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Zoran Brkanac, MD

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Zoran Brkanac, MD

Psychiatry and Behavioral Health, Autism Center

On staff since July 2005

Academic Title: Assistant Professor

Overview

Board Certification(s)
Psychiatry
Child and Adolescent Psychiatry
Medical/Professional School
University of Zagreb, Zagreb
University of Texas Medical School at San Antonio, San Antonio
Residency
Psychiatry, University of Washington School of Medicine, Seattle
Child Psychiatry, University of Washington School of Medicine, Seattle
Clinical Interests

Psychaitry, behavioral genetics

Publications

IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23.
American journal of human genetics , 2009 May: 692-7
Pharmacology and genetics of autism: implications for diagnosis and treatment.
Personalized medicine , 2008 Nov: 599-607
Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci.
Behavior genetics , 2008 Sep: 462-75
Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics , 2007 Jun 5: 556-60
Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics , 2006 Jan 5: 15-27
Genetic determinants of addiction to opioids and cocaine.
Harvard review of psychiatry , 2005 Jul-Aug: 218-32
Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics , 2004 Nov 15: 67-75
Prazosin in PTSD.
Journal of the American Academy of Child and Adolescent Psychiatry , 2003 Apr: 384-5
Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.
American journal of human genetics , 2003 Apr: 839-49
A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.
Archives of neurology , 2002 Aug: 1291-5
Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
American journal of medical genetics , 2002 May 8: 450-7

Primary Office

University of Washington
UW Box 356560 - Psychiatry
1959 NE Pacific St
Seattle, WA 98195-6560
206-685-1240

Additional Offices

Seattle Children's
OA.5.154 - Child Psychiatry
4800 Sand Point Way NE
Seattle, WA 98105
206-987-2164

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