Search Results

There are 10836 results for: content related to: Erratum: Sequence analysis of 17 NRXN1 deletions

  1. Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 4, June 2014, Pages: 303–313, Abdul Noor, Anath C. Lionel, Sarah Cohen-Woods, Narges Moghimi, James Rucker, Alanna Fennell, Bhooma Thiruvahindrapuram, Liana Kaufman, Bryan Degagne, John Wei, Sagar V. Parikh, Pierandrea Muglia, Julia Forte, Stephen W. Scherer, James L. Kennedy, Wei Xu, Peter McGuffin, Anne Farmer, John Strauss and John B. Vincent

    Version of Record online : 3 APR 2014, DOI: 10.1002/ajmg.b.32232

  2. You have full text access to this OnlineOpen article
    Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: A genome-wide association and polygenic scoring study

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 5, July 2014, Pages: 428–437, Niamh Mullins, Nader Perroud, Rudolf Uher, Amy W. Butler, Sarah Cohen-Woods, Margarita Rivera, Karim Malki, Jack Euesden, Robert A. Power, Katherine E. Tansey, Lisa Jones, Ian Jones, Nick Craddock, Michael J. Owen, Ania Korszun, Michael Gill, Ole Mors, Martin Preisig, Wolfgang Maier, Marcella Rietschel, John P. Rice, Bertram Müller-Myhsok, Elisabeth B. Binder, Susanne Lucae, Marcus Ising, Ian W. Craig, Anne E. Farmer, Peter McGuffin, Gerome Breen and Cathryn M. Lewis

    Version of Record online : 25 JUN 2014, DOI: 10.1002/ajmg.b.32247

  3. Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 168, Issue 5, July 2015, Pages: 363–373, Joey W. Trampush, Todd Lencz, Emma Knowles, Gail Davies, Saurav Guha, Itsik Pe'er, David C. Liewald, John M. Starr, Srdjan Djurovic, Ingrid Melle, Kjetil Sundet, Andrea Christoforou, Ivar Reinvang, Semanti Mukherjee, Pamela DeRosse, Astri Lundervold, Vidar M. Steen, Majnu John, Thomas Espeseth, Katri Räikkönen, Elisabeth Widen, Aarno Palotie, Johan G. Eriksson, Ina Giegling, Bettina Konte, Masashi Ikeda, Panos Roussos, Stella Giakoumaki, Katherine E. Burdick, Antony Payton, William Ollier, Mike Horan, Matthew Scult, Dwight Dickinson, Richard E. Straub, Gary Donohoe, Derek Morris, Aiden Corvin, Michael Gill, Ahmad Hariri, Daniel R. Weinberger, Neil Pendleton, Nakao Iwata, Ariel Darvasi, Panos Bitsios, Dan Rujescu, Jari Lahti, Stephanie Le Hellard, Matthew C. Keller, Ole A. Andreassen, Ian J. Deary, David C. Glahn and Anil K. Malhotra

    Version of Record online : 7 MAY 2015, DOI: 10.1002/ajmg.b.32319

  4. RGS2 genetic variation: Association analysis with panic disorder and dimensional as well as intermediate phenotypes of anxiety

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 168, Issue 3, April 2015, Pages: 211–222, Christa Hohoff, Heike Weber, Jan Richter, Katharina Domschke, Peter M. Zwanzger, Patricia Ohrmann, Jochen Bauer, Thomas Suslow, Harald Kugel, Christian Baumann, Benedikt Klauke, Christian P. Jacob, Jürgen Fritze, Borwin Bandelow, Andrew T. Gloster, Alexander L. Gerlach, Tilo Kircher, Thomas Lang, Georg W. Alpers, Andreas Ströhle, Lydia Fehm, Hans-Ulrich Wittchen, Volker Arolt, Paul Pauli, Alfons Hamm, Andreas Reif and Jürgen Deckert

