Search Results

There are 272475 results for: content related to: Genetic studies indicate a potential target 5-HTR 3B for Drug Therapy in Schizophrenia Patients

  1. Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 131B, Issue 1, 15 November 2004, Pages: 1–5, Bernd Frank, Beate Niesler, Markus M. Nöthen, Helge Neidt, Peter Propping, Brigitta Bondy, Marcella Rietschel, Wolfgang Maier, Margot Albus and Gudrun Rappold

    Article first published online : 6 JUL 2004, DOI: 10.1002/ajmg.b.30070

  2. Identification of rare copy number variants in high burden schizophrenia families

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 3, April 2013, Pages: 273–282, Maarten J. Van Den Bossche, Mojca Strazisar, Sophia Cammaerts, Anthony M. Liekens, Geert Vandeweyer, Veerle Depreeuw, Maria Mattheijssens, An-Sofie Lenaerts, Sonia De Zutter, Peter De Rijk, Bernard Sabbe and Jurgen Del-Favero

    Article first published online : 15 MAR 2013, DOI: 10.1002/ajmg.b.32146

  3. Associations of the 5-hydroxytryptamine (serotonin) Receptor 1B gene (HTR1B) with alcohol, cocaine, and heroin abuse

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 2, March 2013, Pages: 169–176, Jian Cao, Emily LaRocque and Dawei Li

    Article first published online : 17 JAN 2013, DOI: 10.1002/ajmg.b.32128

  4. Association of KIBRA with episodic and working memory: A meta-analysis

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 8, December 2012, Pages: 958–969, Annette Milnik, Angela Heck, Christian Vogler, Hans-Jochen Heinze, Dominique J.-F. de Quervain and Andreas Papassotiropoulos

    Article first published online : 12 OCT 2012, DOI: 10.1002/ajmg.b.32101

  5. ANK3 as a risk gene for schizophrenia: New data in han Chinese and meta analysis

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 8, December 2012, Pages: 997–1005, Aihua Yuan, Zhenghui Yi, Qiang Wang, Jinhua Sun, Zhiqiang Li, Yasong Du, Chen Zhang, Tao Yu, Juan Fan, Huafang Li and Shunying Yu

    Article first published online : 25 OCT 2012, DOI: 10.1002/ajmg.b.32112

  6. CSF1R mutations identified in three families with autosomal dominantly inherited leukoencephalopathy

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 8, December 2012, Pages: 951–957, Jun Mitsui, Takashi Matsukawa, Hiroyuki Ishiura, Koichiro Higasa, Jun Yoshimura, Taro L. Saito, Budrul Ahsan, Yuji Takahashi, Jun Goto, Atsushi Iwata, Yuki Niimi, Yuuichi Riku, Yoji Goto, Kazuo Mano, Mari Yoshida, Shinichi Morishita and Shoji Tsuji

    Article first published online : 4 OCT 2012, DOI: 10.1002/ajmg.b.32100

  7. Effectiveness of a web-based protocol for the screening and phenotyping of individuals with tourette syndrome for genetic studies

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 8, December 2012, Pages: 987–996, Crystelle A. Egan, Susan E. Marakovitz, Julia A. O'Rourke, Lisa Osiecki, Cornelia Illmann, Lauren Barton, Elizabeth McLaughlin, Rachel Proujansky, Justin Royal, Heather Cowley, Martha Rangel-Lugo, David L. Pauls, Jeremiah M. Scharf, Carol A. Mathews and for the Tourette Syndrome Association International Consortium for Genetics

    Article first published online : 22 OCT 2012, DOI: 10.1002/ajmg.b.32107

  8. Polymorphisms of the HTR3B gene are associated with post-surgery emesis in a Chinese Han population

    Journal of Clinical Pharmacy and Therapeutics

    Volume 38, Issue 2, April 2013, Pages: 150–155, Xiao-Xu Ma, Qi-Xing Chen, Shui-Jing Wu, Yan Hu and Xiang-Ming Fang

    Article first published online : 7 MAR 2013, DOI: 10.1111/jcpt.12033

  9. Mitochondrial DNA (mtDNA) in brain samples from patients with major psychiatric disorders: Gene expression profiles, MtDNA content and presence of the MtDNA common deletion

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 2, March 2013, Pages: 213–223, Helena Torrell, Elena Montaña, Nerea Abasolo, Bàrbara Roig, Ana M. Gaviria, Elisabet Vilella and Lourdes Martorell

    Article first published online : 25 JAN 2013, DOI: 10.1002/ajmg.b.32134

  10. Refinement of chromosome 3p22.3 region and identification of a susceptibility gene for bipolar affective disorder

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 2, March 2013, Pages: 163–168, Rodrigo Secolin, Claudio E.M. Banzato, Lucas F.B. Mella, Marilza L. Santos, Paulo Dalgalarrondo and Iscia Lopes-Cendes

