeida‐Souza et al. · The American Journal of Human Genetics · 2013 · 137 citations · Full text

Kinesiology, Mendelian Disorder, Genetic Disorder +5

Recessive mutations in<i>SLC13A5</i>result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia

Katia Hardies, Carolien G. F. de Kovel, Sarah Weckhuysen et al. · Brain · 2015 · 111 citations · Full text

Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel Mutations

Andoni Echaniz‐Laguna, Thomas Geuens, Philippe Petiot et al. · Human Mutation · 2017 · 69 citations

Genetics, Neurochemical Biomarkers, Disease Gene Identification +17

Thiol-ene cross-linked alginate hydrogel encapsulation modulates the extracellular matrix of kidney organoids by reducing abnormal type 1a1 collagen deposition

Thomas Geuens, Floor A.A. Ruiter, Anika Schumacher et al. · Biomaterials · 2021 · 65 citations · Full text

Molecular Chaperones in the Pathogenesis of Amyotrophic Lateral Sclerosis: The Role of HSPB1

Simona Capponi, Thomas Geuens, Alessandro Geroldi et al. · Human Mutation · 2016 · 59 citations · Full text

Neurodegenerative Diseases, Molecular Chaperones, Amyotrophic Lateral Sclerosis +14