Alterations of Superficial White Matter in Schizophrenia and Relationship to Cognitive Performance

Por Nazeri, Arash, Chakravarty, M Mallar, Felsky, Daniel, Lobaugh, Nancy J, Rajji, Tarek K, Mulsant, Benoit H, Voineskos, Aristotle N
Publicado em 2013

Functional Consequences of Neurite Orientation Dispersion and Density in Humans across the Adult Lifespan

Por Nazeri, Arash, Chakravarty, M. Mallar, Rotenberg, David J., Rajji, Tarek K., Rathi, Yogesh, Michailovich, Oleg V., Voineskos, Aristotle N.
Publicado no J Neurosci (2015)

Myelin-Associated Glycoprotein Gene and Brain Morphometry in Schizophrenia

Por Felsky, Daniel, Voineskos, Aristotle N., Lerch, Jason P., Nazeri, Arash, Shaikh, Sajid A., Rajji, Tarek K., Mulsant, Benoit H., Kennedy, James L.
Publicado em 2012

White Matter Deficits in Psychopathic Offenders and Correlation with Factor Structure

Por Hoppenbrouwers, Sylco S., Nazeri, Arash, de Jesus, Danilo R., Stirpe, Tania, Felsky, Daniel, Schutter, Dennis J. L. G., Daskalakis, Zafiris J., Voineskos, Aristotle N.
Publicado em 2013

A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family

Por Shearer, A. Eliot, Hildebrand, Michael S., Bromhead, Catherine, Kahrizi, Kimia, Webster, Jennifer A., Azadeh, Batool, Kimberling, William J., Anousheh, Ali, Nazeri, Arash, Stephan, Dietrich, Najmabadi, Hossein, Smith, Richard J.H., Bahlo, Melanie
Publicado em 2009

Prefrontal White Matter Structure Mediates the Influence of GAD1 on Working Memory

Por Lett, Tristram A, Kennedy, James L, Radhu, Natasha, Dominguez, Luis G, Chakravarty, M Mallar, Nazeri, Arash, Farzan, Faranak, Walter, Henrik, Heinz, Andreas, Mulsant, Benoit H, Daskalakis, Zafiris J, Voineskos, Aristotle N
Publicado no Neuropsychopharmacology (2016)

Classification algorithms with multi-modal data fusion could accurately distinguish neuromyelitis optica from multiple sclerosis

Por Eshaghi, Arman, Riyahi-Alam, Sadjad, Saeedi, Roghayyeh, Roostaei, Tina, Nazeri, Arash, Aghsaei, Aida, Doosti, Rozita, Ganjgahi, Habib, Bodini, Benedetta, Shakourirad, Ali, Pakravan, Manijeh, Ghana'ati, Hossein, Firouznia, Kavous, Zarei, Mojtaba, Azimi, Amir Reza, Sahraian, Mohammad Ali
Publicado no Neuroimage Clin (2015)

Channelopathy-related SCN10A gene variants predict cerebellar dysfunction in multiple sclerosis

Por Roostaei, Tina, Sadaghiani, Shokufeh, Park, Min Tae M., Mashhadi, Rahil, Nazeri, Aria, Noshad, Sina, Salehi, Mohammad Javad, Naghibzadeh, Maryam, Moghadasi, Abdorreza Naser, Owji, Mahsa, Doosti, Rozita, Taheri, Amir Pejman Hashemi, Rad, Ali Shakouri, Azimi, Amirreza, Chakravarty, M. Mallar, Voineskos, Aristotle N., Nazeri, Arash, Sahraian, Mohammad Ali
Publicado no Neurology (2016)