Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11

The sentence on page 540 of this article ‘A silent exonic gCt → gTt substitution (Ala → Ala) at nucleotide 1412 was found by SSCP analysis’ is incorrect. The correct sentence should read ‘A silent exonic GCT → GCC substitution (Ala → Ala) at nucleotide 1412 was found by SSCP analysis’.

[1]  M. Baron,et al.  Erythrocyte catechol O-methyltransferase activity in schizophrenia: analysis of family data. , 1984, The American journal of psychiatry.

[2]  T. Sekiya,et al.  Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[3]  P B Herdson,et al.  Ethnic differences. , 1990, The New Zealand medical journal.

[4]  R. Shprintzen,et al.  Late-onset psychosis in the velo-cardio-facial syndrome. , 1992, American journal of medical genetics.

[5]  R. Shprintzen,et al.  The velo-cardio-facial syndrome is associated with chromosome 22 deletions which encompass the DiGeorge syndrome locus , 1992 .

[6]  P. Scambler,et al.  Possible role for COMT in psychosis associated with velo-cardio-facial syndrome , 1992, The Lancet.

[7]  P. O'Connell,et al.  Linkage disequilibrium in the neurofibromatosis 1 (NF1) region: implications for gene mapping. , 1993, American journal of human genetics.

[8]  W. Ewens,et al.  Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). , 1993, American journal of human genetics.

[9]  D. Glavač,et al.  Optimization of the single‐strand conformation polymorphism (SSCP) technique for detection of point mutations , 1993, Human mutation.

[10]  W. Evans,et al.  Ethnic differences in erythrocyte catechol-O-methyltransferase activity in black and white Americans. , 1994, The Journal of pharmacology and experimental therapeutics.

[11]  E. Lander,et al.  Genetic dissection of complex traits science , 1994 .

[12]  T. Kiviluoto,et al.  Genomic organization of the human catechol O-methyltransferase gene and its expression from two distinct promoters. , 1994, European Journal of Biochemistry.

[13]  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.

[14]  D. Curtis,et al.  An extended transmission/disequilibrium test (TDT) for multi‐allele marker loci , 1995, Annals of human genetics.

[15]  I. Ulmanen,et al.  Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme. , 1995, Biochemistry.

[16]  M. Carrington,et al.  Discordant patterns of linkage disequilibrium of the peptide-transporter loci within the HLA class II region. , 1995, American journal of human genetics.

[17]  J. Todd,et al.  Analysis of the CD3 gene region and type 1 diabetes: application of fluorescence-based technology to linkage disequilibrium mapping. , 1995, Human molecular genetics.

[18]  E. Lander,et al.  Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results , 1995, Nature Genetics.

[19]  J. Long,et al.  An E-M algorithm and testing strategy for multiple-locus haplotypes. , 1995, American journal of human genetics.

[20]  J. Todd,et al.  Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31–q33 , 1995, Nature Genetics.

[21]  R. Shprintzen,et al.  Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

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

[23]  M. Owen,et al.  No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity. , 1996, The American journal of psychiatry.

[24]  E. Lander The New Genomics: Global Views of Biology , 1996, Science.

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

[26]  N Risch,et al.  The Future of Genetic Studies of Complex Human Diseases , 1996, Science.

[27]  R. Murray,et al.  Catechol‐O‐methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families , 1997, Psychiatric genetics.

[28]  M. Karayiorgou,et al.  Dissecting the genetic complexity of schizophrenia , 1997, Molecular Psychiatry.

[29]  John P. Rice,et al.  Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 3, 5, 15, 16, 17, and 22. , 1997, American journal of medical genetics.

[30]  G. Kirov,et al.  No association between bipolar disorder and alleles at a functional polymorphism in the COMT gene , 1997, British Journal of Psychiatry.

[31]  R. Kucherlapati,et al.  Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome. , 1997, Genomics.

[32]  R. Kucherlapati,et al.  Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders. , 1997, American journal of human genetics.

[33]  F. Collins,et al.  Applications of DNA chips for genomic analysis , 1998, Molecular Psychiatry.

[34]  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.

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

[36]  J M Trent,et al.  Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired". , 1998, American journal of medical genetics.

[37]  N. Schork,et al.  The future of genetic epidemiology. , 1998, Trends in genetics : TIG.

[38]  A. Chakravarti It's raining SNPs, hallelujah? , 1998, Nature Genetics.

[39]  D G Clayton,et al.  Fine genetic mapping using haplotype analysis and the missing data problem , 1998, Annals of human genetics.

[40]  T. Crow,et al.  A genome-wide search for schizophrenia susceptibility genes. , 1998, American journal of medical genetics.

[41]  E. Boerwinkle,et al.  DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene , 1998, Nature Genetics.