American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Cover image for American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

December 2013

Volume 162, Issue 8

Pages 779–906

  1. Rapid Publication

    1. Top of page
    2. Rapid Publication
    3. Review Articles
    4. Research Articles
    1. Genetic predictors of risk and resilience in psychiatric disorders: A cross-disorder genome-wide association study of functional impairment in major depressive disorder, bipolar disorder, and schizophrenia (pages 779–788)

      Lauren M. McGrath, Marilyn C. Cornelis, Phil H. Lee, Elise B. Robinson, Laramie E. Duncan, Jennifer H. Barnett, Jie Huang, Gloria Gerber, Pamela Sklar, Patrick Sullivan, Roy H. Perlis and Jordan W. Smoller

      Article first published online: 13 SEP 2013 | DOI: 10.1002/ajmg.b.32190

  2. Review Articles

    1. Top of page
    2. Rapid Publication
    3. Review Articles
    4. Research Articles
    1. You have full text access to this OnlineOpen article
  3. Research Articles

    1. Top of page
    2. Rapid Publication
    3. Review Articles
    4. Research Articles
    1. Microduplication of 15q13.3 and Xq21.31 in a family with tourette syndrome and comorbidities (pages 825–831)

      Linea Melchior, Birgitte Bertelsen, Nanette Mol Debes, Camilla Groth, Liselotte Skov, Jens D Mikkelsen, Karen Brøndum-Nielsen and Zeynep Tümer

      Article first published online: 27 JUL 2013 | DOI: 10.1002/ajmg.b.32186

    2. SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay (pages 832–840)

      Yu An, Sami S. Amr, Alcy Torres, Laura Weissman, Peter Raffalli, Gerald Cox, Xiaoming Sheng, Va Lip, Weimin Bi, Ankita Patel, Pawel Stankiewicz, Bai-Lin Wu and Yiping Shen

      Article first published online: 6 SEP 2013 | DOI: 10.1002/ajmg.b.32187

    3. A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability (pages 847–854)

      Eske M. Derks, Muhammad Ayub, Kimberly Chambert, Jurgen Del Favero, Mandy Johnstone, Stuart MacGregor, Alan Maclean, Andrew G. McKechanie, Allan F. McRae, Jennifer L. Moran, Benjamin S. Pickard, Shaun Purcell, Pamela Sklar, David M. StCLair, Naomi R. Wray, Peter M. Visscher and Douglas H. R. Blackwood

      Article first published online: 25 SEP 2013 | DOI: 10.1002/ajmg.b.32189

    4. Haplotype co-segregation with attention deficit-hyperactivity disorder in unrelated german multi-generation families (pages 855–863)

      Michelle K. Lin, Christine M. Freitag, Andrea B. Schote, Haukur Pálmason, Christiane Seitz, Tobias J. Renner, Marcel Romanos, Susanne Walitza, Christian P. Jacob, Andreas Reif, Andreas Warnke, Rita M. Cantor, Klaus-Peter Lesch and Jobst Meyer

      Article first published online: 3 SEP 2013 | DOI: 10.1002/ajmg.b.32192

    5. High frequency of intermediate alleles on huntington disease-associated haplotypes in British Columbia's general population (pages 864–871)

      Alicia Semaka, Chris Kay, Crystal N. Doty, Jennifer A. Collins, Natalie Tam and Michael R. Hayden

      Article first published online: 30 AUG 2013 | DOI: 10.1002/ajmg.b.32193

    6. High rates of comorbid depressive and anxiety disorders among women with premutation of the FMR1 gene (pages 872–878)

      Heather A. Kenna, Molly Tartter, Scott S. Hall, Amy A. Lightbody, Quynh Nguyen, C. Paula de los Angeles, Allan L. Reiss and Natalie L. Rasgon

      Article first published online: 3 SEP 2013 | DOI: 10.1002/ajmg.b.32196

    7. Mood disorders in individuals with distal 18q deletions (pages 879–888)

      William B. Daviss, Louise O'Donnell, Bridgette T. Soileau, Patricia Heard, Erika Carter, Steven R. Pliszka, Jonathan A. L. Gelfond, Daniel E. Hale and Jannine D. Cody

      Article first published online: 4 SEP 2013 | DOI: 10.1002/ajmg.b.32197

    8. Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia (pages 889–897)

      Avinash M. Veerappa, Marita Saldanha, Prakash Padakannaya and Nallur B. Ramachandra

      Article first published online: 20 SEP 2013 | DOI: 10.1002/ajmg.b.32199

    9. Association study of 83 candidate genes for bipolar disorder in chromosome 6q selected using an evidence-based prioritization algorithm (pages 898–906)

      T. Bernard Bigdeli, Brion S. Maher, Zhongming Zhao, Jingchun Sun, Helena Medeiros, Nirmala Akula, Francis J. McMahon, Celia Carvalho, Susana R. Ferreira, Maria H. Azevedo, James A. Knowles, Michele T. Pato, Carlos N. Pato and Ayman H. Fanous

      Article first published online: 30 SEP 2013 | DOI: 10.1002/ajmg.b.32200