Möller, Claes G.

Top Publications

Top Publications Authored or Co-Authored by "Möller, Claes G."

• CDH23 mutation and phenotype heterogeneity: A profile of 107 diverse families with Usher syndrome and nonsyndromic deafness

  American Journal of Human Genetics, Volume 71, No. 2, Year 2002, Citations 213
• Genomic structure and identification of novel mutations in Usherin, the gene responsible for usher syndrome type IIa

  American Journal of Human Genetics, Volume 66, No. 4, Year 2000, Citations 180
• Genetic heterogeneity of usher syndrome: Analysis of 151 families with usher type I

  American Journal of Human Genetics, Volume 67, No. 6, Year 2000, Citations 69
• Gene mapping of Usher syndrome type IIa: Localization of the gene to a 2.1-cM segment on chromosome 1q41

  American Journal of Human Genetics, Volume 56, No. 1, Year 1995, Citations 68
• The ICF core sets for hearing loss project: Functioning and disability from the patient perspective

  International Journal of Audiology, Volume 53, No. 11, Year 2014, Citations 65