Manoj Raghavan

发表

Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias.

T. Lister, M. Raghavan, B. Young, 2005, Cancer research.

Magnetoencephalography in the Preoperative Evaluation for Epilepsy Surgery

Zhimin Li, Chad E Carlson, M. Raghavan, 2014, Current Neurology and Neuroscience Reports.

Nonseizure SUDEP: Sudden unexpected death in epilepsy without preceding epileptic seizures

Orrin Devinsky, Nuria Lacuey, Bilal Zonjy, 2016, Epilepsia.

A comparison of two fMRI methods for predicting verbal memory decline after left temporal lobectomy: Language lateralization versus hippocampal activation asymmetry

J. Binder, T. Hammeke, W. Mueller, 2010, Epilepsia.

Generation and propagation of the action potential.

P. Barkhaus, M. Raghavan, D. Fee, 2019, Handbook of clinical neurology.

Language lateralization by fMRI and Wada testing in 229 patients with epilepsy: Rates and predictors of discordance

Jeffrey R Binder, Thomas A Hammeke, J. Binder, 2013, Epilepsia.

Altered Frontal Lobe Network Function in Temporal Lobe Epilepsy Revealed by Graph Theory Analysis (P1.279)

Colin Humphries, Jeffrey R. Binder, Vivek Prabhakaran, 2018 .

3D visualization of subdural electrode shift as measured at craniotomy reopening

Peter S. LaViolette, Kathleen M. Schmainda, Benjamin M. Ellingson, 2011, Epilepsy Research.

Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event.

Diana Blaydon, D. Kelsell, C. Proby, 2005, Cancer research.