The Clinical Core established earlier has been combined with the Brain Bank Core. This newly formed core will recruit new subjects for brain tissue and neuroimaging studies. It will clinically follow previously recruited subjects and will perform a single neuropsychological and diagnostic assessment of newly recruited subjects who are likely to come to autopsy. Those subjects who come to autopsy without the benefit of antemortem diagnosis and assessment will receive expert review of medical records and informant interviews to complete a structured psychological autopsy. The Mount Sinai School of Medicine (MSSM) / Bronx Veterans Affairs Medical Center Brain Bank (BB) has been operating for approximately 23 years. The schizophrenia component of the bank has been in operation since 1989. Over 1380 brain tissue specimens have been banked and include 147 confirmed schizophrenia cases with no significant neuropathology or psychiatric comorbidity. In addition, 145 control cases are also available. In the past 18 months this cohort has been expanded to include 21 cases of schizophrenia under the age of 61 and 25 similarly aged controls. In addition, a cohort or 48 cases with major depression or bipolar disease has been added. Additional schizophrenic and control cases are accrued on a continual basis and the enrollment projections and objectives of the Clinical Assessment Core indicate that the number of schizophrenic cases available for autopsy will continue or grow during the next 5 years. All specimens are collected with the absolute minimum postmortem delay as possible (mode PMI = 6 hours for cases with legal next of kin present (65%)). Each brain specimen is banked in both flash-frozen and fixed form and receives a full state-of-the-art neuropathology assessment. Clinical records are searched for every case and all medical conditions and medications received during at least the last 12 months of life are recorded. This core has collaborated with Dr. Dwark (Columbia) and has confirm the initial schizophrenia-associated myelin gene expression deficit findings of the CCNMD in the brains of persons dying at younger ages (mean age 51).
The aim of this core is to continue to perform state-of-the-art clinical assessments and brain banking to meet the needs of projects 1 (Hof), 2 (O'Donovan), 3 (Buxbaum) and 4 (Buchsbaum) of the CCNMD, the schizophrenia-associated funded projects that are dependent on the CCNMD, as well as to meet the needs of future, as yet, unspecified studies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Specialized Center (P50)
Project #
5P50MH066392-07
Application #
7847701
Study Section
Special Emphasis Panel (ZMH1)
Project Start
Project End
Budget Start
2009-06-01
Budget End
2010-05-31
Support Year
7
Fiscal Year
2009
Total Cost
$401,367
Indirect Cost
Name
Icahn School of Medicine at Mount Sinai
Department
Type
DUNS #
078861598
City
New York
State
NY
Country
United States
Zip Code
10029
Amiri, Anahita; Coppola, Gianfilippo; Scuderi, Soraya et al. (2018) Transcriptome and epigenome landscape of human cortical development modeled in organoids. Science 362:
Giambartolomei, Claudia; Zhenli Liu, Jimmy; Zhang, Wen et al. (2018) A Bayesian framework for multiple trait colocalization from summary association statistics. Bioinformatics 34:2538-2545
Toker, Lilah; Mancarci, Burak Ogan; Tripathy, Shreejoy et al. (2018) Transcriptomic Evidence for Alterations in Astrocytes and Parvalbumin Interneurons in Subjects With Bipolar Disorder and Schizophrenia. Biol Psychiatry 84:787-796
Huckins, L M; Hatzikotoulas, K; Southam, L et al. (2018) Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa. Mol Psychiatry 23:1169-1180
Wang, Daifeng; Liu, Shuang; Warrell, Jonathan et al. (2018) Comprehensive functional genomic resource and integrative model for the human brain. Science 362:
Mitchell, A C; Javidfar, B; Pothula, V et al. (2018) MEF2C transcription factor is associated with the genetic and epigenetic risk architecture of schizophrenia and improves cognition in mice. Mol Psychiatry 23:123-132
Bryois, Julien; Garrett, Melanie E; Song, Lingyun et al. (2018) Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia. Nat Commun 9:3121
Fazio, Leonardo; Pergola, Giulio; Papalino, Marco et al. (2018) Transcriptomic context of DRD1 is associated with prefrontal activity and behavior during working memory. Proc Natl Acad Sci U S A 115:5582-5587
Gusev, Alexander; Mancuso, Nicholas; Won, Hyejung et al. (2018) Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights. Nat Genet 50:538-548
Mitelman, Serge A; Bralet, Marie-Cecile; Mehmet Haznedar, M et al. (2018) Positron emission tomography assessment of cerebral glucose metabolic rates in autism spectrum disorder and schizophrenia. Brain Imaging Behav 12:532-546

Showing the most recent 10 out of 153 publications