American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Cover image for Vol. 153B Issue 5

July 2010

Volume 153B, Issue 5

Pages 983–1117

  1. Research Articles

    1. Top of page
    2. Research Articles
    3. Brief Research Communications
    1. Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay (pages 983–993)

      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 and Paweł Stankiewicz

      Version of Record online: 16 FEB 2010 | DOI: 10.1002/ajmg.b.31064

    2. 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 (pages 1008–1015)

      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 and Jan Haavik

      Version of Record online: 8 MAR 2010 | DOI: 10.1002/ajmg.b.31067

    3. Case–control association study of TGOLN2 in attempted suicide (pages 1016–1023)

      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 and Virginia L. Willour

      Version of Record online: 31 MAR 2010 | DOI: 10.1002/ajmg.b.31068

    4. BDNF Val66Met polymorphism alters sympathovagal balance in healthy subjects (pages 1024–1030)

      Albert C. Yang, Tai-Jui Chen, Shih-Jen Tsai, Chen-Jee Hong, Chung-Hsun Kuo, Cheng-Hung Yang and Ko-Pei Kao

      Version of Record online: 8 MAR 2010 | DOI: 10.1002/ajmg.b.31069

    5. Evidence for three loci modifying age-at-onset of Alzheimer's disease in early-onset PSEN2 families (pages 1031–1041)

      Elizabeth E. Marchani, Thomas D. Bird, Ellen J. Steinbart, Elisabeth Rosenthal, Chang-En Yu, Gerard D. Schellenberg and Ellen M. Wijsman

      Version of Record online: 23 MAR 2010 | DOI: 10.1002/ajmg.b.31072

    6. Severe mental retardation, seizures, and hypotonia due to deletions of MEF2C (pages 1042–1051)

      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 and Paweł Stankiewicz

      Version of Record online: 23 MAR 2010 | DOI: 10.1002/ajmg.b.31071

    7. A functional variant provided further evidence for the association of ARVCF with schizophrenia (pages 1052–1059)

      Sergi Mas, Miquel Bernardo, Patricia Gassó, Santi Álvarez, Clemente Garcia-Rizo, Miquel Bioque, Brian Kirkpatrick and Amalia Lafuente

      Version of Record online: 23 MAR 2010 | DOI: 10.1002/ajmg.b.31073

    8. Genetic pathway-based hierarchical clustering analysis of older adults with cognitive complaints and amnestic mild cognitive impairment using clinical and neuroimaging phenotypes (pages 1060–1069)

      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 and Andrew J. Saykin

      Version of Record online: 31 MAR 2010 | DOI: 10.1002/ajmg.b.31078

    9. Association study of 182 candidate genes in anorexia nervosa (pages 1070–1080)

      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 and D. Blake Woodside

      Version of Record online: 7 APR 2010 | DOI: 10.1002/ajmg.b.31082

    10. Perception, experience, and response to genetic discrimination in Huntington disease: The international RESPOND-HD study (pages 1081–1093)

      Cheryl Erwin, Janet K. Williams, Andrew R. Juhl, Michelle Mengeling, James A. Mills, Yvonne Bombard, Michael R. Hayden, Kimberly Quaid, Ira Shoulson, Sandra Taylor and Jane S. Paulsen

      Version of Record online: 31 MAR 2010 | DOI: 10.1002/ajmg.b.31079

  2. Brief Research Communications

    1. Top of page
    2. Research Articles
    3. Brief Research Communications
    1. No association of alcohol dependence with HOMER 1 and 2 genetic variants (pages 1102–1109)

      U.W. Preuss, M. Ridinger, D. Rujescu, C. Fehr, G. Koller, N. Wodarz, B. Bondy, M. Soyka, W.M. Wong and P. Zill

      Version of Record online: 23 MAR 2010 | DOI: 10.1002/ajmg.b.31074

    2. A new susceptibility locus for bipolar affective disorder in PAR1 on Xp22.3/Yp11.3 (pages 1110–1114)

      Antònia Flaquer, Rami Abou Jamra, Karolin Etterer, Guillermo Orozco Díaz, Fabio Rivas, Marcella Rietschel, Sven Cichon, Markus M. Nöthen and Konstantin Strauch

      Version of Record online: 23 MAR 2010 | DOI: 10.1002/ajmg.b.31075

    3. No association of the serotonin transporter polymorphisms 5-HTTLPR and RS25531 with schizophrenia or neurocognition (pages 1115–1117)

      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 and Patrick F. Sullivan

      Version of Record online: 31 MAR 2010 | DOI: 10.1002/ajmg.b.31077