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Author Details

Linda M Brzustowicz
The State University of New Jersey
1983
103
39
PMIDPaper TitleJournal TitlePublished Year
36251081Common genetic risk factors in ASD and ADHD co-occurring families.Hum Genet2023
37686052Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments.Int J Mol Sci2023
37761888The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait.Genes (Basel)2023
35893067MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders.Genes (Basel)2022
35830838Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses.Stem Cell Reports2022
35623351Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses.Stem Cell Reports2022
32987141Characterization hiPSC-derived neural progenitor cells and neurons to investigate the role of NOS1AP isoforms in human neuron dendritogenesis.Mol Cell Neurosci2020
32629297Childhood maltreatment, serotonin transporter gene, and risk for callous and unemotional traits: A prospective investigation.Psychiatry Res2020
30931583Social (Pragmatic) Communication Disorder: Another name for the Broad Autism Phenotype?Autism2019
31519145Within-task variability on standardized language tests predicts autism spectrum disorder: a pilot study of the Response Dispersion Index.J Neurodev Disord2019
29601869d-Serine administration affects nitric oxide synthase 1 adaptor protein and DISC1 expression in sex-specific manner.Mol Cell Neurosci2018
29529098Validation of a microRNA target site polymorphism in H3F3B that is potentially associated with a broad schizophrenia phenotype.PLoS One2018
29553565Rapid Detection of Neurodevelopmental Phenotypes in Human Neural Precursor Cells (NPCs).J Vis Exp2018
27826669Behavioral and Molecular Genetics of Reading-Related AM and FM Detection Thresholds.Behav Genet2017
26869880Overexpression of Isoforms of Nitric Oxide Synthase 1 Adaptor Protein, Encoded by a Risk Gene for Schizophrenia, Alters Actin Dynamics and Synaptic Function.Front Cell Neurosci2016
26774966Reply to: Reproducibility and Visual Inspection of Data.Biol Psychiatry2016
25542305Nitric oxide synthase 1 adaptor protein, a protein implicated in schizophrenia, controls radial migration of cortical neurons.Biol Psychiatry2015
25700779Childhood maltreatment predicts allostatic load in adulthood.Child Abuse Negl2015
24170272A genome scan for loci shared by autism spectrum disorder and language impairment.Am J Psychiatry2014
25484875MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome.Front Neurol2014
24969307The value of regenotyping older linkage data sets with denser marker panels.Hum Hered2014
24520327Autism associated gene, engrailed2, and flanking gene levels are altered in post-mortem cerebellum.PLoS One2014
24454738Meta-analysis of repository data: impact of data regularization on NIMH schizophrenia linkage results.PLoS One2014
24170318Revisiting schizophrenia linkage data in the NIMH Repository: reanalysis of regularized data across multiple studies.Am J Psychiatry2014
23393157Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.Hum Mol Genet2013
23613727Chronological changes in microRNA expression in the developing human brain.PLoS One2013
22030358Child abuse and neglect, MAOA, and mental health outcomes: a prospective examination.Biol Psychiatry2012
23248646miRNA-mediated risk for schizophrenia in 22q11.2 deletion syndrome.Front Genet2012
22704665Gene ÿ gene interaction in shared etiology of autism and specific language impairment.Biol Psychiatry2012
22381191Early environmental exposures influence schizophrenia expression even in the presence of strong genetic predisposition.Schizophr Res2012
21183010Altered microRNA expression profiles in postmortem brain samples from individuals with schizophrenia and bipolar disorder.Biol Psychiatry2011
21969044Digging more deeply for genetic effects in psychiatric illness.Am J Psychiatry2011
21611176Validation of a cost-efficient multi-purpose SNP panel for disease based research.PLoS One2011
21193955Genetic covariation underlying reading, language and related measures in a sample selected for specific language impairment.Behav Genet2011
20605702NOS1AP protein levels are altered in BA46 and cerebellum of patients with schizophrenia.Schizophr Res2010
21125004Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci.J Neurodev Disord2010
20948219Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families.Hum Hered2010
20541371Childhood trauma and genetic factors in familial schizophrenia associated with the NOS1AP gene.Schizophr Res2010
20439386Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease.Am J Psychiatry2010
20638248Reduced gray matter in the anterior cingulate gyrus in familial schizophrenia: a preliminary report.Schizophr Res2010
19255043Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.Am J Psychiatry2009
19615670Autism-associated haplotype affects the regulation of the homeobox gene, ENGRAILED 2.Biol Psychiatry2009
19349958Meta-analysis of 32 genome-wide linkage studies of schizophrenia.Mol Psychiatry2009
19553464NOS1AP regulates dendrite patterning of hippocampal neurons through a carboxypeptidase E-mediated pathway.J Neurosci2009
19077434Evidence for a role of the NOS1AP (CAPON) gene in schizophrenia and its clinical dimensions: an association study in a South American population isolate.Hum Hered2009
19255048Conflict of interest-- an issue for every psychiatrist.Am J Psychiatry2009
18474209NOS1AP in schizophrenia.Curr Psychiatry Rep2008
18765489Phenotype matters: the case for careful characterization of relevant traits.Am J Psychiatry2008
19007340Improvements to bead-based oligonucleotide ligation SNP genotyping assays.Biotechniques2008
17267776Size matters: the unexpected challenge of detecting linkage in large cohorts.Am J Psychiatry2007
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Collaborators

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Co-authored papers 31
College of Medicine, The Ohio State University
Co-authored papers 16
The State University of New Jersey
Co-authored papers 14
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Co-authored papers 13
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Co-authored papers 10
Rutgers Robert Wood Johnson Medical School, The State University of New Jersey
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New York State Psychiatric Institute
Co-authored papers 7
Center for Advanced Biotechnology and Medicine, Rutgers University
Co-authored papers 7
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Harrison International Peace Hospital
Co-authored papers 4
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Virginia Commonwealth University
Co-authored papers 3
The State University of New Jersey
Co-authored papers 3
The Ohio State University.
Co-authored papers 3
West Virginia University
Co-authored papers 3
Research Institute at Nationwide Childrens Hospital, University of Iowa
Co-authored papers 3
Rutgers University Department of Genetics
Co-authored papers 3
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Stanford University School of Medicine
Co-authored papers 2
The Hospital for Sick Children
Co-authored papers 2
Hospital for Sick Children, University of Toronto
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University of California san francisco
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University of Pittsburgh
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Lieber Institute for Brain Development
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