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Child Neuropsychology
A Journal on Normal and Abnormal Development in Childhood and Adolescence
Volume 11, 2005 - Issue 1
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Brief report

Effects of Comt Genotype on Behavioral Symptomatology in the 22q11.2 Deletion Syndrome

Carrie E. Bearden Department of Psychiatry & Biobehavioral Sciences, University of California, Los Angeles, USACorrespondence[email protected]
,
Abbas F. Jawad Department of Biostatistics
,
David R. Lynch Department of Neurology at the Children’s Hospital of Philadelphia, Pennsylvania, USA
,
John R. Monterossso Department of Psychiatry & Biobehavioral Sciences, University of California, Los Angeles, USA
,
Set Sokol Department of Neurology at the Children’s Hospital of Philadelphia, Pennsylvania, USA
,
Donna M. McDonald-McGinn Department of Human Genetics and Molecular Biology
,
Sulagna C. Saitta Department of Human Genetics and Molecular Biology
,
Stacy E. Harris Department of Human Genetics and Molecular Biology
,
Edward Moss Department of Child Development
,
Paul P. Wang Department of Child Development
,
Elaine Zackai Department of Human Genetics and Molecular Biology
,
Beverly S. Emanuel Department of Human Genetics and Molecular Biology
&
Tony J. Simon Department of Child Development
 show all
Pages 109-117 | Published online: 16 Feb 2007