    Version of Record online : 4 MAR 2015, DOI: 10.1002/ajmg.b.32299

  5. You have free access to this content
    Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

    American Journal of Medical Genetics Part A

    Volume 167, Issue 2, February 2015, Pages: 296–312, Yanick J. Crow, Diana S. Chase, Johanna Lowenstein Schmidt, Marcin Szynkiewicz, Gabriella M.A. Forte, Hannah L. Gornall, Anthony Oojageer, Beverley Anderson, Amy Pizzino, Guy Helman, Mohamed S. Abdel-Hamid, Ghada M. Abdel-Salam, Sam Ackroyd, Alec Aeby, Guillermo Agosta, Catherine Albin, Stavit Allon-Shalev, Montse Arellano, Giada Ariaudo, Vijay Aswani, Riyana Babul-Hirji, Eileen M. Baildam, Nadia Bahi-Buisson, Kathryn M. Bailey, Christine Barnerias, Magalie Barth, Roberta Battini, Michael W. Beresford, Geneviève Bernard, Marika Bianchi, Thierry Billette de Villemeur, Edward M. Blair, Miriam Bloom, Alberto B. Burlina, Maria Luisa Carpanelli, Daniel R. Carvalho, Manuel Castro-Gago, Anna Cavallini, Cristina Cereda, Kate E. Chandler, David A. Chitayat, Abigail E. Collins, Concepcion Sierra Corcoles, Nuno J.V. Cordeiro, Giovanni Crichiutti, Lyvia Dabydeen, Russell C. Dale, Stefano D′Arrigo, Christian G.E.L. De Goede, Corinne De Laet, Liesbeth M.H. De Waele, Ines Denzler, Isabelle Desguerre, Koenraad Devriendt, Maja Di Rocco, Michael C. Fahey, Elisa Fazzi, Colin D. Ferrie, António Figueiredo, Blanca Gener, Cyril Goizet, Nirmala R. Gowrinathan, Kalpana Gowrishankar, Donncha Hanrahan, Bertrand Isidor, Bülent Kara, Nasaim Khan, Mary D. King, Edwin P. Kirk, Ram Kumar, Lieven Lagae, Pierre Landrieu, Heinz Lauffer, Vincent Laugel, Roberta La Piana, Ming J. Lim, Jean-Pierre S.-M. Lin, Tarja Linnankivi, Mark T. Mackay, Daphna R. Marom, Charles Marques Lourenço, Shane A. McKee, Isabella Moroni, Jenny E.V. Morton, Marie-Laure Moutard, Kevin Murray, Rima Nabbout, Sheela Nampoothiri, Noemi Nunez-Enamorado, Patrick J. Oades, Ivana Olivieri, John R. Ostergaard, Belén Pérez-Dueñas, Julie S. Prendiville, Venkateswaran Ramesh, Magnhild Rasmussen, Luc Régal, Federica Ricci, Marlène Rio, Diana Rodriguez, Agathe Roubertie, Elisabetta Salvatici, Karin A. Segers, Gyanranjan P. Sinha, Doriette Soler, Ronen Spiegel, Tommy I. Stödberg, Rachel Straussberg, Kathryn J. Swoboda, Mohnish Suri, Uta Tacke, Tiong Y. Tan, Johann te Water Naude, Keng Wee Teik, Maya Mary Thomas, Marianne Till, Davide Tonduti, Enza Maria Valente, Rudy Noel Van Coster, Marjo S. van der Knaap, Grace Vassallo, Raymon Vijzelaar, Julie Vogt, Geoffrey B. Wallace, Evangeline Wassmer, Hannah J. Webb, William P. Whitehouse, Robyn N. Whitney, Maha S. Zaki, Sameer M. Zuberi, John H. Livingston, Flore Rozenberg, Pierre Lebon, Adeline Vanderver, Simona Orcesi and Gillian I. Rice

    Version of Record online : 16 JAN 2015, DOI: 10.1002/ajmg.a.36887

  6. You have free access to this content
    A genome-wide approach to children's aggressive behavior: The EAGLE consortium

