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There are 9155 results for: content related to: The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects

  1. Follow-up association studies of chromosome region 9q and nonsyndromic cleft lip/palate

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 7, July 2010, Pages: 1701–1710, Ariadne Letra, Renato Menezes, Manika Govil, Renata F. Fonseca, Toby McHenry, José M. Granjeiro, Eduardo E. Castilla, Iêda M. Orioli, Mary L. Marazita and Alexandre R. Vieira

    Version of Record online : 25 JUN 2010, DOI: 10.1002/ajmg.a.33482

  2. Systematic enrichment analysis of potentially functional regions for 103 prostate cancer risk-associated loci

    The Prostate

    Volume 75, Issue 12, September 1, 2015, Pages: 1264–1276, Haitao Chen, Hongjie Yu, Jianqing Wang, Zheng Zhang, Zhengrong Gao, Zhuo Chen, Yulan Lu, Wennuan Liu, Deke Jiang, S.Lilly Zheng, Gong-hong Wei, William B. Issacs, Junjie Feng and Jianfeng Xu

    Version of Record online : 25 MAY 2015, DOI: 10.1002/pros.23008

  3. You have free access to this content
    Clinical characteristics of comorbid obsessive-compulsive disorder and bipolar disorder in children and adolescents

    Bipolar Disorders

    Volume 12, Issue 2, March 2010, Pages: 185–195, Gagan Joshi, Janet Wozniak, Carter Petty, Fe Vivas, Dayna Yorks, Joseph Biederman and Daniel Geller

    Version of Record online : 25 MAR 2010, DOI: 10.1111/j.1399-5618.2010.00795.x

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    Anorectal atresia and Variants at Predicted Regulatory Sites in Candidate Genes

    Annals of Human Genetics

    Volume 77, Issue 1, January 2013, Pages: 31–46, Tonia C. Carter, Denise M. Kay, Marilyn L. Browne, Aiyi Liu, Paul A. Romitti, Devon Kuehn, Mary R. Conley, Michele Caggana, Charlotte M. Druschel, Lawrence C. Brody and James L. Mills

    Version of Record online : 6 NOV 2012, DOI: 10.1111/j.1469-1809.2012.00734.x

  5. Fine mapping of a calving QTL on Bos taurus autosome 18 in Holstein cattle

    Journal of Animal Breeding and Genetics

    Volume 133, Issue 3, June 2016, Pages: 207–218, X. Mao, N.K. Kadri, J.R. Thomasen, D.J. De Koning, G. Sahana and B. Guldbrandtsen

    Version of Record online : 20 OCT 2015, DOI: 10.1111/jbg.12187

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    Meta-Analysis of Genome-wide Linkage Studies in BMI and Obesity


    Volume 15, Issue 9, September 2007, Pages: 2263–2275, Catherine L. Saunders, Benedetta D. Chiodini, Pak Sham, Cathryn M. Lewis, Victor Abkevich, Adebowale A. Adeyemo, Mariza de Andrade, Rector Arya, Gerald S. Berenson, John Blangero, Michael Boehnke, Ingrid B. Borecki, Yvon C. Chagnon, Wei Chen, Anthony G. Comuzzie, Hong-Wen Deng, Ravindranath Duggirala, Mary F. Feitosa, Philippe Froguel, Robert L. Hanson, Johannes Hebebrand, Patricia Huezo-Dias, Ahmed H. Kissebah, Weidong Li, Amy Luke, Lisa J. Martin, Matthew Nash, Miina Öhman, Lyle J. Palmer, Leena Peltonen, Markus Perola, R. Arlen Price, Susan Redline, Sathanur R. Srinivasan, Michael P. Stern, Steven Stone, Heather Stringham, Stephen Turner, Cisca Wijmenga and David A. Collier

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2007.269

  7. Constitutional FLCN mutations in patients with suspected Birt–Hogg–Dubé syndrome ascertained for non-cutaneous manifestations

    Clinical Genetics

    Volume 79, Issue 4, April 2011, Pages: 345–354, A Maffé, B Toschi, G Circo, D Giachino, S Giglio, A Rizzo, A Carloni, V Poletti, S Tomassetti, C Ginardi, S Ungari and M Genuardi

    Version of Record online : 7 JUN 2010, DOI: 10.1111/j.1399-0004.2010.01480.x

  8. 8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients

    American Journal of Medical Genetics Part A

    Volume 161, Issue 3, March 2013, Pages: 487–500, John C.K. Barber, Jill A. Rosenfeld, Nicola Foulds, Sophie Laird, Mark S. Bateman, N. Simon Thomas, Samantha Baker, Viv K. Maloney, Arayamparambil Anilkumar, Wendy E. Smith, Valerie Banks, Sara Ellingwood, Yara Kharbutli, Lakshmi Mehta, Keith A. Eddleman, Michael Marble, Regina Zambrano, John A. Crolla and Allen N. Lamb

