Genetic heterogeneity in schizophrenia II: conditional analyses of affected schizophrenia sibling pairs provide evidence for an interaction between markers on chromosome 8p and 14q

[1]  T. Beaty,et al.  Multipoint analysis using affected sib pairs: Incorporating linkage evidence from unlinked regions , 2001, Genetic epidemiology.

[2]  T. Beaty,et al.  Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma. , 2001, American journal of human genetics.

[3]  M. Baron,et al.  Genetics of schizophrenia and the new millennium: progress and pitfalls. , 2001, American journal of human genetics.

[4]  D. Housman,et al.  Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes , 2000, Molecular Psychiatry.

[5]  K Y Liang,et al.  A Robust Identity-by-Descent Procedure Using Affected Sib Pairs: Multipoint Mapping for Complex Diseases , 2000, Human Heredity.

[6]  M. Karvonen,et al.  Suicidal behavior in patients with schizophrenia is related to COMT polymorphism , 2000, Psychiatric genetics.

[7]  R. Murray,et al.  Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11 , 2000, Molecular Psychiatry.

[8]  R. Elston,et al.  Multilocus linkage tests based on affected relative pairs. , 2000, American journal of human genetics.

[9]  R. Ebstein,et al.  Homicidal behavior in schizophrenia associated with a genetic polymorphism determining low catechol O-methyltransferase (COMT) activity. , 1999, American journal of medical genetics.

[10]  Nancy J. Cox,et al.  Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans , 1999, Nature Genetics.

[11]  R. Elston,et al.  Improving the power for disease locus detection in affected‐sib‐pair studies by using two‐locus analysis and multiple regression methods , 1999, Genetic epidemiology.

[12]  C. Stefanis,et al.  Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21 , 1998, Nature Genetics.

[13]  J Volavka,et al.  Association between catechol O-methyltransferase genotype and violence in schizophrenia and schizoaffective disorder. , 1998, The American journal of psychiatry.

[14]  D. Housman,et al.  Identification of Sequence Variants and Analysis of the Role of the Catechol-O-Methyl-Transferase Gene in Schizophrenia Susceptibility , 1998, Biological Psychiatry.

[15]  J. Volavka,et al.  Analysis of a functional catechol-O-methyltransferase gene polymorphism in schizophrenia: evidence for association with aggressive and antisocial behavior , 1997, Psychiatry Research.

[16]  R Kucherlapati,et al.  Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome. , 1996, American journal of medical genetics.

[17]  R. Weinshilboum,et al.  Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders. , 1996, Pharmacogenetics.

[18]  L Kruglyak,et al.  Parametric and nonparametric linkage analysis: a unified multipoint approach. , 1996, American journal of human genetics.

[19]  R. Murray,et al.  Preferential transmission of the high activity allele of COMT in schizophrenia , 1996, Psychiatric genetics.

[20]  D. Housman,et al.  Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives. , 1994, The Journal of nervous and mental disease.

[21]  N. Risch Linkage strategies for genetically complex traits. II. The power of affected relative pairs. , 1990, American journal of human genetics.

[22]  D. Rao,et al.  Availability of schizophrenic patients and their families for genetic linkage studies: Findings from the Maryland epidemiology sample , 1989, Genetic epidemiology.