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J. Wauters · SciRah

Researcher profile · Semantic Scholar

J. Wauters

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J. Wauters — researcher profile on SciRah

h-index: 24
Works: 58
Citations: 2,322

Most-cited papers

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy.
K. Sleegers, N. Brouwers, I. Gijselinck, J. Theuns +6 more
2006Brain : a journal of neurology398 citations Open access
Semantic Scholar
Nonsyndromic hearing impairment is associated with a mutation in DFNA5
L. Van Laer, E. Huizing, M. Verstreken, D. V. van Zuijlen +9 more
1998Nature Genetics364 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
Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene family.
W. Van Hul, W. Wuyts, J. Hendrickx, F. Speleman +5 more
1998Genomics129 citations
Semantic Scholar
Microdeletions involving the SCN1A gene may be common in SCN1A‐mutation‐negative SMEI patients
A. Suls, K. Claeys, D. Goossens, Boris Harding +16 more
2006Human Mutation126 citations Open access
Semantic Scholar
Subtelomeric deletions detected in patients with idiopathic mental retardation using multiplex ligation‐dependent probe amplification (MLPA)
L. Rooms, E. Reyniers, R. van Luijk, Stefaan Scheers +5 more
2004Human Mutation106 citations Open access
Semantic Scholar
Identification and Characterization of a Novel Member of the EXT Gene Family, EXTL2
W. Wuyts, W. Van Hul, J. Hendrickx, F. Speleman +6 more
1997European Journal of Human Genetics98 citations
Semantic Scholar
High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.
D. Callen, H. Eyre, S. Lane, Y. Shen +6 more
1993Journal of Medical Genetics62 citations Open access
Semantic Scholar
Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype
Y. van Bever, L. Rooms, A. Laridon, E. Reyniers +4 more
2005American Journal of Medical Genetics. Part A60 citations
Semantic Scholar
A subterminal deletion of the long arm of chromosome 10: A clinical report and review
W. Courtens, W. Wuyts, L. Rooms, Sarah Barbera Pera +1 more
2006American Journal of Medical Genetics. Part A53 citations
Semantic Scholar
Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3).
E. Holinski-Feder, E. Reyniers, S. Uhrig, A. Golla +12 more
2000American Journal of Human Genetics50 citations Open access
Semantic Scholar
Four generations of epilepsy caused by an inherited microdeletion of the SCN1A gene
A. Suls, R. Velizarova, I. Yordanova, L. Deprez +7 more
2010Neurology49 citations
Semantic Scholar
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus
G. Van Camp, H. Kunst, K. Flothmann, W. Mcguirt +10 more
1999Journal of Medical Genetics46 citations Open access
Semantic Scholar
Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion.
W. Wuyts, D. Roland, H. Lüdecke, J. Wauters +3 more
2002American journal of medical genetics44 citations
Semantic Scholar
TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions
L. Rooms, E. Reyniers, Stefaan Scheers, R. van Luijk +8 more
2006European Journal of Human Genetics42 citations
Semantic Scholar
Phenotypic expression and frequency of familial defective apolipoprotein B-100 in Belgian hypercholesterolemics.
M. Kotze, A. Peeters, E. Langenhoven, J. Wauters +1 more
1994Atherosclerosis40 citations
Semantic Scholar
A nonmosaic 45,X karyotype in a mother with Turner's syndrome and in her daughter.
M. Cools, Raoul Rooman, J. Wauters, Yves Jacqemyn +1 more
2004Fertility and Sterility39 citations Open access
Semantic Scholar
Specificity of antigen assays of plasminogen activator inhibitor in plasma: Innotest PAI-1 immunoassay evaluated.
P. Meijer, D. E. Pollet, J. Wauters, C. Kluft
1994Clinical Chemistry38 citations Open access
Semantic Scholar
Expression profile of telomerase subunits in human pleural mesothelioma
K. Dhaene, J. Wauters, B. Weyn, J. Timmermans +1 more
2000Journal of Pathology33 citations
Semantic Scholar
Hypoparathyroidism‐retardation‐dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation—clinical report and review
W. Courtens, W. Wuyts, M. Poot, K. Szuhai +6 more
2006American Journal of Medical Genetics. Part A31 citations
Semantic Scholar
Molecular cloning and characterization of human chondrolectin, a novel type I transmembrane protein homologous to C-type lectins.
Lin Weng, P. Smits, J. Wauters, J. Merregaert
2002Genomics30 citations
Semantic Scholar
Isolation and characterization of chondrolectin (Chodl), a novel C-type lectin predominantly expressed in muscle cells.
Lin Weng, R. Hübner, An Claessens, P. Smits +4 more
2003Gene27 citations
Semantic Scholar
Incidence of low-fluorescence alpha satellite region on chromosome 21 escaping detection of aneuploidy at interphase by FISH.
P. Bossuyt, M.-N. Van Tienen, L. De Gruyter, V. Smets +2 more
1995Cytogenetics and Cell Genetics26 citations
Semantic Scholar
Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly.
W. Courtens, W. Tjalma, L. Messiaen, E. Vamos +5 more
1998American journal of medical genetics25 citations
Semantic Scholar
Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion
J. Wauters, P. Bossuyt, L. Roelen, B. Roy +1 more
1993Clinical Genetics24 citations
Semantic Scholar
An interstitial deletion of chromosome 7 at band q21: A case report and review
W. Courtens, S. Vermeulen, W. Wuyts, L. Messiaen +6 more
2005American Journal of Medical Genetics. Part A23 citations
Semantic Scholar
Molecular and clinical examination of an Italian DEFECT 11 family
W. Wuyts, G. Di Gennaro, F. Bianco, J. Wauters +5 more
1999European Journal of Human Genetics21 citations
Semantic Scholar
Regional mapping of a liver alpha-subunit gene of phosphorylase kinase (PHKA) to the distal region of human chromosome Xp.
J. Wauters, P. Bossuyt, J. Davidson, J. Hendrickx +2 more
1992Cytogenetics and Cell Genetics19 citations
Semantic Scholar
A Novel Alternative Spliced Chondrolectin Isoform Lacking the Transmembrane Domain Is Expressed during T Cell Maturation*
Lin Weng, D. V. van Bockstaele, J. Wauters, E. Van Marck +3 more
2003Journal of Biological Chemistry16 citations Open access
Semantic Scholar
Screening for subtelomeric rearrangements using genetic markers in 70 patients with unexplained mental retardation.
L. Rooms, E. Reyniers, R. van Luijk, Stefan Scheers +2 more
2004Annales de Genetique15 citations
Semantic Scholar
X-linked liver glycogenosis: localization and isolation of a candidate gene.
J. Hendrickx, P. Coucke, P. Bossuyt, J. Wauters +13 more
1993Human Molecular Genetics15 citations
Semantic Scholar
Fully automated FISH examination of amniotic fluid cells
J. Wauters, E. van Assche, A. Antsaklis, J. Tepperberg +4 more
2007Prenatal Diagnosis12 citations
Semantic Scholar
A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.
W. Courtens, W. Wuyts, Stefaan Scheers, R. van Luijk +5 more
2006European Journal of Medical Genetics9 citations
Semantic Scholar
A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review
W. Courtens, J. Wauters, M. Wojciechowski, E. Reyniers +5 more
2007Clinical Dysmorphology8 citations
Semantic Scholar
18q-Syndrome with coeliac disease
W. Lipschutz, S. Cadranel, B. Lipschutz, L. Martin +5 more
1999European Journal of Pediatrics8 citations
Semantic Scholar
In vitro expression of α-l-fucosidase activity polymorphism observed in plasma
A. V. van Elsen, J. Leroy, J. Wauters, P. Willems +2 more
2004Human Genetics6 citations
Semantic Scholar
Molecular and clinical examination of an Italian DEFECT11 family.
W. Wuyts, G. Di Gennaro, F. Bianco, J. Wauters +5 more
1999European Journal of Human Genetics6 citations
Semantic Scholar
In vitro expression of alpha-L-fucosidase activity polymorphism observed in plasma.
A. V. van Elsen, J. Leroy, J. Wauters, P. Willems +2 more
1983Human Genetics6 citations
Semantic Scholar
Expression and localization of CHODLΔE/CHODLfΔE, the soluble isoform of chondrolectin
An Claessens, K. K. van de Vijver, D. V. van Bockstaele, J. Wauters +3 more
20075 citations
Semantic Scholar
Expression and localization of CHODLDeltaE/CHODLfDeltaE, the soluble isoform of chondrolectin.
An Claessens, K. K. van de Vijver, D. V. van Bockstaele, J. Wauters +3 more
2007Cell Biology International3 citations
Semantic Scholar
α-l-Fucosidase in human fibroblasts. I. The enzyme activity polymorphism
J. Wauters, K. Stuer, A. V. van Elsen, P. Willems
2004Biochemical Genetics3 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
Calendar of Events 1992
G. G. M. Habets, R. A. van der Kammen, T. Serikawa, J. Yamada +114 more
19922 citations Open access
Semantic Scholar
α-l-Fucosidase in human fibroblasts. I. The enzyme activity polymorphism
J. Wauters, K. Stuer, A. V. van Elsen, P. Willems
1992Biochemical Genetics2 citations
Semantic Scholar
Precise mapping of the fragile site FRA12A on chromosome 12q13.1
B. Winnepenninckx, E. Reyniers, P. Bossuyt, A. Smits +2 more
20011 citations
Semantic Scholar
Identification of a new connexin gene GJA11 (Cx59) using degenerate PCR primers
P. Coucke, L. Van Laer, Johan Meyers, P. Van Hauwe +5 more
20001 citations
Semantic Scholar
Contents Vol. 60, 1999
G. Habets, R. A. van der Kammen, T. Serikawa, J. Yamada +114 more
1999Digestion1 citations Open access
Semantic Scholar
Abstracts of the 12th European Colloquium on Cytogenetics of Domestic Animals
M. Ribaudo, A. Dileonardo, P. Rubino, A. Giallongo +68 more
19961 citations
Semantic Scholar
Assignment of the human integral transmembrane protein 1 gene (ITM1) to human chromosome band 11q23.3 by in situ hybridization and YAC mapping.
W. Van Hul, G. Hong, J. Wauters, E. Van Hul +4 more
1996Cytogenetics and Cell Genetics1 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

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