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There are 160981 results for: content related to: Common Susceptibility Variants Examined for Association with Dilated Cardiomyopathy

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    The 2015 Annual Meeting of the International Genetic Epidemiology Society

    Genetic Epidemiology

    Volume 39, Issue 7, November 2015, Pages: 529–599,

    Version of Record online : 14 SEP 2015, DOI: 10.1002/gepi.21916

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    Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy

    Clinical and Translational Science

    Volume 1, Issue 1, May 2008, Pages: 21–26, Ray E. Hershberger, Sharie B. Parks, Jessica D. Kushner, Duanxiang Li, Susan Ludwigsen, Petra Jakobs, Deirdre Nauman, Donna Burgess, Julie Partain and Michael Litt

    Version of Record online : 21 MAY 2008, DOI: 10.1111/j.1752-8062.2008.00017.x

  3. Epilepsy-Related Sudden Unexpected Death: Targeted Molecular Analysis of Inherited Heart Disease Genes Using Next-Generation DNA Sequencing

    Brain Pathology

    Yukiko Hata, Koji Yoshida, Koshi Kinoshita and Naoki Nishida

    Version of Record online : 20 JUN 2016, DOI: 10.1111/bpa.12390

  4. Barth syndrome associated with compound hemizygosity and heterozygosity of the TAZ and LDB3 genes

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 9, 1 May 2007, Pages: 907–915, Nicola Marziliano, Savina Mannarino, Luisa Nespoli, Marta Diegoli, Michele Pasotti, Clara Malattia, Maurizia Grasso, Andrea Pilotto, Emanuele Porcu, Arturo Raisaro, Claudia Raineri, Roberto Dore, Pietro Paolo Maggio, Agnese Brega and Eloisa Arbustini

    Version of Record online : 29 MAR 2007, DOI: 10.1002/ajmg.a.31653

  5. Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies

    Genetic Epidemiology

    Volume 35, Issue 8, December 2011, Pages: 790–799, Dalin Li, Juan Pablo Lewinger, William J. Gauderman, Cassandra Elizabeth Murcray and David Conti

    Version of Record online : 15 SEP 2011, DOI: 10.1002/gepi.20628

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    Expression, purification, and characterization of the functional dimeric cytoplasmic domain of human erythrocyte band 3 in Escherichia coli

    Protein Science

    Volume 1, Issue 9, September 1992, Pages: 1206–1214, Cheng C. Wang, Ryuichi Moriyama, Philip S. Low, Janine A. Badylak, Jack E. Dixon and Samuel E. Lux

    Version of Record online : 31 DEC 2008, DOI: 10.1002/pro.5560010913

  7. Detecting Association of Rare and Common Variants by Testing an Optimally Weighted Combination of Variants

    Genetic Epidemiology

    Volume 36, Issue 6, September 2012, Pages: 561–571, Qiuying Sha, Xuexia Wang, Xinli Wang and Shuanglin Zhang

    Version of Record online : 19 JUN 2012, DOI: 10.1002/gepi.21649

  8. Annual Research Review: The (epi)genetics of neurodevelopmental disorders in the era of whole-genome sequencing – unveiling the dark matter

    Journal of Child Psychology and Psychiatry

    Volume 56, Issue 3, March 2015, Pages: 278–295, Dominik P. Kiser, Olga Rivero and Klaus-Peter Lesch

    Version of Record online : 11 FEB 2015, DOI: 10.1111/jcpp.12392

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    Genetic basis of end-stage hypertrophic cardiomyopathy

    European Journal of Heart Failure

    Volume 13, Issue 11, November 2011, Pages: 1193–1201, Pablo Garcia-Pavia, Maria E. Vázquez, Javier Segovia, Clara Salas, Patricia Avellana, Manuel Gómez-Bueno, Carlos Vilches, M. Esther Gallardo, Rafael Garesse, Jesús Molano, Belén Bornstein and Luis Alonso-Pulpon

    Version of Record online : 18 FEB 2014, DOI: 10.1093/eurjhf/hfr110

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    A systematic evaluation of the ataxia telangiectasia mutated gene does not show an association with non-Hodgkin lymphoma

