Anne S Bassett

Ontology type: schema:Person     

Person Info


Anne S



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
  • JSON-LD is the canonical representation for SciGraph data.

    TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT

        "@context": "", 
        "affiliation": [
            "affiliation": {
              "id": "", 
              "type": "Organization"
            "isCurrent": true, 
            "type": "OrganizationRole"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
            "id": "", 
            "type": "Organization"
        "familyName": "Bassett", 
        "givenName": "Anne S", 
        "id": "sg:person.01260453616.49", 
        "sameAs": [
        "sdDataset": "persons", 
        "sdDatePublished": "2019-03-07T13:16", 
        "sdLicense": "", 
        "sdPublisher": {
          "name": "Springer Nature - SN SciGraph project", 
          "type": "Organization"
        "sdSource": "s3://com-uberresearch-data-dimensions-researchers-20181010/20181011/dim_researchers/base/researchers_1088.json", 
        "type": "Person"

    Download the RDF metadata as:  json-ld nt turtle xml License info


    JSON-LD is a popular format for linked data which is fully compatible with JSON.

    curl -H 'Accept: application/ld+json' ''

    N-Triples is a line-based linked data format ideal for batch operations.

    curl -H 'Accept: application/n-triples' ''

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' ''

    RDF/XML is a standard XML format for linked data.

    curl -H 'Accept: application/rdf+xml' ''


    This table displays all metadata directly associated to this object as RDF triples.

    32 TRIPLES      10 PREDICATES      19 URIs      7 LITERALS      2 BLANK NODES

    Subject Predicate Object
    1 sg:person.01260453616.49 schema:affiliation N15956c017dc1411dbcba173668b94c42
    10 schema:familyName Bassett
    11 schema:givenName Anne S
    12 schema:sameAs
    13 schema:sdDatePublished 2019-03-07T13:16
    14 schema:sdLicense
    15 schema:sdPublisher N9857ae6babad4e45884de05743068675
    16 sgo:license sg:explorer/license/
    17 sgo:sdDataset persons
    18 rdf:type schema:Person
    19 N15956c017dc1411dbcba173668b94c42 schema:affiliation
    20 sgo:isCurrent true
    21 rdf:type schema:OrganizationRole
    22 N9857ae6babad4e45884de05743068675 schema:name Springer Nature - SN SciGraph project
    23 rdf:type schema:Organization
    24 schema:Organization
    25 schema:Organization
    26 schema:Organization
    27 schema:Organization
    28 schema:Organization
    29 schema:Organization
    30 schema:Organization
    31 schema:Organization
    32 schema:Organization

    Preview window. Press ESC to close (or click here)