|
| 22182939 | Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability. | Mol Psychiatry | 2012 |
| 22547139 | Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia. | Psychiatr Genet | 2012 |
| 22182939 | Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability. | Mol Psychiatry | 2012 |
| 22547139 | Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia. | Psychiatr Genet | 2012 |
| 20628343 | Common functional polymorphisms of DISC1 and cortical maturation in typically developing children and adolescents. | Mol Psychiatry | 2011 |
| 23074677 | A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband. | Case Rep Genet | 2011 |
| 20628343 | Common functional polymorphisms of DISC1 and cortical maturation in typically developing children and adolescents. | Mol Psychiatry | 2011 |
| 21620981 | Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls. | Neuroimage | 2011 |
| 23074677 | A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband. | Case Rep Genet | 2011 |
| 21620981 | Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls. | Neuroimage | 2011 |
| 19955556 | Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals. | J Med Genet | 2010 |
| 20841422 | Longitudinally mapping the influence of sex and androgen signaling on the dynamics of human cortical maturation in adolescence. | Proc Natl Acad Sci U S A | 2010 |
| 20157310 | A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication. | Mol Psychiatry | 2010 |
| 19955556 | Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals. | J Med Genet | 2010 |
| 20841422 | Longitudinally mapping the influence of sex and androgen signaling on the dynamics of human cortical maturation in adolescence. | Proc Natl Acad Sci U S A | 2010 |
| 20157310 | A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication. | Mol Psychiatry | 2010 |
| 19346217 | Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function. | J Med Genet | 2009 |
| 19346217 | Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function. | J Med Genet | 2009 |
| 17879154 | Sequencing and analyzing the t(1;7) reciprocal translocation breakpoints associated with a case of childhood-onset schizophrenia/autistic disorder. | J Autism Dev Disord | 2008 |
| 17879154 | Sequencing and analyzing the t(1;7) reciprocal translocation breakpoints associated with a case of childhood-onset schizophrenia/autistic disorder. | J Autism Dev Disord | 2008 |
| 18800051 | Sex chromosome anomalies in childhood onset schizophrenia: an update. | Mol Psychiatry | 2008 |
| 18369103 | Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. | Science | 2008 |
| 18800051 | Sex chromosome anomalies in childhood onset schizophrenia: an update. | Mol Psychiatry | 2008 |
| 18369103 | Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. | Science | 2008 |
| 17033632 | Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories. | Mol Psychiatry | 2007 |
| 17033632 | Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories. | Mol Psychiatry | 2007 |
| 16199538 | Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype. | J Med Genet | 2006 |
| 16199538 | Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype. | J Med Genet | 2006 |
| 15365816 | FISH diagnosis of the common 57-kb deletion in CTNS causing cystinosis. | Hum Genet | 2004 |
| 15365816 | FISH diagnosis of the common 57-kb deletion in CTNS causing cystinosis. | Hum Genet | 2004 |
| 12729595 | Phosphomannomutase activity in congenital disorders of glycosylation type Ia determined by direct analysis of the interconversion of mannose-1-phosphate to mannose-6-phosphate by high-pH anion-exchange chromatography with pulsed amperometric detection. | Anal Biochem | 2003 |
| 12729595 | Phosphomannomutase activity in congenital disorders of glycosylation type Ia determined by direct analysis of the interconversion of mannose-1-phosphate to mannose-6-phosphate by high-pH anion-exchange chromatography with pulsed amperometric detection. | Anal Biochem | 2003 |
| 12108805 | Cytogenetic abnormalities in attention-deficit/hyperactivity disorder. | J Am Acad Child Adolesc Psychiatry | 2002 |
| 12108805 | Cytogenetic abnormalities in attention-deficit/hyperactivity disorder. | J Am Acad Child Adolesc Psychiatry | 2002 |
| 11121174 | Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21. | Am J Med Genet | 2000 |
| 11121174 | Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21. | Am J Med Genet | 2000 |
| 10523812 | Castellanos replies | Mol Psychiatry | 1999 |
| 10523812 | Castellanos replies | Mol Psychiatry | 1999 |
| 9861003 | A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish. | Proc Natl Acad Sci U S A | 1998 |
| 9861003 | A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish. | Proc Natl Acad Sci U S A | 1998 |
| 9657416 | HLA antigens in childhood onset schizophrenia. | Psychiatry Res | 1998 |
| 9781019 | The characterization and sequence analysis of thirty CTG-repeat containing genomic cosmid clones. | Eur J Hum Genet | 1998 |
| 9585604 | A triplet repeat on 17q accounts for most expansions detected by the repeat-expansion-detection technique. | Am J Hum Genet | 1998 |
| 9514586 | Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired". | Am J Med Genet | 1998 |
| 9774777 | Lack of an association between a dopamine-4 receptor polymorphism and attention-deficit/hyperactivity disorder: genetic and brain morphometric analyses. | Mol Psychiatry | 1998 |
| 9702740 | Large CAG/CTG repeats are associated with childhood-onset schizophrenia. | Mol Psychiatry | 1998 |
| 9514586 | Chromosome 22q11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired". | Am J Med Genet | 1998 |
| 9657416 | HLA antigens in childhood onset schizophrenia. | Psychiatry Res | 1998 |
| 9585604 | A triplet repeat on 17q accounts for most expansions detected by the repeat-expansion-detection technique. | Am J Hum Genet | 1998 |
| 9702740 | Large CAG/CTG repeats are associated with childhood-onset schizophrenia. | Mol Psychiatry | 1998 |