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 5, July 2016, Pages: 562–572, Irene Pappa, Beate St Pourcain, Kelly Benke, Alana Cavadino, Christian Hakulinen, Michel G. Nivard, Ilja M. Nolte, Carla M. T. Tiesler, Marian J. Bakermans-Kranenburg, Gareth E. Davies, David M. Evans, Marie-Claude Geoffroy, Harald Grallert, Maria M. Groen-Blokhuis, James J. Hudziak, John P. Kemp, Liisa Keltikangas-Järvinen, George McMahon, Viara R. Mileva-Seitz, Ehsan Motazedi, Christine Power, Olli T. Raitakari, Susan M. Ring, Fernando Rivadeneira, Alina Rodriguez, Paul A. Scheet, Ilkka Seppälä, Harold Snieder, Marie Standl, Elisabeth Thiering, Nicholas J. Timpson, René Veenstra, Fleur P. Velders, Andrew J. O. Whitehouse, George Davey Smith, Joachim Heinrich, Elina Hypponen, Terho Lehtimäki, Christel M. Middeldorp, Albertine J. Oldehinkel, Craig E. Pennell, Dorret I. Boomsma and Henning Tiemeier

    Version of Record online : 18 JUN 2015, DOI: 10.1002/ajmg.b.32333

  7. You have full text access to this OnlineOpen article
    Evaluating the role of a galanin enhancer genotype on a range of metabolic, depressive and addictive phenotypes

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 8, December 2014, Pages: 654–664, Tom G. Richardson, Camelia Minica, Jon Heron, Jeremy Tavare, Alasdair MacKenzie, Ian Day, Glyn Lewis, Matthew Hickman, Jacqueline M. Vink, Joel Gelernter, Henry R. Kranzler, Lindsay A Farrer, Marcus Munafò and David Wynick

    Version of Record online : 16 SEP 2014, DOI: 10.1002/ajmg.b.32270

  8. A preliminary analysis of microRNA as potential clinical biomarker for schizophrenia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 168, Issue 3, April 2015, Pages: 170–178, Xin-yang Sun, Jin Zhang, Wei Niu, Wei Guo, Hong-tao Song, Heng-yu Li, Hui-min Fan, Lin Zhao, Ai-fang Zhong, Yun-hua Dai, Zhong-min Guo, Li-yi Zhang, Jim Lu and Qiao-li Zhang

    Version of Record online : 5 FEB 2015, DOI: 10.1002/ajmg.b.32292

  9. Genetic variation at the CELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesity

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 4, June 2014, Pages: 283–293, Anke Hinney, Özgür Albayrak, Jochen Antel, Anna-Lena Volckmar, Rebecca Sims, Jade Chapman, Denise Harold, Amy Gerrish, Iris M. Heid, Thomas W. Winkler, André Scherag, Jens Wiltfang, Julie Williams, Johannes Hebebrand, GERAD Consortium, IGAP Consortium and GIANT Consortium

    Version of Record online : 1 MAY 2014, DOI: 10.1002/ajmg.b.32234

  10. Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 8, December 2014, Pages: 627–634, Yimin Sun, Yong Gao, Yuxi Zhou, Huan Chen, Guoqing Wang, Junquan Xu, Jiguang Xia, Michael S.Y. Huen, Wai Ting Siok, Yuyang Jiang and Li Hai Tan

    Version of Record online : 17 SEP 2014, DOI: 10.1002/ajmg.b.32267

  11. You have full text access to this OnlineOpen article
    Altered DNA methylation status of human brain derived neurotrophis factor gene could be useful as biomarker of depression

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 4, June 2014, Pages: 357–364, Yixuan Song, Koichi Miyaki, Tomoko Suzuki, Yasuharu Sasaki, Akizumi Tsutsumi, Norito Kawakami, Akihito Shimazu, Masaya Takahashi, Akiomi Inoue, Chiemi Kan, Sumiko Kurioka and Takuro Shimbo

    Version of Record online : 7 MAY 2014, DOI: 10.1002/ajmg.b.32238

  12. You have full text access to this OnlineOpen article
    Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 168, Issue 2, March 2015, Pages: 135–143, Eliana Marisa Ramos, Tammy Gillis, Jayalakshmi S. Mysore, Jong-Min Lee, Martin Gögele, Yuri D'Elia, Irene Pichler, Jorge Sequeiros, Peter P. Pramstaller, James F. Gusella, Marcy E. MacDonald and Isabel Alonso

    Version of Record online : 5 FEB 2015, DOI: 10.1002/ajmg.b.32289

  13. Association study of 83 candidate genes for bipolar disorder in chromosome 6q selected using an evidence-based prioritization algorithm

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 8, December 2013, 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

