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Vijay S. Ganesh

Affiliations: 
2012 Biology: Medical Sciences, Division of Harvard University, Cambridge, MA, United States 
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"Vijay Ganesh"
Mean distance: 14.84 (cluster 46)
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Chris A. Walsh grad student 2012 Harvard
 (Identification and Characterization of Genes Essential for Human Brain Development.)

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Publications

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Wojcik MH, Lemire G, Zaki MS, et al. (2023) Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis. Medrxiv : the Preprint Server For Health Sciences
Lemire G, Sanchis-Juan A, Russell K, et al. (2023) Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease. Medrxiv : the Preprint Server For Health Sciences
Akula SK, Chen AY, Neil JE, et al. (2023) Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria. Jama Neurology
Deng X, Achari A, Federman S, et al. (2020) Metagenomic sequencing with spiked primer enrichment for viral diagnostics and genomic surveillance. Nature Microbiology
Smith RS, Kenny CJ, Ganesh V, et al. (2018) Sodium Channel SCN3A (Na1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development. Neuron
Coulter ME, Dorobantu CM, Lodewijk GA, et al. (2018) The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles. Cell Reports. 24: 973-986.e8
Piantadosi A, Mukerji S, Ye S, et al. (2018) 868. Prospective Pathogen Detection in Patients With Central Nervous System Inflammation Using Metagenomic Sequencing Open Forum Infectious Diseases. 5: S23-S23
Piantadosi A, Kanjilal S, Ganesh V, et al. (2017) Rapid detection of Powassan virus in a patient with encephalitis by metagenomic sequencing. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America
Mochida GH, Ganesh VS, de Michelena MI, et al. (2012) CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development. Nature Genetics. 44: 1260-4
Clapham KR, Yu TW, Ganesh VS, et al. (2012) FLNA genomic rearrangements cause periventricular nodular heterotopia. Neurology. 78: 269-78
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