American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Cover image for Vol. 171 Issue 5

Early View (Online Version of Record published before inclusion in an issue)

Edited By: Ming T. Tsuang and Stephen V. Faraone

Impact Factor: 3.391

ISI Journal Citation Reports © Ranking: 2015: 41/140 (Psychiatry); 53/165 (Genetics & Heredity)

Online ISSN: 1552-485X

Associated Title(s): American Journal of Medical Genetics Part A, American Journal of Medical Genetics Part C: Seminars in Medical Genetics


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  1. Research Articles

    1. Associations of rare nicotinic cholinergic receptor gene variants to nicotine and alcohol dependence

      Lingjun Zuo, Yunlong Tan, Chiang-Shan R. Li, Zhiren Wang, Kesheng Wang, Xiangyang Zhang, Xiandong Lin, Xiangning Chen, Chunlong Zhong, Xiaoping Wang, Jijun Wang, Lu Lu and Xingguang Luo

      Version of Record online: 30 JUL 2016 | DOI: 10.1002/ajmg.b.32476

    2. Heritability of major depressive and comorbid anxiety disorders in multi-generational families at high risk for depression

      Guia Guffanti, Marc J. Gameroff, Virginia Warner, Ardesheer Talati, Charles E. Glatt, Priya Wickramaratne and Myrna M. Weissman

      Version of Record online: 25 JUL 2016 | DOI: 10.1002/ajmg.b.32477

    3. Whole genome sequencing of a dizygotic twin suggests a role for the serotonin receptor HTR7 in autism spectrum disorder

      Céline Helsmoortel, Sigrid M.A. Swagemakers, Geert Vandeweyer, Andrew P. Stubbs, Ivo Palli, Geert Mortier, R. Frank Kooy and Peter J. van der Spek

      Version of Record online: 6 JUL 2016 | DOI: 10.1002/ajmg.b.32473

    4. You have full text access to this OnlineOpen article
      Genetic variation in the endocannabinoid system and response to Cognitive Behavior Therapy for child anxiety disorders

      Kathryn J. Lester, Jonathan R. I. Coleman, Susanna Roberts, Robert Keers, Gerome Breen, Susan Bögels, Cathy Creswell, Jennifer L. Hudson, Anna McKinnon, Maaike Nauta, Ronald M. Rapee, Silvia Schneider, Wendy K. Silverman, Mikael Thastum, Polly Waite, Gro Janne H. Wergeland and Thalia C. Eley

      Version of Record online: 27 JUN 2016 | DOI: 10.1002/ajmg.b.32467

    5. Reduced gamma-aminobutyric acid is associated with emotional and behavioral problems in Prader–Willi syndrome

      Lauren J. Rice, Jim Lagopoulos, Michael Brammer and Stewart L. Einfeld

      Version of Record online: 24 JUN 2016 | DOI: 10.1002/ajmg.b.32472

    6. Fragile X syndrome screening in pregnant women and women planning pregnancy shows a remarkably high FMR1 premutation prevalence in the Balearic Islands

      Ramona Alfaro Arenas, Jordi Rosell Andreo, Dami Heine Suñer and Group for the study of FXS in the Balearic Islands

      Version of Record online: 22 JUN 2016 | DOI: 10.1002/ajmg.b.32470

    7. You have full text access to this OnlineOpen article
      A novel CCM2 variant in a family with non-progressive cognitive complaints and cerebral microbleeds

      Petra E. Cohn-Hokke, Henne Holstege, Marjan M. Weiss, Wiesje M. van der Flier, Frederik Barkhof, Erik A. Sistermans, Yolande A. L. Pijnenburg, John C. van Swieten, Hanne Meijers-Heijboer and Philip Scheltens

      Version of Record online: 8 JUN 2016 | DOI: 10.1002/ajmg.b.32468

    8. You have full text access to this OnlineOpen article
      A balanced translocation disrupting BCL2L10 and PNLDC1 segregates with affective psychosis

      Christian G. Bouwkamp, Anneke J. A. Kievit, Simone Olgiati, Guido J. Breedveld, Michiel Coesmans, Vincenzo Bonifati and Steven A. Kushner

