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There are 24516 results for: content related to: Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, ift27 and parvalbumin

  1. You have full text access to this OnlineOpen article
    Assessment of first and second degree relatives of individuals with bipolar disorder shows increased genetic risk scores in both affected relatives and young At-Risk Individuals

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 168, Issue 7, October 2015, Pages: 617–629, Janice M. Fullerton, Daniel L. Koller, Howard J. Edenberg, Tatiana Foroud, Hai Liu, Anne L. Glowinski, Melvin G. McInnis, Holly C. Wilcox, Andrew Frankland, Gloria Roberts, Peter R. Schofield, Philip B. Mitchell, John I. Nurnberger and Bipolar High Risk Study Group, BiGS Consortium

    Version of Record online : 16 JUL 2015, DOI: 10.1002/ajmg.b.32344

  2. 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

    Version of Record online : 22 DEC 2008, DOI: 10.1002/ajmg.b.30899

  3. Identification of susceptibility loci at 7q31 and 9p13 for bipolar disorder in an isolated population

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 153B, Issue 3, April 2010, Pages: 723–735, Outi M. Palo, Pia Soronen, Kaisa Silander, Teppo Varilo, Katja Tuononen, Tuula Kieseppä, Timo Partonen, Jouko Lönnqvist, Tiina Paunio and Leena Peltonen

    Version of Record online : 22 OCT 2009, DOI: 10.1002/ajmg.b.31039

  4. A review of association and linkage studies for genetical analyses of learning disorders

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 7, 5 October 2007, Pages: 923–943, Emrah Caylak

    Version of Record online : 17 MAY 2007, DOI: 10.1002/ajmg.b.30537

  5. Affected sibling pair linkage analysis of qualitative and quantitative traits for schizophrenia on chromosome 22 in a Chinese population

    American Journal of Medical Genetics

    Volume 105, Issue 4, 8 May 2001, Pages: 321–327, Guiqing Cai, Tao Li, Hong Deng, Jinghua Zhao, Xun Hu, Robin M. Murray, Xiehe Liu, Pak C. Sham and David A. Collier

    Version of Record online : 30 APR 2001, DOI: 10.1002/ajmg.1346

  6. Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy

    Annals of Neurology

    Volume 57, Issue 6, June 2005, Pages: 866–873, Ulrike Tauer, Susanne Lorenz, Kirsten P. Lenzen, Armin Heils, Hiltrud Muhle, Meike Gresch, Bernd A. Neubauer, Stephan Waltz, Gabrielle Rudolf, Manuel Mattheisen, Konstantin Strauch, Peter Nürnberg, Bettina Schmitz, Ulrich Stephani and Thomas Sander

    Version of Record online : 31 MAY 2005, DOI: 10.1002/ana.20500

  7. What drives the dating game of executive options exercise? Evidence from Taiwan

    Accounting & Finance

    Volume 52, Issue 2, June 2012, Pages: 605–625, Ming-Cheng Wu, Hung-Gay Fung and Yi-Ting Huang

    Version of Record online : 16 FEB 2011, DOI: 10.1111/j.1467-629X.2011.00406.x

  8. Thirteenth Annual Meeting of the International Genetic Epidemiology Society

    Genetic Epidemiology

    Volume 27, Issue 3, November 2004, Pages: 258–316,

    Version of Record online : 5 OCT 2004, DOI: 10.1002/gepi.20029

  9. Suggestive evidence for association of the circadian genes PERIOD3 and ARNTL with bipolar disorder

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 141B, Issue 3, 5 April 2006, Pages: 234–241, Caroline M. Nievergelt, Daniel F. Kripke, Thomas B. Barrett, Elyssa Burg, Ronald A. Remick, A. Dessa Sadovnick, Susan L. McElroy, Paul E. Keck Jr, Nicholas J. Schork and John R. Kelsoe

    Version of Record online : 9 MAR 2006, DOI: 10.1002/ajmg.b.30252

  10. Alcohol Dependence Genetics: Lessons Learned From Genome-Wide Association Studies (GWAS) and Post-GWAS Analyses

    Alcoholism: Clinical and Experimental Research

    Volume 39, Issue 8, August 2015, Pages: 1312–1327, Amy B. Hart and Henry R. Kranzler

    Version of Record online : 25 JUN 2015, DOI: 10.1111/acer.12792

  11. You have free access to this content
    Association of dopamine transporter gene variants with childhood ADHD features in bipolar disorder

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 2, March 2013, Pages: 137–145, Tiffany A. Greenwood, Eun-Jeong Joo, Tatyana Shekhtman, A. Dessa Sadovnick, Ronald A. Remick, Paul E. Keck, Susan L. McElroy and John R. Kelsoe

    Version of Record online : 19 DEC 2012, DOI: 10.1002/ajmg.b.32108

  12. You have free access to this content
    Gene-based SNP mapping of a psychotic bipolar affective disorder linkage region on 22q12.3: Association with HMG2L1 and TOM1

