Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jessica Kaczorowski"'
Autor:
Kathryn Kemp, Jessica Kaczorowski, Chris J Burgin, Michael Raulin, Donald Lynam, Chelsea Sleep, Josh Miller, Neus Barrantes-Vidal, Thomas Richard Kwapil
The underlying vulnerability for schizophrenia-spectrum disorders is expressed across a continuum of clinical and subclinical symptoms and impairment referred to as schizotypy. Schizotypy is a multidimensional construct with positive, negative, and d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::960ffae944581c9609ed0c0cc027c20a
https://doi.org/10.31234/osf.io/97tpw
https://doi.org/10.31234/osf.io/97tpw
Autor:
Matcheri S. Keshavan, Jessica Kaczorowski, Stephen R. Hooper, Kelly Schoch, Allyn McConkie-Rosell, Vandana Shashi, Thomas R. Kwapil, Kathryn E. Lewandowski
Publikováno v:
Journal of Genetic Counseling. 19:535-544
The purpose of this study is to examine the association between parental socio-economic status (SES) and childhood neurocognition and behavior in children with chromosome 22q11.2 deletion syndrome (22q11DS). Although undoubtedly, the deletion of gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::712eec370991938b17aed655926ec061
https://doi.org/10.1007/s10897-010-9309-x
https://doi.org/10.1007/s10897-010-9309-x
Autor:
Vandana Shashi, Thomas R. Kwapil, Margaret N. Berry, Kelly Schoch, Matcheri S. Keshavan, Edward J. Spence, Timothy D. Howard, Jessica Kaczorowski
Publikováno v:
Psychiatry Research. 178:433-436
The COMT gene is thought to contribute to the cognitive/psychiatric phenotypes in 22q11.2 deletion syndrome. We measured these manifestations against the Val/Met alleles of the COMT gene, in 40 nonpsychotic 22q11DS children. The Val allele was associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5066d9c6e42fe1aad37ba2ab42452681
https://doi.org/10.1016/j.psychres.2010.04.048
https://doi.org/10.1016/j.psychres.2010.04.048
Autor:
Margaret N. Berry, Jessica Kaczorowski, Vandana Shashi, Thomas R. Kwapil, Matcheri S. Keshavan, Timothy D. Howard, Rajaprabhakaran Rajarethinam, Edward J. Spence, Diwadkar Vaibhav, Konasale M. Prasad, Dhruman D. Goradia, Cesar S. Santos
Publikováno v:
Psychiatry Research: Neuroimaging. 181:1-8
Chromosome 22q11.2 deletion syndrome (22q11DS) is associated with cognitive deficits and morphometric brain abnormalities in childhood and a markedly elevated risk of schizophrenia in adolescence/early adulthood. Determining the relationship between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0e2c054581f6c298d9c3a5e9ec7645b
https://doi.org/10.1016/j.pscychresns.2009.07.003
https://doi.org/10.1016/j.pscychresns.2009.07.003
Publikováno v:
Schizophrenia research. 115(2-3)
Patients with schizophrenia often exhibit structural brain abnormalities, as well as neurological soft signs (NSS), consistent with its conceptualization as a neurodevelopmental disorder. NSS are mild, presumably nonlocalizing, neurological impairmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4caf97a78c939b0a77747f4764282139
https://pubmed.ncbi.nlm.nih.gov/19651490
https://pubmed.ncbi.nlm.nih.gov/19651490