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L. Vits · SciRah

Researcher profile · Semantic Scholar

L. Vits

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L. Vits — researcher profile on SciRah

h-index: 20
Works: 38
Citations: 2,731

Most-cited papers

A point mutation in the FMR-1 gene associated with fragile X mental retardation
K. De Boulle, A. Verkerk, E. Reyniers, L. Vits +6 more
1993Nature Genetics636 citations
Semantic Scholar
The full mutation in the FMR–1 gene of male fragile X patients is absent in their sperm
E. Reyniers, L. Vits, K. De Boulle, B. V. van Roy +7 more
1993Nature Genetics269 citations
Semantic Scholar
CRASH Syndrome: Clinical Spectrum of Corpus Callosum Hypoplasia, Retardation, Adducted Thumbs, Spastic Paraparesis and Hydrocephalus Due to Mutations in One Single Gene, L1
E. Fransen, V. Lemmon, G. Van Camp, L. Vits +2 more
1995European Journal of Human Genetics236 citations
Semantic Scholar
L1-associated diseases: clinical geneticists divide, molecular geneticists unite.
Erik Fransen, G. Van Camp, L. Vits, P. Willems
1997Human Molecular Genetics212 citations Open access
Semantic Scholar
Positional cloning of a gene involved in hereditary multiple exostoses.
W. Wuyts, W. Van Hul, J. Wauters, M. Nemtsova +18 more
1996Human Molecular Genetics194 citations
Semantic Scholar
Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm.
G. Jansen, P. J. Willems, M. Coerwinkel, Willy M. Nillesen +5 more
1994American Journal of Human Genetics181 citations
Semantic Scholar
MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM
L. Vits, G. Camp, P. Coucke, E. Fransen +9 more
1994Nature Genetics157 citations
Semantic Scholar
Genotype-phenotype correlation in L1 associated diseases.
Erik Fransen, G. Van Camp, R. D'Hooge, L. Vits +1 more
1998Journal of Medical Genetics104 citations Open access
Semantic Scholar
A duplication in the L1CAM gene associated with X–linked hydrocephalus
G. Van Camp, L. Vits, P. Coucke, S. Lyonnet +5 more
1993Nature Genetics97 citations
Semantic Scholar
The clinical spectrum of mutations in L1, a neuronal cell adhesion molecule.
Erik Fransen, L. Vits, G. Van Camp, P. Willems
1996American journal of medical genetics88 citations
Semantic Scholar
X-linked hydrocephalus and MASA syndrome present in one family are due to a single missense mutation in exon 28 of the L1CAM gene.
Erik Fransen, C. Schrander-Stumpel, L. Vits, P. Coucke +2 more
1994Human Molecular Genetics69 citations
Semantic Scholar
Assignment of X-linked hydrocephalus to Xq28 by linkage analysis.
P. Willems, I. Dijkstra, B. J. Van der Auwera, L. Vits +11 more
1990Genomics67 citations
Semantic Scholar
Segregation of the fragile X mutation from an affected male to his normal daughter.
Patrick J. Willems, B. V. van Roy, K. De Boulle, L. Vits +5 more
1992Human Molecular Genetics59 citations
Semantic Scholar
A locus‐specific mutation database for the neural cell adhesion molecule L1CAM (Xq28)
G. Van Camp, E. Fransen, L. Vits, G. Raes +1 more
1996Human Mutation54 citations Open access
Semantic Scholar
Further localization of X-linked hydrocephalus in the chromosomal region Xq28.
P. Willems, L. Vits, P. Raeymaekers, J. Beuten +14 more
1992American Journal of Human Genetics54 citations
Semantic Scholar
A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11.
E. Reyniers, P. Van Bogaert, Nils Peeters, L. Vits +4 more
1999American Journal of Human Genetics38 citations Open access
Semantic Scholar
An optimized DHPLC protocol for molecular testing of the EXT1 and EXT2 genes in hereditary multiple osteochondromas
W. Wuyts, R. Radersma, K. Storm, L. Vits
2005Clinical Genetics37 citations Open access
Semantic Scholar
Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus family.
P. Coucke, L. Vits, G. Van Camp, F. Serville +6 more
1994Human Molecular Genetics34 citations
