• Issue

    American Journal of Medical Genetics: Volume 96, Issue 6

    707-893
    4 December 2000
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Brief Research Communication

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Tardive dyskinesia is not associated with the serotonin gene polymorphism (5-HTTLPR) in Chinese

Siow-Ann Chong,  Ene-Choo Tan,  Chay-Hoon Tan,  Rathi Mahendren,  Agnes Hou-Ngee Tay,  Hong-Choon Chua, 
  • Pages: 712-715
  • First Published: 23 October 2002
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Mutation and association analysis of the Fyn kinase gene with alcoholism and schizophrenia

Hiroki Ishiguro,  Toshikazu Saito,  Haruo Shibuya,  Michio Toru,  Tadao Arinami, 
  • Pages: 716-720
  • First Published: 23 October 2002
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Association between homozygosity at the COMT gene locus and obsessive compulsive disorder

Kim M. Schindler,  M.A. Richter,  James L. Kennedy,  Michele T. Pato,  Carlos N. Pato, 
  • Pages: 721-724
  • First Published: 23 October 2002
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Support for an association between HLA-DR1 and schizophrenia in the Japanese population

Rie Akaho,  Ikumi Matsushita,  Kaori Narita,  Yuji Okazaki,  Yuriko Okabe,  Masaki Matsushita,  Hirohiko Hohjoh,  Katsushi Tokunaga,  Tsukasa Sasaki, 
  • Pages: 725-727
  • First Published: 23 October 2002
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Search for bipolar disorder susceptibility loci: The application of a modified genome scan concentrating on gene-rich regions

V.E. Murphy,  L.A. Mynett-Johnson,  E. Claffey,  P. Bergin,  M. McAuliffe,  C. Kealey,  P. McKeon, 
  • Pages: 728-732
  • First Published: 23 October 2002

Brief Research Communication

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Association analysis of CAG repeats at the KCNN3 locus in Indian patients with bipolar disorder and schizophrenia

Quasar Saleem,  V.S. Sreevidya,  J. Sudhir,  J. Vijaya Savithri,  Y. Gowda,  Chandrika B-Rao,  V. Benegal,  Partha P. Majumder,  Anuranjan Anand,  Samir K. Brahmachari,  Sanjeev Jain, 
  • Pages: 744-748
  • First Published: 23 October 2002
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Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: Identification of a BAC contig spanning the translocation breakpoint at 7q21†

WenLiang Yan,  Xin-Yuan Guan,  Eric D. Green,  Rob Nicolson,  Tieng K. Yap,  Jinghui Zhang,  Leslie K. Jacobsen,  Donna M. Krasnewich,  Sanjiv Kumra,  Marge C. Lenane,  Peter Gochman,  Patricia J. Damschroder-Williams,  Lisa E. Esterling,  Robert T. Long,  Brian M. Martin,  Ellen Sidransky,  Judith L. Rapoport,  Edward I. Ginns, 
  • Pages: 749-753
  • First Published: 23 October 2002
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Influence of ascertainment strategy on finding sex differences in genetic estimates from twin studies of alcoholism

Carol A. Prescott,  Kenneth S. Kendler, 
  • Pages: 754-761
  • First Published: 23 October 2002
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The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine

Hisanori Kowa,  Kenichi Yasui,  Takao Takeshima,  Katsuya Urakami,  Fumihiko Sakai,  Kenji Nakashima, 
  • Pages: 762-764
  • First Published: 23 October 2002
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Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: Identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13

Moyra Smith,  Pauline A. Filipek,  Charles Wu,  Maureen Bocian,  Simin Hakim,  Charlotte Modahl,  M. Anne Spence, 
  • Pages: 765-770
  • First Published: 23 October 2002

Brief Research Communication

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Exploratory association study between catechol-O-methyltransferase (COMT) high/low enzyme activity polymorphism and hypnotizability

Pesach Lichtenberg,  Rachel Bachner-Melman,  Inga Gritsenko,  Richard P. Ebstein, 
  • Pages: 771-774
  • First Published: 23 October 2002
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Identical distribution of the α2-macroglobulin pentanucleotide deletion in subjects with alzheimer disease and controls in a German population

Metin Bagli,  Andreas Papassotiropoulos,  Frank Jessen,  Sandra Schmitz,  Marie Luise Rao,  Wolfgang Maier,  Reinhard Heun, 
  • Pages: 775-777
  • First Published: 23 October 2002