    Version of Record online : 23 JAN 2013, DOI: 10.1002/ajmg.a.35767

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    Comorbidity of body dysmorphic disorder and eating disorders: Severity of psychopathology and body image disturbance

    International Journal of Eating Disorders

    Volume 39, Issue 1, January 2006, Pages: 11–19, Jessica S. Ruffolo, Katharine A. Phillips, William Menard, Christina Fay and Risa B. Weisberg

    Version of Record online : 27 OCT 2005, DOI: 10.1002/eat.20219

  10. The transcription factor 7-like 2 (TCF7L2) gene is associated with Type 2 diabetes in UK community-based cases, but the risk allele frequency is reduced compared with UK cases selected for genetic studies

    Diabetic Medicine

    Volume 24, Issue 10, October 2007, Pages: 1067–1072, N. M. G. De Silva, A. Steele, B. Shields, B. Knight, K. Parnell, M. N. Weedon, A. T. Hattersley and T. M. Frayling

    Version of Record online : 24 AUG 2007, DOI: 10.1111/j.1464-5491.2007.02253.x

  11. 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


    ANZ Journal of Surgery

    Volume 76, Issue 1-2, January 2006, Pages: 14–19, Lincoln A. Rothwell, E. Leslie Bokey, Anil Keshava, Pierre H. Chapuis and Owen F. Dent

    Version of Record online : 16 FEB 2006, DOI: 10.1111/j.1445-2197.2006.03556.x

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    Exercise-induced TBC1D1 Ser237 phosphorylation and 14-3-3 protein binding capacity in human skeletal muscle

    The Journal of Physiology

    Volume 588, Issue 22, November 2010, Pages: 4539–4548, Christian Frøsig, Christian Pehmøller, Jesper B. Birk, Erik A. Richter and Jørgen F. P. Wojtaszewski

    Version of Record online : 15 NOV 2010, DOI: 10.1113/jphysiol.2010.194811

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    Long QT syndrome: beyond the causal mutation

    The Journal of Physiology

    Volume 591, Issue 17, September 2013, Pages: 4125–4139, Ahmad S. Amin, Yigal M. Pinto and Arthur A. M. Wilde

    Version of Record online : 19 JUL 2013, DOI: 10.1113/jphysiol.2013.254920

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    ETS Research Bulletin Series

    Volume 1976, Issue 2, December 1976, Pages: i–177, Lawrence J. Stricker

    Version of Record online : 8 AUG 2014, DOI: 10.1002/j.2333-8504.1976.tb01116.x

  16. Role of chromosome aberrations in recurrent abortion: A study of 269 balanced translocations

    American Journal of Medical Genetics

    Volume 24, Issue 2, June 1986, Pages: 341–356, Mauro Campana, Dr. Angelo Serra, Giovanni Neri and James F. Reynolds

    Version of Record online : 3 JUN 2005, DOI: 10.1002/ajmg.1320240214

  17. Autoimmune thyroid disease in type I diabetic families

    Genetic Epidemiology

    Volume 6, Issue 1, 1989, Pages: 137–141, H. Payami, S. Joe and G. Thomson

    Version of Record online : 3 JUN 2005, DOI: 10.1002/gepi.1370060126


    Journal of Food Quality

    Volume 29, Issue 3, June 2006, Pages: 282–293, CRISTINA PATANÈ

    Version of Record online : 22 MAY 2006, DOI: 10.1111/j.1745-4557.2006.00074.x

  19. Reproductive risks for translocation carriers: Cytogenetic study and analysis of pregnancy outcome in 58 families

    American Journal of Medical Genetics

    Volume 16, Issue 4, December 1983, Pages: 535–561, Dr. Giovanni Neri, Angelo Serra, Mauro Campana and Bruna Tedeschi

    Version of Record online : 2 JUN 2005, DOI: 10.1002/ajmg.1320160412

  20. Results of a SNP genome screen in a large Costa Rican pedigree segregating for severe bipolar disorder

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 141B, Issue 4, 5 June 2006, Pages: 367–373, Susan Service, Julio Molina, Joseph DeYoung, Damini Jawaheer, Ileana Aldana, Thuy Vu, Julio Bejarano, Eduardo Fournier, Magui Ramirez, Carol A. Mathews, Pablo Davanzo, Gabriel Macaya, Lodewijk Sandkuijl, Chiara Sabatti, Victor Reus and Nelson Freimer

    Version of Record online : 1 MAY 2006, DOI: 10.1002/ajmg.b.30323