• Issue

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics: Volume 137B, Issue 1

    1-58
    5 August 2005
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Brief Research Communications

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Functional COMT variant predicts response to high dose pyridoxine in Parkinson's disease

Eng-King Tan,  Sin-Yun Cheah,  Stephanie Fook-Chong,  Kenneth Yew,  V.R. Chandran,  Sau-Ying Lum,  Zhao Yi, 
  • Pages: 1-4
  • First Published: 21 July 2005

Articles

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Transcriptional analysis of multiple brain regions in Parkinson's disease supports the involvement of specific protein processing, energy metabolism, and signaling pathways, and suggests novel disease mechanisms†‡

Yanli Zhang,  Michael James,  Frank A. Middleton,  Richard L. Davis, 
  • Pages: 5-16
  • First Published: 21 July 2005

Research Articles

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Direct genomic PCR sequencing of the high affinity thiamine transporter (SLC19A2) gene identifies three genetic variants in Wernicke Korsakoff syndrome (WKS)

Irene Guerrini,  Allan D. Thomson,  Cristopher C.H. Cook,  Andrew McQuillin,  Vishal Sharma,  Michael Kopelman,  Gerald Reynolds,  Pramod Jauhar,  Clive Harper,  Hugh M.D. Gurling, 
  • Pages: 17-19
  • First Published: 21 July 2005
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A high predisposition to depression and anxiety in mothers and other matrilineal relatives of children with presumed maternally inherited mitochondrial disorders†

Richard G. Boles,  Brittany B. Burnett,  Katrina Gleditsch,  Stacey Wong,  Ariela Guedalia,  Anneli Kaariainen,  Judy Eloed,  Alan Stern,  Virdette Brumm, 
  • Pages: 20-24
  • First Published: 21 July 2005
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An association analysis of microsatellite markers across the Prader–Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder

Sarah Curran,  Sian Roberts,  Simon Thomas,  Marijcke Veltman,  Josie Browne,  Emanuela Medda,  Andrew Pickles,  Pak Sham,  Patrick F. Bolton, 
  • Pages: 25-28
  • First Published: 21 July 2005

Brief Research Communications

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Evidence for a common biological basis of the absorption trait, hallucinogen effects, and positive symptoms: Epistasis between 5-HT2a and COMT polymorphisms

Ulrich Ott,  Martin Reuter,  Juergen Hennig,  Dieter Vaitl, 
  • Pages: 29-32
  • First Published: 21 July 2005

Research Articles

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5-HT1A polymorphism and self-transcendence in mood disorders

Cristina Lorenzi,  Alessandro Serretti,  Laura Mandelli,  Viviana Tubazio,  Cristina Ploia,  Enrico Smeraldi, 
  • Pages: 33-35
  • First Published: 21 July 2005
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Insomnia improvement during antidepressant treatment and CLOCK gene polymorphism

Alessandro Serretti,  Cristina Cusin,  Francesco Benedetti,  Laura Mandelli,  Adele Pirovano,  Raffaella Zanardi,  Cristina Colombo,  Enrico Smeraldi, 
  • Pages: 36-39
  • First Published: 21 July 2005
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Association of the promoter polymorphism −1438G/A of the 5-HT2A receptor gene with behavioral impulsiveness and serotonin function in women with bulimia nervosa

Kenneth R. Bruce,  Howard Steiger,  Ridha Joober,  N.M.K. Ng Ying Kin,  Mimi Israel,  Simon N. Young, 
  • Pages: 40-44
  • First Published: 21 July 2005
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Association study of CREB1 and childhood-onset mood disorders

I. Burcescu,  K. Wigg,  N. King,  Á. Vetró,  E. Kiss,  L. Katay,  J.L. Kennedy,  M. Kovacs,  C.L. Barr,  The International Consortium for Childhood-Onset Mood Disorders , 
  • Pages: 45-50
  • First Published: 21 July 2005

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Population-based and family-based association study of 5′UTR polymorphism of the reelin gene and schizophrenia

Céline Goldberger,  David Gourion,  Sophie Leroy,  Franck Schürhoff,  Marie-Chantal Bourdel,  Marion Leboyer,  Marie-Odile Krebs, 
  • Pages: 51-55
  • First Published: 21 July 2005

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Cytosolic PLA2 genes possibly contribute to the etiology of schizophrenia

Ran Tao,  Yaqin Yu,  Xiaojuan Zhang,  Yingjun Guo,  Jieping Shi,  Xuan Zhang,  Lin Xie,  Shuzheng Liu,  Guizhi Ju,  Qi Xu,  Yan Shen,  Jun Wei, 
  • Pages: 56-58
  • First Published: 21 July 2005