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 · 557 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

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 · 520 citations · Full text

Language Studies, American Sign Language, Neuroscience +15

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 · 235 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

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 · 205 citations · Full text

Medicine, Genetics, Molecular Genetics +13

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

Medicine, Pediatrics, Radiology +13