American Journal of Medical Genetics

Cover image for American Journal of Medical Genetics

8 April 2002

Volume 114, Issue 3

Pages 255–359

Currently known as: American Journal of Medical Genetics Part A

  1. Research Articles

    1. Top of page
    2. Research Articles
    3. Meeting Report
    4. Research Articles
    5. Brief Research Communication
    6. Research Articles
    7. Letter to the Editor
    8. Research Articles
    9. Brief Research Communication
    10. Research Articles
    1. The norepinephrine transporter gene and attention-deficit hyperactivity disorder (pages 255–259)

      Cathy L. Barr, Jamie Kroft, Yu Feng, Karen Wigg, Wendy Roberts, Molly Malone, Abel Ickowicz, Russell Schachar, Rosemary Tannock and James L. Kennedy

      Version of Record online: 14 MAR 2002 | DOI: 10.1002/ajmg.10193

    2. Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorder (pages 260–268)

      Erik G. Willcutt, Bruce F. Pennington, Shelley D. Smith, Lon R. Cardon, Javier Gayán, Valerie S. Knopik, Richard K. Olson and John C. DeFries

      Version of Record online: 7 FEB 2002 | DOI: 10.1002/ajmg.10205

    3. Association study of a SNAP-25 microsatellite and attention deficit hyperactivity disorder (pages 269–271)

      Jonathan Mill, Sarah Curran, Lindsey Kent, Alison Gould, Louise Huckett, Sandra Richards, Eric Taylor and Philip Asherson

      Version of Record online: 18 JAN 2002 | DOI: 10.1002/ajmg.10253

  2. Meeting Report

    1. Top of page
    2. Research Articles
    3. Meeting Report
    4. Research Articles
    5. Brief Research Communication
    6. Research Articles
    7. Letter to the Editor
    8. Research Articles
    9. Brief Research Communication
    10. Research Articles
  3. Research Articles

    1. Top of page
    2. Research Articles
    3. Meeting Report
    4. Research Articles
    5. Brief Research Communication
    6. Research Articles
    7. Letter to the Editor
    8. Research Articles
    9. Brief Research Communication
    10. Research Articles
    1. Transmission disequilibrium studies of the serotonin 5-HT2A receptor gene (HTR2A) in autism (pages 277–283)

      Jeremy Veenstra-VanderWeele, Soo-Jeong Kim, Catherine Lord, Rachel Courchesne, Natasha Akshoomoff, Bennett L. Leventhal, Eric Courchesne and Edwin H. Cook Jr.

      Version of Record online: 14 MAR 2002 | DOI: 10.1002/ajmg.10192

  4. Brief Research Communication

    1. Top of page
    2. Research Articles
    3. Meeting Report
    4. Research Articles
    5. Brief Research Communication
    6. Research Articles
    7. Letter to the Editor
    8. Research Articles
    9. Brief Research Communication
    10. Research Articles
    1. Family-based and population study of a functional promoter-region monoamine oxidase A polymorphism in autism: Possible association with IQ (pages 284–287)

      Nurit Yirmiya, Tammy Pilowsky, Sigal Tidhar, Lubov Nemanov, Larissa Altmark and Richard P. Ebstein

      Version of Record online: 14 FEB 2002 | DOI: 10.1002/ajmg.10189

    2. ApoE ϵ3-haplotype modulates Alzheimer beta-amyloid deposition in the brain (pages 288–291)

      Liisa Myllykangas, Tuomo Polvikoski, Karoliina Reunanen, Fabienne Wavrant-De Vrieze, Clare Ellis, Dena Hernandez, Raimo Sulkava, Kimmo Kontula, Auli Verkkoniemi, Irma-Leena Notkola, John Hardy, Jordi Perez-Tur, Matti J. Haltia and Pentti J. Tienari

      Version of Record online: 9 JAN 2002 | DOI: 10.1002/ajmg.10202

  5. Research Articles

    1. Top of page
    2. Research Articles
    3. Meeting Report
    4. Research Articles
    5. Brief Research Communication
    6. Research Articles
    7. Letter to the Editor
    8. Research Articles
    9. Brief Research Communication
    10. Research Articles
    1. Molecular evidence of presenilin 1 mutation in familial early onset dementia (pages 292–298)

      Miho Matsubara-Tsutsui, Minoru Yasuda, Hidehisa Yamagata, Takuo Nomura, Keiko Taguchi, Katsuhiko Kohara, Koho Miyoshi and Tetsuro Miki

      Version of Record online: 18 JAN 2002 | DOI: 10.1002/ajmg.10250

    2. Paternal age and sporadic schizophrenia: Evidence for de novo mutations (pages 299–303)

      Dolores Malaspina, Cheryl Corcoran, Cherine Fahim, Ariela Berman, Jill Harkavy-Friedman, Scott Yale, Deborah Goetz, Raymond Goetz, Susan Harlap and Jack Gorman

      Version of Record online: 20 FEB 2002 | DOI: 10.1002/ajmg.1701

    3. Novel polymorphisms in the promoter region of the neurotrophin-3 gene and their associations with schizophrenia (pages 304–309)

      Mineko Hattori, Hiroshi Kunugi, Akihisa Akahane, Hiroshi Tanaka, Sugiko Ishida, Tetsuya Hirose, Ryoji Morita, Kazuhiro Yamakawa and Shinichiro Nanko

