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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 12, 2011
Argininosuccinate lyase deficiency-argininosuccinic aciduria and beyondAyelet Erez, Sandesh C Sreenath Nagamani, Brendan LeeMolecular Genetics and Metabolism|August 2, 2011
Arginase I deficiency: severe infantile presentation with hyperammonemia: more common than reported?Shailly Jain-Ghai, Sandesh C Sreenath Nagamani, Susan Blaser, et al.European Journal of Human Genetics : EJHG|September 22, 2011
Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43-q44Sandesh C Sreenath Nagamani, Ayelet Erez, Carolyn Bay, et al.European Journal of Human Genetics : EJHG|December 15, 2010
Phenotypic manifestations of copy number variation in chromosome 16p13.11Sandesh C Sreenath Nagamani, Ayelet Erez, Patricia Bader, et al.Human Molecular Genetics|March 1, 2011
Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplicationsPengfei Liu, Ayelet Erez, Sandesh C Sreenath Nagamani, et al.Cell|September 20, 2011
Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangementsPengfei Liu, Ayelet Erez, Sandesh C Sreenath Nagamani, et al.Pageof 1