ThomasFernandezMD

PubMed

• 209 citations
  Partitioning the heritability of tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture
  Lea K. Davis, Dongmei Yu, Clare L. Keenan, Eric R. Gamazon, Anuar Konkashbaev
  Plos Genetics. 2013-10-24
• 915 citations
  Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
  Stephen Sanders, A. Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T. Murtha
  Neuron. 2011-06-09
• 17 citations
  Whole-exome sequencing identifies genes associated with Tourette's disorder in multiplex families.
  Xiaolong Cao, Yeting Zhang, Mohamed Abdulkadir, Li Deng, Thomas V. Fernandez
  Molecular Psychiatry. 2021-04-09

Journal Articles

• Investigation of Previously Implicated Genetic Variants in Chronic Tic Disorders: A Transmission Disequilibrium Test Approach  
  Barbara J Coffey, Donald L Gilbert, Lawrence W Brown, Dorothy E Grice, Thomas V Fernandez, Samuel Kuperman, Samuel H Zinner, European Archives of Psychiatry and Clinical Neuroscience
• Transcranial Magnetic Stimulation of Wernicke’s and right homologous sites to curtail “voices”: A randomized trial.  
  Hoffman RE, Wu K, Pittman B, Cahill JD, Hawkins KA, Fernandez T, Hannestad J, Biological Psychiatry, 1/1/2013
• Genome-wide association study of Tourette syndrome.  
  Scharf JM, Yu D, Matthews CA, Neale BM, et al., Molecular Psychiatry, 1/1/2012
• Rare copy number variants in Tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.  
  Fernandez TV, Sanders SJ, Yurkiewicz IR, et al., Biological Psychiatry, 1/1/2012
• Multiple recurrent de novo copy number variations (CNVs), including duplications of the 7q11.23 Williams-Buren syndrome region, are strongly associated with autism.  
  Sanders SJ, Ercan-Sencicek AG, Hus V, et al., Neuron, 1/1/2011
• Elevated functional connectivity along a corticostriatal loop and the mechanism of auditory/verbal hallucinations in patients with schizophrenia.  
  Hoffman RE, Fernandez T, Pittman B, Hampson M, Biological Psychiatry, 1/1/2011
• L-histidine decarboxylase and Tourette’s syndrome.  
  Ercan-Sencicek AG, Stillman AA, etl., New England Journal of Medicine, 1/1/2010
• 3p deletion and (skewed) literature review (reply).  
  Fernandez TV, State MW, Davalos-Rodriguez NO., American Journal of Medical Genetics, 1/1/2010
• Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.  
  Fernandez TV, et al., American Journal of Medical Genetics, 1/1/2008
• Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.  
  Fernandez T, Morgan T, Davis N, Klin A, Morris A, Farhi A, Lifton RP, State MW, American Journal of Human Genetics, 1/1/2004
• Genetics and Genomics of Neurobehavioral Disorders.  
  Fernandez TV, State MW, Journal of the American Academy of Child and Adolescent Psychiatry, 1/1/2004
• Lessons from childhood-onset schizophrenia.  
  Nicolson R, Lenane M, Hamburger SD, Fernandez T, Bedwell J, Rapoport JL, Brain Research Reviews, 1/1/2000
• Premorbid speech and language impairments in childhood-onset schizophrenia:association with risk factors.  
  Nicolson R, Lenane M, Singaracharlu S, Malaspina D, Giedd JN, Hamburger SD, Gochman P, Bedwell J, Thaker GK, Fernandez T, Wudarsky M, Hommer DW, Rapoport JL, American Journal of Psychiatry, 1/1/2000
• Progressive cortical change during adolescence in childhood-onset schizophrenia. A longitudinal magnetic resonance imaging study.  
  Rapoport JL, Giedd JN, Blumenthal J, Hamburger S, Jeffries N, Fernandez T, Nicolson R, Bedwell J, Lenane M, Zijdenbos A, Paus T, Evans A, Archives of General Psychiatry, 1/1/1999
• Apolipoprotein E alleles in childhood-onset schizophrenia.  
  Fernandez T, Yan WL, Hamburger S, Rapoport JL, Saunders AM, Schapiro M, Ginns EI, Sidransky E, American Journal of Medical Genetics: Neuropsychiatric Genetics, 1/1/1999
• Childhood-onset schizophrenia: progressive brain changes during adolescence.  
  Giedd JN, Jeffries NO, Blumenthal J, Castellanos FX, Vaituzis AC, Fernandez T, Hamburger SD, Liu H, Nelson J, Bedwell J, Tran L, Lenane M, Nicolson R, Rapoport JL, Biological Psychiatry, 1/1/1999
• Obstetrical complications and childhood-onset schizophrenia.  
  Nicolson R, Malaspina D, Giedd JN, Hamburger S, Lenane M, Bedwell J, Fernandez T, Berman A, Susser E, Rapoport JL, American Journal of Psychiatry, 1/1/1999
• Clinical and neurobiological correlates of cytogenetic abnormalities in childhood-onset schizophrenia.  
  Nicolson R, Giedd JN, Lenane M, Hamburger S, Singaracharlu S, Bedwell J, Fernandez T, Thaker GK, Malaspina D, Rapoport JL, American Journal of Psychiatry, 1/1/1999
• Functional differentiation along the anterior-posterior axis of the hippocampus in monkeys.  
  Colombo M, Fernandez T, Nakamura K, Gross CG, Neurophysiology, 1/1/1998
• Brief report: association of sex chromosome anomalies with childhood-onset psychotic disorders.  
  Kumra S, Wiggs E, Krasnewich D, Meck J, Smith A, Bedwell J, Fernandez T, Jacobsen L, Lenane M, Rapoport J, Journal of the American Academy of Child and Adolescent Psychiatry, 1/1/1998
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Books/Book Chapters

