Kumar N. Alagramam

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene

Kumar N. Alagramam, Crystal L. Murcia, Heajoon Y. Kwon et al. · Nature Genetics · 2001 · 315 citations

Medicine, Genetics, Molecular Genetics +13

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

Kumar N. Alagramam · Human Molecular Genetics · 2001 · 285 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Interactions in the network of Usher syndrome type 1 proteins

Avital Adato, Vincent Michel, Yoshiaki Kikkawa et al. · Human Molecular Genetics · 2004 · 239 citations

Life Sciences, Cell Biology, Molecular Biology +13

Mutations in Protocadherin 15 and Cadherin 23 Affect Tip Links and Mechanotransduction in Mammalian Sensory Hair Cells

Kumar N. Alagramam, Richard J. Goodyear, Ruishuang Geng et al. · PLoS ONE · 2011 · 138 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation

Rui Geng, Scott Geller, Toshinori Hayashi et al. · Human Molecular Genetics · 2009 · 84 citations · Full text

Medicine, Genetics, Neuroscience +17