The NIMH Genetics Initiative is driven by the need to understand the inherited (genetic), environmental and physiologic causes of mental disorders, such as schizophrenia, bipolar disorder, depression, and autism. This goal will be most readily attained if annotated clinical data and biological materials (i.e., DNA, RNA, plasma proteins, and cell lines) produced from the blood of affected and unaffected individuals in large cohorts or families are shared among many researchers. To this end, the NIMH has established a central resource for producing and banking biological materials and associated clinical data. Per NIH data sharing policies, this resource, currently known as the NIMH Center for Collaborative Genetic Studies of Mental Disorders (""""""""the Center""""""""), has distributed these biological samples and clinical data to a large number of qualified researchers investigating the causes of mental disorders. We have maintained the Center since September 1998, during which 70,797 blood samples were submitted to the Center, including an unprecedented 52,578 samples since July 2003. Due to technical improvements the Center has processed submitted blood samples into lymphoblast cell lines with an unprecedented 99.7% success. Since July 2003, the Center has distributed 306,423 DNA samples and 4,006 lymphoblast cell lines, and made more than 400 distributions of clinical and genetic data to ~300 mental health researchers. The scope and quality of these distributed resources have empowered the field of mental health genetics to produce a better understanding of the biology of mental disorders. Herein, we propose to continue as the Center for Genomic Studies on Mental Disorders. The Biologics Core will continue to produce and distribute renewable biologic research resources from blood and cell lines. The Data Management and Genomics Core will continue improvements to the web-based repository of clinical and genotype data and associated bioinformatics and computational genomics tools. The Analysis Core will produce methodology designed to integrate and analyze large, independent sets of genetic and clinical data. The overriding aim of the Center is to continue to serve the scientific needs of NIMH and other mental health researchers in a flexible and innovative manner while respecting human subject confidentiality, informed consent issues, and PI prerogatives.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Resource-Related Research Projects--Cooperative Agreements (U24)
Project #
3U24MH068457-07S1
Application #
7937467
Study Section
Special Emphasis Panel (ZMH1-ERB-C (07))
Program Officer
Lehner, Thomas
Project Start
2003-07-01
Project End
2013-05-31
Budget Start
2009-06-01
Budget End
2010-05-31
Support Year
7
Fiscal Year
2009
Total Cost
$3,370,690
Indirect Cost
Name
Rutgers University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
001912864
City
New Brunswick
State
NJ
Country
United States
Zip Code
08901
Zhang, Tianxiao; Hou, Liping; Chen, David T et al. (2018) Exome sequencing of a large family identifies potential candidate genes contributing risk to bipolar disorder. Gene 645:119-123
Sun, N; Nasello, C; Deng, L et al. (2018) The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family. Mol Psychiatry 23:1487-1495
VAN DER Mee, Denise J; Fedko, Iryna O; Hottenga, Jouke-Jan et al. (2018) Dopaminergic Genetic Variants and Voluntary Externally Paced Exercise Behavior. Med Sci Sports Exerc 50:700-708
Abdulkadir, Mohamed; Londono, Douglas; Gordon, Derek et al. (2018) Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach. Eur Arch Psychiatry Clin Neurosci 268:301-316
Culverhouse, R C; Saccone, N L; Horton, A C et al. (2018) Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression. Mol Psychiatry 23:133-142
Thornton, Laura M; Munn-Chernoff, Melissa A; Baker, Jessica H et al. (2018) The Anorexia Nervosa Genetics Initiative (ANGI): Overview and methods. Contemp Clin Trials 74:61-69
Smit, Dirk J A; Wright, Margaret J; Meyers, Jacquelyn L et al. (2018) Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. Hum Brain Mapp 39:4183-4195
Hysi, Pirro G; Valdes, Ana M; Liu, Fan et al. (2018) Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability. Nat Genet 50:652-656
Van der Auwera, Sandra; Peyrot, Wouter J; Milaneschi, Yuri et al. (2018) Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes: The childhood trauma working-group of PGC-MDD. Am J Med Genet B Neuropsychiatr Genet 177:40-49
Wain, Louise V (see original citation for additional authors) (2017) Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. Hypertension :

Showing the most recent 10 out of 107 publications