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There are 19027 results for: content related to: Copy number variation prevalence in known asthma genes and their impact on asthma susceptibility

  1. You have free access to this content
    Clinical and Histological Aspects of CNV Formation: Studies in an Animal Model

    Acta Ophthalmologica

    Volume 86, Issue thesis2, September 2008, Pages: 1–28, Nathan Lassota

    Article first published online : 4 SEP 2008, DOI: 10.1111/j.1755-3768.2008.01412.x

  2. Copy number variation in the genomes of domestic animals

    Animal Genetics

    Volume 43, Issue 5, October 2012, Pages: 503–517, A. Clop, O. Vidal and M. Amills

    Article first published online : 6 MAR 2012, DOI: 10.1111/j.1365-2052.2012.02317.x

  3. You have full text access to this OnlineOpen article
    Increased rate of sporadic and recurrent rare genic copy number variants in Parkinson's disease among Ashkenazi Jews

    Molecular Genetics & Genomic Medicine

    Volume 1, Issue 3, September 2013, Pages: 142–154, Xinmin Liu, Rong Cheng, Xin Ye, Miguel Verbitsky, Sergey Kisselev, Helen Mejia-Santana, Elan D. Louis, Lucien J. Cote, Howard F. Andrews, Cheryl H. Waters, Blair Ford, Stanley Fahn, Karen Marder, Joseph H. Lee and Lorraine N. Clark

    Article first published online : 7 JUN 2013, DOI: 10.1002/mgg3.18

  4. Inheritance Model Introduces Differential Bias in CNV Calls Between Parents and Offspring

    Genetic Epidemiology

    Volume 36, Issue 5, July 2012, Pages: 488–498, Sulgi Kim, Steven P. Millard, Chang-En Yu, Lesley Leong, Allen Radant, Dorcas Dobie, Debby W. Tsuang and Ellen M. Wijsman

    Article first published online : 24 MAY 2012, DOI: 10.1002/gepi.21643

  5. A genome-wide scan for copy number variations using high-density single nucleotide polymorphism array in Simmental cattle

    Animal Genetics

    Volume 46, Issue 3, June 2015, Pages: 289–298, Yang Wu, Huizhong Fan, Shengyun Jing, Jiangwei Xia, Yan Chen, Lupei Zhang, Xue Gao, Junya Li, Huijiang Gao and Hongyan Ren

    Article first published online : 27 APR 2015, DOI: 10.1111/age.12288

  6. Detection of Clinically Relevant Copy Number Variants with Whole-Exome Sequencing

    Human Mutation

    Volume 34, Issue 10, October 2013, Pages: 1439–1448, Joep de Ligt, Philip M. Boone, Rolph Pfundt, Lisenka E.L.M. Vissers, Todd Richmond, Joel Geoghegan, Kathleen O'Moore, Nicole de Leeuw, Christine Shaw, Han G. Brunner, James R. Lupski, Joris A. Veltman and Jayne Y. Hehir-Kwa

    Article first published online : 30 AUG 2013, DOI: 10.1002/humu.22387

  7. An MLPA-Based Strategy for Discrete CNV Genotyping: CNV-miRNAs as an Example

    Human Mutation

    Volume 34, Issue 5, May 2013, Pages: 763–773, Malgorzata Marcinkowska-Swojak, Barbara Uszczynska, Marek Figlerowicz and Piotr Kozlowski

    Article first published online : 8 MAR 2013, DOI: 10.1002/humu.22288

  8. An Evaluation of Copy Number Variation Detection Tools from Whole-Exome Sequencing Data

    Human Mutation

    Volume 35, Issue 7, July 2014, Pages: 899–907, Renjie Tan, Yadong Wang, Sarah E. Kleinstein, Yongzhuang Liu, Xiaolin Zhu, Hongzhe Guo, Qinghua Jiang, Andrew S. Allen and Mingfu Zhu

    Article first published online : 1 MAY 2014, DOI: 10.1002/humu.22537

  9. Movement related cortical potentials of cued versus self-initiated movements: Double dissociated modulation by dorsal premotor cortex versus supplementary motor area rTMS

    Human Brain Mapping

    Volume 33, Issue 4, April 2012, Pages: 824–839, Ming-Kuei Lu, Noritoshi Arai, Chon-Haw Tsai and Ulf Ziemann

