• Issue

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics: Volume 153B, Issue 5

    983-1117
    July 2010
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Research Articles

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Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay†‡

Barbara Wiśniowiecka-Kowalnik,  Monika Nesteruk,  Sarika U. Peters,  Zhilian Xia,  M. Lance Cooper,  Sarah Savage,  R. Stephen Amato,  Patricia Bader,  Marsha F. Browning,  Christa L. Haun,  Andrew Walter Duda III,  Sau Wai Cheung,  Paweł Stankiewicz, 
  • Pages: 983-993
  • First Published: 24 June 2010
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Limited genetic covariance between autistic traits and intelligence: Findings from a longitudinal twin study†

Rosa A. Hoekstra,  Francesca Happé,  Simon Baron-Cohen,  Angelica Ronald, 
  • Pages: 994-1007
  • First Published: 24 June 2010
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Common variants in the TPH1 and TPH2 regions are not associated with persistent ADHD in a combined sample of 1,636 adult cases and 1,923 controls from four European populations†

Stefan Johansson,  Anne Halmøy,  Thegna Mavroconstanti,  Kaya K. Jacobsen,  Elisabeth T. Landaas,  Andreas Reif,  Christian Jacob,  Andrea Boreatti-Hümmer,  Susanne Kreiker,  Klaus-Peter Lesch,  Cornelis C. Kan,  J.J. Sandra Kooij,  Lambertus A. Kiemeney,  Jan K. Buitelaar,  Barbara Franke,  Marta Ribasés,  Rosa Bosch,  Mònica Bayés,  Miguel Casas,  Josep Antoni Ramos-Quiroga,  Bru Cormand,  Per Knappskog,  Jan Haavik, 
  • Pages: 1008-1015
  • First Published: 24 June 2010
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Case–control association study of TGOLN2 in attempted suicide†‡

Pamela B. Mahon,  Adrian M. Stütz,  Fayaz Seifuddin,  Yuqing Huo,  Fernando S. Goes,  Dubravka Jancic,  Jennifer T. Judy,  J. Raymond DePaulo Jr,  Elliot S. Gershon,  Francis J. McMahon,  Peter P. Zandi,  James B. Potash,  Virginia L. Willour, 
  • Pages: 1016-1023
  • First Published: 24 June 2010
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BDNF Val66Met polymorphism alters sympathovagal balance in healthy subjects†

Albert C. Yang,  Tai-Jui Chen,  Shih-Jen Tsai,  Chen-Jee Hong,  Chung-Hsun Kuo,  Cheng-Hung Yang,  Ko-Pei Kao, 
  • Pages: 1024-1030
  • First Published: 24 June 2010
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Evidence for three loci modifying age-at-onset of Alzheimer's disease in early-onset PSEN2 families†

Elizabeth E. Marchani,  Thomas D. Bird,  Ellen J. Steinbart,  Elisabeth Rosenthal,  Chang-En Yu,  Gerard D. Schellenberg,  Ellen M. Wijsman, 
  • Pages: 1031-1041
  • First Published: 24 June 2010
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Severe mental retardation, seizures, and hypotonia due to deletions of MEF2C†

Beata A. Nowakowska,  Ewa Obersztyn,  Krystyna Szymańska,  Monika Bekiesińska-Figatowska,  Zhilian Xia,  Christian B. Ricks,  Ewa Bocian,  David W. Stockton,  Krzysztof Szczałuba,  Magdalena Nawara,  Ankita Patel,  Daryl A. Scott,  Sau Wai Cheung,  Timothy P. Bohan,  Paweł Stankiewicz, 
  • Pages: 1042-1051
  • First Published: 24 June 2010
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A functional variant provided further evidence for the association of ARVCF with schizophrenia†

Sergi Mas,  Miquel Bernardo,  Patricia Gassó,  Santi Álvarez,  Clemente Garcia-Rizo,  Miquel Bioque,  Brian Kirkpatrick,  Amalia Lafuente, 
  • Pages: 1052-1059
  • First Published: 24 June 2010
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Genetic pathway-based hierarchical clustering analysis of older adults with cognitive complaints and amnestic mild cognitive impairment using clinical and neuroimaging phenotypes†

Chantel D. Sloan,  Li Shen,  John D. West,  Heather A. Wishart,  Laura A. Flashman,  Laura A. Rabin,  Robert B. Santulli,  Stephen J. Guerin,  C. Harker Rhodes,  Gregory J. Tsongalis,  Thomas W. McAllister,  Tim A. Ahles,  Stephen L. Lee,  Jason H. Moore,  Andrew J. Saykin, 
  • Pages: 1060-1069
  • First Published: 24 June 2010
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Association study of 182 candidate genes in anorexia nervosa†

Andrea Poyastro Pinheiro,  Cynthia M. Bulik,  Laura M. Thornton,  Patrick F. Sullivan,  Tammy L. Root,  Cinnamon S. Bloss,  Wade H. Berrettini,  Nicholas J. Schork,  Walter H. Kaye,  Andrew W. Bergen,  Pierre Magistretti,  Harry Brandt,  Steve Crawford,  Scott Crow,  Manfred M. Fichter,  David Goldman,  Katherine A. Halmi,  Craig Johnson,  Allan S. Kaplan,  Pamela K. Keel,  Kelly L. Klump,  Maria La Via,  James E. Mitchell,  Michael Strober,  Alessandro Rotondo,  Janet Treasure,  D. Blake Woodside, 
  • Pages: 1070-1080
  • First Published: 24 June 2010
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Perception, experience, and response to genetic discrimination in Huntington disease: The international RESPOND-HD study†

Cheryl Erwin,  Janet K. Williams,  Andrew R. Juhl,  Michelle Mengeling,  James A. Mills,  Yvonne Bombard,  Michael R. Hayden,  Kimberly Quaid,  Ira Shoulson,  Sandra Taylor,  Jane S. Paulsen,  the I-RESPOND-HD Investigators of the Huntington Study Group , 
  • Pages: 1081-1093
  • First Published: 24 June 2010

Brief Research Communications

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Intra-individual variability in genetic and environmental models of attention-deficit/hyperactivity disorder†

G.M.L. Perry,  T. Sagvolden,  S.V. Faraone, 
  • Pages: 1094-1101
  • First Published: 24 June 2010
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No association of alcohol dependence with HOMER 1 and 2 genetic variants†

U.W. Preuss,  M. Ridinger,  D. Rujescu,  C. Fehr,  G. Koller,  N. Wodarz,  B. Bondy,  M. Soyka,  W.M. Wong,  P. Zill, 
  • Pages: 1102-1109
  • First Published: 24 June 2010
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A new susceptibility locus for bipolar affective disorder in PAR1 on Xp22.3/Yp11.3†

Antònia Flaquer,  Rami Abou Jamra,  Karolin Etterer,  Guillermo Orozco Díaz,  Fabio Rivas,  Marcella Rietschel,  Sven Cichon,  Markus M. Nöthen,  Konstantin Strauch, 
  • Pages: 1110-1114
  • First Published: 24 June 2010
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No association of the serotonin transporter polymorphisms 5-HTTLPR and RS25531 with schizophrenia or neurocognition†

Thomas I. Konneker,  James J. Crowley,  Corey R. Quackenbush,  Richard S.E. Keefe,  Diana O. Perkins,  T. Scott Stroup,  Jeffrey A. Lieberman,  Edwin van den Oord,  Patrick F. Sullivan, 
  • Pages: 1115-1117
  • First Published: 24 June 2010