    International Journal of Cancer

    Volume 121, Issue 9, 1 November 2007, Pages: 1967–1975, Payal Sipahimalani, John J. Spinelli, Amy C. MacArthur, Agnes Lai, Stephen R. Leach, Rozmin T. Janoo-Gilani, Diana L. Palmquist, Joseph M. Connors, Randy D. Gascoyne, Richard P. Gallagher and Angela R. Brooks-Wilson

    Version of Record online : 19 JUL 2007, DOI: 10.1002/ijc.22888

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    Animal Models of Congenital Cardiomyopathies Associated With Mutations in Z-Line Proteins

    Journal of Cellular Physiology

    Volume 232, Issue 1, January 2017, Pages: 38–52, Marie-Louise Bang

    Version of Record online : 2 JUN 2016, DOI: 10.1002/jcp.25424

  12. Joint Association Testing of Common and Rare Genetic Variants Using Hierarchical Modeling

    Genetic Epidemiology

    Volume 36, Issue 6, September 2012, Pages: 642–651, Niall J. Cardin, Joel A. Mefford and John S. Witte

    Version of Record online : 16 JUL 2012, DOI: 10.1002/gepi.21659

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    Current understanding of human genetics and genetic analysis of psoriasis

    The Journal of Dermatology

    Volume 39, Issue 3, March 2012, Pages: 231–241, Akira OKA, Tomotaka MABUCHI, Akira OZAWA and Hidetoshi INOKO

    Version of Record online : 21 FEB 2012, DOI: 10.1111/j.1346-8138.2012.01504.x

  14. A mutation in the Z-line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathy

    Clinical Genetics

    Volume 88, Issue 2, August 2015, Pages: 172–176, J. M. Lopez-Ayala, M. Ortiz-Genga, I. Gomez-Milanes, D. Lopez-Cuenca, F. Ruiz-Espejo, J. J. Sanchez-Munoz, M. J. Oliva-Sandoval, L. Monserrat and J. R. Gimeno

    Version of Record online : 8 SEP 2014, DOI: 10.1111/cge.12458

  15. Functional Linear Models for Association Analysis of Quantitative Traits

    Genetic Epidemiology

    Volume 37, Issue 7, November 2013, Pages: 726–742, Ruzong Fan, Yifan Wang, James L. Mills, Alexander F. Wilson, Joan E. Bailey-Wilson and Momiao Xiong

    Version of Record online : 15 OCT 2013, DOI: 10.1002/gepi.21757

  16. Synaptic connections of DB3 diffuse bipolar cell axons in macaque retina

    Journal of Comparative Neurology

    Volume 416, Issue 1, 3 January 2000, Pages: 19–29, Roy A. Jacoby and David W. Marshak

    Version of Record online : 7 FEB 2000, DOI: 10.1002/(SICI)1096-9861(20000103)416:1<19::AID-CNE3>3.0.CO;2-H

  17. Left ventricular non-compaction revealed by aortic regurgitation due to Kawasaki disease in a boy with LDB3 mutation

    Pediatrics International

    Volume 58, Issue 8, August 2016, Pages: 797–800, Akira Hachiya, Noriko Motoki, Yohei Akazawa, Satoshi Matsuzaki, Keiichi Hirono, Yukiko Hata, Naoki Nishida, Fukiko Ichida and Kenichi Koike

    Version of Record online : 23 AUG 2016, DOI: 10.1111/ped.12983

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    Anti-anti-idiotypic (Ab3) antibodies that bind progesterone-11α–bovine serum albumin differ in their combining sites from antibodies raised directly against the antigen


    Volume 100, Issue 2, June 2000, Pages: 152–164, R. D. Kirsch, D. Beale, M. He, A. L. Corper, U. Krawinkel-Brenig and M. J. Taussig

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1365-2567.2000.00006.x

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    Journal of Thrombosis and Haemostasis

    Volume 13, Issue S2, June 2015, Pages: 1–997,

    Version of Record online : 3 JUN 2015, DOI: 10.1111/jth.12993

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    Genome-wide association studies and the genetic dissection of complex traits

    American Journal of Hematology

    Volume 84, Issue 8, August 2009, Pages: 504–515, Paola Sebastiani, Nadia Timofeev, Daniel A. Dworkis, Thomas T. Perls and Martin H. Steinberg

    Version of Record online : 16 APR 2009, DOI: 10.1002/ajh.21440