Rare copy number variants in individuals at clinical high risk for psychosis: Enrichment of synaptic/brain‐related functional pathways-Reference-Cited by-同舟云学术

Rare copy number variants in individuals at clinical high risk for psychosis: Enrichment of synaptic/brain‐related functional pathways

Published:2019-11-19 Issue:2 Volume:183 Page:140-151
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am J Med Genet

Author:

Jagannath Vinita¹^ORCID,Grünblatt Edna¹²³^ORCID,Theodoridou Anastasia⁴⁵,Oneda Beatrice⁶,Roth Alexander¹,Gerstenberg Miriam¹,Franscini Maurizia¹,Traber‐Walker Nina¹,Correll Christoph U.⁷⁸⁹¹⁰,Heekeren Karsten⁴⁵,Rössler Wulf⁴¹¹,Rauch Anita²³⁶^ORCID,Walitza Susanne¹²³⁴^ORCID

Affiliation:

1. Department of Child and Adolescent Psychiatry and Psychotherapy, University Hospital of PsychiatryUniversity of Zurich Zurich Switzerland

2. Neuroscience Center Zurich, University of Zurich and ETH Zurich Zurich Switzerland

3. Zurich Center for Integrative Human PhysiologyUniversity of Zurich Zurich Switzerland

4. The Zurich Program for Sustainable Development of Mental Health Services (ZInEP)University Hospital of Psychiatry Zurich Zurich Switzerland

5. Department of Psychiatry, Psychotherapy and Psychosomatics, University Hospital of PsychiatryUniversity of Zurich Zurich Switzerland

6. Institute of Medical GeneticsUniversity of Zurich Schlieren Switzerland

7. Department of PsychiatryThe Zucker Hillside Hospital, Northwell Health Glen Oaks New York

8. Department of Psychiatry and Molecular MedicineZucker School of Medicine at Hofstra/Northwell Hempstead New York

9. The Feinstein Institute for Medical Research Manhasset New York

10. Department of Child and Adolescent PsychiatryCharité Universitätsmedizin Berlin Germany

11. Department of Psychiatry and PsychotherapyCharité Universitätsmedizin Berlin Berlin Germany

Funder

ZInEP

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.b.32770

Reference104 articles.

1. Reliability and validity of a depression rating scale for schizophrenics

2. Genome-wide linkage in Utah autism pedigrees

3. The clinical significance of small copy number variants in neurodevelopmental disorders

4. Gene Ontology: tool for the unification of biology

5. Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and Disease

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