Ioana L. Coman, Ph.D.
Affiliations: | 2000 | Wayne State University, Detroit, MI, United States |
Area:
Computer Science, Information ScienceGoogle:
"Ioana Coman"Parents
Sign in to add mentorIshwar K. Sethi | grad student | 2000 | Wayne State | |
(Algorithms for efficient management and retrieval of visual documents.) |
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Publications
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Tylee DS, Kikinis Z, Quinn TP, et al. (2017) Machine-learning classification of 22q11.2 deletion syndrome: A diffusion tensor imaging study. Neuroimage. Clinical. 15: 832-842 |
Olszewski AK, Kikinis Z, Gonzalez CS, et al. (2017) The social brain network in 22q11.2 deletion syndrome: a diffusion tensor imaging study. Behavioral and Brain Functions : Bbf. 13: 4 |
Kikinis Z, Cho KI, Coman IL, et al. (2016) Abnormalities in brain white matter in adolescents with 22q11.2 deletion syndrome and psychotic symptoms. Brain Imaging and Behavior |
Mattiaccio LM, Coman IL, Schreiner MJ, et al. (2016) Atypical functional connectivity in resting-state networks of individuals with 22q11.2 deletion syndrome: associations with neurocognitive and psychiatric functioning. Journal of Neurodevelopmental Disorders. 8: 2 |
Kikinis Z, Cho KK, Coman IL, et al. (2015) Developmental abnormalities in brain white matter in prodromes with 22q11.2 Deletion Syndrome: A tract based spatial statistics study. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 47: 88-9 |
Kates WR, Olszewski AK, Gnirke MH, et al. (2015) White matter microstructural abnormalities of the cingulum bundle in youths with 22q11.2 deletion syndrome: associations with medication, neuropsychological function, and prodromal symptoms of psychosis. Schizophrenia Research. 161: 76-84 |
Perlstein MD, Chohan MR, Coman IL, et al. (2014) White matter abnormalities in 22q11.2 deletion syndrome: preliminary associations with the Nogo-66 receptor gene and symptoms of psychosis. Schizophrenia Research. 152: 117-23 |
Radoeva PD, Coman IL, Antshel KM, et al. (2012) Atlas-based white matter analysis in individuals with velo-cardio-facial syndrome (22q11.2 deletion syndrome) and unaffected siblings. Behavioral and Brain Functions : Bbf. 8: 38 |
Coman IL, Gnirke MH, Middleton FA, et al. (2010) The effects of gender and catechol O-methyltransferase (COMT) Val108/158Met polymorphism on emotion regulation in velo-cardio-facial syndrome (22q11.2 deletion syndrome): An fMRI study. Neuroimage. 53: 1043-50 |
Unlu MZ, Krol A, Magri A, et al. (2010) Computerized method for nonrigid MR-to-PET breast-image registration. Computers in Biology and Medicine. 40: 37-53 |