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There are 298532 results for: content related to: Actimetric evidence that CLOCK 3111 T/C SNP influences sleep and activity patterns in patients affected by bipolar depression

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    Clock genes beyond the clock: CLOCK genotype biases neural correlates of moral valence decision in depressed patients

    Genes, Brain and Behavior

    Volume 7, Issue 1, February 2008, Pages: 20–25, F. Benedetti, D. Radaelli, A. Bernasconi, S. Dallaspezia, A. Falini, G. Scotti, C. Lorenzi, C. Colombo and E. Smeraldi

    Article first published online : 13 FEB 2007, DOI: 10.1111/j.1601-183X.2007.00312.x

  2. A polymorphism at the 3′-untranslated region of the CLOCK gene is associated with adult attention-deficit hyperactivity disorder

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 3, 5 April 2008, Pages: 333–338, Christian Kissling, Wolfgang Retz, Stefan Wiemann, Andrew N. Coogan, R. Marc Clement, Regina Hünnerkopf, Alex C. Conner, Christine M. Freitag, Michael Rösler and Johannes Thome

    Article first published online : 18 OCT 2007, DOI: 10.1002/ajmg.b.30602

  3. Evaluation of association of SNPs in the TNF alpha gene region with schizophrenia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 3, 5 April 2007, Pages: 318–324, B. Morar, S.G. Schwab, M. Albus, W. Maier, B. Lerer and D.B. Wildenauer

    Article first published online : 14 DEC 2006, DOI: 10.1002/ajmg.b.30451

  4. HTR2C and HTR1A gene variants in German and Italian suicide attempters and completers

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 3, 5 April 2007, Pages: 291–299, Alessandro Serretti, Laura Mandelli, Ina Giegling, Barbara Schneider, Annette M. Hartmann, Axel Schnabel, Konrad Maurer, Hans-Jürgen Möller and Dan Rujescu

    Article first published online : 27 DEC 2006, DOI: 10.1002/ajmg.b.30432

  5. A locus for Bowen–Conradi syndrome maps to chromosome region 12p13.3

    American Journal of Medical Genetics Part A

    Volume 132A, Issue 2, 15 January 2005, Pages: 136–143, Ryan E. Lamont, JC. Loredo-Osti, Nicole M. Roslin, Jill Mauthe, Gail Coghlan, Edward Nylen, Danielle Frappier, A. Micheil Innes, Edward G. Lemire, R. Brian Lowry, Cheryl R. Greenberg, Barbara L. Triggs-Raine, Kenneth Morgan, Klaus Wrogemann, T. Mary Fujiwara and Teresa Zelinski

    Article first published online : 2 DEC 2004, DOI: 10.1002/ajmg.a.30420

  6. Insomnia improvement during antidepressant treatment and CLOCK gene polymorphism

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 137B, Issue 1, 5 August 2005, Pages: 36–39, Alessandro Serretti, Cristina Cusin, Francesco Benedetti, Laura Mandelli, Adele Pirovano, Raffaella Zanardi, Cristina Colombo and Enrico Smeraldi

    Article first published online : 10 JUN 2005, DOI: 10.1002/ajmg.b.30130

  7. Effect of 5-HT1A gene polymorphisms on antidepressant response in major depressive disorder

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 1, 5 January 2009, Pages: 115–123, Masaki Kato, Tsuyoshi Fukuda, Masataka Wakeno, Gaku Okugawa, Yoshiteru Takekita, Syunsuke Watanabe, Megumi Yamashita, Yuka Hosoi, Junichi Azuma, Toshihiko Kinoshita and Alessandro Serretti

    Article first published online : 15 MAY 2008, DOI: 10.1002/ajmg.b.30783

  8. An association analysis of Alzheimer disease candidate genes detects an ancestral risk haplotype clade in ACE and putative multilocus association between ACE, A2M, and LRRTM3

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 5, 5 July 2009, Pages: 721–735, Todd L. Edwards, Margaret Pericak-Vance, Johnny R. Gilbert, Jonathan L. Haines, Eden R. Martin and Marylyn D. Ritchie

    Article first published online : 22 DEC 2008, DOI: 10.1002/ajmg.b.30899

  9. Dopaminergic polymorphisms in Tourette syndrome: Association with the DAT gene (SLC6A3)

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 5, 5 July 2007, Pages: 605–610, Dustin Y. Yoon, Christopher A. Rippel, Andrew J. Kobets, Christina M. Morris, Jennifer E. Lee, Phillip N. Williams, Dana D. Bridges, David J. Vandenbergh, Yin Y. Shugart and Harvey S. Singer

    Article first published online : 14 DEC 2006, DOI: 10.1002/ajmg.b.30466

  10. Autosomal linkage analysis of a Japanese single multiplex schizophrenia pedigree reveals two candidate loci on chromosomes 4q and 3q

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 6, 5 September 2007, Pages: 735–742, Naoshi Kaneko, Tatsuyuki Muratake, Hideki Kuwabara, Takanori Kurosaki, Mitsuru Takei, Tsuyuka Ohtsuki, Tadao Arinami, Shoji Tsuji and Toshiyuki Someya

    Article first published online : 1 AUG 2007, DOI: 10.1002/ajmg.b.30488

  11. Sleep quality and diurnal preference in a sample of young adults: Associations with 5HTTLPR, PER3, and CLOCK 3111

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 156, Issue 6, September 2011, Pages: 681–690, Nicola L. Barclay, Thalia C. Eley, Jonathan Mill, Chloe C. Y. Wong, Helena M. S. Zavos, Simon N. Archer and Alice M. Gregory

