American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 1552-4841

Journal

11 - 17 out of 17Page size: 10

Publications

  1. 2002
  2. Published

    The Role of DRD4 in Children wit ADHD and Comorbid Disturbance

    Lindsey Kent, 1 Jan 2002, In: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 114, p. 150-153 4 p.

    Research output: Contribution to journal › Article

  3. 2001
  4. Published

    Allelic variation of a Bal1 polymorphism in the DRD3 gene does not influence suceptibility to bipolar disorder: Results of analysis and meta-analysis

    Ian Jones & Nick Craddock, 8 May 2001, In: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 105, p. 307-311 5 p.

    Research output: Contribution to journal › Article

  5. Published

    Scanning of estrogen receptor a (ER a) and thyroid hormone receptor a (TR a) genes in patients with psychiatric diseases: Four missense mutations identified in ER a gene

    Nick Craddock, Ian Jones, 8 May 2001, In: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 105, p. 369-374 6 p.

    Research output: Contribution to journal › Article

  6. Published

    Is the estrogen regulated expression of the serotonin transporter gene modulated by the VNTR polymorphism: A possible mechanism for increased risk for bipolar affective puerperal psychosis

    Jean-Charles Lambert, Fiona Middle, Emma Robertson, Ian Jones, Nick Craddock & Corinne Lendon, 1 Jan 2001, In: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 105, 619, p. 77 1 p.

    Research output: Contribution to journal › Article

  7. 2000
  8. Published

    Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the wolfram gene

    Fiona Middle, Farhat Khanim, Corinne Lendon & Nick Craddock, 3 Apr 2000, In: American Journal of Medical Genetics - Neuropsychiatric Genetics. 96, 2, p. 154-157 4 p.

    Research output: Contribution to journal › Article › peer-review

  9. 1999
  10. Published

    The CALL gene is haploinsufficient in a 3p-syndrome patient

    Farida Latif, 29 Oct 1999, In: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 86, p. 482-485 4 p.

    Research output: Contribution to journal › Article

  11. Published

    Mutation and preliminary genotype/phenotype analysis in 19 Wolfram syndrome (Didmoad) kindreds

    Carol Hardy, Farhat Khanim, Farida Latif & Timothy Barrett, 1 Jan 1999, In: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 65, p. 1279-1290 12 p.

    Research output: Contribution to journal › Article

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