      Version of Record online: 17 JAN 2002 | DOI: 10.1002/ajmg.10248

    4. Angiotensin converting enzyme gene insertion/deletion polymorphism: Case-control association studies in schizophrenia, major affective disorder, and tardive dyskinesia and a family-based association study in schizophrenia (pages 310–314)

      Ronnen H. Segman, Yami Shapira, Ilan Modai, Adnan Hamdan, Joseph Zislin, Uriel Heresco-Levy, Kyra Kanyas, Shmuel Hirschmann, Osnat Karni, Boris Finkel, Michael Schlafman, Arturo Lerner, Baruch Shapira, Fabio Macciardi and Bernard Lerer

      Version of Record online: 18 JAN 2002 | DOI: 10.1002/ajmg.10255

    5. Investigation of linkage and association/linkage disequilibrium of HLA A-, DQA1-, DQB1-, and DRB1-alleles in 69 sib-pair- and 89 trio-families with schizophrenia (pages 315–320)

      Sibylle G. Schwab, Joachim Hallmayer, Julia Freimann, Bernard Lerer, Margot Albus, Margitta Borrmann-Hassenbach, Ronnen H. Segman, Matyas Trixler, Marcella Rietschel, Wolfgang Maier and Dieter B. Wildenauer

      Version of Record online: 20 FEB 2002 | DOI: 10.1002/ajmg.10307

  6. Letter to the Editor

    1. Top of page
    2. Research Articles
    3. Meeting Report
    4. Research Articles
    5. Brief Research Communication
    6. Research Articles
    7. Letter to the Editor
    8. Research Articles
    9. Brief Research Communication
    10. Research Articles
  7. Research Articles

    1. Top of page
    2. Research Articles
    3. Meeting Report
    4. Research Articles
    5. Brief Research Communication
    6. Research Articles
    7. Letter to the Editor
    8. Research Articles
    9. Brief Research Communication
    10. Research Articles
    1. Correlation between serotonin uptake in human blood platelets with the 44-bp polymorphism and the 17-bp variable number of tandem repeat of the serotonin transporter (pages 323–328)

      Rolf Kaiser, Bruno Müller-Oerlinghausen, Diana Filler, Pierre-Benoit Tremblay, Anne Berghöfer, Ivar Roots and Jürgen Brockmöller

      Version of Record online: 7 FEB 2002 | DOI: 10.1002/ajmg.10119

    2. Allelic association analysis of the dopamine D2, D3, 5-HT2A, and GABAAγ2 receptors and serotonin transporter genes with heroin abuse in Chinese subjects (pages 329–335)

      Tao Li, Xiehe Liu, Jinghua Zhao, Xun Hu, David M. Ball, El-Wui Loh, Pak C. Sham and David A. Collier

      Version of Record online: 17 JAN 2002 | DOI: 10.1002/ajmg.10200

  8. Brief Research Communication

    1. Top of page
    2. Research Articles
    3. Meeting Report
    4. Research Articles
    5. Brief Research Communication
    6. Research Articles
    7. Letter to the Editor
    8. Research Articles
    9. Brief Research Communication
    10. Research Articles
    1. Serotonin 2a receptor T102C polymorphism and impaired impulse control (pages 336–339)

      James M. Bjork, F. Gerard Moeller, Donald M. Dougherty, Alan C. Swann, Mirta A. Machado and Craig L. Hanis

      Version of Record online: 20 FEB 2002 | DOI: 10.1002/ajmg.10206

    2. No evidence of an association between a functional monoamine oxidase a gene polymorphism and completed suicides (pages 340–342)

      Hisae Ono, Osamu Shirakawa, Naoki Nishiguchi, Akiyoshi Nishimura, Hideyuki Nushida, Yasuhiro Ueno and Kiyoshi Maeda

      Version of Record online: 18 JAN 2002 | DOI: 10.1002/ajmg.10237

  9. Research Articles

    1. Top of page
    2. Research Articles
    3. Meeting Report
    4. Research Articles
    5. Brief Research Communication
    6. Research Articles
    7. Letter to the Editor
    8. Research Articles
    9. Brief Research Communication
    10. Research Articles
    1. Is there a relationship between Wolfram syndrome carrier status and suicide? (pages 343–346)

      Joanna Crawford, Marta A. Zielinski, Laura J. Fisher, Grant R. Sutherland and Robert D. Goldney

      Version of Record online: 12 FEB 2002 | DOI: 10.1002/ajmg.10256

    2. Exploratory factor analysis of obsessive-compulsive patients and association with 5-HTTLPR polymorphism (pages 347–353)

      Maria Cristina Cavallini, Daniela Di Bella, Francesca Siliprandi, Francesca Malchiodi and Laura Bellodi

      Version of Record online: 20 FEB 2002 | DOI: 10.1002/ajmg.1700

    3. Sequencing of the GRIK1 gene in patients with juvenile absence epilepsy does not reveal mutations affecting receptor structure (pages 354–359)

      Claudia Izzi, Alessandro Barbon, Rebekka Kretz, Thomas Sander and Sergio Barlati

      Version of Record online: 18 JAN 2002 | DOI: 10.1002/ajmg.10254

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