      Version of Record online: 3 JUN 2016 | DOI: 10.1002/ajmg.b.32465

    9. Common variants in CACNA1C and MDD susceptibility: A comprehensive meta-analysis

      Shuquan Rao, Yao Yao, Chuan Zheng, Joanne Ryan, Canquan Mao, Fuquan Zhang, David Meyre and Qi Xu

      Version of Record online: 3 JUN 2016 | DOI: 10.1002/ajmg.b.32466

    10. Whole-exome sequencing implicates DGKH as a risk gene for panic disorder in the Faroese population

      Noomi O. Gregersen, Francesco Lescai, Jieqin Liang, Qibin Li, Thomas Als, Henriette N. Buttenschøn, Anne Hedemand, Marjun Biskopstø, Jun Wang, August G. Wang, Anders D. Børglum, Ole Mors and Ditte Demontis

      Version of Record online: 3 JUN 2016 | DOI: 10.1002/ajmg.b.32464

    11. Whole-gene sequencing investigation of SAT1 in attempted suicide

      Eric T. Monson, Kelly de Klerk, Sophia C. Gaynor, Alex H. Wagner, Marie E. Breen, Meredith Parsons, Thomas L. Casavant, Peter P. Zandi, James B. Potash and Virginia L. Willour

      Version of Record online: 27 MAY 2016 | DOI: 10.1002/ajmg.b.32462

    12. You have full text access to this OnlineOpen article
      Testing for the mediating role of endophenotypes using molecular genetic data in a twin study of ADHD traits

      Rebecca Pinto, Philip Asherson, Nicholas Ilott, Celeste H.M. Cheung and Jonna Kuntsi

      Version of Record online: 27 MAY 2016 | DOI: 10.1002/ajmg.b.32463

  2. Review Articles

    1. The genetics of anxiety-related negative valence system traits

      Jeanne E. Savage, Chelsea Sawyers, Roxann Roberson-Nay and John M. Hettema

      Version of Record online: 19 MAY 2016 | DOI: 10.1002/ajmg.b.32459

  3. Research Articles

    1. FKBP5 genotype interacts with early life trauma to predict heavy drinking in college students

      Richard Lieberman, Stephen Armeli, Denise M. Scott, Henry R. Kranzler, Howard Tennen and Jonathan Covault

      Version of Record online: 19 MAY 2016 | DOI: 10.1002/ajmg.b.32460

    2. The role of protein intrinsic disorder in major psychiatric disorders

      Luciana Tovo-Rodrigues, Mariana Recamonde-Mendoza, Vanessa Rodrigues Paixão-Côrtes, Estela M. Bruxel, Jaqueline B. Schuch, Deise C. Friedrich, Luis A. Rohde and Mara H. Hutz

      Version of Record online: 17 MAY 2016 | DOI: 10.1002/ajmg.b.32455

    3. Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy

      Ingo Kurth, Manuela Baumgartner, Maria Schabhüttl, Cecilia Tomni, Reinhard Windhager, Tim M. Strom, Thomas Wieland, Kurt Gremel and Michaela Auer-Grumbach

      Version of Record online: 17 MAY 2016 | DOI: 10.1002/ajmg.b.32458

    4. Preliminary examination of microRNA expression profiling in bipolar disorder I patients during antipsychotic treatment

      Chor Hong Lim, Nor Zuraida Zainal, Sharmilla Kanagasundram, Shamsul Mohd Zain and Zahurin Mohamed

      Version of Record online: 13 MAY 2016 | DOI: 10.1002/ajmg.b.32457

    5. The ANK3 gene and facial affect processing: An ERP study

      Wan Zhao, Qiumei Zhang, Ping Yu, Zhifang Zhang, Xiongying Chen, Huang Gu, Jinguo Zhai, Min Chen, Boqi Du, Xiaoxiang Deng, Feng Ji, Chuanyue Wang, Yu-Tao Xiang, Dawei Li, Hongjie Wu, Qi Dong, Yuejia Luo, Jun Li and Chuansheng Chen