    Article first published online : 28 JUN 2011, DOI: 10.1002/ajmg.b.31210

  12. A splicing mutation in the α/β GlcNAc-1-phosphotransferase gene results in an adult onset form of mucolipidosis III associated with sensory neuropathy and cardiomyopathy

    American Journal of Medical Genetics Part A

    Volume 132A, Issue 4, 1 February 2005, Pages: 369–375, Richard A. Steet, Roger Hullin, Mariko Kudo, Michele Martinelli, Nils U. Bosshard, Thomas Schaffner, Stuart Kornfeld and Beat Steinmann

    Article first published online : 4 JAN 2005, DOI: 10.1002/ajmg.a.30498

  13. Increase in GSK3β gene copy number variation in bipolar disorder

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 3, 5 April 2007, Pages: 259–265, Herbert M. Lachman, Erika Pedrosa, Oriana A. Petruolo, Melissa Cockerham, Alexander Papolos, Tomas Novak, Demitri F. Papolos and Pavla Stopkova

    Article first published online : 13 MAR 2007, DOI: 10.1002/ajmg.b.30498

  14. Clinical and genetic epidemiology of Bardet–Biedl syndrome in Newfoundland: A 22-year prospective, population-based, cohort study

    American Journal of Medical Genetics Part A

    Volume 132A, Issue 4, 1 February 2005, Pages: 352–360, Susan J. Moore, Jane S. Green, Yanli Fan, Ashvinder K. Bhogal, Elizabeth Dicks, Bridget A. Fernandez, Mark Stefanelli, Christopher Murphy, Benvon C. Cramer, John C.S. Dean, Philip L. Beales, Nicholas Katsanis, Anne S. Bassett, William S. Davidson and Patrick S. Parfrey

    Article first published online : 6 JAN 2005, DOI: 10.1002/ajmg.a.30406

  15. Polymorphisms in the potential functional regions of the TGF-β 1 and TGF-β receptor genes and disease susceptibility in HBV-related hepatocellular carcinoma patients

    Molecular Carcinogenesis

    Volume 51, Issue S1, October 2012, Pages: E123–E131, Zhenhui Xin, Wei Zhang, Aiqiang Xu, Li Zhang, Tao Yan, Zhuo Li, Xiaopan Wu, Xilin Zhu, Juan Ma, Ke Li, Hui Li and Ying Liu

    Article first published online : 30 JAN 2012, DOI: 10.1002/mc.21876

  16. The influence of four serotonin-related genes on decision-making in suicide attempters

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 5, 5 July 2007, Pages: 615–624, Fabrice Jollant, Catherine Buresi, Sébastien Guillaume, Isabelle Jaussent, Frank Bellivier, Marion Leboyer, Didier Castelnau, Alain Malafosse and Philippe Courtet

    Article first published online : 12 JAN 2007, DOI: 10.1002/ajmg.b.30467

  17. Shprintzen–Goldberg syndrome: Fourteen new patients and a clinical analysis

    American Journal of Medical Genetics Part A

    Volume 135A, Issue 3, 15 June 2005, Pages: 251–262, Peter N. Robinson, Luitgard M. Neumann, Stephanie Demuth, Herbert Enders, Ursula Jung, Rainer König, Beate Mitulla, Dietmar Müller, Petra Muschke, Lutz Pfeiffer, Bettina Prager, Mirja Somer and Sigrid Tinschert

    Article first published online : 9 MAY 2005, DOI: 10.1002/ajmg.a.30431

  18. Girl with monosomy 1p36 and Angelman syndrome due to unbalanced der(1) transmission of a maternal translocation t(1;15)(p36.3;q13.1)

    American Journal of Medical Genetics Part A

    Volume 131A, Issue 1, 15 November 2004, Pages: 94–98, Hiroyuki Torisu, Toshiyuki Yamamoto, Takehisa Fujiwaki, Mitsutaka Kadota, Mitsuo Oshimura, Kenji Kurosawa, Shinjiro Akaboshi and Akira Oka

    Article first published online : 21 SEP 2004, DOI: 10.1002/ajmg.a.30413

  19. The tryptophan hydroxylase 1 (TPH1) gene, schizophrenia susceptibility, and suicidal behavior: A multi-centre case–control study and meta-analysis

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 2, March 2010, Pages: 387–396, Peter Saetre, Per Lundmark, August Wang, Thomas Hansen, Henrik B. Rasmussen, Srdjan Djurovic, Ingrid Melle, Ole A. Andreassen, Thomas Werge, Ingrid Agartz, Håkan Hall, Lars Terenius and Erik G. Jönsson

    Article first published online : 12 JUN 2009, DOI: 10.1002/ajmg.b.30991

  20. PhenoChipping of psychotic disorders: A novel approach for deconstructing and quantitating psychiatric phenotypes

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 141B, Issue 6, 5 September 2006, Pages: 653–662, Alexander B. Niculescu, Len L. Lulow, Corey A. Ogden, Helen Le-Niculescu, Daniel R. Salomon, Nicholas J. Schork, Michael P. Caligiuri and James B. Lohr

    Article first published online : 12 JUL 2006, DOI: 10.1002/ajmg.b.30404