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 1, 5 January 2008, Pages: 59–67, James B. Potash, Silvia Buervenich, Nancy J. Cox, Peter P. Zandi, Nirmala Akula, Jo Steele, Jennifer A. Rathe, Dimitrios Avramopoulos, Sevilla D. Detera-Wadleigh, Elliot S. Gershon, J. Raymond DePaulo Jr., Andrew P. Feinberg and Francis J. McMahon

    Version of Record online : 1 AUG 2007, DOI: 10.1002/ajmg.b.30574

  13. Analysis of the dopamine beta hydroxylase gene in Gilles de la tourette syndrome

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 141B, Issue 6, 5 September 2006, Pages: 673–677, Fatih Ozbay, Karen G. Wigg, Eda Tahir Turanli, Phil Asherson, Yanki Yazgan, Paul Sandor and Cathy L. Barr

    Version of Record online : 12 JUL 2006, DOI: 10.1002/ajmg.b.30393

  14. Failure to confirm association between RGS4 haplotypes and schizophrenia in Caucasians

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 139B, Issue 1, 5 November 2005, Pages: 23–27, Janet L. Sobell, Christian Richard, Donna A. Wirshing and Leonard L. Heston

    Version of Record online : 4 AUG 2005, DOI: 10.1002/ajmg.b.30221

  15. Evidence of gene-environment interaction for the RUNX2 gene and environmental tobacco smoke in controlling the risk of cleft lip with/without cleft palate

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 94, Issue 2, February 2012, Pages: 76–83, Tao Wu, M. Daniele Fallin, Min Shi, Ingo Ruczinski, Kung Yee Liang, Jacqueline B. Hetmanski, Hong Wang, Roxann G. Ingersoll, Shangzhi Huang, Xiaoqian Ye, Yah-Huei Wu-Chou, Philip K. Chen, Ethylin Wang Jabs, Bing Shi, Richard Redett, Alan F. Scott, Jeffrey C. Murray, Mary L. Marazita, Ronald G. Munger and Terri H. Beaty

    Version of Record online : 12 JAN 2012, DOI: 10.1002/bdra.22885

  16. Analysis of familial aggregation studies with complex ascertainment schemes

    Statistics in Medicine

    Volume 27, Issue 24, 30 October 2008, Pages: 5076–5092, Abigail G. Matthews, Dianne M. Finkelstein and Rebecca A. Betensky

    Version of Record online : 10 JUL 2008, DOI: 10.1002/sim.3327

  17. A new measure of the effective number of tests, a practical tool for comparing families of non-independent significance tests

    Genetic Epidemiology

    Volume 33, Issue 7, November 2009, Pages: 559–568, Nicholas W. Galwey

    Version of Record online : 13 FEB 2009, DOI: 10.1002/gepi.20408

  18. You have free access to this content
    Exploration of a Putative Susceptibility Locus for Idiopathic Generalized Epilepsy on Chromosome 8p12

    Epilepsia

    Volume 44, Issue 1, January 2003, Pages: 32–39, Thomas Sander, Christine Windemuth, Herbert Schulz, Kathrin Saar, Elena Gennaro, Concetta Riggio, Amedeo Bianchi, Federico Zara, Gabrielle Rudolf, Fabienne Picard, Christine Bulteau, Anna Kaminska, Cécile Cieuta, Jean-François Prud'homme, Olivier Dulac, Louise Bate, Robert Robinson, R. Mark Gardiner, Athanasios Covanis, Gerrit-Jan De Haan, Guus A. M. A. J. Janssen, M. Gerard Van Erp, Eduard H. J. F. Boezeman, Dick Lindhout, Armin Heils, Peter Nürnberg and Diéter Janz

    Version of Record online : 17 JAN 2003, DOI: 10.1046/j.1528-1157.2003.51501.x

  19. Common and rare variants of DAOA in bipolar disorder

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 7, 5 October 2009, Pages: 960–966, Manjula Maheshwari, Jiajun Shi, Judith A. Badner, Andrew Skol, Virginia L. Willour, Donna M. Muzny, David A. Wheeler, Fowler R. Gerald, Sevilla Detera-Wadleigh, Francis J. McMahon, James B. Potash, Elliot S. Gershon, Chunyu Liu and Richard A. Gibbs

    Version of Record online : 4 FEB 2009, DOI: 10.1002/ajmg.b.30925

  20. Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 150B, Issue 4, 5 June 2009, Pages: 560–569, Michael E. Talkowski, Lora McClain, Trina Allen, L. DiAnne Bradford, Monica Calkins, Neil Edwards, Lyudmila Georgieva, Rodney Go, Ruben Gur, Raquel Gur, George Kirov, Kodavali Chowdari, Joseph Kwentus, Paul Lyons, Hader Mansour, Joseph McEvoy, Michael C. O'Donovan, Judith O'Jile, Michael J. Owen, Alberto Santos, Robert Savage, Draga Toncheva, Gerard Vockley, Joel Wood, Bernie Devlin and Vishwajit L. Nimgaonkar

    Version of Record online : 20 OCT 2008, DOI: 10.1002/ajmg.b.30862