Published in J Psychiatr Res on November 01, 2010
Structural MRI of pediatric brain development: what have we learned and where are we going? Neuron (2010) 3.74
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia. Am J Hum Genet (2010) 2.70
Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications. JAMA Neurol (2013) 1.81
Copy number variable microRNAs in schizophrenia and their neurodevelopmental gene targets. Biol Psychiatry (2014) 1.46
Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays. Hum Mol Genet (2013) 1.44
Diverse types of genetic variation converge on functional gene networks involved in schizophrenia. Nat Neurosci (2012) 1.34
Copy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: risk and transmission in extended pedigrees. Biol Psychiatry (2011) 1.25
Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome. Behav Genet (2011) 1.11
Response to clozapine in a clinically identifiable subtype of schizophrenia. Br J Psychiatry (2015) 1.09
Evaluating genetic counseling for family members of individuals with schizophrenia in the molecular age. Schizophr Bull (2012) 1.08
Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular era. Appl Clin Genet (2012) 1.07
Child psychiatry branch of the National Institute of Mental Health longitudinal structural magnetic resonance imaging study of human brain development. Neuropsychopharmacology (2014) 1.06
Association of schizophrenia in 22q11.2 deletion syndrome and gray matter volumetric deficits in the superior temporal gyrus. Am J Psychiatry (2011) 1.03
Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome. J Intellect Disabil Res (2011) 1.01
Evaluating genetic counseling for individuals with schizophrenia in the molecular age. Schizophr Bull (2012) 0.96
Functional outcomes of adults with 22q11.2 deletion syndrome. Genet Med (2012) 0.94
Social cognition in 22q11.2 microdeletion syndrome: relevance to psychosis? Schizophr Res (2012) 0.94
Structural abnormalities in cortical volume, thickness, and surface area in 22q11.2 microdeletion syndrome: Relationship with psychotic symptoms. Neuroimage Clin (2013) 0.93
Copy number variants: a new molecular frontier in clinical psychiatry. Curr Psychiatry Rep (2011) 0.89
Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain. Hum Mol Genet (2012) 0.88
22q11.2 deletion syndrome. Nat Rev Dis Prim (2015) 0.87
Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome. Clin Endocrinol (Oxf) (2014) 0.83
Parental origin, DNA structure, and the schizophrenia spectrum. Am J Psychiatry (2011) 0.83
MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome. Front Neurol (2014) 0.82
Perceived burden and neuropsychiatric morbidities in adults with 22q11.2 deletion syndrome. J Intellect Disabil Res (2012) 0.78
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data. Lancet Neurol (2016) 0.77
iCLIP identifies novel roles for SAFB1 in regulating RNA processing and neuronal function. BMC Biol (2015) 0.75
Accumulation of minor alleles and risk prediction in schizophrenia. Sci Rep (2017) 0.75
Large-scale copy number polymorphism in the human genome. Science (2004) 34.64
Origins and functional impact of copy number variation in the human genome. Nature (2009) 23.63
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science (2008) 20.68
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet (2010) 13.70
Strong association of de novo copy number mutations with sporadic schizophrenia. Nat Genet (2008) 10.19
Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes. PLoS Genet (2005) 7.60
Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database. Nat Genet (2008) 6.71
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc Natl Acad Sci U S A (1995) 5.62
22q11 deletion syndrome: a genetic subtype of schizophrenia. Biol Psychiatry (1999) 2.43
A population study of chromosome 22q11 deletions in infancy. Arch Dis Child (1998) 2.15
Chromosome 22qII deletions. An under-recognised cause of idiopathic learning disability. Br J Psychiatry (1998) 2.03
Schizophrenia and 22q11.2 deletion syndrome. Curr Psychiatry Rep (2008) 2.02
Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease. Am J Psychiatry (2010) 1.95
Genomic microarrays in mental retardation: a practical workflow for diagnostic applications. Hum Mutat (2009) 1.71
Elevated prevalence of generalized anxiety disorder in adults with 22q11.2 deletion syndrome. Am J Psychiatry (2010) 1.57
Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies. Ann N Y Acad Sci (2009) 1.44
Premature death in adults with 22q11.2 deletion syndrome. J Med Genet (2009) 1.42
Genetic counselling for schizophrenia in the era of molecular genetics. Can J Psychiatry (2001) 1.41
Genetic insights into schizophrenia. Can J Psychiatry (2001) 1.38
Chromosomal abnormalities and schizophrenia. Am J Med Genet (2000) 1.36
A survey of the 22q11 microdeletion in a large cohort of schizophrenia patients. Schizophr Res (2005) 1.30
Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis. Molecular genetic study. Br J Psychiatry (2003) 1.27
Genetic insights into the neurodevelopmental hypothesis of schizophrenia. Schizophr Bull (2001) 1.23
Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans. Expert Rev Mol Diagn (2009) 1.22
Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia. Schizophr Res (2007) 1.16
Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease. Int J Cardiol (2008) 1.12
Screening for 22q11 deletions in a schizophrenia population. Schizophr Res (2001) 1.05
Application of array-based comparative genome hybridization in children with developmental delay or mental retardation. Pediatr Neonatol (2008) 0.93
Systematic mutation analysis of the catechol O-methyltransferase gene as a candidate gene for schizophrenia. Am J Psychiatry (1999) 0.89
Clinical application of microarray-based molecular cytogenetics: an emerging new era of genomic medicine. J Pediatr (2009) 0.87
