Pages that link to "Q58277465"

The following pages link to 22q11 deletion syndrome in childhood onset schizophrenia: an update (Q58277465):

Displaying 42 items.

• Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited (Q24647915) (← links)
• Hyperprolinemia is a risk factor for schizoaffective disorder (Q28288735) (← links)
• Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders (Q30458768) (← links)
• Analysis of TBX1 variation in patients with psychotic and affective disorders (Q30545900) (← links)
• Schizophrenia and 22q11.2 deletion syndrome (Q31155236) (← links)
• Trajectories of anatomic brain development as a phenotype (Q31156275) (← links)
• Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome (Q33352752) (← links)
• Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia (Q33608652) (← links)
• Velo-Cardio-Facial Syndrome (Q33612908) (← links)
• Psychotic features as the first manifestation of 22q11.2 deletion syndrome (Q33766603) (← links)
• 22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis (Q34393037) (← links)
• Subtyping schizophrenia: implications for genetic research (Q34542103) (← links)
• Sex chromosome anomalies in childhood onset schizophrenia: an update. (Q35048190) (← links)
• Genomic Copy Number Variation in Disorders of Cognitive Development (Q35109761) (← links)
• An interictal schizophrenia-like psychosis in an adult patient with 22q11.2 deletion syndrome (Q35353595) (← links)
• Anxiety Disorders and Perceptual Disturbances in Adolescents with 22q11.2 Deletion Syndrome Treated with SSRI: A Case Series (Q35568668) (← links)
• Glutamatergic markers, age, intellectual functioning and psychosis in 22q11 deletion syndrome (Q35956869) (← links)
• The neurodevelopmental model of schizophrenia: update 2005. (Q36034203) (← links)
• Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia (Q36062961) (← links)
• Annotation: velo-cardio-facial syndrome (Q36118609) (← links)
• No age effect in the prevalence and clinical significance of ultra-high risk symptoms and criteria for psychosis in 22q11 deletion syndrome: Confirmation of the genetically driven risk for psychosis? (Q36345854) (← links)
• Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular era (Q36380279) (← links)
• Genomic structural variation and schizophrenia (Q37161534) (← links)
• Ultra high risk status and transition to psychosis in 22q11.2 deletion syndrome (Q37274686) (← links)
• Clinical perspectives on the genetics of schizophrenia: a bottom-up orientation (Q37346463) (← links)
• The genetics of childhood-onset schizophrenia: when madness strikes the prepubescent (Q37390402) (← links)
• Associations between social cognition, skills, and function and subclinical negative and positive symptoms in 22q11.2 deletion syndrome (Q37419446) (← links)
• Psychosis in children with velocardiofacial syndrome (22q11.2 deletion syndrome). (Q37419572) (← links)
• Neurobiology and phenotypic expression in early onset schizophrenia (Q37832780) (← links)
• Schizophrenia genetics: progress, at last (Q37994371) (← links)
• Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature. (Q38084601) (← links)
• Development of novel therapy of schizophrenia in children and adolescents. (Q38223714) (← links)
• Accumulation of minor alleles and risk prediction in schizophrenia (Q41718177) (← links)
• Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome (Q46400538) (← links)
• Clozapine treatment of psychosis associated with velo-cardio-facial syndrome: benefits and risks (Q46556675) (← links)
• Genetic findings in schizophrenia (Q46598637) (← links)
• 22q11.2 deletion and schizophrenia in childhood and adolescence (Q46854411) (← links)
• Transcriptional signatures of schizophrenia in hiPSC-derived NPCs and neurons are concordant with post-mortem adult brains. (Q47098607) (← links)
• Longitudinal study of premorbid adjustment in 22q11.2 deletion (velocardiofacial) syndrome and association with psychosis (Q47889196) (← links)
• Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories. (Q48399002) (← links)
• Psychiatric Features in Children with Genetic Syndromes: Toward Functional Phenotypes (Q48941588) (← links)
• Childhood-Onset Schizophrenia: A Systematic Overview of Its Genetic Heterogeneity From Classical Studies to the Genomic Era (Q92539390) (← links)