2013 - Fellow of the American Association for the Advancement of Science (AAAS)
Genetics connects with themes related to Exon in her study. Her studies link Genetics with Exon. Her Gene study frequently involves adjacent topics like Linkage (software). She performs multidisciplinary studies into Locus (genetics) and Phenotype in her work. Linda M. Brzustowicz performs integrative Phenotype and Locus (genetics) research in her work. Psychiatry connects with themes related to Schizophrenia (object-oriented programming) in her study. Her research on Schizophrenia (object-oriented programming) frequently connects to adjacent areas such as Psychiatry. Single-nucleotide polymorphism and Haplotype are two areas of study in which Linda M. Brzustowicz engages in interdisciplinary research. Linda M. Brzustowicz undertakes multidisciplinary studies into Haplotype and Linkage disequilibrium in her work.
Linda M. Brzustowicz connects relevant research areas such as Schizophrenia (object-oriented programming) and Psychosis in the realm of Psychiatry. Her work on Schizophrenia (object-oriented programming) is being expanded to include thematically relevant topics such as Psychiatry. Her Gene study frequently links to adjacent areas such as Linkage (software). Linda M. Brzustowicz merges Genetics with Neuroscience in her research. She undertakes multidisciplinary investigations into Neuroscience and Genetics in her work. Linda M. Brzustowicz combines Locus (genetics) and Chromosome in her research. By researching both Chromosome and Locus (genetics), she produces research that crosses academic boundaries. Her Linkage disequilibrium research extends to the thematically linked field of Genotype. Her research brings together the fields of Genotype and Linkage disequilibrium.
By researching both Gene and Serine, Linda M. Brzustowicz produces research that crosses academic boundaries. With her scientific publications, her incorporates both Serine and Phosphorylation. She performs integrative study on Phosphorylation and Signal transducing adaptor protein in her works. Signal transducing adaptor protein is frequently linked to Receptor in her study. She integrates Receptor and Biochemistry in her research. Her Biochemistry study frequently links to other fields, such as DISC1. Her work often combines DISC1 and Gene studies. Her research on Genetics often connects related topics like Multiplex. Much of her study explores Multiplex relationship to Genetics.
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The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene.
R E Tanzi;K Petrukhin;I Chernov;J L Pellequer.
Nature Genetics (1993)
Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia
Cathryn M. Lewis;Douglas F. Levinson;Lesley H. Wise;Lynn E. DeLisi.
American Journal of Human Genetics (2003)
Location of a Major Susceptibility Locus for Familial Schizophrenia on Chromosome 1q21-q22
Linda M. Brzustowicz;Kathleen A. Hodgkinson;Eva W. C. Chow;Eva W. C. Chow;William G. Honer.
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3
L. M. Brzustowicz;L. M. Brzustowicz;T. Lehner;T. Lehner;L. H. Castilla;L. H. Castilla;G. K. Penchaszadeh;G. K. Penchaszadeh.
Mapping, Cloning and Genetic Characterization of the Region Containing the Wilson Disease Gene
K Petrukhin;S G Fischer;M Pirastu;R E Tanzi.
Nature Genetics (1993)
MAOA and the "cycle of violence:" childhood abuse and neglect, MAOA genotype, and risk for violent and antisocial behavior.
Cathy Spatz Widom;Linda M. Brzustowicz;Linda M. Brzustowicz.
Biological Psychiatry (2006)
Genetic homogeneity between acute and chronic forms of spinal muscular atrophy.
T C Gilliam;L M Brzustowicz;L H Castilla;T Lehner.
Meta-analysis of 32 genome-wide linkage studies of schizophrenia
M Y M Ng;D F Levinson;S Faraone;B K Suarez.
Molecular Psychiatry (2009)
A Major Susceptibility Locus for Specific Language Impairment Is Located on 13q21
Christopher W. Bartlett;Judy F. Flax;Mark W. Logue;Veronica J. Vieland.
American Journal of Human Genetics (2002)
Linkage of familial schizophrenia to chromosome 13q32.
Linda M. Brzustowicz;Linda M. Brzustowicz;William G. Honer;Eva W.C. Chow;Dawn Little.
American Journal of Human Genetics (1999)
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