• Issue

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics: Volume 174, Issue 8

    i, 765-853
    December 2017
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Cover Image, Volume 174B, Number 8, December 2017

Edmund C. Jenkins,  Elaine J. Marchi,  Milen T. Velinov,  Lingling Ye,  Sharon J. Krinsky-McHale,  Warren B. Zigman,  Nicole Schupf,  Wayne P. Silverman, 
  • Page: i
  • First Published: 14 November 2017
Cover Image, Volume 174B, Number 8, December 2017

COVER FIGURE

The cover image, by Edmund C. Jenkins et al., is based on the Research Article Longitudinal telomere shortening and early Alzheimer's disease progression in adults with down syndrome, DOI: 10.1002/ajmg.b.32575.

Issue Information - TOC

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Issue Information - TOC

  • Pages: 765-766
  • First Published: 14 November 2017

RESEARCH ARTICLES

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Genome-wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type

Elaine K. Green,  Arianna Di Florio,  Liz Forty,  Katherine Gordon-Smith,  Detelina Grozeva,  Christine Fraser,  Alexander L. Richards,  Jennifer L. Moran,  Shaun Purcell,  Pamela Sklar,  George Kirov,  Michael J. Owen,  Michael C. O'Donovan,  Nick Craddock,  Lisa Jones,  Ian R. Jones, 
  • Pages: 767-771
  • First Published: 29 August 2017
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Longitudinal telomere shortening and early Alzheimer's disease progression in adults with down syndrome

Edmund C. Jenkins,  Elaine J. Marchi,  Milen T. Velinov,  Lingling Ye,  Sharon J. Krinsky-McHale,  Warren B. Zigman,  Nicole Schupf,  Wayne P. Silverman, 
  • Pages: 772-778
  • First Published: 30 August 2017
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The clinical features of alcohol use disorders in biological and step-fathers that predict risk for alcohol use disorders in offspring

Kenneth S. Kendler MD,  Henrik Ohlsson PhD,  Alexis Edwards,  Jan Sundquist MD, PhD,  Kristina Sundquist MD, PhD, 
  • Pages: 779-785
  • First Published: 29 August 2017
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Genomewide association studies of suicide attempts in US soldiers

Murray B. Stein MD, MPH,  Erin B. Ware PhD, MPH,  Colter Mitchell PhD,  Chia-Yen Chen ScD,  Susan Borja PhD,  Tianxi Cai ScD,  Catherine L. Dempsey PhD, MPH,  Carol S. Fullerton PhD,  Joel Gelernter MD,  Steven G. Heeringa PhD,  Sonia Jain PhD,  Ronald C. Kessler PhD,  James A. Naifeh PhD,  Matthew K. Nock PhD,  Stephan Ripke MD,  Xiaoying Sun MS,  Jean C. Beckham PhD,  Nathan A. Kimbrel PhD,  VA Mid-Atlantic Mental Illness Research, Education, and Clinical Center (MIRECC) Workgroup ,  Robert J Ursano MD,  Jordan W. Smoller MD, ScD, 
  • Pages: 786-797
  • First Published: 13 September 2017
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Genetic and molecular risk factors within the newly identified primate-specific exon of the SAP97/DLG1 gene in the 3q29 schizophrenia-associated locus

Akihito Uezato,  Naoki Yamamoto,  Daisuke Jitoku,  Emiko Haramo,  Eri Hiraaki,  Yoshimi Iwayama,  Tomoko Toyota,  Masakazu Umino,  Asami Umino,  Yasuhide Iwata,  Katsuaki Suzuki,  Mitsuru Kikuchi,  Tasuku Hashimoto,  Nobuhisa Kanahara,  Akeo Kurumaji,  Takeo Yoshikawa,  Toru Nishikawa, 
  • Pages: 798-807
  • First Published: 09 October 2017
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A functional polymorphism of the OXTR gene is associated with autistic traits in Caucasian and Asian populations

Christian Montag,  Cornelia Sindermann,  Martin Melchers,  Sonja Jung,  Ruixue Luo,  Benjamin Becker,  Jiang Xie,  Wenming Xu,  Adam J. Guastella,  Keith M. Kendrick, 
  • Pages: 808-816
  • First Published: 13 October 2017
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Exome sequences of multiplex, multigenerational families reveal schizophrenia risk loci with potential implications for neurocognitive performance

Mark Z. Kos,  Melanie A. Carless,  Juan Peralta,  Joanne E. Curran,  Ellen E. Quillen,  Marcio Almeida,  August Blackburn,  Lucy Blondell,  David R. Roalf,  Michael F. Pogue-Geile,  Ruben C. Gur,  Harald H.H. Göring,  Vishwajit L. Nimgaonkar,  Raquel E. Gur,  Laura Almasy, 
  • Pages: 817-827
  • First Published: 13 September 2017
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Nhe5 deficiency enhances learning and memory via upregulating Bdnf/TrkB signaling in mice

Xuejiao Chen,  Xiyi Wang,  Lingyun Tang,  Jinjin Wang,  Chunling Shen,  Jianbing Liu,  Shunyuan Lu,  Hongxin Zhang,  Ying Kuang,  Jian Fei,  Zhugang Wang, 
  • Pages: 828-838
  • First Published: 05 October 2017
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Identification of a novel homozygous TRAPPC9 gene mutation causing non-syndromic intellectual disability, speech disorder, and secondary microcephaly

Ansar A. Abbasi,  Kathrin Blaesius,  Hao Hu,  Zahid Latif,  Sylvie Picker-Minh,  Muhammad N. Khan,  Sundas Farooq,  Muzammil A. Khan,  Angela M. Kaindl, 
  • Pages: 839-845
  • First Published: 14 October 2017
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Ancestry-specific and sex-specific risk alleles identified in a genome-wide gene-by-alcohol dependence interaction study of risky sexual behaviors

Renato Polimanti,  Hongyu Zhao,  Lindsay A. Farrer,  Henry R. Kranzler,  Joel Gelernter, 
  • Pages: 846-853
  • First Published: 09 October 2017