    Version of Record online : 30 SEP 2013, DOI: 10.1002/ajmg.b.32200

  14. A genome-wide linkage scan of bipolar disorder in Latino families identifies susceptibility loci at 8q24 and 14q32

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 6, September 2014, Pages: 479–491, Suzanne Gonzalez, Cynthia Camarillo, Marco Rodriguez, Mercedes Ramirez, Juan Zavala, Regina Armas, Salvador A. Contreras, Javier Contreras, Albana Dassori, Laura Almasy, Deborah Flores, Alvaro Jerez, Henriette Raventós, Alfonso Ontiveros, Humberto Nicolini and Michael Escamilla

    Version of Record online : 17 JUL 2014, DOI: 10.1002/ajmg.b.32251

  15. Genetic association of ACSM1 variation with schizophrenia and major depressive disorder in the Han Chinese population

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 168, Issue 2, March 2015, Pages: 144–149, Wenjin Li, Weidong Ji, Zhiqiang Li, Kuanjun He, Qingzhong Wang, Jianhua Chen, Yu Qiang, Guoyin Feng, Xingwang Li, Jiawei Shen, Zujia Wen, Jue Ji and Yongyong Shi

    Version of Record online : 5 FEB 2015, DOI: 10.1002/ajmg.b.32291

  16. Prevalence and heritability of obsessive-compulsive spectrum and anxiety disorder symptoms: A survey of the Australian Twin Registry

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 4, June 2014, Pages: 314–325, Clara López-Solà, Leonardo F. Fontenelle, Pino Alonso, Daniel Cuadras, Debra L. Foley, Christos Pantelis, Jesus Pujol, Murat Yücel, Narcís Cardoner, Carles Soriano-Mas, José M. Menchón and Ben J. Harrison

    Version of Record online : 23 APR 2014, DOI: 10.1002/ajmg.b.32233

  17. Sequence analysis of 17 NRXN1 deletions

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 1, January 2014, Pages: 52–61, Louise Kristine Enggaard Hoeffding, Thomas Hansen, Andrés Ingason, Linh Doung, Johan H. Thygesen, Rikke S. Møller, Niels Tommerup, George Kirov, Dan Rujescu, Lars A. Larsen and Thomas Werge

    Version of Record online : 25 SEP 2013, DOI: 10.1002/ajmg.b.32204

    Corrected by:

    Erratum: Erratum: Sequence analysis of 17 NRXN1 deletions

    Vol. 165, Issue 3, 261, Version of Record online: 12 MAR 2014

  18. You have free access to this content
    Association of CDH11 with non-syndromic ASD

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 5, July 2014, Pages: 391–398, An Crepel, Veerle De Wolf, Nathalie Brison, Berten Ceulemans, Didier Walleghem, Gilian Peuteman, Diether Lambrechts, Jean Steyaert, Ilse Noens, Koen Devriendt and Hilde Peeters

    Version of Record online : 18 MAY 2014, DOI: 10.1002/ajmg.b.32243

  19. The interaction effect between BDNF val66met polymorphism and obesity on executive functions and frontal structure

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 3, April 2014, Pages: 245–253, Idoia Marqués-Iturria, Maite Garolera, Roser Pueyo, Bàrbara Segura, Imma Hernan, Isabel García-García, Consuelo Sánchez-Garre, María Vernet-Vernet, María José Sender-Palacios, Ana Narberhaus, Mar Ariza, Carme Junqué and María Ángeles Jurado

    Version of Record online : 12 MAR 2014, DOI: 10.1002/ajmg.b.32229

  20. Novel QTL at chromosome 6p22 for alcohol consumption: Implications for the genetic liability of alcohol use disorders

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 4, June 2014, Pages: 294–302, Mark Z. Kos, David C. Glahn, Melanie A. Carless, Rene Olvera, D. Reese McKay, Ellen E. Quillen, Joel Gelernter, Xiang-Ding Chen, Hong-Wen Deng, Jack W. Kent, Thomas D. Dyer, Harald H.H. Göring, Joanne E. Curran, Ravi Duggirala, John Blangero and Laura Almasy

    Version of Record online : 1 APR 2014, DOI: 10.1002/ajmg.b.32231