M M Lesperance

Author PubWeight™ 11.37‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. Hum Mol Genet 2001 1.57
2 The sequence and antiapoptotic functional domains of the human cytomegalovirus UL37 exon 1 immediate early protein are conserved in multiple primary strains. Virology 2001 1.30
3 A gene responsible for autosomal dominant auditory neuropathy (AUNA1) maps to 13q14-21. J Med Genet 2004 1.02
4 Presence of human papillomavirus predicts recurrence of inverted papilloma. Otolaryngol Head Neck Surg 1995 0.96
5 Human papillomavirus types important in progression of inverted papilloma. Otolaryngol Head Neck Surg 1995 0.94
6 Pediatric myofibromatosis of the head and neck. Arch Otolaryngol Head Neck Surg 1999 0.93
7 DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24. Am J Hum Genet 2000 0.89
8 The carboxyl terminus of the human cytomegalovirus UL37 immediate-early glycoprotein is conserved in primary strains and is important for transactivation. J Gen Virol 2001 0.85
9 Interpretation of linkage data for a Huntington-like disorder mapping to 4p15.3. Am J Hum Genet 2000 0.79
10 A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus. J Med Genet 1999 0.79
11 Outcome of newborn hearing screening by ABR compared with four different DPOAE pass criteria. Am J Audiol 2000 0.78
12 Substituting a telephone call for pediatric adenotonsillectomy postoperative visits. Arch Otolaryngol Head Neck Surg 2001 0.75
13 Evidence in support of a different model of universal newborn hearing loss identification. Am J Audiol 2001 0.75
14 No association between DFNA6 and Pro250Arg mutation in FGFR3. Am J Med Genet 1999 0.75
15 Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13. Adv Otorhinolaryngol 2000 0.75