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There are 5382 results for: content related to: Replication of Genome-Wide association studies ( GWAS ) loci for sleep in the British G1219 cohort

  1. Genetic analysis of SNPs in CACNA1C and ANK3 gene with schizophrenia: A comprehensive meta-analysis

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 168, Issue 8, December 2015, Pages: 637–648, Fayi Nie, Xiaoli Wang, Panpan Zhao, Hao Yang, Wenhua Zhu, Yaling Zhao, Bo Chen, Robert K. Valenzuela, Rui Zhang, Amelia L. Gallitano and Jie Ma

    Version of Record online : 31 JUL 2015, DOI: 10.1002/ajmg.b.32348

  2. The impact of CACNA1C allelic variation on regional gray matter volume in Chinese population

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 3, April 2016, Pages: 396–401, Liang Huang, Yin Mo, Xuejin Sun, Hualin Yu, Hao Li, Lichuan Wu and Ming Li

    Version of Record online : 12 JAN 2016, DOI: 10.1002/ajmg.b.32418

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    Disorders and borders: Psychiatric genetics and nosology

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 7, October 2013, Pages: 559–578, Jordan W. Smoller

    Version of Record online : 17 OCT 2013, DOI: 10.1002/ajmg.b.32174

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

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 6, September 2016, Pages: 896–903, 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

  5. Timothy syndrome 1 genotype without syndactyly and major extracardiac manifestations

    American Journal of Medical Genetics Part A

    Volume 173, Issue 3, March 2017, Pages: 784–789, Róbert Sepp, Lidia Hategan, Attila Bácsi, Judit Cseklye, László Környei, János Borbás, Márta Széll, Tamás Forster, István Nagy and Zoltán Hegedűs

    Version of Record online : 17 FEB 2017, DOI: 10.1002/ajmg.a.38084

  6. Expanding the phenotype of Timothy syndrome type 2: An adolescent with ventricular fibrillation but normal development

    American Journal of Medical Genetics Part A

    Volume 167, Issue 3, March 2015, Pages: 629–634, Anita Hiippala, Jonna Tallila, Samuel Myllykangas, Juha W Koskenvuo and Tero-Pekka Alastalo

    Version of Record online : 18 FEB 2015, DOI: 10.1002/ajmg.a.36924

  7. Currently recognized genes for schizophrenia: High-resolution chromosome ideogram representation

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 2, March 2016, Pages: 181–202, Merlin G. Butler, Austen B. McGuire, Humaira Masoud and Ann M. Manzardo

    Version of Record online : 13 OCT 2015, DOI: 10.1002/ajmg.b.32391

  8. A genome-wide association study of sleep habits and insomnia

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 5, July 2013, Pages: 439–451, Enda M. Byrne, Philip R. Gehrman, Sarah E. Medland, Dale R. Nyholt, Andrew C. Heath, Pamela A. F. Madden, Ian B. Hickie, Cornelia M. Van Duijn, Anjali K. Henders, Grant W. Montgomery, Nicholas G. Martin, Naomi R. Wray and The Chronogen Consortium

    Version of Record online : 31 MAY 2013, DOI: 10.1002/ajmg.b.32168

  9. Deletion of psychiatric risk gene Cacna1c impairs hippocampal neurogenesis in cell-autonomous fashion

    Glia

    Volume 65, Issue 5, May 2017, Pages: 817–827, Bianca Völkening, Kai Schönig, Golo Kronenberg, Dusan Bartsch and Tillmann Weber

    Version of Record online : 23 FEB 2017, DOI: 10.1002/glia.23128

  10. Incomplete Timothy syndrome secondary to a mosaic mutation of the CACNA1C gene diagnosed using next-generation sequencing

    American Journal of Medical Genetics Part A

    Volume 173, Issue 2, February 2017, Pages: 531–536, Amandine Baurand, Sylvie Falcon-Eicher, Gabriel Laurent, Elisabeth Villain, Caroline Bonnet, Christel Thauvin-Robinet, Caroline Jacquot, Jean-Christophe Eicher, Jean-Baptiste Gourraud, Sébastien Schmitt, Stéphane Bézieau, Mathilde Giraud, Solenne Dumont, Paul Kuentz, Vincent Probst, Antoine Burguet, Florence Kyndt and Laurence Faivre

    Version of Record online : 21 NOV 2016, DOI: 10.1002/ajmg.a.38045

  11. Long QT syndrome with craniofacial, digital, and neurologic features: Is it useful to distinguish between timothy syndrome types 1 and 2?

