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One or more keywords matched the following items that are connected to Faraone, Stephen
Item TypeName
Academic Article Further investigation of a chromosome 15 locus in schizophrenia: analysis of affected sibpairs from the NIMH Genetics Initiative.
Academic Article Family-based tests of association and linkage that use unaffected sibs, covariates, and interactions.
Academic Article Genome-wide search for schizophrenia susceptibility loci: the NIMH Genetics Initiative and Millennium Consortium.
Academic Article An overview of the genetics of psychotic mood disorders.
Academic Article No association of G72 and D-amino acid oxidase genes with schizophrenia.
Academic Article Suggestive linkage of chromosome 10p to schizophrenia is not due to transmission ratio distortion.
Academic Article A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16.
Academic Article RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function.
Academic Article The genetics of schizophrenia.
Academic Article Genetic influences on attention deficit hyperactivity disorder.
Academic Article Genetic transmission of major affective disorders: quantitative models and linkage analyses.
Academic Article Population differences in the International Multi-Centre ADHD Gene Project.
Academic Article Family-based association study of markers on chromosome 22 in schizophrenia using African-American, European-American, and Chinese families.
Academic Article Linkage of chromosome 13q32 to schizophrenia in a large veterans affairs cooperative study sample.
Academic Article Evidence for linkage between regulatory enzymes in glycolysis and schizophrenia in a multiplex sample.
Academic Article Genome scan of schizophrenia families in a large Veterans Affairs Cooperative Study sample: evidence for linkage to 18p11.32 and for racial heterogeneity on chromosomes 6 and 14.
Academic Article NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees.
Academic Article HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention.
Academic Article Genome scan of European-American schizophrenia pedigrees: results of the NIMH Genetics Initiative and Millennium Consortium.
Academic Article Evidence for the multigenic inheritance of schizophrenia.
Academic Article No association evidence between schizophrenia and dystrobrevin-binding protein 1 (DTNBP1) in Taiwanese families.
Academic Article Association of SNPs and haplotypes in APOL1, 2 and 4 with schizophrenia.
Academic Article Clustering by neurocognition for fine mapping of the schizophrenia susceptibility loci on chromosome 6p.
Academic Article Genome-wide linkage analysis of heroin dependence in Han Chinese: results from wave one of a multi-stage study.
Academic Article Linkage analysis of attention deficit hyperactivity disorder.
Academic Article Genome-wide linkage analysis of heroin dependence in Han Chinese: results from Wave Two of a multi-stage study.
Academic Article A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication.
Academic Article Manic symptoms and behavioral dysregulation in youth with velocardiofacial syndrome (22q11.2 deletion syndrome).
Academic Article Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder.
Academic Article Examination of genetic linkage of chromosome 15 to schizophrenia in a large Veterans Affairs Cooperative Study sample.
Academic Article Schizophrenia: a review of genetic studies.
Academic Article Three potential susceptibility loci shown by a genome-wide scan for regions influencing the age at onset of mania.
Academic Article Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q.
Academic Article Early onset bipolar disorder: possible linkage to chromosome 9q34.
Academic Article Multivariate genomewide linkage scan of neurocognitive traits and ADHD symptoms: suggestive linkage to 3q13.
Academic Article Whole-genome association study of bipolar disorder.
Academic Article Association between the 5HT1B receptor gene (HTR1B) and the inattentive subtype of ADHD.
Academic Article The case for heterogeneity in the etiology of schizophrenia.
Academic Article Genome scan of three quantitative traits in schizophrenia pedigrees.
Academic Article Deletion at the SLC1A1 glutamate transporter gene co-segregates with schizophrenia and bipolar schizoaffective disorder in a 5-generation family.
Academic Article Ordered subsets linkage analysis of antisocial behavior in substance use disorder among participants in the Collaborative Study on the Genetics of Alcoholism.
Academic Article Linkage disequilibrium mapping of the chromosome 6q21-22.31 bipolar I disorder susceptibility locus.
Academic Article Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach.
Academic Article ANXA7, PPP3CB, DNAJC9, and ZMYND17 genes at chromosome 10q22 associated with the subgroup of schizophrenia with deficits in attention and executive function.
Academic Article The corticotropin-releasing hormone gene and behavioral inhibition in children at risk for panic disorder.
Academic Article Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings.
Academic Article Neuropsychological intra-individual variability explains unique genetic variance of ADHD and shows suggestive linkage to chromosomes 12, 13, and 17.
Academic Article Sex differences in affective disorder: genetic transmission.
Academic Article Genome scan of Han Chinese schizophrenia families from Taiwan: confirmation of linkage to 10q22.3.
Academic Article Genome-wide scan of homogeneous subtypes of NIMH genetics initiative schizophrenia families.
Academic Article Neuropsychological endophenotype approach to genome-wide linkage analysis identifies susceptibility loci for ADHD on 2q21.1 and 13q12.11.
Academic Article Suggestive linkage of the child behavior checklist juvenile bipolar disorder phenotype to 1p21, 6p21, and 8q21.
Concept Chromosomes, Human, Pair 7
Concept Chromosome Aberrations
Concept Chromosome Deletion
Concept Chromosomes, Human, Pair 10
Concept Chromosomes, Human, Pair 3
Concept Chromosomes, Human, Pair 20
Concept Chromosomes, Human, Pair 14
Concept Physical Chromosome Mapping
Concept Chromosomes, Human, Pair 11
Concept Chromosomes, Human, Pair 1
Concept Chromosomes, Human, Pair 19
Concept Chromosomes, Human, Pair 4
Concept Chromosome Segregation
Concept Chromosomes, Human, Pair 8
Concept Chromosome Mapping
Concept Chromosomes, Human, Pair 2
Concept X Chromosome
Concept Chromosomes, Human, Pair 13
Concept Chromosomes, Human, Pair 9
Concept Chromosomes, Human, Pair 6
Concept Chromosomes, Human, Pair 18
Concept Chromosomes, Human, Pair 12
Concept Chromosomes, Human, Pair 15
Concept Sex Chromosome Aberrations
Concept Chromosomes, Human, Pair 16
Concept Chromosome Disorders
Concept Chromosomes, Human, Pair 22
Concept Chromosomes, Human, Pair 17
Academic Article Copy number variants in attention-deficit hyperactive disorder: identification of the 15q13 deletion and its functional role.
Academic Article Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome.
Search Criteria
  • Chromosomes Human Pair 9
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.