No evidence of increased risk for schizophrenia or bipolar affective disorder in persons with aneuploidies of the sex chromosomes. Psychol Med (2001) 0.84
Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia. Behav Brain Funct (2008) 0.83
[A study on the occurrence of the deletion 22q11.2 in patients affected with a psychiatric disease]. Psychiatr Pol (2007) 0.83
Clinical features of 78 adults with 22q11 Deletion Syndrome. Am J Med Genet A (2005) 3.13
The schizophrenia phenotype in 22q11 deletion syndrome. Am J Psychiatry (2003) 3.04
Incidence of schizophrenia and other psychoses in ethnic minority groups: results from the MRC AESOP Study. Psychol Med (2006) 2.79
Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome. Hum Mol Genet (2008) 2.76
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia. Am J Hum Genet (2010) 2.70
Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. Am J Psychiatry (2014) 2.15
A male phenotype with Aicardi syndrome. J Child Neurol (2009) 2.07
A method for accurate detection of genomic microdeletions using real-time quantitative PCR. BMC Genomics (2005) 2.04
Schizophrenia and 22q11.2 deletion syndrome. Curr Psychiatry Rep (2008) 2.02
The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome. Am J Med Genet A (2009) 1.82
Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications. JAMA Neurol (2013) 1.81
Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome. Biol Psychiatry (2007) 1.63
Elevated prevalence of generalized anxiety disorder in adults with 22q11.2 deletion syndrome. Am J Psychiatry (2010) 1.57
Canadian anaplastic lymphoma kinase study: a model for multicenter standardization and optimization of ALK testing in lung cancer. J Thorac Oncol (2014) 1.55
Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22. Am J Hum Genet (2004) 1.55
Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways. PLoS Genet (2012) 1.44
Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays. Hum Mol Genet (2013) 1.44
Bone marrow stem and progenitor cell contribution to neovasculogenesis is dependent on model system with SDF-1 as a permissive trigger. Blood (2009) 1.15
Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletions. J Med Genet (2011) 1.13
Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease. Int J Cardiol (2008) 1.12
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures. Hum Mol Genet (2013) 1.11
Childhood head injury and expression of schizophrenia in multiply affected families. Arch Gen Psychiatry (2003) 1.08
Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion. Schizophr Res (2012) 1.08
Fine mapping of the schizophrenia susceptibility locus on chromosome 1q22. Hum Hered (2002) 1.06
Temperament pathways to childhood disruptive behavior and adolescent substance abuse: testing a cascade model. J Abnorm Child Psychol (2009) 1.04
Hippocampal malrotation is associated with chromosome 22q11.2 microdeletion. Can J Neurol Sci (2013) 0.99
Heritability of neurocognitive traits in familial schizophrenia. Am J Med Genet B Neuropsychiatr Genet (2009) 0.97
Postal survey of physicians and laboratories: practices and perceptions of molecular oncology testing. BMC Health Serv Res (2009) 0.95
Novel exon 1 mutations in MECP2 implicate isoform MeCP2_e1 in classical Rett syndrome. Am J Med Genet A (2009) 0.95
Functional outcomes of adults with 22q11.2 deletion syndrome. Genet Med (2012) 0.94
Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome. Am J Med Genet A (2015) 0.91
Premorbid adjustment and schizophrenia in individuals with 22q11.2 deletion syndrome. Schizophr Res (2013) 0.90
Childhood trauma and genetic factors in familial schizophrenia associated with the NOS1AP gene. Schizophr Res (2010) 0.89
Voxel-based morphometry and automated lobar volumetry: the trade-off between spatial scale and statistical correction. Neuroimage (2009) 0.87
Determination of 3-dimensional zonal renal volumes using contrast-enhanced computed tomography. J Comput Assist Tomogr (2007) 0.87
Mutations in MECP2 exon 1 in classical Rett patients disrupt MECP2_e1 transcription, but not transcription of MECP2_e2. Am J Med Genet B Neuropsychiatr Genet (2011) 0.87
Prenatal genetic testing with chromosomal microarray analysis identifies major risk variants for schizophrenia and other later-onset disorders. Am J Psychiatry (2013) 0.86
Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome. Clin Endocrinol (Oxf) (2014) 0.83
Complex congenital heart disease in unaffected relatives of adults with 22q11.2 deletion syndrome. Am J Cardiol (2011) 0.82
Early environmental exposures influence schizophrenia expression even in the presence of strong genetic predisposition. Schizophr Res (2012) 0.81
Concerns about the heritability of serious mental illness: a not-so-strange interlude. Am J Psychiatry (2014) 0.80
Acute ischemic stroke caused by paradoxical air embolism following injection sclerotherapy for varicose veins. Neurol India (2013) 0.79
Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. Am J Med Genet A (2012) 0.79
Reproductive genetic testing and human genetic variation in the era of genomic medicine. Am J Bioeth (2015) 0.77
Reduced gray matter in the anterior cingulate gyrus in familial schizophrenia: a preliminary report. Schizophr Res (2010) 0.77
Reproductive fitness and genetic transmission of tetralogy of Fallot in the molecular age. Circ Cardiovasc Genet (2014) 0.76
Adult expression of a 3q13.31 microdeletion. Mol Cytogenet (2014) 0.76
Sibship characteristics in a familial sample with genetic susceptibility to schizophrenia. Schizophr Res (2007) 0.75
Is schizophrenia linked to chromosome 1q? Science (2002) 0.75
Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader-Willi syndrome: a new case and review of the literature. Am J Med Genet A (2004) 0.75
Acantholysis: worth a second look? Dermatol Surg (2014) 0.75