A
Anil K. Lalwani
Researcher at Columbia University
Publications - 301
Citations - 10655
Anil K. Lalwani is an academic researcher from Columbia University. The author has contributed to research in topics: Hearing loss & Sensorineural hearing loss. The author has an hindex of 53, co-authored 296 publications receiving 9519 citations. Previous affiliations of Anil K. Lalwani include NewYork–Presbyterian Hospital & National Institutes of Health.
Papers
More filters
Journal ArticleDOI
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 M. Peters,Saima Riazuddin,Saima Riazuddin,S. L. Bernstein,Zubair M. Ahmed,Zubair M. Ahmed,Seth L. Ness,Robert C. Polomeno,Arabandi Ramesh,Arabandi Ramesh,Melvin D. Schloss,C. R. Srikumari Srisailpathy,C. R. Srikumari Srisailpathy,Sigrid Wayne,Susan Bellman,Dilip Desmukh,Zahoor Ahmed,Shaheen N. Khan,Vazken M. Der Kaloustian,X. Cindy Li,Anil K. Lalwani,Sheikh Riazuddin,Maria Bitner-Glindzicz,Walter E. Nance,Xue-Zhong Liu,Graeme Wistow,Richard J.H. Smith,Andrew J. Griffith,Edward R. Wilcox,Thomas B. Friedman,Robert J. Morell +31 more
TL;DR: Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular dysfunction (USH1D) were previously mapped to overlapping regions of chromosome 10q21-q22, but mutations in a novel cadherin-like gene, CDH23, were found both in families with DFNB12 and in Families with USH1D.
Journal ArticleDOI
Cerebral organization for language in deaf and hearing subjects: Biological constraints and effects of experience
Helen J. Neville,Daphne Bavelier,David P. Corina,Josef P. Rauschecker,Avi Karni,Anil K. Lalwani,Allen R. Braun,Vince Clark,Peter Jezzard,Robert Turner +9 more
TL;DR: Results suggest that the early acquisition of a natural language is important in the expression of the strong bias for these areas to mediate language, independently of the form of the language.
Journal ArticleDOI
A mutation in PDS causes non-syndromic recessive deafness.
Journal ArticleDOI
Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9.
Anil K. Lalwani,Jayne A. Goldstein,Michael J. Kelley,William M. Luxford,Caley M. Castelein,Anand N. Mhatre +5 more
TL;DR: Both the precise role of MYH9 in the cochlea and the mechanism by which the R705H mutation leads to the DFNA17 phenotype (progressive hearing impairment and cochchleosaccular degeneration) remain to be elucidated.
Journal ArticleDOI
Use of laboratory evaluation and radiologic imaging in the diagnostic evaluation of children with sensorineural hearing loss.
TL;DR: The aim of this study was to examine the yield of laboratory tests and radiologic imaging commonly used in the diagnostic evaluation of SNHL in children.