Semantic Scholar
Founder effect in a Belgian-Dutch fragile X population
S. Buyle, E. Reyniers, L. Vits, K. De Boulle +6 more
1993Human Genetics22 citations
Semantic Scholar
Localization of a gene responsible for nonspecific mental retardation (MRX9) to the pericentromeric region of the X chromosome.
P. Willems, L. Vits, I. Buntinx, P. Raeymaekers +2 more
1993Genomics20 citations
Semantic Scholar
Evidence for somatic and germline mosaicism in CRASH syndrome
L. Vits, D. Chitayat, G. Van Camp, J. A. Holden +2 more
1998Human Mutation18 citations
Semantic Scholar
CAG repeat contraction in the androgen receptor gene in three brothers with mental retardation.
R. Kooy, E. Reyniers, K. Storm, L. Vits +5 more
1999American journal of medical genetics15 citations
Semantic Scholar
Apparent regression of the CGG repeat in FMR1 to an allele of normal size
L. Vits, K. De Boulle, E. Reyniers, I. Handig +3 more
1994Human Genetics15 citations
Semantic Scholar
Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22.
P. Willems, J. Hendrickx, B. J. Van der Auwera, L. Vits +9 more
1991Genomics14 citations
Semantic Scholar
Identification of novel and recurrent glucokinase mutations in Belgian and Luxembourg maturity onset diabetes of the young patients
L. Vits, D. Beckers, M. Craen, C. D. de Beaufort +16 more
2006Clinical Genetics12 citations Open access
Semantic Scholar
Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the same family.
P. Willems, L. Vits, R. Wanders, P. Coucke +6 more
1990Archives of Neurology11 citations
Semantic Scholar
High incidence of the CFTR mutations 3272-26A-->G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A-->G, E588V, and 1671insTATCA).
K. Storm, Els Moens, L. Vits, Haike De Vlieger +7 more
2007Journal of Cystic Fibrosis7 citations Open access
Semantic Scholar
Two brothers with mental retardation discordant for the fragile-X syndrome.
B. V. van Roy, Patrick J. Willems, L. Vits, B. Ceulemans +4 more
1990American journal of medical genetics5 citations
Semantic Scholar
Frequency of the phenylalanine deletion (ΔF508) in the CF gene of Belgian cystic fibrosis patients
J. Wauters, J. Hendrickx, P. Coucke, L. Vits +6 more
1991Clinical Genetics3 citations
Semantic Scholar
MspI RFLP in the L1 CAM gene in Xq28.
P. Willems, L. Vits, K. De Boulle
1991Nucleic Acids Research2 citations Open access
Semantic Scholar
DXS89 (pTAK10) detects a homologous sequence on the Y chromosome.
Jan Hendrickx, L. Vits, Patrick J. Willems
1992Genomics1 citations
Semantic Scholar
DNA Diagnosis of Cystic Fibrosis by Direct Detection of the Af508 Mutation.
J. Hendrickx, J. Wauters, P. Coucke, L. Vits +2 more
1991Acta Clinica Belgica1 citations
Semantic Scholar
Erratum to “High incidence of the CFTR mutations 3272-26A→G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A→G, E588V, and 1671insTATCA)” [Journal of Cystic Fibrosis 6(2007)371–375]
K. Storm, Els Moens, L. Vits, Haike De Vlieger +7 more
20080 citations Open access
Semantic Scholar
Erratum to: CRASH syndrome: Clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1
E. Fransen, V. Lemmon, G. Camp, L. Vits +2 more
19960 citations
Semantic Scholar
BglII RFLP in DXS498 between the pigment gene repeat unit, RCP and GCP
L. Vits, Patrick J. Willems
1992Human Genetics0 citations
Semantic Scholar
PCR detection of a BclI RFLP in the G6PD gene of Caucasians
Patrick J. Willems, L. Vits
1992Human Genetics0 citations
Semantic Scholar
DNA diagnosis of cystic fibrosis by direct detection of the delta F508 mutation.
J. Hendrickx, J. Wauters, P. Coucke, L. Vits +2 more
1991Acta Clinica Belgica0 citations
Semantic Scholar
Genotype-phenotype correlation in Li associated diseases
E. Fransen, G. Van Camp, R. D'Hooge, L. Vits +1 more
0 citations
Semantic Scholar

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