• Lewis’s Child and Adolescent Psychiatry: A Comprehensive Textbook 
  Chapter: Assessing Risk: Gene Discovery In Child Psychiatric Disorders. 
  Fernandez TV, State MWEditors: Martin A, Volkmar FR.Lippincott Williams & Wilkins, Philadelphia, PAEdition 4th,2007

Abstracts/Posters

• Searching for the genes of Tourette’s: The Tourette International Collaborative Genetics (TIC Genetics) Study.
  Heiman GA, Fernandez TV, Hoekstra PJ, Dietrich A, king RA, State MW, Tischfield JA, and the TIC Genetics Team, Annual Meeting of the American Society of Human Genetics., 1/1/2012
• Rare Structural and Sequence Variation in Tourette Syndrome and Autism.
  Fernandez TV, 1st Joint Meeting of the European Network for the Study of Gilles de la Tourette Syndrome (EUNetGTS), 12/14/2011
• Rare copy number variants in Tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.
  Fernandez TV, Sanders SJ, Song Y, Leckman JF, King RA, Gilbert DL, Heiman GA, Tischfield JA, Hoekstra PJ, State MW, 50th Annual Meeting of the American College of Neuropsychopharmacology, 1/1/2011
• Rare copy number variants in Tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.
  Fernandez TV, Sanders SJ, Song Y, Leckman JF, King RA, Gilbert DL, Heiman GA, Tischfield JA, Hoekstra PJ, State MW, American Academy of Child and Adolescent Psychiatry Scientific Proceedings, 1/1/2011
• Genetic Investigation of Complex Motor Stereotypies.
  Fernandez T, Sanders S, Mason C, Singer H, Hakonarson H, State MW, American Academy of Child and Adolescent Psychiatry Scientific Proceedings, 1/1/2009
• Elevated functional connectivity in a corticostriatal loop and the mechanism of auditory/verbal hallucinations in patients with schizophrenia.
  Hoffman RE, Fernandez T, Pittman B, Hampson M, Schizophrenia Bulletin, 1/1/2009
• Stereotactically positioned rTMS delivered to optimized Wernicke’s and right superior temporal sites for auditory/verbal hallucinations.
  Hoffman RE, Wu K, Fulbright R, Buchanan R, Fernandez T, Hawkins KA, Constable T, Hampson M, Biological Psychiatry, 1/1/2008
• Screening autism candidate genes based on a balanced translocation.
  Fernandez T, Klin A, Davis N, Koenig K, State M, American Academy of Child and Adolescent Psychiatry Scientific Proceedings, 1/1/2007
• Characterization of contactin 4, a gene involved in mental retardation.
  State MW, Kwan K, Stillman A, Fernandez T, Morgan T, Davis N, Sestan N, American Academy of Child and Adolescent Psychiatry Scientific Proceedings, 1/1/2004
• Analysis of a balanced (4;11) translocation in three autistic siblings.
  Fernandez T, Klin A, Davis N, Koenig K, Farhi A, Volkmar F, State M, American Academy of Child and Adolescent Psychiatry Scientific Proceedings, 1/1/2004
• Premorbid speech and language impairments in childhood-onset schizophrenia: association with risk factors.
  Nicholson R, Lenane M, Singaracharlu S, Bedwell J, Giedd JN, Hamburger SD, Thaker GK, Malaspina D, Fernandez T, Wudarsky M, Hommer DW, Rapoport JL, Schizophrenia Research, 1/1/2000
• HLA alleles in attention-deficit hyperactivity disorder.
  Fernandez T, Lewczyk CM, Castellanos FX, Simonis T, Jacobsen LK, Rapoport JL, Biological Psychiatry, 1/1/1999
• Lack of an association between dopamine transporter (DAT1) & ADHD.
  Castellanos FX, Lewczyk CM, Fernandez T, Koprivica V, Kashani A, Tayebi N, Ginns EI, Rapoport JL, Sidransky E, Molecular Psychiatry, 1/1/1999
• Lack of an association between dopamine transporter (DAT1) and ADHD.
  Lewczyk CM, Fernandez T, Castellanos FX, Koprivica V, Kashani A, Tayebi N, Ginns EI, Rapoport JL, Sidransky E, Biological Psychiatry, 1/1/1999
• Obstetrical complications in childhood-onset schizophrenia.
  Nicolson R, Giedd J, Malaspina D, Lenane M, Fernandez T, Bedwell J, Berman A, Susser E, Rapoport JL, Schizophrenia Research, 1/1/1999
• Premorbid impairments in childhood-onset schizophrenia: association with risk factors.
  Nicolson R, Singaracharlu S, Lenane M, Giedd JN, Hamburger SD, Bedwell J, Fernandez T, Rapoport JL, Biological Psychiatry, 1/1/1999
• Smooth pursuit eye tracking in the relatives of patients with childhood-onset schizophrenia.
  Nicolson R, Hommer D, Thaker G, Brown M, Bedwell J, Lenane M, Fernandez T, Rapoport JL, Schizophrenia Research, 1/1/1999
• Clinical and biological correlates of cytogenetic abnormalities in childhood-onset psychosis.
  Nicolson R, Kumra S, Giedd J, Fernandez T, Bedwell J, Lenane M, Rapoport JL, Biological Psychiatry, 1/1/1998
• Functional differentiation along the anterior-posterior axis of the hippocampus in monkeys.
  Colombo M, Fernandez T, Nakamura K, Gross CG, European Journal of Neuroscience, 1/1/1998
• A comparison of bimodal, visual-tactile neurons in parietal area 7b and ventral premotor cortex of the monkey brain.
  Graziano MSA, Gross CG, Fernandez TV, Society for Neuroscience Abstracts, 1/1/1996
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Lectures

