• Issue

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics: Volume 150B, Issue 7

    893-1023
    5 October 2009
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Research Articles

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Evidence that putative ADHD low risk alleles at SNAP25 may increase the risk of schizophrenia†

L.S. Carroll,  K. Kendall,  M.C. O'Donovan,  M.J. Owen,  N.M. Williams, 
  • Pages: 893-899
  • First Published: 08 January 2009
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Genetic variation in 5HTTLPR is associated with emotional resilience†‡

Murray B. Stein,  Laura Campbell-Sills,  Joel Gelernter, 
  • Pages: 900-906
  • First Published: 16 January 2009
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Gender moderates the relationship between mania spectrum and serotonin transporter polymorphisms in depression†‡

P. Rucci,  V.L. Nimgaonkar,  H. Mansour,  M. Miniati,  I. Masala,  A. Fagiolini,  G.B. Cassano,  E. Frank, 
  • Pages: 907-913
  • First Published: 05 January 2009
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Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33–q26.13 in Arab Israeli families†

A. Alkelai,  Y. Kohn,  T. Olender,  K. Sarner-Kanyas,  A. Rigbi,  A. Hamdan,  E. Ben-Asher,  D. Lancet,  B. Lerer, 
  • Pages: 914-925
  • First Published: 16 January 2009
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Variants in nicotinic acetylcholine receptors α5 and α3 increase risks to nicotine dependence†

Xiangning Chen,  Jingchun Chen,  Vernell S. Williamson,  Seon-Sook An,  John M. Hettema,  Steven H. Aggen,  Michael C. Neale,  Kenneth S. Kendler, 
  • Pages: 926-933
  • First Published: 08 January 2009
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Profiling brain expression of the spermidine/spermine N1-acetyltransferase 1 (SAT1) gene in suicide†

Timothy A. Klempan,  Dan Rujescu,  Chantal Mérette,  Carla Himmelman,  Adolfo Sequeira,  Lilian Canetti,  Laura M. Fiori,  Barbara Schneider,  Alexandre Bureau,  Gustavo Turecki, 
  • Pages: 934-943
  • First Published: 16 January 2009
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A twin concordance study of trichotillomania†

Carol E. Novak,  Nancy J. Keuthen,  S. Evelyn Stewart,  David L. Pauls, 
  • Pages: 944-949
  • First Published: 17 September 2009
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Genetic linkage findings for DSM-IV nicotine withdrawal in two populations†‡

Michele L. Pergadia,  Arpana Agrawal,  Anu Loukola,  Grant W. Montgomery,  Ulla Broms,  Scott F. Saccone,  Jen C. Wang,  Alexandre A. Todorov,  Kauko Heikkilä,  Dixie J. Statham,  Anjali K. Henders,  Megan J. Campbell,  John P. Rice,  Richard D. Todd,  Andrew C. Heath,  Alison M. Goate,  Leena Peltonen,  Jaakko Kaprio,  Nicholas G. Martin,  Pamela A.F. Madden, 
  • Pages: 950-959
  • First Published: 29 January 2009
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Common and rare variants of DAOA in bipolar disorder†‡

Manjula Maheshwari,  Jiajun Shi,  Judith A. Badner,  Andrew Skol,  Virginia L. Willour,  Donna M. Muzny,  David A. Wheeler,  Fowler R. Gerald,  Sevilla Detera-Wadleigh,  Francis J. McMahon,  James B. Potash,  Elliot S. Gershon,  Chunyu Liu,  Richard A. Gibbs, 
  • Pages: 960-966
  • First Published: 04 February 2009
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Association studies and gene expression analyses of the DISC1-interacting molecules, pericentrin 2 (PCNT2) and DISC1-binding zinc finger protein (DBZ), with schizophrenia and with bipolar disorder†‡

Ayyappan Anitha,  Kazuhiko Nakamura,  Kazuo Yamada,  Yoshimi Iwayama,  Tomoko Toyota,  Nori Takei,  Yasuhide Iwata,  Katsuaki Suzuki,  Yoshimoto Sekine,  Hideo Matsuzaki,  Masayoshi Kawai,  Ismail Thanseem,  Ko Miyoshi,  Taiichi Katayama,  Shinsuke Matsuzaki,  Kousuke Baba,  Akiko Honda,  Tsuyoshi Hattori,  Shoko Shimizu,  Natsuko Kumamoto,  Mitsuru Kikuchi,  Masaya Tohyama,  Takeo Yoshikawa,  Norio Mori, 
  • Pages: 967-976
  • First Published: 03 February 2009
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Family-based association of YWHAH in psychotic bipolar disorder†

