Wim Wuyts

Overview

Best Publications

• Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)

  W Balemans;M Ebeling;N Patel;E Van Hul

  1291
  Citations

• Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease.

  W Balemans;N Patel;M Ebeling;E Van Hul

  790
  Citations

• Diagnosis of Hypersensitivity Pneumonitis in Adults. An Official ATS/JRS/ALAT Clinical Practice Guideline.

  Ganesh Raghu;Martine Remy-Jardin;Christopher J Ryerson;Jeffrey L Myers

  682
  Citations

• A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment

  F. J. Del Castillo;M. Rodriguez-Ballesteros;A. Alvarez;T. Hutchin

  432
  Citations

• Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease

  Lynne J. Hocking;Gavin J.A. Lucas;Anna Daroszewska;Jon Mangion

  382
  Citations

• The pathogenesis of pulmonary fibrosis: a moving target

  Wim A Wuyts;Carlo Agostini;Katerina M Antoniou;Demosthenes Bouros

  376
  Citations

• Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study

  Ignacio Del Castillo;Miguel A. Moreno-Pelayo;Francisco J. Del Castillo;Zippora Brownstein

  365
  Citations

• Molecular basis of multiple exostoses: mutations in the EXT1 and EXT2 genes.

  Wim Wuyts;Wim Van Hul

  281
  Citations

• Positional Cloning of a Gene Involved in Hereditary Multiple Exostoses

  W. Wuyts;W. Van Hul;J. Wauters;M. Nemtsova

  279
  Citations

• Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses

  W. Wuyts;W. van Hul;K. de Boulle;J.J. Hendrickx

  252
  Citations

• Phenotypes of organ involvement in sarcoidosis.

  Jonas Christian Schupp;Sandra Freitag-Wolf;Elena Bargagli;Violeta Mihailović-Vučinić

  238
  Citations

• EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas.

  Judith V.M.G. Bovée;Anne-Marie Cleton-Jansen;Wim Wuyts;Goedele Caethoven

  234
  Citations

• Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb).

  Ivy Jennes;Elena Pedrini;Monia Zuntini;Marina Mordenti

  214
  Citations

• Two-color multiplex ligation-dependent probe amplification: detecting genomic rearrangements in hereditary multiple exostoses.

  Stefan J. White;Geraldine R. Vink;Marjolein Kriek;Wim Wuyts

  201
  Citations

• Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene family

  W. Van Hul;W. Wuyts;J. Hendrickx;F. Speleman

  197
  Citations

• Evaluation of the role of RANK and OPG genes in Paget’s disease of bone

  W Wuyts;L Van Wesenbeeck;A Morales-Piga;S Ralston

  179
  Citations

• Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35.

  Lynne J. Hocking;Craig A. Herbert;Rosie K. Nicholls;Fiona Williams

  165
  Citations

• The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)

  Wim Wuyts;Erna Cleiren;Tessa Homfray;Alberto Rasore-Quartino

  151
  Citations

• Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: Identification of "protective" and "risk" factors

  Elena Pedrini;Ivy Jennes;Morena Tremosini;Annamaria Milanesi

  140
  Citations

• Identification and characterization of a novel member of the EXT gene family, EXTL2.

  W. Wuyts;W. van Hul;J. Hendrickx;F. Speleman

  136
  Citations