Morell, Robert J.

Top Publications

Top Publications Authored or Co-Authored by "Morell, Robert J."

• 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
• Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: First report of the WS consortium

  American Journal of Human Genetics, Volume 50, No. 5, Year 1992, Citations 173
• Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

  Nature Genetics, Volume 40, No. 11, Year 2008, Citations 74
• CDC14A phosphatase is essential for hearing and male fertility in mouse and human

  Human Molecular Genetics, Volume 27, No. 5, Year 2018, Citations 45
• Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome

  Clinical Genetics, Volume 91, No. 2, Year 2017, Citations 38