• Issue

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics: Volume 177, Issue 1

    i, 1-109
    January 2018
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COVER IMAGE

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Cover Image, Volume 177B, Number 1, January 2018

Sali M. K. Farhan,  Tania F. Gendron,  Leonard Petrucelli,  Robert A. Hegele,  Michael J. Strong, 
  • Page: i
  • First Published: 12 December 2017
Cover Image, Volume 177B, Number 1, January 2018

The cover image, by Sali M. K. Farhan et al., is based on the Research Article OPTN p.Met468Arg and ATXN2 intermediate length polyQ extension in families with C9orf72 mediated amyotrophic lateral sclerosis and frontotemporal dementia, DOI: 10.1002/ajmg.b.32606.

ISSUE INFORMATION - TOC

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Issue Information - TOC

  • Pages: 1-2
  • First Published: 12 December 2017

RESEARCH ARTICLES

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Association study of NDST3 gene for schizophrenia, bipolar disorder, major depressive disorder in the Han Chinese population

Lin Wang,  Jianhua Chen,  Zhiqiang Li,  Weiming Sun,  Boyu Chen,  Sining Li,  Weidong Li,  Dajiang Lu,  Yonggang Wang,  Yongyong Shi, 
  • Pages: 3-9
  • First Published: 15 November 2017
Open Access

Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability

Jin J. Zhao,  Jonatan Halvardson,  Cecilia S. Zander,  Ammar Zaghlool,  Patrik Georgii-Hemming,  Else Månsson,  Göran Brandberg,  Helena E. Sävmarker,  Carina Frykholm,  Ekaterina Kuchinskaya,  Ann-Charlotte Thuresson,  Lars Feuk, 
  • Pages: 10-20
  • First Published: 09 October 2017
Open Access

A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains

Siri Ranlund,  Stella Calafato,  Johan H. Thygesen,  Kuang Lin,  Wiepke Cahn,  Benedicto Crespo-Facorro,  Sonja M.C. de Zwarte,  Álvaro Díez,  Marta Di Forti,  GROUP ,  Conrad Iyegbe,  Assen Jablensky,  Rebecca Jones,  Mei-Hua Hall,  Rene Kahn,  Luba Kalaydjieva,  Eugenia Kravariti,  Colm McDonald,  Andrew M. McIntosh,  Andrew McQuillin,  PEIC ,  Marco Picchioni,  Diana P. Prata,  Dan Rujescu,  Katja Schulze,  Madiha Shaikh,  Timothea Toulopoulou,  Neeltje van Haren,  Jim van Os,  Evangelos Vassos,  Muriel Walshe,  WTCCC2 ,  Cathryn Lewis,  Robin M. Murray,  John Powell,  Elvira Bramon, 
  • Pages: 21-34
  • First Published: 29 August 2017
Full Access

Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences

Oliver W. Quarrell,  Angus J. Clarke,  Cecilia Compton,  Christine E.M. de Die-Smulders,  Alan Fryer,  Sian Jenkins,  Nayana Lahiri,  Rhona MacLeod,  Zosia Miedzybrodzka,  Patrick J. Morrison,  Hannah Musgrave,  Mary O'Driscoll,  Mark Strong,  Martine J. van Belzen,  Sascha Vermeer,  Corien C. Verschuuren-Bemelmans,  Emilia K. Bijlsma, 
  • Pages: 35-39
  • First Published: 02 November 2017
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Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes: The childhood trauma working-group of PGC-MDD

Sandra Van der Auwera,  Wouter J. Peyrot,  Yuri Milaneschi,  Johannes Hertel,  Bernhard Baune,  Gerome Breen,  Enda Byrne,  Erin C. Dunn,  Helen Fisher,  Georg Homuth,  Douglas Levinson,  Cathryn Lewis,  Natalie Mills,  Niamh Mullins,  Matthias Nauck,  Giorgio Pistis,  Martin Preisig,  Marcella Rietschel,  Stephan Ripke,  Patrick Sullivan,  Alexander Teumer,  Henry Völzke,  Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium ,  Dorret I. Boomsma,  Naomi R. Wray,  Brenda Penninx,  Hans Grabe, 
  • Pages: 40-49
  • First Published: 21 November 2017
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Contribution of genes in the GABAergic pathway to bipolar disorder and its executive function deficit in the Chinese Han population

Hongyan Ren,  Lijie Guan,  Liansheng Zhao,  Yin Lin,  Yincheng Wang,  Zhenxing Yang,  Xuan Li,  Xiaohong Ma,  Xiongchao Cheng,  Wenhao Deng,  Katherine J. Aitchison,  Liping Cao,  Tao Li, 
  • Pages: 50-67
  • First Published: 14 November 2017
Full Access

Estimation of minimal disease prevalence from population genomic data: Application to primary familial brain calcification

Gaël Nicolas,  Camille Charbonnier,  Dominique Campion,  Joris A. Veltman, 
  • Pages: 68-74
  • First Published: 20 November 2017
Full Access

OPTN p.Met468Arg and ATXN2 intermediate length polyQ extension in families with C9orf72 mediated amyotrophic lateral sclerosis and frontotemporal dementia

Sali M. K. Farhan,  Tania F. Gendron,  Leonard Petrucelli,  Robert A. Hegele,  Michael J. Strong, 
  • Pages: 75-85
  • First Published: 28 October 2017
Full Access

Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population

Hongsheng Gui,  Miaoxin Li,  Pak C. Sham,  Larry Baum,  International League Against Epilepsy Consortium on Complex Epilepsies ,  Patrick Kwan,  Stacey S. Cherny, 
  • Pages: 86-92
  • First Published: 17 November 2017
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Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis

Yanqing Zhang,  Yi Liu,  Mehdi Zarrei,  Winnie Tong,  Rui Dong,  Ying Wang,  Haiyan Zhang,  Xiaomeng Yang,  Jeffrey R. MacDonald,  Mohammed Uddin,  Stephen W. Scherer,  Zhongtao Gai, 
  • Pages: 93-100
  • First Published: 20 November 2017
Full Access

Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTEN hamartoma tumor syndrome

Tugce B. Balci,  Jorge Davila,  Denice Lewis,  Addo Boafo,  Erick Sell,  Julie Richer,  Sarah M. Nikkel,  Christine M. Armour,  Eva Tomiak,  Matthew A. Lines,  Sarah L. Sawyer, 
  • Pages: 101-109
  • First Published: 20 November 2017