    Article first published online : 31 DEC 2012, DOI: 10.1002/ajmg.b.32127

  11. Schizophrenia two-hit hypothesis in velo-cardio facial syndrome

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 2, March 2013, Pages: 177–182, Hywel J. Williams, Stephen Monks, Kieran C. Murphy, George Kirov, Michael C. O'Donovan and Michael J. Owen

    Article first published online : 17 JAN 2013, DOI: 10.1002/ajmg.b.32129

  12. Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: An integrated meta-analysis

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 8, December 2012, Pages: 970–976, Li Zou, Wei Chen, Shanshan Shao, Zhao Sun, Rong Zhong, Junxin Shi, Xiaoping Miao and Ranran Song

    Article first published online : 12 OCT 2012, DOI: 10.1002/ajmg.b.32102

  13. Oculocerebrocutaneous syndrome: An update

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 5, 1 March 2008, Page: 674, Alasdair Hunter

    Article first published online : 1 FEB 2008, DOI: 10.1002/ajmg.a.32185

  14. A combined study of genetic association and brain imaging on the DAOA gene in schizophrenia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 2, March 2013, Pages: 191–200, Jun Chen, Yong Xu, Juan Zhang, Zhifen Liu, Cheng Xu, Kerang Zhang, Yan Shen and Qi Xu

    Article first published online : 17 JAN 2013, DOI: 10.1002/ajmg.b.32131

  15. Association of aggression with a novel microRNA binding site polymorphism in the wolframin gene

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 4, June 2013, Pages: 404–412, Reka Kovacs-Nagy, Zsuzsanna Elek, Anna Szekely, Tibor Nanasi, Maria Sasvari-Szekely and Zsolt Ronai

    Article first published online : 3 MAY 2013, DOI: 10.1002/ajmg.b.32157

  16. Catechol-O-methyltransferase gene val158met polymorphism and depressive symptoms during early childhood

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 3, April 2013, Pages: 245–252, Haroon I. Sheikh, Katie R. Kryski, Heather J. Smith, Lea R. Dougherty, Daniel N. Klein, Sara J. Bufferd, Shiva M. Singh and Elizabeth P. Hayden

    Article first published online : 8 MAR 2013, DOI: 10.1002/ajmg.b.32141

  17. A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 2, March 2013, Pages: 146–156, C. Tran, F. Gagnon, K.G. Wigg, Y. Feng, L. Gomez, T.D. Cate-Carter, E.N. Kerr, L.L. Field, B.J. Kaplan, M.W. Lovett and Dr. C.L. Barr

    Article first published online : 22 JAN 2013, DOI: 10.1002/ajmg.b.32123

  18. Meta-analysis of association between obsessive-compulsive disorder and the 3′ region of neuronal glutamate transporter gene SLC1A1

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 4, June 2013, Pages: 367–379, S.E. Stewart, C. Mayerfeld, P.D. Arnold, J.R. Crane, C. O'Dushlaine, J.A. Fagerness, D. Yu, J.M. Scharf, E. Chan, F. Kassam, P.R. Moya, J.R. Wendland, R. Delorme, M.A. Richter, J.L. Kennedy, J. Veenstra-VanderWeele, J. Samuels, B.D. Greenberg, J.T. McCracken, J.A. Knowles, A.J. Fyer, S.L. Rauch, M.A. Riddle, M.A. Grados, O.J. Bienvenu, B. Cullen, Y. Wang, Y.Y. Shugart, J. Piacentini, S. Rasmussen, G. Nestadt, D.L. Murphy, M.A. Jenike, E.H. Cook, D.L. Pauls, G.L. Hanna and C.A. Mathews

    Article first published online : 18 APR 2013, DOI: 10.1002/ajmg.b.32137

  19. Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 4, June 2013, Pages: 388–403, Frédérique Béna, Damien L. Bruno, Mats Eriksson, Conny van Ravenswaaij-Arts, Zornitza Stark, Trijnie Dijkhuizen, Erica Gerkes, Stefania Gimelli, Devika Ganesamoorthy, Ann Charlotte Thuresson, Audrey Labalme, Marianne Till, Frédéric Bilan, Laurent Pasquier, Alain Kitzis, Christele Dubourgm, Massimiliano Rossi, Armand Bottani, Maryline Gagnebin, Damien Sanlaville, Brigitte Gilbert-Dussardier, Michel Guipponi, Arie van Haeringen, Marjolein Kriek, Claudia Ruivenkamp, Stylianos E. Antonarakis, Britt Marie Anderlid, Howard R. Slater and Jacqueline Schoumans

    Article first published online : 26 MAR 2013, DOI: 10.1002/ajmg.b.32148

  20. You have free access to this content
    Bromodeoxyuridine Induces Senescence in Neural Stem and Progenitor Cells

    STEM CELLS

    Volume 26, Issue 12, December 2008, Pages: 3218–3227, Heather H. Ross, Lindsay H. Levkoff, Gregory P. Marshall II, Maria Caldeira, Dennis A. Steindler, Brent A. Reynolds and Eric D. Laywell

    Article first published online : 18 SEP 2008, DOI: 10.1634/stemcells.2008-0299