Marijcke W M Veltman

Summary

Affiliation: University of Cambridge
Country: UK

Publications

  1. ncbi request reprint A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family study
    Marijcke W M Veltman
    Developmental Psychiatry Section, University of Cambridge, Cambridge, UK
    J Autism Dev Disord 35:117-27. 2005
  2. ncbi request reprint Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review
    Marijcke W M Veltman
    Department of Psychiatry, Section of Developmental Psychiatry, University of Cambridge, Cambridge, UK
    Psychiatr Genet 15:243-54. 2005
  3. ncbi request reprint Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders
    Marijcke W M Veltman
    Developmental Psychiatry Section, University of Cambridge, Douglas House, 18b Trumpington Road, Cambridge, CB2 2AH, UK
    Eur Child Adolesc Psychiatry 13:42-50. 2004
  4. pmc Effect on health-related outcomes of interventions to alter the interaction between patients and practitioners: a systematic review of trials
    Simon J Griffin
    General Practice and Primary Care Research Unit, Department of Public Health and Primary Care, Institute of Public Health, University Forvie Site, Robinson Way, Cambridge, CB2 2SR, UK
    Ann Fam Med 2:595-608. 2004
  5. ncbi request reprint Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype
    Katja M Milner
    Child and Adolescent Psychiatry Department and MRC Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, London, UK
    J Child Psychol Psychiatry 46:1089-96. 2005
  6. ncbi request reprint Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders
    Patrick F Bolton
    Department of Child Psychiatry and MRC Centre for Social, Genetic and Developmental Psychiatry, The Institute of Psychiatry, Kings College, London, UK
    Psychiatr Genet 14:131-7. 2004

Collaborators

Detail Information

Publications6

  1. ncbi request reprint A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family study
    Marijcke W M Veltman
    Developmental Psychiatry Section, University of Cambridge, Cambridge, UK
    J Autism Dev Disord 35:117-27. 2005
    ..More research is required to determine whether paternally derived duplications that involve 15q11-13 are associated with developmental impairments...
  2. ncbi request reprint Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review
    Marijcke W M Veltman
    Department of Psychiatry, Section of Developmental Psychiatry, University of Cambridge, Cambridge, UK
    Psychiatr Genet 15:243-54. 2005
    ..0176). Thus, the limited available evidence supported the prediction that overexpression of maternally imprinted genes in 15q11-13 confers a risk for ASD. Further research will be required to confirm these findings...
  3. ncbi request reprint Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders
    Marijcke W M Veltman
    Developmental Psychiatry Section, University of Cambridge, Douglas House, 18b Trumpington Road, Cambridge, CB2 2AH, UK
    Eur Child Adolesc Psychiatry 13:42-50. 2004
    ..They also suggest that there may be cognitive differences between the groups in processing visuo-spatial information...
  4. pmc Effect on health-related outcomes of interventions to alter the interaction between patients and practitioners: a systematic review of trials
    Simon J Griffin
    General Practice and Primary Care Research Unit, Department of Public Health and Primary Care, Institute of Public Health, University Forvie Site, Robinson Way, Cambridge, CB2 2SR, UK
    Ann Fam Med 2:595-608. 2004
    ....
  5. ncbi request reprint Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype
    Katja M Milner
    Child and Adolescent Psychiatry Department and MRC Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, London, UK
    J Child Psychol Psychiatry 46:1089-96. 2005
    ..We also tested reports that PWS cases due to the larger type I (TI) form of deletion show differences to cases with the smaller type II (TII) deletion...
  6. ncbi request reprint Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders
    Patrick F Bolton
    Department of Child Psychiatry and MRC Centre for Social, Genetic and Developmental Psychiatry, The Institute of Psychiatry, Kings College, London, UK
    Psychiatr Genet 14:131-7. 2004
    ..The frequency of abnormalities of 15q11-q13 and other possibly causal medical disorders including karyotypic abnormalities was investigated in an unselected series of children who were referred to one of two autism assessment centres...