Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Ioana L Coman"'
Autor:
Christopher eMcCarthy, Avinash eRamprashad, Carlie eThompson, Jo-Anna eBotti, Ioana L Coman, Wendy R. Kates
Publikováno v:
Frontiers in Neuroscience, Vol 9 (2015)
This paper examined whether FreeSurfer - generated data differed between a fully – automated, unedited pipeline and an edited pipeline that included the application of control points to correct errors in white matter segmentation. In a sample of 30
Externí odkaz:
https://doaj.org/article/7b29de7cbce3436d807ac72414c20420
Autor:
Daniel S. Tylee, Zora Kikinis, Thomas P. Quinn, Kevin M. Antshel, Wanda Fremont, Muhammad A. Tahir, Anni Zhu, Xue Gong, Stephen J. Glatt, Ioana L. Coman, Martha E. Shenton, Wendy R. Kates, Nikos Makris
Publikováno v:
NeuroImage: Clinical, Vol 15, Iss , Pp 832-842 (2017)
Chromosome 22q11.2 deletion syndrome (22q11.2DS) is a genetic neurodevelopmental syndrome that has been studied intensively in order to understand relationships between the genetic microdeletion, brain development, cognitive function, and the emergen
Externí odkaz:
https://doaj.org/article/cb3aa6b71cf44449a17b7e94312ce4eb
Autor:
Marek Kubicki, Ioana L. Coman, Nikos Makris, Sylvain Bouix, Zora Kikinis, Carina Heller, Saskia Steinmann, Kevin M. Antshel, Thomas Weiß, Stefan R. Schweinberger, Wendy R. Kates, James J. Levitt, Wanda Fremont
Publikováno v:
Schizophr Res
Background Abnormalities in fronto-striatal-thalamic (FST) sub-circuits are present in schizophrenia and are associated with cognitive impairments. However, it remains unknown whether abnormalities in FST sub-circuits are present before psychosis ons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ab4eea1275a3e2ca74cb6348b469407
https://doi.org/10.1016/j.schres.2020.09.008
https://doi.org/10.1016/j.schres.2020.09.008
Autor:
Kevin M. Antshel, Ioana L. Coman, Wanda Fremont, Thomas Weiss, Sylvain Bouix, Marek Kubicki, Wendy R. Kates, Sophia Swago, Elisabetta C. del Re, Carina Heller, Zora Kikinis
Publikováno v:
Psychiatry research. 301
The 22q11.2 deletion syndrome (22q11DS) is a developmental genetic syndrome associated with a 30% risk for developing schizophrenia. Lateral ventricles and subcortical structures are abnormal in this syndrome as well as in schizophrenia. Here, we inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::785f9ee7a81803da3a739eb9d0e4f5a8
https://pubmed.ncbi.nlm.nih.gov/33993037
https://pubmed.ncbi.nlm.nih.gov/33993037
Autor:
Marek Kubicki, Stefan R. Schweinberger, Wendy R. Kates, Carina Heller, Lily Charron, Saskia Steinmann, Thomas Weiß, Sylvain Bouix, Ioana L. Coman, Nikos Makris, Zora Kikinis, Wanda Fremont, Kevin M. Antshel, Martha E. Shenton, James J. Levitt
Publikováno v:
Schizophrenia Bulletin
Background Cognitive decline is considered a fundamental component in schizophrenia. Abnormalities in fronto-striatal-thalamic (FST) sub-circuits are present in schizophrenia and are associated with cognitive impairments. However, it remains unknown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17f3199337218f212d1e350e217db84d
http://europepmc.org/articles/PMC7234482
http://europepmc.org/articles/PMC7234482
Autor:
Sylvain Bouix, Carina Heller, Kevin M. Antshel, Zora Kikinis, Marek Kubicki, Wendy R. Kates, Wanda Fremont, Ioana L. Coman, Sophia Swago, Thomas Weiss, Elisabetta C. del Re
Publikováno v:
Biological Psychiatry. 89:S370
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::317ae6f2c78dfc6c175603f434703d6a
https://doi.org/10.1016/j.biopsych.2021.02.920
https://doi.org/10.1016/j.biopsych.2021.02.920
Autor:
Martha E. Shenton, Yingying Tang, Sylvain Bouix, Nikos Makris, Wendy R. Kates, Kang Ik K. Cho, Ioana L. Coman, Petya D. Radoeva, Marek Kubicki, Wanda Fremont, Kevin M. Antshel, Jun Soo Kwon, Zora Kikinis, Ryan Eckbo
Publikováno v:
Brain Imaging and Behavior. 11:1353-1364
22q11.2 Deletion Syndrome (22q11DS) is considered to be a promising cohort to explore biomarkers of schizophrenia risk based on a 30 % probability of developing schizophrenia in adulthood. In this study, we investigated abnormalities in the microstru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b7a4f06f198d9c95bdb325fa80aaa5f
https://doi.org/10.1007/s11682-016-9602-x
https://doi.org/10.1007/s11682-016-9602-x
Autor:
Ioana L. Coman, Wanda Fremont, Sylvain Bouix, Ofer Pasternak, Yogesh Rathi, Marek Kubicki, Wendy R. Kates, Martha E. Shenton, Valerie J. Sydnor, Kevin M. Antshel, Zora Kikinis, Nikos Makris
Publikováno v:
NeuroImage : Clinical
NeuroImage: Clinical, Vol 21, Iss, Pp-(2019)
NeuroImage: Clinical, Vol 21, Iss, Pp-(2019)
Background 22q11.2 Deletion Syndrome (22q11DS) is a genetic, neurodevelopmental disorder characterized by a chromosomal deletion and a distinct cognitive profile. Although abnormalities in the macrostructure of the cortex have been identified in indi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d7a94940a21abb7e6b1872e8fd2186d
http://europepmc.org/articles/PMC6411601
http://europepmc.org/articles/PMC6411601
Autor:
Ioana L. Coman, Carlie A. Thompson, Wendy R. Kates, Leah M. Mattiaccio, Wanda Fremont, Kevin M. Antshel
Publikováno v:
Behavioral and Brain Functions : BBF
Behavioral and Brain Functions, Vol 14, Iss 1, Pp 1-11 (2018)
Behavioral and Brain Functions, Vol 14, Iss 1, Pp 1-11 (2018)
Background 22q11.2 deletion syndrome (22q11DS) is a neurodevelopmental syndrome associated with deficits in cognitive and emotional processing. This syndrome represents one of the highest risk factors for the development of schizophrenia. Previous st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8043677ca5e4bb4d88d758314de42e21
http://europepmc.org/articles/PMC5775582
http://europepmc.org/articles/PMC5775582
Autor:
Carrie E. Bearden, Katherine H. Karlsgodt, Jennifer K. Forsyth, Lucina Q. Uddin, Nurit Hirsh, Wendy R. Kates, Leila Kushan, Ioana L. Coman, Leah Mattiacio, Ariana Anderson, Matthew J. Schreiner
Publikováno v:
Cerebral cortex (New York, N.Y. : 1991), vol 27, iss 6
22q11.2 Deletion syndrome (22q11DS) is a genetic disorder associated with numerous phenotypic consequences and is one of the greatest known risk factors for psychosis. We investigated intrinsic-connectivity-networks (ICNs) as potential biomarkers for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83c0e6cd17ba2e072eb01419b336927b
https://escholarship.org/uc/item/91b245dw
https://escholarship.org/uc/item/91b245dw