Brief Research Communication

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Drawbacks of GENEHUNTER for larger pedigrees: Application to panic disorder

R. Goedken,  E. Ludington,  R. Crowe,  A.J. Fyer,  S.E. Hodge,  J.A. Knowles,  V.J. Vieland,  M.M Weissman, 
  • Pages: 781-783
  • First Published: 23 October 2002

Brief Research Communication

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Association of 5HT2A receptor gene polymorphism and alcohol abuse with behavior problems

Hai-Gwo Hwu,  Chia-Hsiang Chen, 
  • Pages: 797-800
  • First Published: 23 October 2002
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Association between a functional polymorphism in the monoamine oxidase A gene promoter and major depressive disorder

Thomas G. Schulze,  Daniel J. Müller,  Harald Krauss,  Harald Scherk,  Stephanie Ohlraun,  Yana V. Syagailo,  Christine Windemuth,  Helge Neidt,  Markus Grässle,  Andreas Papassotiropoulos,  Reinhard Heun,  Markus M. Nöthen,  Wolfgang Maier,  Klaus-Peter Lesch,  Marcella Rietschel, 
  • Pages: 801-803
  • First Published: 23 October 2002

Brief Research Communication

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NURR1 Mutations in cases of schizophrenia and manic-depressive disorder

Silvia Buervenich,  Andrea Carmine,  Mariette Arvidsson,  Fengqing Xiang,  Zhiping Zhang,  Olof Sydow,  Erik G. Jönsson,  Göran C. Sedvall,  Sherry Leonard,  Randal G. Ross,  Robert Freedman,  Kodavali V. Chowdari,  Vishwajit L. Nimgaonkar,  Thomas Perlmann,  Maria Anvret,  Lars Olson, 
  • Pages: 808-813
  • First Published: 23 October 2002
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Failure to replicate association between the gene for the neuronal nicotinic acetylcholine receptor α4 subunit (CHRNA4) and IGE

B. Chioza,  H. Goodwin,  J. Blower,  D. McCormick,  L. Nashef,  P. Asherson,  A.J. Makoff, 
  • Pages: 814-816
  • First Published: 23 October 2002
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Implications of comorbidity and ascertainment bias for identifying disease genes

Jordan W. Smoller,  Kathryn L. Lunetta,  James Robins, 
  • Pages: 817-822
  • First Published: 23 October 2002
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Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease: The NIMH Alzheimer disease genetics initiative

Julianne S. Collins,  Rodney T. Perry,  Bracie Watson Jr,  Lindy E. Harrell,  Ronald T. Acton,  Deborah Blacker,  Marilyn S. Albert,  Rudolph E. Tanzi,  Susan S. Bassett,  Melvin G. McInnis,  R. Duncan Campbell,  Rodney C.P. Go, 
  • Pages: 823-830
  • First Published: 23 October 2002
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Lack of association of serotonin-2A receptor gene polymorphism (T102C) with suicidal ideation and suicide

Brigitta Bondy,  Joachim Kuznik,  Thomas Baghai,  Cornelius Schüle,  Peter Zwanzger,  Christo Minov,  Sylvia de Jonge,  Rainer Rupprecht,  Harald Meyer,  Rolf R. Engel,  Wolfgang Eisenmenger,  Manfred Ackenheil, 
  • Pages: 831-835
  • First Published: 23 October 2002
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Evidence for linkage by transmission disequilibrium test analysis of a chromosome 22 microsatellite marker D22S278 and bipolar disorder in a Palestinian Arab population

Mustafa Mujaheed,  Marilys Corbex,  Pesach Lichtenberg,  Douglas F. Levinson,  Jean-Francois Deleuze,  Jacques Mallet,  Richard P. Ebstein, 
  • Pages: 836-838
  • First Published: 23 October 2002
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Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH

Cyril Goizet,  Elsa Excoffier,  Laurence Taine,  Emmanuelle Taupiac,  Azza Abd El Moneim,  Benoit Arveiler,  Manuel Bouvard,  Didier Lacombe, 
  • Pages: 839-844
  • First Published: 23 October 2002

Brief Research Communication

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Multimarkerhaplotypes within the serotonin transporter gene suggest evidence of an association with bipolar disorder

L. Mynett-Johnson,  C. Kealey,  E. Claffey,  D. Curtis,  L. Bouchier-Hayes,  C. Powell,  P. McKeon, 
  • Pages: 845-849
  • First Published: 23 October 2002
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Molecular genetic studies of bipolar disorder and puerperal psychosis at two polymorphisms in the estrogen receptor α gene (ESR 1)