      Version of Record online: 13 MAY 2016 | DOI: 10.1002/ajmg.b.32456

    6. PARK16 is associated with PD in the Malaysian population

      Aroma Agape Gopalai, Azlina Ahmad-Annuar, Hui-Hua Li, Yi Zhao, Shen-Yang Lim, Ai Huey Tan, Thien Thein Lim, Gaik Bee Eow, Puvanarajah Santhi, Viswanathan Shanthi, Mohamed Ibrahim Norlinah, Zariah Abdul Aziz, Soo Kun Lim, Chong Tin Tan and Eng-King Tan

      Version of Record online: 13 MAY 2016 | DOI: 10.1002/ajmg.b.32454

    7. Genome-wide association study of generalized anxiety symptoms in the Hispanic Community Health Study/Study of Latinos

      Erin C. Dunn, Tamar Sofer, Linda C. Gallo, Stephanie M. Gogarten, Kathleen F. Kerr, Chia-Yen Chen, Murray B. Stein, Robert J. Ursano, Xiuqing Guo, Yucheng Jia, Qibin Qi, Jerome I. Rotter, Maria Argos, Jianwen Cai, Frank J. Penedo, Krista Perreira, Sylvia Wassertheil-Smoller and Jordan W. Smoller

      Version of Record online: 9 MAY 2016 | DOI: 10.1002/ajmg.b.32448

    8. The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot

      Ignacio F. Mata, Marie Y. Davis, Alexis N. Lopez, Michael O. Dorschner, Erica Martinez, Dora Yearout, Brenna A. Cholerton, Shu-Ching Hu, Karen L. Edwards, Thomas D. Bird and Cyrus P. Zabetian

      Version of Record online: 25 APR 2016 | DOI: 10.1002/ajmg.b.32452

    9. Polymorphisms of the TCF4 gene are associated with the risk of schizophrenia in the Han Chinese

      Jingjie Li, Zhengshuai Chen, Fengjiao Wang, Yongri Ouyang, Ning Zhang, Min Yang, Mengdan Yan, Xikai Zhu, Xue He, Dongya Yuan and Tianbo Jin

      Version of Record online: 22 APR 2016 | DOI: 10.1002/ajmg.b.32449

    10. Transcriptome analysis of genes and gene networks involved in aggressive behavior in mouse and zebrafish

      Karim Malki, Ebba Du Rietz, Wim E. Crusio, Oliver Pain, Jose Paya-Cano, Rezhaw L. Karadaghi, Frans Sluyter, Sietse F. de Boer, Kenneth Sandnabba, Leonard C. Schalkwyk, Philip Asherson and Maria Grazia Tosto

      Version of Record online: 19 APR 2016 | DOI: 10.1002/ajmg.b.32451

    11. Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach

      Michael A. Mooney, Shannon K. McWeeney, Stephen V. Faraone, Anke Hinney, Johannes Hebebrand, IMAGE2 Consortium, German ADHD GWAS Group, Joel T. Nigg and Beth Wilmot

      Version of Record online: 22 MAR 2016 | DOI: 10.1002/ajmg.b.32446

    12. You have full text access to this OnlineOpen article
      Genome-wide significant schizophrenia risk variation on chromosome 10q24 is associated with altered cis-regulation of BORCS7, AS3MT, and NT5C2 in the human brain

      Rodrigo R. R. Duarte, Claire Troakes, Matthew Nolan, Deepak P. Srivastava, Robin M. Murray and Nicholas J. Bray

      Version of Record online: 22 MAR 2016 | DOI: 10.1002/ajmg.b.32445

    13. Unusually long duration and delayed penetrance in a family with FTD and mutation in MAPT (V337M)

      Kimiko Domoto-Reilly, Marie Y. Davis, C. Dirk Keene and Thomas D. Bird

      Version of Record online: 16 MAR 2016 | DOI: 10.1002/ajmg.b.32443

    14. Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case–control study

      Jun Egawa, Satoshi Hoya, Yuichiro Watanabe, Ayako Nunokawa, Masako Shibuya, Masashi Ikeda, Emiko Inoue, Shujiro Okuda, Kenji Kondo, Takeo Saito, Naoshi Kaneko, Tatsuyuki Muratake, Hirofumi Igeta, Nakao Iwata and Toshiyuki Someya

      Version of Record online: 14 MAR 2016 | DOI: 10.1002/ajmg.b.32444

    15. You have full text access to this OnlineOpen article
      15q13.3 duplication in two patients with childhood-onset schizophrenia

      Dale Zhou, Peter Gochman, Diane D. Broadnax, Judith L. Rapoport and Kwangmi Ahn

      Version of Record online: 10 MAR 2016 | DOI: 10.1002/ajmg.b.32439

  4. Review Articles

    1. You have full text access to this OnlineOpen article
      An examination of the language construct in NIMH's research domain criteria: Time for reconceptualization!

