Antoon Vandenberghe

Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse

Annachiara De Sandre‐Giovannoli, Malika Chaouch, Serguei Kozlov et al. · The American Journal of Human Genetics · 2002 · 542 citations · Full text

Neurodegenerative Diseases, Homozygous Defects, Molecular Neuroscience +8

Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability

Feng Zhang, Pavel Seeman, Pengfei Liu et al. · The American Journal of Human Genetics · 2010 · 161 citations · Full text

Genome Instability, Genetic Disorder, Genetics +8

Nucleotide sequence of a crustacean 18S ribosomal RNA gene and secondary structure of eukaryotic small subunit ribosoraal RNAs

L Nelles, Bao-Ling Fang, Guido Volckaert et al. · Nucleic Acids Research · 1984 · 142 citations · Full text

Conservation of secondary structure in 5 S ribosomal RNA : a uniform model for eukaryotic, eubacterial, archaebacterial and organelle sequences is energetically favourable

Rupert De Wächter, Min-Wei Chen, Antoon Vandenberghe · Biochimie · 1982 · 111 citations

Biology, S Ribosomal Rna, Natural Sciences +10

Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene

Eva Nelis, Vincent Timmerman, Peter De Jonghe et al. · Human Genetics · 1994 · 98 citations

Mendelian Disorder, Genetic Disorder, Medicine +11