• Genomic Investigations of Tourette Disorder. 
  Annual Meeting for the European Society for the Study of Tourette Syndrome / COST International Conf - 4/26/2013
• From Bedside to Bench: Translational Clinical Science and Tourette Syndrome. 
  Yale Child Study Center Grand Rounds. New Haven, CT. - 1/15/2013
• Previews from the Pipeline: A Data Blitz Featuring Early Career Investigators. 
  American Academy of Child and Adolescent Psychiatry 59th Annual Meeting. San Francisco, CA. - 10/24/2012
• New findings about the Genetics of Tourette Syndrome. 
  5/22/2012
• Update on the Genetics of Tourette Syndrome. 
  Tourette Syndrome Association National Conference. Arlington, VA - 4/20/2012
• Detecting Rare Structural Variants in Neuropsychiatric Disorders. 
  Columbia University Seminar in Genetic Epidemiology. New York, NY. - 2/9/2012
• Genetic Variation in Childhood Movement Disorders. 
  Yale Child Study Center Grand Rounds. New Haven, CT. - 3/15/2011
• Lost In Translation: Challenges in Linking Basic Science with Clinical Practice in Psychiatry. 
  European Research Training Seminar in Child and Adolescent Psychiatry. Siena, Italy. - 11/21/2010
• Genetic Variation in Tourette Syndrome. 
  Yale Department of Psychiatry Grand Rounds. New Haven, CT. - 6/4/2010
• Genetics in Autism Spectrum Disorders: Obstacles and Promising Alternatives for the Future 
  13th International Congress of the European Society of Child & Adolescent Psychiatry. Florence, Ital - 8/25/2007
• The Gene Hunter. 
  Annual meeting of the Donald J. Cohen Medical Student Training Program. Harvard Medical School, Bost - 1/27/2007
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