    American Journal of Medical Genetics Part A

    Volume 167, Issue 11, November 2015, Pages: 2780–2785, Vinson Diep and Laurie H. Seaver

    Version of Record online : 31 JUL 2015, DOI: 10.1002/ajmg.a.37258

  12. Neurophysiologic effect of GWAS derived schizophrenia and bipolar risk variants

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 1, January 2014, Pages: 9–18, Mei-Hua Hall, Deborah L. Levy, Dean F. Salisbury, Steve Haddad, Patience Gallagher, Mary Lohan, Bruce Cohen, Dost Öngür and Jordan W. Smoller

    Version of Record online : 8 NOV 2013, DOI: 10.1002/ajmg.b.32212

  13. Reduced levels of Cacna1c attenuate mesolimbic dopamine system function

    Genes, Brain and Behavior

    C. E. Terrillion, D. T. Dao, R. Cachope, M. K. Lobo, A. C. Puche, J. F. Cheer and T. D. Gould

    Version of Record online : 13 MAR 2017, DOI: 10.1111/gbb.12371

  14. Working memory genetics in schizophrenia and related disorders: An RDoC perspective

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 1, January 2016, Pages: 121–131, Emanuel Schwarz, Heike Tost and Andreas Meyer-Lindenberg

    Version of Record online : 14 SEP 2015, DOI: 10.1002/ajmg.b.32353

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    Sex-dependent modulation of age-related cognitive decline by the L-type calcium channel gene Cacna1c (Cav1.2)

    European Journal of Neuroscience

    Volume 42, Issue 8, October 2015, Pages: 2499–2507, Panos Zanos, Shambhu Bhat, Chantelle E. Terrillion, Robert J. Smith, Leonardo H. Tonelli and Todd D. Gould

    Version of Record online : 23 JUN 2015, DOI: 10.1111/ejn.12952

  16. L-type Ca2+ channels in mood, cognition and addiction: integrating human and rodent studies with a focus on behavioural endophenotypes

    The Journal of Physiology

    Volume 594, Issue 20, 15 October 2016, Pages: 5823–5837, Z. D. Kabir, A. S. Lee and A. M. Rajadhyaksha

    Version of Record online : 24 APR 2016, DOI: 10.1113/JP270673

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

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 174, Issue 2, March 2017, Pages: 156–177, 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

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    Ca2+–calmodulin-dependent protein kinase II represses cardiac transcription of the L-type calcium channel α1C-subunit gene (Cacna1c) by DREAM translocation

    The Journal of Physiology

    Volume 589, Issue 11, June 2011, Pages: 2669–2686, Jarkko J. Ronkainen, Sandra L. Hänninen, Topi Korhonen, Jussi T. Koivumäki, Reka Skoumal, Sini Rautio, Veli-Pekka Ronkainen and Pasi Tavi

    Version of Record online : 1 JUN 2011, DOI: 10.1113/jphysiol.2010.201400

  19. RDoC and translational perspectives on the genetics of trauma-related psychiatric disorders

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 171, Issue 1, January 2016, Pages: 81–91, Janitza L. Montalvo-Ortiz, Joel Gelernter, James Hudziak and Joan Kaufman

    Version of Record online : 22 NOV 2015, DOI: 10.1002/ajmg.b.32395

  20. Risk and information evaluation of prioritized genes for complex traits: Application to bipolar disorder

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 7, October 2014, Pages: 596–606, Chung-Feng Kao, Li-Chung Chuang and Po-Hsiu Kuo

    Version of Record online : 13 AUG 2014, DOI: 10.1002/ajmg.b.32263