Deepak Grover,  Ranjana Verma,  Fernando S. Goes,  Pamela L. Belmonte Mahon,  Elliot S. Gershon,  Francis J. McMahon,  James B. Potash, 
  • Pages: 977-983
  • First Published: 21 January 2009
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SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration†‡

Hanna Örlén,  Atle Melberg,  Raili Raininko,  Eva Kumlien,  Miriam Entesarian,  Per Söderberg,  Magnus Påhlman,  Niklas Darin,  Mårten Kyllerman,  Eva Holmberg,  Henry Engler,  Urban Eriksson,  Niklas Dahl, 
  • Pages: 984-992
  • First Published: 04 February 2009
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Homozygosity mapping through whole genome analysis identifies a COL18A1 mutation in an Indian family presenting with an autosomal recessive neurological disorder†‡

Coro Paisán-Ruiz,  Geoff Scopes,  Philip Lee,  Henry Houlden, 
  • Pages: 993-997
  • First Published: 21 January 2009
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A narrow and highly significant linkage signal for severe bipolar disorder in the chromosome 5q33 region in Latin American pedigrees†

A.J. Jasinska,  S. Service,  D. Jawaheer,  J. DeYoung,  M. Levinson,  Z. Zhang,  B. Kremeyer,  H. Muller,  I. Aldana,  J. Garcia,  G. Restrepo,  C. Lopez,  C. Palacio,  C. Duque,  M. Parra,  J. Vega,  D. Ortiz,  G. Bedoya,  C. Mathews,  P. Davanzo,  E. Fournier,  J. Bejarano,  M. Ramirez,  C. Araya Ortiz,  X. Araya,  J. Molina,  C. Sabatti,  V. Reus,  J. Ospina,  G. Macaya,  A. Ruiz-Linares,  N.B. Freimer, 
  • Pages: 998-1006
  • First Published: 24 March 2009

Brief Research Communications

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G72/G30 (DAOA) and juvenile-onset mood disorders†

Lissette Gomez,  Karen Wigg,  Yu Feng,  Eniko Kiss,  Krisztina Kapornai,  Zsuzsa Tamás,  László Mayer,  Ildikó Baji,  Gabriella Daróczi,  István Benák,  Viola Osváth Kothencné,  Edit Dombovári,  Emília Kaczvinszk,  Márta Besnyő,  Julia Gádoros,  Nicole King,  Judit Székely,  Maria Kovacs,  Ágnes Vetró,  James L Kennedy,  Cathy L Barr, 
  • Pages: 1007-1012
  • First Published: 16 December 2008
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Association of major depression with rare functional variants in norepinephrine transporter and serotonin1A receptor genes†‡

Britta Haenisch,  Karoline Linsel,  Michael Brüss,  Ralf Gilsbach,  Peter Propping,  Markus M. Nöthen,  Marcella Rietschel,  Rolf Fimmers,  Wolfgang Maier,  Astrid Zobel,  Susanne Höfels,  Vera Guttenthaler,  Manfred Göthert,  Heinz Bönisch, 
  • Pages: 1013-1016
  • First Published: 22 December 2008
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Variation in P2RX7 candidate gene (rs2230912) is not associated with bipolar I disorder and unipolar major depression in four European samples†

Maria Grigoroiu-Serbanescu,  Stefan Herms,  Thomas W. Mühleisen,  Alexander Georgi,  Carmen C. Diaconu,  Jana Strohmaier,  Piotr Czerski,  Joanna Hauser,  Anna Leszczynska-Rodziewicz,  Rami Abou Jamra,  Gulia Babadjanova,  A. Tiganov,  V. Krasnov,  Sofia Kapiletti,  Ana Iulia Neagu,  Jennifer Vollmer,  René Breuer,  Marcella Rietschel,  Markus M. Nöthen,  Sven Cichon,  Peter Propping, 
  • Pages: 1017-1021
  • First Published: 27 March 2009

Letters to the Editor

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LRRK2 G2385R modulates age at onset in Parkinson's disease: A multi-center pooled analysis†

E.K. Tan,  R. Peng,  Y.R. Wu,  R.M. Wu,  Y.H. Wu-Chou,  L.C. Tan,  X.K. An,  C.M. Chen,  S. Fook-Chong,  C.S. Lu, 
  • Pages: 1022-1023
  • First Published: 16 January 2009