Tim Ziermans

Dr. Tim Ziermans

orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2006 in Biological Psychiatry
Verified
Journal Article
Closed access
SDSarah Durston
Sarah Durston
MMMartijn Mulder
Martijn Mulder
BCB.J. Casey
B.J. Casey
TZTim Ziermans
Tim Ziermans
HEHerman van Engeland
Herman van Engeland

7 October 2010 in Schizophrenia Bulletin
Verified
Journal Article
Open access
TZTim Ziermans
Tim Ziermans
PSPatricia F. Schothorst
Patricia F. Schothorst
HSHugo G. Schnack
Hugo G. Schnack
PKP. Cédric M. P. Koolschijn
P. Cédric M. P. Koolschijn
RKRené S. Kahn
René S. Kahn
SDSarah Durston
Sarah Durston
Ultra-high risk (UHR) for psychosis has been associated with widespread structural brain changes in young adults. The onset of these changes and their subsequent progression over time are not well understood. Rate of brain change over time was investigated in 43 adolescents at UHR for psychosis compared with 30 healthy controls. Brain volumes (total brain, gray matter, white matter [WM], cerebellum, and ventricles), cortical thickness, and voxel-based morphometry were measured at baseline and at follow-up (2 y after baseline) and compared between UHR individuals and controls. Post hoc analyses were done for UHR individuals who became psychotic (N = 8) and those who did not (N = 35). UHR individuals showed a smaller increase in cerebral WM over time than controls and more cortical thinning in the left middle temporal gyrus. Post hoc, a more pronounced decrease over time in total brain and WM volume was found for UHR individuals who became psychotic relative to controls and a greater decrease in total brain volume than individuals who were not psychotic. Furthermore, UHR individuals with subsequent psychosis displayed more thinning than controls in widespread areas in the left anterior cingulate, precuneus, and temporo-parieto-occipital area. Volume loss in the individuals who developed psychosis could not be attributed to medication use. The development of psychosis during adolescence is associated with progressive structural brain changes around the time of onset. These changes cannot be attributed to (antipsychotic) medication use and are therefore likely to reflect a pathophysiological process related to clinical manifestation of psychosis.

1 August 2011 in Biological Psychiatry
Verified
Journal Article
Closed access
IDIroise Dumontheil
Iroise Dumontheil
CRChantal Roggeman
Chantal Roggeman
TZTim Ziermans
Tim Ziermans
MPMyriam Peyrard-Janvid
Myriam Peyrard-Janvid
HMHans Matsson
Hans Matsson
TKTorkel Klingberg
Torkel Klingberg

1 March 2011 in Schizophrenia Research
Verified
Journal Article
Closed access
TZTim Ziermans
Tim Ziermans
PSPatricia F. Schothorst
Patricia F. Schothorst
MSMirjam Sprong
Mirjam Sprong
HEHerman van Engeland
Herman van Engeland

11 July 2016 in Autism
Verified
Journal Article
Open access
RDRenee R Dijkhuis
Renee R Dijkhuis
TZTim Ziermans
Tim Ziermans
SRSophie Van Rijn
Sophie Van Rijn
WSWouter G Staal
Wouter G Staal
HSHanna Swaab
Hanna Swaab
Background: Autism is generally associated with poor functional outcome but little is known about predictors of quality of life, especially during early adulthood. This study was conducted to assess subjective quality of life during early adulthood in high-functioning autism spectrum disorder and its relation with self-regulating abilities. Individuals with high-functioning autism spectrum disorder who progressed into post-secondary higher education (N = 75) were compared to a typical peer control group (N = 28) based on behavioral self-report questionnaires. The results indicated that individuals with high-functioning autism spectrum disorder reported significantly lower subjective quality of life than typical controls (p < 0.001, effect size (d) = 1.84). In addition, individuals with high-functioning autism spectrum disorder reported more problems with emotion processing (p < 0.05, effect size (d) = 0.79) and daily executive functioning (p < 0.001, effect size (d) = 1.29) than controls. A higher level of executive functioning problems was related to lower quality of life in the high-functioning autism spectrum disorder group, but no significant relation between level of emotion processing and subjective quality of life became apparent in the regression analysis. Our findings show that even in high-functioning young adults with autism, executive functioning, emotion processing, and subjective quality of life are low compared to typically developing peers. Furthermore, these results emphasize the importance of targeting executive functioning problems in individuals with autism to improve subjective quality of life.

1 January 2008 in Journal of the American Academy of Child & Adolescent Psychiatry
Verified
Journal Article
Closed access
PDF file
SDSarah Durston
Sarah Durston
JFJohn A. Fossella
John A. Fossella
MMMartijn J. Mulder
Martijn J. Mulder
BCB.J. Casey
B.J. Casey
TZTim Ziermans
Tim Ziermans
HEHerman VAN Engeland
Herman VAN Engeland