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Linda E. Campbell, Rayna Azuma, Fiona Ambery, Angela Stevens, Anna Smith, Robin G. Morris, Declan G.M. Murphy & Kieran C. Murphy. (2010) Executive functions and memory abilities in children with 22q11.2 deletion syndrome. Australian and New Zealand Journal of Psychiatry 44:4, pages 364-371.
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Kathryn E. Lewandowski. (2007) Relationship of Catechol-O-Methyltransferase to Schizophrenia and Its Correlates: Evidence for Associations and Complex Interactions. Harvard Review of Psychiatry 15:5, pages 233-244.
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Michela Menghi, Ginevra Micangeli, Francesca Tarani, Carolina Putotto, Federica Pirro, Alessandro Mariani, Carla Petrella, Federica Pulvirenti, Bianca Cinicola, Fiorenza Colloridi, Luigi Tarani & Marco Fiore. (2023) Neuroinflammation and Oxidative Stress in Individuals Affected by DiGeorge Syndrome. International Journal of Molecular Sciences 24:4, pages 4242.
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Arianna Benedetti, Cinzia Molent, Weronika Barcik & Francesco Papaleo. (2021) Social behavior in 16p11.2 and 22q11.2 copy number variations: Insights from mice and humans. Genes, Brain and Behavior 21:5.
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Tuana Kant, Emiko Koyama, Clement C. Zai, Joseph H. Beitchman & James L. Kennedy. (2022) COMT Val/Met and Psychopathic Traits in Children and Adolescents: A Systematic Review and New Evidence of a Developmental Trajectory toward Psychopathy. International Journal of Molecular Sciences 23:3, pages 1782.
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Giok Kim, Eunsoo Moon, Je Min Park, Byung Dae Lee, Young Min Lee, Hee Jeong Jeong, Soo Yeon Kim, Kangyoon Lee & Hwagyu Suh. (2020) Various Psychiatric Manifestation in DiGeorge Syndrome (22q11.2 Deletion Syndrome): A Case Report. Clinical Psychopharmacology and Neuroscience 18:3, pages 458-462.
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Sami Boussetta, Lotfi Cherni, Andrew J. Pakstis, Nesrine Ben Salem, Sarra Elkamel, Houssein Khodjet-el-Khil, Kenneth K. Kidd & Amel Ben Ammar Elgaaied. (2019) Usefulness of COMT gene polymorphisms in North African populations. Gene 696, pages 186-196.
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Amanda Oliveira Santos, Natalia Freitas Rossi, Maria da Conceição Faria Freitas Tandel, Antonio Richieri-Costa & Célia Maria Giacheti. (2016) Aspectos da fluência em tarefa de narrativa oral na síndrome del22q11.2. CoDAS 28:4, pages 373-378.
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Asit B. Biswas & Frederick Furniss. (2016) Cognitive phenotype and psychiatric disorder in 22q11.2 deletion syndrome: A review. Research in Developmental Disabilities 53-54, pages 242-257.
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Rayna Azuma, Quinton Deeley, Linda E Campbell, Eileen M Daly, Vincent Giampietro, Michael J Brammer, Kieran C Murphy & Declan GM Murphy. (2015) An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders 7:1.
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Omri Weisman, Ruth Feldman, Merav Burg-Malki, Miri Keren, Ronny Geva, Gil Diesendruck & Doron Gothelf. (2015) Mother–Child Interaction as a Window to a Unique Social Phenotype in 22q11.2 Deletion Syndrome and in Williams Syndrome. Journal of Autism and Developmental Disorders 45:8, pages 2567-2577.
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Aline Santos Sampaio, Ana Gabriela Hounie, Kátia Petribú, Carolina Cappi, Ivanil Morais, Homero Vallada, Maria Conceição do Rosário, S. Evelyn Stewart, Jesen Fargeness, Carol Mathews, Paul Arnold, Gregory L. Hanna, Margaret Richter, James Kennedy, Leonardo Fontenelle, Carlos Alberto de Bragança Pereira, David L. Pauls & Eurípedes Constantino Miguel. (2015) COMT and MAO-A Polymorphisms and Obsessive-Compulsive Disorder: A Family-Based Association Study. PLOS ONE 10:3, pages e0119592.
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Matthew J. Schreiner, Maria T. Lazaro, Maria Jalbrzikowski & Carrie E. Bearden. (2013) Converging levels of analysis on a genomic hotspot for psychosis: Insights from 22q11.2 Deletion Syndrome. Neuropharmacology 68, pages 157-173.
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V. Shashi, A. Veerapandiyan, K. Schoch, T. Kwapil, M. Keshavan, E. Ip & S. Hooper. (2011) Social skills and associated psychopathology in children with chromosome 22q11.2 deletion syndrome: implications for interventions. Journal of Intellectual Disability Research 56:9, pages 865-878.
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Maude Schneider, Martial Van der Linden, Bronwyn Glaser, Eleonora Rizzi, Sophie P. Dahoun, Christine Hinard, Lucia Bartoloni, Stylianos E. Antonarakis, Martin Debbané & Stephan Eliez. (2012) Preliminary structure and predictive value of attenuated negative symptoms in 22q11.2 deletion syndrome. Psychiatry Research 196:2-3, pages 277-284.
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Michael R. Hunsaker. (2012) Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders. Progress in Neurobiology 96:2, pages 220-241.
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Katherine H. Karlsgodt, Peter Bachman, Anderson M. Winkler, Carrie E. Bearden & David C. Glahn. (2011) Genetic influence on the working memory circuitry: Behavior, structure, function and extensions to illness. Behavioural Brain Research 225:2, pages 610-622.
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Frederick Furniss, Asit B. Biswas, Rohit Gumber & Niraj Singh. (2011) Cognitive phenotype of velocardiofacial syndrome: A review. Research in Developmental Disabilities 32:6, pages 2206-2213.
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Rungnapa Ittiwut, Jennifer B. Listman, Chupong Ittiwut, Joseph F. Cubells, Roger D. Weiss, Kathleen Brady, David Oslin, Lindsay A. Farrer, Henry R. Kranzler & Joel Gelernter. (2011) Association between polymorphisms in catechol‐ O ‐methyltransferase ( COMT ) and cocaine‐induced paranoia in European‐American and African‐American populations . American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156:6, pages 651-660.
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Elena L. Grigorenko, Alexander E. Urban & Einar Mencl. (2010) Behavior, Brain, and Genome in Genomic Disorders: Finding the Correspondences. Journal of Developmental & Behavioral Pediatrics 31:7, pages 602-609.
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Vandana Shashi, Timothy D. Howard, Matcheri S. Keshavan, Jessica Kaczorowski, Margaret N. Berry, Kelly Schoch, Edward J. Spence & Thomas R. Kwapil. (2010) COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome. Psychiatry Research 178:2, pages 433-436.
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John A. Fossella, Kevin Guise & Jin Fan. (2010) Genetics as a tool for the dissociation of mental operations over the course of development. Annals of the New York Academy of Sciences 1191:1, pages 110-132.
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Kevin M. Antshel, Eileen Marrinan, Wendy R. Kates, Wanda Fremont & Robert J. Shprintzen. (2009) Language and Literacy Development in Individuals With Velo-cardio-facial Syndrome. Topics in Language Disorders 29:2, pages 170-186.
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Christina Sobin, Karen Kiley-Brabeck, Samantha Hadley Monk, Jananne Khuri & Maria Karayiorgou. (2009) Sex differences in the behavior of children with the 22q11 deletion syndrome. Psychiatry Research 166:1, pages 24-34.
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Carrie E. Bearden, David C. Glahn, Agatha D. Lee, Ming-Chang Chiang, Theo G.M. van Erp, Tyrone D. Cannon, Allan L. Reiss, Arthur W. Toga & Paul M. Thompson. (2008) Neural phenotypes of common and rare genetic variants. Biological Psychology 79:1, pages 43-57.
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Beverly N. Hay. (2007) Deletion 22q11: Spectrum of Associated Disorders. Seminars in Pediatric Neurology 14:3, pages 136-139.
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Anne S. Bassett, Oana Caluseriu, Rosanna Weksberg, Donald A. Young & Eva W.C. Chow. (2007) Catechol-O-methyl Transferase and Expression of Schizophrenia in 73 Adults with 22q11 Deletion Syndrome. Biological Psychiatry 61:10, pages 1135-1140.
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Gene S. Fisch. (2006) Animal Models and Human Neuropsychiatric Disorders. Behavior Genetics 37:1, pages 1-10.
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Alka AnejaWanda P. FremontKevin M. AntshelStephen V. FaraoneNuria AbdulSaburAnne Marie HigginsRobert ShprintzenWendy R. Kates. (2007) Manic Symptoms and Behavioral Dysregulation in Youth with Velocardiofacial Syndrome (22q11.2 Deletion Syndrome). Journal of Child and Adolescent Psychopharmacology 17:1, pages 105-114.
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Wendy R. Kates, Kevin M. Antshel, Nuria AbdulSabur, Deirdre Colgan, Birgit Funke, Wanda Fremont, Anne Marie Higgins, Raju Kucherlapati & Robert J. Shprintzen. (2006) A gender‐moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo‐cardio‐facial syndrome (22q11.2 deletion syndrome) . American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B:3, pages 274-280.
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