Identification of DNA copy-number aberrations by array-comparative genomic hybridization in patients with schizophrenia.
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Woon Kyu Lee | Young Hoon Kim | S. Yim | Young Hoon Kim | Sang-Ick Han | H. Rha | W. Lee | Kweon-Haeng Lee | Hyoung Kyun Rha | Ho Jin Moon | Sung-Vin Yim | Yang-Whan Jeon | Young Jin Ko | Kwang-Soo Lee | Sang-Ick Han | Y-W Jeon | Y. Ko | Kweon-haeng Lee | H. Moon | Kwang-Soo Lee
[1] M. Providenti,et al. The copy-number of plasmids and other genetic elements can be determined by SYBR-Green-based quantitative real-time PCR. , 2006, Journal of microbiological methods.
[2] M Somerville,et al. Submicroscopic deletions and duplications in individuals with intellectual disability detected by array‐CGH , 2005, American journal of medical genetics. Part A.
[3] Stine H. Kresse,et al. Mapping and characterization of the amplicon near APOA2 in 1q23 in human sarcomas by FISH and array CGH , 2005, Molecular Cancer.
[4] R. Weksberg,et al. Clinical features of 78 adults with 22q11 deletion syndrome , 2005, American journal of medical genetics. Part A.
[5] Stephan Eliez,et al. COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome , 2005, Nature Neuroscience.
[6] J. Gécz,et al. Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males. , 2005, American journal of human genetics.
[7] R. Borgatti,et al. A 2.3 Mb duplication of chromosome 8q24.3 associated with severe mental retardation and epilepsy detected by standard karyotype , 2005, European Journal of Human Genetics.
[8] S. McCarthy,et al. Serotonin receptor 2C (HTR2C) and schizophrenia: Examination of possible medication and genetic influences on expression levels , 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[9] I. Gottesman,et al. Theories of schizophrenia: a genetic-inflammatory-vascular synthesis , 2005, BMC Medical Genetics.
[10] Yuedong Wang,et al. Genomic alterations in the endometrium may be a proximate cause for endometriosis. , 2004, European journal of obstetrics, gynecology, and reproductive biology.
[11] B. McGillivray,et al. Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array‐CGH , 2004, American journal of medical genetics. Part A.
[12] M. O’Donovan,et al. Multicenter linkage study of schizophrenia loci on chromosome 22q , 2004, Molecular Psychiatry.
[13] Thomas Liehr,et al. Rapid detection of subtelomeric deletion/duplication by novel real‐time quantitative PCR using SYBR‐green dye , 2004, Human mutation.
[14] M Bobrow,et al. Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features , 2004, Journal of Medical Genetics.
[15] N. Carter,et al. High-resolution analysis of genomic copy number alterations in bladder cancer by microarray-based comparative genomic hybridization , 2004, Oncogene.
[16] D. Babovic‐Vuksanovic,et al. Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation , 2004, American journal of medical genetics. Part A.
[17] S. Küry,et al. Mutation analysis of the zinc transporter gene SLC30A4 reveals no association with periodic catatonia on chromosome 15q15 , 2003, Journal of Neural Transmission.
[18] S. Minchin,et al. A DNA expression array to detect toxic stress response in European flounder (Platichthys flesus). , 2003, Aquatic toxicology.
[19] Michael C O'Donovan,et al. A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain. , 2003, American journal of human genetics.
[20] M. Hauser,et al. Evaluation of a homemade SYBR green I reaction mixture for real-time PCR quantification of gene expression. , 2002, BioTechniques.
[21] H. Horigome,et al. Screening for 22q11 deletions in a schizophrenia population , 2001, Schizophrenia Research.
[22] Ajay N. Jain,et al. Assembly of microarrays for genome-wide measurement of DNA copy number , 2001, Nature Genetics.
[23] R. Straub,et al. Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[24] M. Hiratsuka,et al. Detection of angiotensin-converting enzyme insertion/deletion polymorphisms using real-time polymerase chain reaction and melting curve analysis with SYBR Green I on a GeneAmp 5700. , 2001, Analytical biochemistry.
[25] T. Wienker,et al. Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15. , 2000, American journal of human genetics.
[26] Alan W. Stitt,et al. Retinal VEGF mRNA measured by SYBR green I fluorescence: A versatile approach to quantitative PCR. , 2000, Molecular vision.
[27] M. Schwarz,et al. The Immune System and Schizophrenia: An Integrative View , 2000, Annals of the New York Academy of Sciences.
[28] M. Owen,et al. High rates of schizophrenia in adults with velo-cardio-facial syndrome (VCFS) , 1999, Schizophrenia Research.
[29] O. Gabrielli,et al. Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome , 1999, European Journal of Human Genetics.
[30] D. Blackwood,et al. Mapping studies on a pericentric inversion (18) (p11.31 q21.1) in a family with both schizophrenia and learning disability. , 1999, Psychiatric genetics.
[31] H. Meltzer. The Role of Serotonin in Antipsychotic Drug Action , 1999, Neuropsychopharmacology.
[32] J. Hallmayer,et al. Chromosome 22 workshop report. , 1999, American journal of medical genetics.
[33] R. Weksberg,et al. 22q11 deletion syndrome in adults with schizophrenia. , 1998, American journal of medical genetics.
[34] G. Nicholson,et al. Determination of gene dosage at the PMP22 and androgen receptor loci by quantitative PCR. , 1998, Clinical chemistry.
[35] H. Döhner,et al. Matrix‐based comparative genomic hybridization: Biochips to screen for genomic imbalances , 1997, Genes, chromosomes & cancer.
[36] P. McGuffin,et al. Genetic basis of schizophrenia , 1995, The Lancet.
[37] R. Shprintzen,et al. Schizophrenia and chromosomal deletions within 22q11.2. , 1995, American journal of human genetics.
[38] 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.
[39] M. First,et al. The Structured Clinical Interview for DSM-III-R (SCID). I: History, rationale, and description. , 1992, Archives of general psychiatry.