Ian Jones,  Fiona Middle,  Fiona McCandless,  Natasha Coyle,  Emma Robertson,  Ian Brockington,  Corinne Lendon,  Nick Craddock, 
  • Pages: 850-853
  • First Published: 23 October 2002
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Detection of expansion regions in Portuguese bipolar families

Carlos N. Pato,  Antonio Macedo,  Alda Ambrosio,  John B. Vincent,  Amy Bauer,  Kim Schindler,  Junzhe Xu,  Isabel Coelho,  Ana Dourado,  Jose Valente,  M. Helena Azevedo,  James L. Kennedy,  Michele T. Pato, 
  • Pages: 854-857
  • First Published: 23 October 2002

Brief Research Communication

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Tryptophan hydroxylase gene polymorphisms are not associated with suicide

Hisae Ono,  Osamu Shirakawa,  Naoki Nishiguchi,  Akiyoshi Nishimura,  Hideyuki Nushida,  Yasuhiro Ueno,  Kiyoshi Maeda, 
  • Pages: 861-863
  • First Published: 23 October 2002
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Second stage of a genome scan of schizophrenia: Study of five positive regions in an expanded sample

Bryan J. Mowry,  Kelly R. Ewen,  Derek J. Nancarrow,  David P. Lennon,  Deborah A. Nertney,  Helen L. Jones,  Matthew S. O'Brien,  Catherine E. Thornley,  Marilyn K. Walters,  Raymond R. Crowe,  Jeremy M. Silverman,  Jean Endicott,  Lawrence Sharpe,  Nicholas K. Hayward,  Madeline M. Gladis,  Simon J. Foote,  Douglas F. Levinson, 
  • Pages: 864-869
  • First Published: 23 October 2002
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Human leukocyte antigen (HLA) DRB1 alleles in Kuwaiti Arabs with schizophrenia

M.Z. Haider,  M.A. Zahid,  H.N. Dalal,  M.A. Razik, 
  • Pages: 870-872
  • First Published: 23 October 2002
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Long repeat tracts at SCA8 in major psychosis

John B. Vincent,  Qiu-Ping Yuan,  Martin Schalling,  R Adolfsson,  M. Helena Azevedo,  Antonio Macedo,  Amy Bauer,  Camille DallaTorre,  Helena M. Medeiros,  Michele T. Pato,  Carlos N. Pato,  Timothy Bowen,  Carol A. Guy,  Michael J. Owen,  Michael C. O'Donovan,  Andrew D. Paterson,  Arturas Petronis,  James L. Kennedy, 
  • Pages: 873-876
  • First Published: 23 October 2002

Letters to the Editor

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No association between suicidal behavior and 5-HT2A-T102C polymorphism in alcohol dependents

U.W. Preuss,  G. Koller,  M. Bahlmann,  M. Soyka,  B. Bondy, 
  • Pages: 877-878
  • First Published: 23 October 2002
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No evidence for association of 5-HT2A receptor polymorphism with suicide

Joanna Crawford,  Grant R. Sutherland,  Robert D. Goldney, 
  • Pages: 879-880
  • First Published: 23 October 2002
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Linkage mapping of bipolar affective disorder

Miron Baron, 
  • Pages: 881-883
  • First Published: 23 October 2002
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Comparison of the number of triplets in SCA1, MJD/SCA3, HD, SBMA, DRPLA, MD, FRAXA and FRDA genes in schizophrenic patients and a healthy population

B. Čuljković,  O. Stojković,  D. Savić,  N. Zamurović,  M. Nešić,  T. Major,  D. Keckarević,  S. Romac,  B. Zamurović,  S. Vukosavić, 
  • Pages: 884-887
  • First Published: 23 October 2002
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Behavioral phenotype in childhood type of dystrophia myotonica

J. Steyaert,  C. de Die-Smulders,  J.P. Fryns,  E. Goossens,  D. Willekens, 
  • Pages: 888-889
  • First Published: 23 October 2002
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MAO-B gene intronic dinucleotide repeat polymorphism revisited

Philipp G. Sand,  Christian Luckhaus, 
  • Pages: 890-891
  • First Published: 23 October 2002
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Suicidal behavior, the serotonin 2A receptor gene, and the media

Gustavo Turecki, 
  • Page: 892
  • First Published: 23 October 2002

Errata

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Erratum

  • Page: 893
  • First Published: 23 October 2002