      Brita Elvevåg, Alex S. Cohen, Maria K. Wolters, Heather C. Whalley, Viktoria-Eleni Gountouna, Ksenia A. Kuznetsova, Andrew R. Watson and Kristin K. Nicodemus

      Version of Record online: 10 MAR 2016 | DOI: 10.1002/ajmg.b.32438

  5. Research Articles

    1. Explaining the variable penetrance of CNVs: parental intelligence modulates expression of intellectual impairment caused by the 22q11.2 deletion

      Petra Klaassen, Sasja Duijff, Henriëtte Swanenburg de Veye, Frits Beemer, Gerben Sinnema, Elemi Breetvelt, Renske Schappin and Jacob Vorstman

      Version of Record online: 8 MAR 2016 | DOI: 10.1002/ajmg.b.32441

    2. Understanding the covariation of tics, attention-deficit/hyperactivity, and obsessive-compulsive symptoms: A population-based adult twin study

      Rebecca Pinto, Benedetta Monzani, James F. Leckman, Christian Rück, Eva Serlachius, Paul Lichtenstein and David Mataix-Cols

      Version of Record online: 27 FEB 2016 | DOI: 10.1002/ajmg.b.32436

    3. Adult neurogenesis and neurodegenerative diseases: A systems biology perspective

      Emrin Horgusluoglu, Kelly Nudelman, Kwangsik Nho and Andrew J. Saykin

      Version of Record online: 16 FEB 2016 | DOI: 10.1002/ajmg.b.32429

    4. Smoking during pregnancy and ADHD risk: A genetically informed, multiple-rater approach

      Valerie S. Knopik, Kristine Marceau, L. Cinnamon Bidwell, Rohan H.C. Palmer, Taylor F. Smith, Alexandre Todorov, Allison Schettini Evans and Andrew C. Heath

      Version of Record online: 22 JAN 2016 | DOI: 10.1002/ajmg.b.32421

  6. Review Articles

    1. Genetics of psychosis of Alzheimer disease

      Chintan Shah, Mary Ann A. DeMichele-Sweet and Robert A. Sweet

      Version of Record online: 12 JAN 2016 | DOI: 10.1002/ajmg.b.32413

  7. Research Articles

    1. Childhood attention-deficit/hyperactivity disorder symptoms and the development of adolescent alcohol problems: A prospective, population-based study of Swedish twins

      Patrick D. Quinn, Erik Pettersson, Sebastian Lundström, Henrik Anckarsäter, Niklas Långström, Clara Hellner Gumpert, Henrik Larsson, Paul Lichtenstein and Brian M. D'Onofrio

      Version of Record online: 30 DEC 2015 | DOI: 10.1002/ajmg.b.32412

    2. Genetic and environmental influences on the relationship between ADHD symptoms and internalizing problems: A Chinese twin study

      Tian-Jiao Chen, Cheng-Ye Ji, Shang-Shang Wang, Paul Lichtenstein, Henrik Larsson and Zheng Chang

      Version of Record online: 29 DEC 2015 | DOI: 10.1002/ajmg.b.32411

    3. A powerful phenotype for gene-finding studies derived from trajectory analyses of symptoms of anxiety and depression between age seven and 18

      Gitta H. Lubke, Patrick J. Miller, Brad Verhulst, Meike Bartels, Toos van Beijsterveldt, Gonneke Willemsen, Dorret I. Boomsma and Christel M. Middeldorp

      Version of Record online: 3 SEP 2015 | DOI: 10.1002/ajmg.b.32375

    4. Genetic and environmental contributions to the inverse association between specific autistic traits and experience seeking in adults

      Ángel Romero-Martínez, Luís Moya-Albiol, Anna A. E. Vinkhuyzen and Tinca J. C. Polderman

      Version of Record online: 18 AUG 2015 | DOI: 10.1002/ajmg.b.32352


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