Rutgers University School of Arts and Sciences Division of Life Sciences
 

Publications

Selected Recent Publications

  • Bartlett CW, Hou L, Flax JF, Hare A, Cheong SY, Fermano Z, Zimmerman-Bier B, Cartwright C, Azaro MA, Buyske S, Brzustowicz LM. A Genome Scan for Loci Shared by Autism Spectrum Disorder and Language Impairment. American Journal of Psychiatry, 2014;171:72-81.
  • Vieland VJ, Walters KA, Lehner T, Azaro M, Tobin K, Huang Y, Brzustowicz LM. Revisiting Schizophrenia Linkage Data in the NIMH Repository: Reanalysis of Regularized Data Across Multiple Studies. American Journal of Psychiatry, 2014;171:350-9.
  • Moreau MP, Bruse S, Jornsten R, Liu Y, Brzustowicz LM. Chronological Changes in microRNA Expression in the Developing Human Brain. PLOS ONE, 2013 8:e60480.
  • Brzustowicz LM, Bassett AS.  miRNA-Mediated Risk for Schizophrenia in 22q11.2 Deletion Syndrome.  Frontiers in Genetics, 2012, 3:291.
  • Bartlett CW, Flax JF, Fermano Z, Hare A, Hou L, Petrill SA, Buyske S, Brzustowicz LM. Gene x Gene Interaction in Shared Etiology of Autism and Specific Language Impairment. Biological Psychiatry, 2012,72:692-9.
  • Husted JA, Ahmed R, Chow EW, Brzustowicz LM, Bassett AS. Early Environmental Exposures Influence Schizophrenia Expression Even in the Presence of Strong Genetic Predisposition. Schizophrenia Research, 2012;137:166-8.
  • Nikulina V, Widom CS, Brzustowicz LM.  Child Abuse and Neglect, MAOA, and Mental Health Outcomes: A Prospective Examination. Biological Psychiatry, 2012;71:350-7.
  • Hou L, Phillips C, Azaro M, Brzustowicz LM, Bartlett CW. Validation of a cost-efficient multi-purpose SNP panel for disease based research. PLoS One, 2011; 6(5):e19699.
  • Logan J, Petrill SA, Flax J, Justice LM, Hou L, Bassett AS, Tallal P, Brzustowicz LM, Bartlett CW. Genetic Covariation Underlying Reading, Language and Related Measures in a Sample Selected for Specific Language Impairment. Behavior Genetics,  2011;41:651-659
  • Moreau MP, Bruse SE, David-Rus R, Buyske S, Brzustowicz LM. Altered microRNA expression profiles in post-mortem brain samples from individuals with schizophrenia and bipolar disorderBiological Psychiatry, 2011; 69:188-93.
  • Flax JF, Hare Am Azaro MA, Vieland VJ, Brzustowicz LM.  Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci. Journal of Neurodevelopmental Disorders, 2010; 2:210-223.
  • Simmons TR, Flax JF, Azaro MA, Hayter JE, Justice LM, Petrill SA, Bassett AS, Tallal P, Brzustowicz LM, Bartlett CW. Increasing Genotype-Phenotype Model Determinism: Application to Bivariate Reading/Language Traits and Epistatic Interactions in Language Impaired Families. Human Heredity,  2010; 70:232-244.
  • Costain G, Ho A, Crawley AP, Mikulis DJ, Brzustowicz LM, Chow EW, Bassett AS. Reduced gray matter in the anterior cingulate gyrus in familial schizophrenia: A preliminary report. Schizophrenia Research, 2010; 122:81-4.
  • Hadzimichalis NM, Previtera ML, Moreau MP, Li B, Lee GH, Dulencin AM, Matteson PG, Buyske S, Millonig JH, Brzustowicz, LM, Firestein, BL.  NOS1AP protein levels are altered in BA46 and cerebellum of patients with schizophrenia. Schizophrenia Research, 2010; 124:248-50.
  • Husted JA, Ahmed R, Chow EWC, Brzustowicz LM, Bassett AS. Childhood Trauma and Genetic Factors in Familial Schizophrenia Associated with the NOS1AP Gene. Schizophrenia Research, 2010; 121:187-92.
  • Bassett AS, Scherer SW, Brzustowicz LM. Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and Disease.  American Journal of Psychiatry, 2010;167:899-914
  • Benayed R, Choi J, Matteson PG, Gharani N, Kamdar S, Brzustowicz LM, Millonig JH.  Autism Associated Haplotype Affects the Regulation of the Homeobox Gene, ENGRAILED 2.  Biological Psychiatry, 2009;66:911-917.
  • Carrel D, Du Y, Komlos D, Hadzimichalis NM, Kwon M, Wang B, Brzustowicz  LM, Firestein BL. NOS1AP regulates dendrite patterning of hippocampal neurons through a CPE-mediated pathway. The Journal of Neuroscience, 2009;29:8248-58.
  • Wratten NS, Memoli H, Huang Y, Dulencin AM, Matteson PG, Cornacchia MA, Azaro MA, Messenger J, Hayter JE, Bassett AS, Buyske S, Millonig JH, Vieland VJ, Brzustowicz LM.  Identification of a schizophrenia associated functional non-coding variant in NOS1APAmerican Journal of Psychiatry, 2009; 166:434-441.
  • Kremeyer B, García J, Kymäläinen H, Wratten N, Restrepo G, Palacio C, Miranda AL, López C, Restrepo M, Bedoya G, Brzustowicz LM, Ospina-Duque J, Arbeláez MP, Ruiz-Linares A. 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;67:163-73