The Clinical Core established earlier has been combined with the Brain Bank Core. This newly formed corewill recruit new subjects for brain tissue and neuroimaging studies. It will clinically follow previously recruitedsubjects and will perform a single neuropsychological and diagnostic assessment of newly recruited subjectswho are likely to come to autopsy. Those subjects who come to autopsy without the benefit of antemortemdiagnosis and assessment will receive expert review of medical records and informant interviews tocomplete a structured psychological autopsy. The Mount Sinai School of Medicine (MSSM) / Bronx VeteransAffairs Medical Center Brain Bank (BB) has been operating for approximately 23 years. The schizophreniacomponent of the bank has been in operation since 1989. Over 1380 brain tissue specimens have beenbanked and include 147 confirmed schizophrenia cases with no significant neuropathology or psychiatriccomorbidity. In addition, 145 control cases are also available. In the past 18 months this cohort has beenexpanded to include 21 cases of schizophrenia under the age of 61 and 25 similarly aged controls. Inaddition, a cohort or 48 cases with major depression or bipolar disease has been added. Additionalschizophrenic and control cases are accrued on a continual basis and the enrollment projections andobjectives of the Clinical Assessment Core indicate that the number of schizophrenic cases available forautopsy will continue or grow during the next 5 years. All specimens are collected with the absoluteminimum 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-artneuropathology assessment. Clinical records are searched for every case and all medical conditions andmedications received during at least the last 12 months of life are recorded. This core has collaborated withDr. Dwark (Columbia) and has confirm the initial schizophrenia-associated myelin gene expression deficitfindings of the CCNMD in the brains of persons dying at younger ages (mean age 51).
The aim of this core isto continue to perform state-of-the-art clinical assessments and brain banking to meet the needs of projects1 (Hof), 2 (O'Donovan), 3 (Buxbaum) and 4 (Buchsbaum) of the CCNMD, the schizophrenia-associatedfunded 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 #
2P50MH066392-05A1
Application #
7332886
Study Section
Special Emphasis Panel (ZMH1-ERB-S (03))
Project Start
2007-08-01
Project End
2012-05-31
Budget Start
2007-07-19
Budget End
2008-05-31
Support Year
5
Fiscal Year
2007
Total Cost
$411,933
Indirect Cost
Name
Mount Sinai School of Medicine
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