E Weisblatt

Summary

Affiliation: University of St Andrews
Country: UK

Publications

  1. ncbi X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits
    L Kent
    Bute Medical School, University of St Andrews, St Andrews KY169TS, UK
    J Med Genet 45:519-24. 2008
  2. ncbi An investigation of mitochondrial haplogroups in autism
    Lindsey Kent
    Developmental Psychiatry, University of Cambridge, Cambridge, UK
    Am J Med Genet B Neuropsychiatr Genet 147:987-9. 2008
  3. ncbi Beckwith Weidemann syndrome: a behavioral phenotype-genotype study
    Lindsey Kent
    Bute Medical School, University of St Andrews, St Andrews, Scotland, UK
    Am J Med Genet B Neuropsychiatr Genet 147:1295-7. 2008

Detail Information

Publications3

  1. ncbi X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits
    L Kent
    Bute Medical School, University of St Andrews, St Andrews KY169TS, UK
    J Med Genet 45:519-24. 2008
    ..Animal work suggests the STS gene may be involved in attentional processes. We have therefore undertaken a systematic study of autism and attention deficit hyperactivity disorder (ADHD) in boys with XLI...
  2. ncbi An investigation of mitochondrial haplogroups in autism
    Lindsey Kent
    Developmental Psychiatry, University of Cambridge, Cambridge, UK
    Am J Med Genet B Neuropsychiatr Genet 147:987-9. 2008
    ..The mtDNA haplogroup was determined in 162 autism probands, and compared to two sets of population controls. Results show no compelling evidence of an association of any mitochondrial haplogroup in autism...
  3. ncbi Beckwith Weidemann syndrome: a behavioral phenotype-genotype study
    Lindsey Kent
    Bute Medical School, University of St Andrews, St Andrews, Scotland, UK
    Am J Med Genet B Neuropsychiatr Genet 147:1295-7. 2008
    ..These findings suggest a potential role for the 11p15.5 imprinted gene cluster in ASD and indicate a need for further investigations of neurobehavioral phenotypes in BWS...