Linda Brzustowicz Department of Genetics Rutgers University Biography Publications Institution JoVE Articles Linda Brzustowicz has not added a biography. If you are Linda Brzustowicz and would like to personalize this page please email our Author Liaison for assistance. Publications Reply To: Reproducibility and Visual Inspection of Data Biological Psychiatry. 09, 2016 | Pubmed ID: 26774966 Childhood Maltreatment Predicts Allostatic Load in Adulthood Child Abuse & Neglect. Sep, 2015 | Pubmed ID: 25700779 Nitric Oxide Synthase 1 Adaptor Protein, a Protein Implicated in Schizophrenia, Controls Radial Migration of Cortical Neurons Biological Psychiatry. Jun, 2015 | Pubmed ID: 25542305 MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome Frontiers in Neurology. 2014 | Pubmed ID: 25484875 The Value of Regenotyping Older Linkage Data Sets with Denser Marker Panels Human Heredity. 2014 | Pubmed ID: 24969307 Autism Associated Gene, Engrailed2, and Flanking Gene Levels Are Altered in Post-mortem Cerebellum PloS One. 2014 | Pubmed ID: 24520327 Meta-analysis of Repository Data: Impact of Data Regularization on NIMH Schizophrenia Linkage Results PloS One. 2014 | Pubmed ID: 24454738 Revisiting Schizophrenia Linkage Data in the NIMH Repository: Reanalysis of Regularized Data Across Multiple Studies The American Journal of Psychiatry. Mar, 2014 | Pubmed ID: 24170318 A Genome Scan for Loci Shared by Autism Spectrum Disorder and Language Impairment The American Journal of Psychiatry. Jan, 2014 | Pubmed ID: 24170272 Chronological Changes in MicroRNA Expression in the Developing Human Brain PloS One. 2013 | Pubmed ID: 23613727 MiRNA-mediated Risk for Schizophrenia in 22q11.2 Deletion Syndrome Frontiers in Genetics. 2012 | Pubmed ID: 23248646 Gene × Gene Interaction in Shared Etiology of Autism and Specific Language Impairment Biological Psychiatry. Oct, 2012 | Pubmed ID: 22704665 Early Environmental Exposures Influence Schizophrenia Expression Even in the Presence of Strong Genetic Predisposition Schizophrenia Research. May, 2012 | Pubmed ID: 22381191 Validation of a Cost-efficient Multi-purpose SNP Panel for Disease Based Research PloS One. 2011 | Pubmed ID: 21611176 Genetic Covariation Underlying Reading, Language and Related Measures in a Sample Selected for Specific Language Impairment Behavior Genetics. Sep, 2011 | Pubmed ID: 21193955 Altered MicroRNA Expression Profiles in Postmortem Brain Samples from Individuals with Schizophrenia and Bipolar Disorder Biological Psychiatry. Jan, 2011 | Pubmed ID: 21183010 Combined Linkage and Linkage Disequilibrium Analysis of a Motor Speech Phenotype Within Families Ascertained for Autism Risk Loci Journal of Neurodevelopmental Disorders. Dec, 2010 | Pubmed ID: 21125004 Increasing Genotype-phenotype Model Determinism: Application to Bivariate Reading/language Traits and Epistatic Interactions in Language-impaired Families Human Heredity. 2010 | Pubmed ID: 20948219 Reduced Gray Matter in the Anterior Cingulate Gyrus in Familial Schizophrenia: a Preliminary Report Schizophrenia Research. Sep, 2010 | Pubmed ID: 20638248 NOS1AP 蛋白水平 BA46 和小脑的精神分裂症病人在发生改变。 Schizophrenia Research. Dec, 2010 | Pubmed ID: 20605702 Childhood Trauma and Genetic Factors in Familial Schizophrenia Associated with the NOS1AP Gene Schizophrenia Research. Aug, 2010 | Pubmed ID: 20541371 Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and Disease The American Journal of Psychiatry. Aug, 2010 | Pubmed ID: 20439386 Autism-associated Haplotype Affects the Regulation of the Homeobox Gene, ENGRAILED 2 Biological Psychiatry. Nov, 2009 | Pubmed ID: 19615670 NOS1AP 规管通过羧肽酶介导电子通路的海马神经元树突阵列。 