Thomas Voit

Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1

Aruto Yoshida, Kazuhiro Kobayashi, Hiroshi Manya et al. · Developmental Cell · 2001 · 707 citations · Full text

Mendelian Disorder, Neuronal Migration Disorder, Genetic Disorder +8

Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan

Martin Brockington, Derek J. Blake, Paola Prandini et al. · The American Journal of Human Genetics · 2001 · 596 citations · Full text

Mendelian Disorder, Abnormal Glycosylation, Medicine +10

G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex

Xianhua Piao, R. Sean Hill, Adria Bodell et al. · Science · 2004 · 519 citations

Developmental Cognitive Neuroscience, Cellular Neurobiology, Social Sciences +16

Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

Marina Raffaele di Barletta, Enzo Ricci, Giuliana Galluzzi et al. · The American Journal of Human Genetics · 2000 · 411 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +7

Lack of myostatin results in excessive muscle growth but impaired force generation

Helge Amthor, Raymond Macharia, Roberto Navarrete et al. · Proceedings of the National Academy of Sciences · 2007 · 402 citations · Full text

Mechanobiology, Muscle Physiology, Muscle Function +15