Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

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Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome

Published:2017-10-08 Issue:1 Volume:39 Page:232-248
ISSN:1065-9471
Container-title:Human Brain Mapping
language:en
Short-container-title:Hum. Brain Mapp.

Author:

Zhan Liang¹^ORCID,Jenkins Lisanne M.²^ORCID,Zhang Aifeng²^ORCID,Conte Giorgio³,Forbes Angus³,Harvey Danielle⁴,Angkustsiri Kathleen⁵,Goodrich-Hunsaker Naomi J.⁶⁷^ORCID,Durdle Courtney⁶,Lee Aaron⁶,Schumann Cyndi⁶,Carmichael Owen⁸^ORCID,Kalish Kristopher⁹,Leow Alex D.²¹⁰,Simon Tony J.⁶

Affiliation:

1. Computer Engineering Program; University of Wisconsin-Stout; Wisconsin

2. Department of Psychiatry; University of Illinois; Chicago Illinois

3. Department of Computer Science; University of Illinois; Chicago Illinois

4. Division of Biostatistics, Department of Public Health Sciences, School of Medicine; University of California; Davis California

5. Department of Pediatrics; University of California; Davis California

6. Department of Psychiatry and Behavioral Sciences; University of California; Davis California

7. Department of Psychology; Brigham Young University; Provo Utah

8. Pennington Biomedical Research Center, Louisiana State University; Baton Rouge Louisiana

9. Department of Neurology; University of California; Davis California

10. Department of Bioengineering; University of Illinois; Chicago Illinois

Funder

National Institute on Aging

National Institute of Mental Health

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Publisher

Wiley

Subject

Neurology (clinical),Neurology,Radiology, Nuclear Medicine and imaging,Radiological and Ultrasound Technology,Anatomy

Reference104 articles.

1. The hallucinating brain: A review of structural and functional neuroimaging studies of hallucinations;Allen;Neurosci Biobehav Rev,2008

2. White matter abnormalities in adults with 22q11 deletion syndrome with and without schizophrenia;Alves;Schizophr Res,2011

3. An integrated approach to correction for off-resonance effects and subject movement in diffusion MR imaging;Andersson;NeuroImage,2016

4. Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): Autism spectrum disorder or a different endophenotype?;Angkustsiri;J Autism Dev Disord,2014

5. An examination of the relationship of anxiety and intelligence to adaptive functioning in children with chromosome 22q11.2 deletion syndrome;Angkustsiri;J Dev Behav Pediatr,2012

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1. Cortical gradient perturbation in attention deficit hyperactivity disorder correlates with neurotransmitter‐, cell type‐specific and chromosome‐ transcriptomic signatures;Psychiatry and Clinical Neurosciences;2024-02-09

2. Opposing white matter microstructure abnormalities in 22q11.2 deletion and duplication carriers;Translational Psychiatry;2021-11-10

3. Brain microstructural abnormalities in 22q11.2 deletion syndrome: A systematic review of diffusion tensor imaging studies;European Neuropsychopharmacology;2021-11

4. Pathways to understanding psychosis through rare – 22q11.2DS - and common variants;Current Opinion in Genetics & Development;2021-06

5. Structural control energy of resting‐state functional brain states reveals less cost‐effective brain dynamics in psychosis vulnerability;Human Brain Mapping;2021-02-10

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