American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Cover image for Vol. 159B Issue 2

March 2012

Volume 159B, Issue 2

Pages 131–253

  1. Rapid Publications

    1. Top of page
    2. Rapid Publications
    3. Review Articles
    4. Research Articles
    1. Neuropsychological intra-individual variability explains unique genetic variance of ADHD and shows suggestive linkage to chromosomes 12, 13, and 17 (pages 131–140)

      Alexis C. Frazier-Wood, Janita Bralten, Alejandro Arias-Vasquez, Marjolein Luman, Jaap Ooterlaan, Joseph Sergeant, Stephen V. Faraone, Jan Buitelaar, Barbara Franke, Jonna Kuntsi and Nanda N. J. Rommelse

      Article first published online: 5 JAN 2012 | DOI: 10.1002/ajmg.b.32018

    2. Coordinated changes in AHRR methylation in lymphoblasts and pulmonary macrophages from smokers (pages 141–151)

      Martha M. Monick, Steven R.H. Beach, Jeff Plume, Rory Sears, Meg Gerrard, Gene H. Brody and Robert A. Philibert

      Article first published online: 9 JAN 2012 | DOI: 10.1002/ajmg.b.32021

  2. Review Articles

    1. Top of page
    2. Rapid Publications
    3. Review Articles
    4. Research Articles
  3. Research Articles

    1. Top of page
    2. Rapid Publications
    3. Review Articles
    4. Research Articles
    1. A twin study of schizoaffective-mania, schizoaffective-depression, and other psychotic syndromes (pages 172–182)

      Alastair G. Cardno, Frühling V. Rijsdijk, Robert M. West, Irving I. Gottesman, Nick Craddock, Robin M. Murray and Peter McGuffin

      Article first published online: 27 DEC 2011 | DOI: 10.1002/ajmg.b.32011

    2. PLA2G6 mutations in PARK14-linked young-onset parkinsonism and sporadic Parkinson's disease (pages 183–191)

      Chin-Song Lu, Szu-Chia Lai, Ruey-Meei Wu, Yi-Hsin Weng, Chia-Ling Huang, Rou-Shayn Chen, Hsiu-Chen Chang, Yah-Huei Wu-Chou and Tu-Hsueh Yeh

      Article first published online: 27 DEC 2011 | DOI: 10.1002/ajmg.b.32012

    3. Longevity candidate genes and their association with personality traits in the elderly (pages 192–200)

      Michelle Luciano, Lorna M. Lopez, Marleen H.M. de Moor, Sarah E. Harris, Gail Davies, Teresa Nutile, Robert F. Krueger, Tõnu Esko, David Schlessinger, Tanaka Toshiko, Jaime L. Derringer, Anu Realo, Narelle K. Hansell, Michele L. Pergadia, Anu-Katriina Pesonen, Serena Sanna, Antonio Terracciano, Pamela A.F. Madden, Brenda Penninx, Philip Spinhoven, Catherina A. Hartman, Ben A. Oostra, A. Cecile J.W. Janssens, Johan G. Eriksson, John M. Starr, Alessandra Cannas, Luigi Ferrucci, Andres Metspalu, Margeret J. Wright, Andrew C. Heath, Cornelia M. van Duijn, Laura J. Bierut, Katri Raikkonen, Nicholas G. Martin, Marina Ciullo, Dan Rujescu, Dorret I. Boomsma and Ian J. Deary

      Article first published online: 27 DEC 2011 | DOI: 10.1002/ajmg.b.32013

    4. Mutations in MECP2 exon 1 in classical rett patients disrupt MECP2_e1 transcription, but not transcription of MECP2_e2 (pages 210–216)

      Peter J. Gianakopoulos, Yuzhi Zhang, Nela Pencea, Marija Orlic-Milacic, Kirti Mittal, Christian Windpassinger, Sara-Jane White, Peter M. Kroisel, Eva W.C. Chow, Carol J. Saunders, Berge A. Minassian and John B. Vincent

      Article first published online: 27 DEC 2011 | DOI: 10.1002/ajmg.b.32015

    5. Beyond the patient: The broader impact of genetic discrimination among individuals at risk of Huntington disease (pages 217–226)

      Yvonne Bombard, JoAnne Palin, Jan M. Friedman, Gerry Veenstra, Susan Creighton, Joan L. Bottorff, Michael R. Hayden and The Canadian Respond-HD Collaborative Research Group

      Article first published online: 9 JAN 2012 | DOI: 10.1002/ajmg.b.32016

    6. Alpha-5 and -3 nicotinic receptor gene variants predict nicotine dependence but not cessation: Findings from the COMMIT cohort (pages 227–235)

      Chad A. Bousman, Cheryl Rivard, Jason Den Haese, Christine Ambrosone and Andrew Hyland

      Article first published online: 5 JAN 2012 | DOI: 10.1002/ajmg.b.32019

    7. Clinical improvement of the aggressive neurobehavioral phenotype in a patient with a deletion of PITX3 and the absence of L-DOPA in the cerebrospinal fluid (pages 236–242)

      Katarzyna Derwińska, Hanna Mierzewska, Alicja Goszczańska, Elżbieta Szczepanik, Zhilian Xia, Katarzyna Kuśmierska, Jolanta Tryfon, Anna Kutkowska-Kaźmierczak, Ewa Bocian, Tadeusz Mazurczak, Ewa Obersztyn and Paweł Stankiewicz

      Article first published online: 5 JAN 2012 | DOI: 10.1002/ajmg.b.32020

    8. The neuroanatomy of genetic subtype differences in Prader–Willi syndrome (pages 243–253)

      Robyn A. Honea, Laura M. Holsen, Rebecca J. Lepping, Rodrigo Perea, Merlin G. Butler, William M. Brooks and Cary R. Savage

      Article first published online: 12 JAN 2012 | DOI: 10.1002/ajmg.b.32022

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