Follow
Vijay S. Ganesh, M.D., Ph.D.
Vijay S. Ganesh, M.D., Ph.D.
Brigham and Women's Hospital, Boston, MA
Verified email at post.harvard.edu
Title
Cited by
Cited by
Year
Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex
VL Sheen, VS Ganesh, M Topcu, G Sebire, A Bodell, RS Hill, PE Grant, ...
Nature genetics 36 (1), 69-76, 2004
3992004
Mutations in PNKP cause microcephaly, seizures and defects in DNA repair
J Shen, EC Gilmore, CA Marshall, M Haddadin, JJ Reynolds, W Eyaid, ...
Nature genetics 42 (3), 245-249, 2010
3372010
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome
VL Sheen, A Jansen, MH Chen, E Parrini, T Morgan, R Ravenscroft, ...
Neurology 64 (2), 254-262, 2005
2052005
Genomic and functional profiling of human Down syndrome neural progenitors implicates S100B and aquaporin 4 in cell injury
G Esposito, J Imitola, J Lu, D De Filippis, C Scuderi, VS Ganesh, ...
Human molecular genetics 17 (3), 440-457, 2008
1512008
Sodium channel SCN3A (NaV1. 3) regulation of human cerebral cortical folding and oral motor development
RS Smith, CJ Kenny, V Ganesh, A Jang, R Borges-Monroy, JN Partlow, ...
Neuron 99 (5), 905-913. e7, 2018
1322018
Metagenomic sequencing with spiked primer enrichment for viral diagnostics and genomic surveillance
X Deng, A Achari, S Federman, G Yu, S Somasekar, I Bártolo, S Yagi, ...
Nature microbiology 5 (3), 443-454, 2020
1262020
CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development
GH Mochida, VS Ganesh, MI De Michelena, H Dias, KD Atabay, ...
Nature genetics 44 (11), 1260-1264, 2012
1042012
A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts
GH Mochida, VS Ganesh, JM Felie, D Gleason, RS Hill, KR Clapham, ...
The American Journal of Human Genetics 87 (6), 882-889, 2010
1042010
The ESCRT-III protein CHMP1A mediates secretion of sonic hedgehog on a distinctive subtype of extracellular vesicles
ME Coulter, CM Dorobantu, GA Lodewijk, F Delalande, S Cianferani, ...
Cell reports 24 (4), 973-986. e8, 2018
862018
A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21
A Rajab, GH Mochida, A Hill, V Ganesh, A Bodell, A Riaz, PE Grant, ...
Neurology 60 (10), 1664-1667, 2003
772003
Autosomal recessive form of periventricular heterotopia
VL Sheen, M Topcu, S Berkovic, D Yalnizoglu, I Blatt, A Bodell, RS Hill, ...
Neurology 60 (7), 1108-1112, 2003
702003
Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus
VL Sheen, L Basel-Vanagaite, JR Goodman, IE Scheffer, A Bodell, ...
Brain and Development 26 (5), 326-334, 2004
572004
Rapid detection of Powassan virus in a patient with encephalitis by metagenomic sequencing
A Piantadosi, S Kanjilal, V Ganesh, A Khanna, EP Hyle, J Rosand, T Bold, ...
Clinical infectious diseases 66 (5), 789-792, 2018
542018
Centers for Mendelian Genomics: A decade of facilitating gene discovery
SM Baxter, JE Posey, NJ Lake, N Sobreira, JX Chong, S Buyske, EE Blue, ...
Genetics in Medicine 24 (4), 784-797, 2022
452022
Enhanced virus detection and metagenomic sequencing in patients with meningitis and encephalitis
A Piantadosi, SS Mukerji, S Ye, MJ Leone, LM Freimark, D Park, G Adams, ...
MBio 12 (4), 10.1128/mbio. 01143-21, 2021
382021
FLNA genomic rearrangements cause periventricular nodular heterotopia
KR Clapham, TW Yu, VS Ganesh, B Barry, Y Chan, D Mei, E Parrini, ...
Neurology 78 (4), 269-278, 2012
242012
Jamestown Canyon virus in Massachusetts: clinical case series and vector screening
CM Kinsella, ML Paras, S Smole, S Mehta, V Ganesh, LH Chen, ...
Emerging Microbes & Infections 9 (1), 903-912, 2020
222020
A form of muscular dystrophy associated with pathogenic variants in JAG2
S Coppens, AM Barnard, S Puusepp, S Pajusalu, K Őunap, ...
The American Journal of Human Genetics 108 (5), 840-856, 2021
212021
Fatal case of chronic Jamestown Canyon virus encephalitis diagnosed by metagenomic sequencing in patient receiving rituximab
IH Solomon, VS Ganesh, G Yu, XD Deng, MR Wilson, S Miller, TA Milligan, ...
Emerging infectious diseases 27 (1), 238, 2021
212021
Diagnostic capabilities of nanopore long‐read sequencing in muscular dystrophy
CC Bruels, HR Littel, AL Daugherty, S Stafki, EA Estrella, ES McGaughy, ...
Annals of clinical and translational neurology 9 (8), 1302-1309, 2022
122022
The system can't perform the operation now. Try again later.
Articles 1–20