Anne S Bassett


Ontology type: schema:Person     


Person Info

NAME

Anne S

SURNAME

Bassett

Publications in SciGraph latest 50 shown

  • 2019-04 Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot in GENETICS IN MEDICINE
  • 2018-09-21 Phenotypic and genetic analysis of an adult cohort with extreme obesity in INTERNATIONAL JOURNAL OF OBESITY
  • 2018-06-13 Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size in MOLECULAR PSYCHIATRY
  • 2017-12 Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia in GENOME MEDICINE
  • 2017-12 A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium in MOLECULAR PSYCHIATRY
  • 2017-11 Genomic Disorders in Psychiatry—What Does the Clinician Need to Know? in CURRENT PSYCHIATRY REPORTS
  • 2017-02 Obesity in adults with 22q11.2 deletion syndrome in GENETICS IN MEDICINE
  • 2017-01 Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression in GENETICS IN MEDICINE
  • 2016-11 The importance of copy number variation in congenital heart disease in NPJ GENOMIC MEDICINE
  • 2016-11 De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients in NPJ GENOMIC MEDICINE
  • 2016-04 Fetal growth and gestational factors as predictors of schizophrenia in 22q11.2 deletion syndrome in GENETICS IN MEDICINE
  • 2016-03 Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome in HUMAN GENETICS
  • 2015-12 Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms in JOURNAL OF NEURODEVELOPMENTAL DISORDERS
  • 2015-11-19 22q11.2 deletion syndrome in NATURE REVIEWS DISEASE PRIMERS
  • 2015-10 Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome in JOURNAL OF GENETIC COUNSELING
  • 2015-08 Practical guidelines for managing adults with 22q11.2 deletion syndrome in GENETICS IN MEDICINE
  • 2015-02 Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature in GENETICS IN MEDICINE
  • 2014-12 Adult expression of a 3q13.31 microdeletion in MOLECULAR CYTOGENETICS
  • 2014-01 Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome in GENETICS IN MEDICINE
  • 2013-04 1q21.1 Microduplication expression in adults in GENETICS IN MEDICINE
  • 2012-12 22q11.2 Deletion Syndrome: Attitudes towards Disclosing the Risk of Psychiatric Illness in JOURNAL OF GENETIC COUNSELING
  • 2012-10 Functional outcomes of adults with 22q11.2 deletion syndrome in GENETICS IN MEDICINE
  • 2011-09 Genetic Covariation Underlying Reading, Language and Related Measures in a Sample Selected for Specific Language Impairment in BEHAVIOR GENETICS
  • 2011-05 Cognitive, Behavioural and Psychiatric Phenotype in 22q11.2 Deletion Syndrome in BEHAVIOR GENETICS
  • 2009-08 Meta-analysis of 32 genome-wide linkage studies of schizophrenia in MOLECULAR PSYCHIATRY
  • 2008-04 Schizophrenia and 22q11.2 deletion syndrome in CURRENT PSYCHIATRY REPORTS
  • 2007-02 Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome in HUMAN GENETICS
  • 2006-06 Heritability of schizophrenia and major affective disorder as a function of age, in the presence of strong cohort effects in EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE
  • 2005-12 A method for accurate detection of genomic microdeletions using real-time quantitative PCR in BMC GENOMICS
  • 2005-04 Tumor necrosis factor promoter haplotype associated with schizophrenia reveals a linked locus on 1q44 in MOLECULAR PSYCHIATRY
  • 2002-08 Schizophrenia and genetics: New insights in CURRENT PSYCHIATRY REPORTS
  • 2002-02 Recent advances in the genetics of schizophrenia in CELLULAR AND MOLECULAR LIFE SCIENCES
  • 2001-05 Mutation screening of the KCNN3 gene reveals a rare frameshift mutation in MOLECULAR PSYCHIATRY
  • 1997-01 NCAM and schizophrenia: genetic studies in MOLECULAR PSYCHIATRY
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