The Journal of Neuroscience : the Official Journal of the Society for Neuroscience. Jun, 2009 | Pubmed ID: 19553464 Identification of a Schizophrenia-associated Functional Noncoding Variant in NOS1AP The American Journal of Psychiatry. Apr, 2009 | Pubmed ID: 19255043 Evidence for a Role of the NOS1AP (CAPON) Gene in Schizophrenia and Its Clinical Dimensions: an Association Study in a South American Population Isolate Human Heredity. 2009 | Pubmed ID: 19077434 Improvements to Bead-based Oligonucleotide Ligation SNP Genotyping Assays BioTechniques. Nov, 2008 | Pubmed ID: 19007340 Phenotype Matters: the Case for Careful Characterization of Relevant Traits The American Journal of Psychiatry. Sep, 2008 | Pubmed ID: 18765489 NOS1AP in Schizophrenia Current Psychiatry Reports. Apr, 2008 | Pubmed ID: 18474209 Association of Synapsin 2 with Schizophrenia in Families of Northern European Ancestry Schizophrenia Research. Nov, 2007 | Pubmed ID: 17766091 Evaluation of a Susceptibility Gene for Schizophrenia: Genotype Based Meta-analysis of RGS4 Polymorphisms from Thirteen Independent Samples Biological Psychiatry. Jul, 2006 | Pubmed ID: 16631129 Support for the Homeobox Transcription Factor Gene ENGRAILED 2 As an Autism Spectrum Disorder Susceptibility Locus American Journal of Human Genetics. Nov, 2005 | Pubmed ID: 16252243 增加背外侧前额叶皮层的表达卡蓬在精神分裂症和躁郁症。 PLoS Medicine. Oct, 2005 | Pubmed ID: 16146415 Examination of Potential Overlap in Autism and Language Loci on Chromosomes 2, 7, and 13 in Two Independent Samples Ascertained for Specific Language Impairment Human Heredity. 2004 | Pubmed ID: 15133308 Linkage Disequilibrium Mapping of Schizophrenia Susceptibility to the CAPON Region of Chromosome 1q22 American Journal of Human Genetics. May, 2004 | Pubmed ID: 15065015 Genome Scan Meta-analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia American Journal of Human Genetics. Jul, 2003 | Pubmed ID: 12802786 Fine Mapping of the Schizophrenia Susceptibility Locus on Chromosome 1q22 Human Heredity. 2002 | Pubmed ID: 12771552 A Major Susceptibility Locus for Specific Language Impairment is Located on 13q21 American Journal of Human Genetics. Jul, 2002 | Pubmed ID: 12048648 Genetic Insights into Schizophrenia Canadian Journal of Psychiatry. Revue Canadienne De Psychiatrie. Mar, 2001 | Pubmed ID: 11280081 Location of a Major Susceptibility Locus for Familial Schizophrenia on Chromosome 1q21-q22 Science (New York, N.Y.). Apr, 2000 | Pubmed ID: 10784452 Linkage of Familial Schizophrenia to Chromosome 13q32 American Journal of Human Genetics. Oct, 1999 | Pubmed ID: 10486329 人脑神经前体细胞神经发育表型的快速检测 (npc) Madeline Williams*1, Smrithi Prem*1, Xiaofeng Zhou1, Paul Matteson2, Percy Luk Yeung3, Chi-Wei Lu3, Zhiping Pang4, Linda Brzustowicz5, James H. Millonig2, Emanuel Dicicco-Bloom1 1Department of Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, 2Center for Advanced Biotechnology and Medicine, Department of Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, 3The Child Health Institute of NJ, Department of Obstetrics, Gynecology, and Reproductive Services, Rutgers Robert Wood Johnson Medical School, 4The Child Health Institute of NJ, Department of Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, 5Department of Genetics, Rutgers University JoVE 56628 Developmental Biology
人脑神经前体细胞神经发育表型的快速检测 (npc) Madeline Williams*1, Smrithi Prem*1, Xiaofeng Zhou1, Paul Matteson2, Percy Luk Yeung3, Chi-Wei Lu3, Zhiping Pang4, Linda Brzustowicz5, James H. Millonig2, Emanuel Dicicco-Bloom1 1Department of Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, 2Center for Advanced Biotechnology and Medicine, Department of Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, 3The Child Health Institute of NJ, Department of Obstetrics, Gynecology, and Reproductive Services, Rutgers Robert Wood Johnson Medical School, 4The Child Health Institute of NJ, Department of Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, 5Department of Genetics, Rutgers University JoVE 56628 Developmental Biology