Anil K. Lalwani

Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

Julie M. Bork, Linda Peters, Saima Riazuddin et al. · The American Journal of Human Genetics · 2001 · 551 citations · Full text

Developmental Biology, Allelic Mutations, Mendelian Disorder +7

Cerebral organization for language in deaf and hearing subjects: Biological constraints and effects of experience

Helen J. Neville, Daphné Bavelier, David P. Corina et al. · Proceedings of the National Academy of Sciences · 1998 · 518 citations

Human Nonsyndromic Hereditary Deafness DFNA17 Is Due to a Mutation in Nonmuscle Myosin MYH9

Anil K. Lalwani, Jayne A. Goldstein, Michael J. Kelley et al. · The American Journal of Human Genetics · 2000 · 232 citations · Full text

Rare Diseases, Genetic Disorder, Nonmuscle Myosin Myh9 +7

OTOF Encodes Multiple Long and Short Isoforms: Genetic Evidence That the Long Ones Underlie Recessive Deafness DFNB9

Shin’ichiro Yasunaga, M’hamed Grati, Sébastien Chardenoux et al. · The American Journal of Human Genetics · 2000 · 203 citations · Full text

Developmental Biology, Short Isoforms, Genetic Disorder +11

Use of Laboratory Evaluation and Radiologic Imaging in the Diagnostic Evaluation of Children With Sensorineural Hearing Loss

Derek D. Mafong, Edward J. Shin, Anil K. Lalwani · The Laryngoscope · 2002 · 198 citations