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Molecular Genetics and Metabolism|July 17, 2007
Three dimensional structure of human biotinidase: computer modeling and functional correlationsKirit Pindolia, Kevin Jensen, Barry WolfHuman Mutation|June 18, 2010
Analysis of mutations causing biotinidase deficiencyKirit Pindolia, Megan Jordan, Barry WolfMolecular Genetics and Metabolism|March 18, 2014
Characterization and functional analysis of cellular immunity in mice with biotinidase deficiencyKirit Pindolia, Hong Li, Cisley Cardwell, et al.Molecular Genetics and Metabolism Reports|October 19, 2016
Differential gene expression during early development in brains of wildtype and biotinidase-deficient miceChristian Brigolin, Nathan McKenty, Kirit Pindolia, et al.Journal of Inherited Metabolic Disease|May 19, 2017
Developmental window of sensorineural deafness in biotinidase-deficient miceKathleen June Maheras, Kirit Pindolia, Barry Wolf, et al.Neurobiology of Disease|May 15, 2012
Neurological deficits in mice with profound biotinidase deficiency are associated with demylination and axonal degenerationKirit Pindolia, Jieli Chen, Cisley Cardwell, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|July 24, 2015
Biotinidase deficiency mimicking neuromyelitis optica: Initially exhibiting symptoms in adulthoodLaure Bottin, Sabine Prud'hon, Stéphanie Guey, et al.Molecular Genetics and Metabolism|September 10, 2005
Evolutionary conservation of biotinidase: implications for the enzyme's structure and subcellular localizationBarry Wolf, Kevin JensenMolecular Genetics and Metabolism|November 6, 2010
Development and characterization of a mouse with profound biotinidase deficiency: a biotin-responsive neurocutaneous disorderKirit Pindolia, Megan Jordan, Caiying Guo, et al.Molecular Genetics and Metabolism Reports|June 28, 2017
Corrigendum to "First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children" [Mol. Genet. Metab. Rep. 2 (2016) 81-84]Danika Nadeen Senanayake, Eresha A Jasinge, Kirit Pindolia, et al.Pageof 6