Michael J. Dixon

Overview

Best Publications

• Cleft lip and palate: understanding genetic and environmental influences.

  Michael J. Dixon;Mary L. Marazita;Terri H. Beaty;Jeffrey C. Murray

  2091
  Citations

• Cleft lip and palate

  Peter A Mossey;Julian Little;Ron G Munger;Mike J Dixon

  1893
  Citations

• Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes.

  Shinji Kondo;Brian C. Schutte;Rebecca J. Richardson;Bryan C. Bjork

  1051
  Citations

• Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis

  C. Toomes;J. James;A. J. Wood;Chu Lee Wu

  631
  Citations

• Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome

  Jill Dixon;Sara J. Edwards;Amanda J. Gladwin

  497
  Citations

• Tcof1/Treacle is required for neural crest cell formation and proliferation deficiencies that cause craniofacial abnormalities

  Jill Dixon;Natalie Carmaline Jones;Lisa L Sandell;Sachintha M Jayasinghe

  485
  Citations

• Prevention of the neurocristopathy Treacher Collins syndrome through inhibition of p53 function

  Natalie Carmaline Jones;Megan L Lynn;Karin Gaudenz;Daisuke Sakai

  467
  Citations

• Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome

  Johannes G. Dauwerse;Jill Dixon;Saskia Seland;Claudia A L Ruivenkamp

  415
  Citations

• The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor

  Benigno C. Valdez;Dale Henning;Rolando B. So;Jill Dixon

  390
  Citations

• Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch

  Rebecca J Richardson;Jill Dixon;Saimon Malhotra;Matthew J Hardman

  371
  Citations

• Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype–phenotype correlation

  Elfride De Baere;Michael J. Dixon;Kent W. Small;Ethylin W. Jabs

  326
  Citations

• Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta

  M. Helen Rajpar;Kathryn Harley;Chris Laing;Robin M. Davies

  308
  Citations

• FOXL2 and BPES: Mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation

  Elfride De Baere;Diane Beysen;Christine Oley;Birgit Lorenz

  288
  Citations

• Treacher Collins syndrome: etiology, pathogenesis and prevention

  Paul A Trainor;Jill Dixon;Michael J Dixon

  277
  Citations

• Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia

  Martin J Barron;Sinead T McDonnell;Iain MacKie;Michael J Dixon

  271
  Citations

• Mutation of the Na-K-Cl Co-Transporter Gene Slc12a2 Results in Deafness in Mice

  Michael J. Dixon;James Gazzard;Shazia S. Chaudhry;Natalie Sampson

  229
  Citations

• Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization

  M. Helen Rajpar;Martin J. Koch;Robin M. Davies;Kieran T. Mellody

  223
  Citations

• Treacher Collins syndrome.

  Michael J. Dixon

  210
  Citations

• A Conserved Pbx-Wnt-p63-Irf6 Regulatory Module Controls Face Morphogenesis by Promoting Epithelial Apoptosis

  Elisabetta Ferretti;Bingsi Li;Rediet Zewdu;Victoria Wells

  190
  Citations

• The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation

  Bianca Gonzales;Dale Henning;Rolando B. So;Jill Dixon

  188
  Citations