A. James Barkovich, MD

Professor in Residence
Departments of Radiology, Pediatrics, Neurology and Neurological Surgery
University of California
E-mail: jim.barkovich@radiology.ucsf.edu
Page: http://cancer.ucsf.edu/people/barkovich_ajames.php

 

Fields of interest:

Brain disorders including correlating genetic defects with brain imaging findings to facilitate diagnosis, early detection of brain injury in newborns with encephalopathy, and early detection and correlation with neurodevelopmental outcome of brain injury in premature newborns

 

Recent publications:

Mellado C., Poduri A., Gleason D., Elhosary P. C., Barry B. J., Partlow J. N., Chang B. S., Shaw G. M., Barkovich A. J., Walsh C. A.:
Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort
Am. J. Med. Genet. A. 2010; 152A(11): 2736-42.

Bonifacio S. L., Glass H. C., Chau V., Berman J. I., Xu D., Brant R., Barkovich A. J., Poskitt K. J., Miller S. P., Ferriero D. M.:
Extreme premature birth is not associated with impaired development of brain microstructure
J. Pediatr. 2010; 157(5): 726-32 e1.

Yu T. W., Mochida G. H., Tischfield D. J., Sgaier S. K., Flores-Sarnat L., Sergi C. M., Topcu M., McDonald M. T., Barry B. J., Felie J. M., Sunu C., Dobyns W. B., Folkerth R. D., Barkovich A. J., Walsh C. A.:
Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture
Nat. Genet. 2010; 42(11): 1015-20.

Habas P. A., Kim K., Corbett-Detig J. M., Rousseau F., Glenn O. A., Barkovich A. J., Studholme C.:
A spatiotemporal atlas of MR intensity, tissue probability and shape of the fetal brain with application to segmentation
Neuroimage 2010; 53(2): 460-70.

Hess C. P., Barkovich A. J.:
Seizures: emergency neuroimaging
Neuroimaging Clin. N. Am. 2010; 20(4): 619-37.

Habas P. A., Kim K., Rousseau F., Glenn O. A., Barkovich A. J., Studholme C.:
Atlas-based segmentation of developing tissues in the human brain with quantitative validation in young fetuses
Hum. Brain Mapp. 2010; 31(9): 1348-58.

Poduri A., Chitsazzadeh V., D'Arrigo S., Fedrizzi E., Pantaleoni C., Riva D., Busse C., Kuster H., Duplessis A., Gaitanis J., Sahin M., Garganta C., Topcu M., Dies K. A., Barry B. J., Partlow J., Barkovich A. J., Walsh C. A., Chang B. S.:
The syndrome of perisylvian polymicrogyria with congenital arthrogryposis
Brain Dev. 2010; 32(7): 550-5.

Glass H. C., Bonifacio S. L., Peloquin S., Shimotake T., Sehring S., Sun Y., Sullivan J., Rogers E., Barkovich A. J., Rowitch D., Ferriero D. M.:
Neurocritical care for neonates
Neurocrit. Care 2010; 12(3): 421-9.

Barkovich A. J.:
Current concepts of polymicrogyria
Neuroradiology 2010; 52(6): 479-87.

Shen J., Gilmore E. C., Marshall C. A., Haddadin M., Reynolds J. J., Eyaid W., Bodell A., Barry B., Gleason D., Allen K., Ganesh V. S., Chang B. S., Grix A., Hill R. S., Topcu M., Caldecott K. W., Barkovich A. J., Walsh C. A.:
Mutations in PNKP cause microcephaly, seizures and defects in DNA repair
Nat. Genet. 2010; 42(3): 245-9.