    Article first published online : 21 MAR 2011, DOI: 10.1002/hbm.21248

  10. You have free access to this content
    Copy-number variation in the pathogenesis of autism spectrum disorder

    Psychiatry and Clinical Neurosciences

    Volume 68, Issue 2, February 2014, Pages: 85–95, Emiko Shishido, Branko Aleksic and Norio Ozaki

    Article first published online : 29 DEC 2013, DOI: 10.1111/pcn.12128

  11. You have free access to this content
    Pathogenic or not? Assessing the clinical relevance of copy number variants

    Clinical Genetics

    Volume 84, Issue 5, November 2013, Pages: 415–421, JY Hehir-Kwa, R Pfundt, JA Veltman and N de Leeuw

    Article first published online : 21 AUG 2013, DOI: 10.1111/cge.12242

  12. Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesions

    Birth Defects Research Part A: Clinical and Molecular Teratology

    Volume 100, Issue 12, December 2014, Pages: 951–964, Peter S. White, Hongbo M. Xie, Petra Werner, Joseph Glessner, Brande Latney, Hakon Hakonarson and Elizabeth Goldmuntz

    Article first published online : 26 JUL 2014, DOI: 10.1002/bdra.23279

  13. Genome-wide copy number profiling using high-density SNP array in chickens

    Animal Genetics

    Volume 46, Issue 2, April 2015, Pages: 148–157, G. Yi, L. Qu, S. Chen, G. Xu and N. Yang

    Article first published online : 6 FEB 2015, DOI: 10.1111/age.12267

  14. Spontaneous deletion enhances movement of a cucumber necrosis virus based chimera expressing the red clover necrotic mosaic virus movement protein gene

    Molecular Plant Pathology

    Volume 2, Issue 1, January 2001, Pages: 13–25, Ron Reade, Karine Delroux, Kim Macdonald, Tim L. Sit, Steven A. Lommel and D’Ann Rochon

    Article first published online : 7 JUL 2008, DOI: 10.1046/j.1364-3703.2001.00045.x

  15. Using Family Data as a Verification Standard to Evaluate Copy Number Variation Calling Strategies for Genetic Association Studies

    Genetic Epidemiology

    Volume 36, Issue 3, April 2012, Pages: 253–262, Xiaojing Zheng, John R. Shaffer, Caitlin P. McHugh, Cathy C. Laurie, Bjarke Feenstra, Mads Melbye, Jeffrey C. Murray, Mary L. Marazita and and Eleanor Feingold

    Article first published online : 24 APR 2012, DOI: 10.1002/gepi.21618

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    Anti-vascular endothelial growth factor for neovascular age-related macular degeneration

    Intervention Review

    The Cochrane Library

    Sharon D Solomon, Kristina Lindsley, Satyanarayana S Vedula, Magdalena G Krzystolik and Barbara S Hawkins

    Published Online : 29 AUG 2014, DOI: 10.1002/14651858.CD005139.pub3

  17. SgD-CNV, a database for common and rare copy number variants in three Asian populations

    Human Mutation

    Volume 32, Issue 12, December 2011, Pages: 1341–1349, Haiyan Xu, Wan-Ting Poh, Xueling Sim, Rick Twee-Hee Ong, Chen Suo, Wan-Ting Tay, Chiea-Chuen Khor, Mark Seielstad, Jianjun Liu, Tin Aung, E-Shyong Tai, Tien-Yin Wong, Kee-Seng Chia and Yik-Ying Teo

    Article first published online : 30 SEP 2011, DOI: 10.1002/humu.21601

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    Copy Number Variations at the Prader-Willi Syndrome Region on Chromosome 15 and associations with Obesity in Whites


    Volume 19, Issue 6, June 2011, Pages: 1229–1234, Yuan Chen, Yong-Jun Liu, Yu-Fang Pei, Tie-Lin Yang, Fei-Yan Deng, Xiao-Gang Liu, Ding-You Li and Hong-Wen Deng

    Article first published online : 6 SEP 2012, DOI: 10.1038/oby.2010.323

  19. Laser photocoagulation for neovascular age-related macular degeneration

    Intervention Review

    The Cochrane Library

    Gianni Virgili and Alessandro Bini

    Published Online : 18 JUL 2007, DOI: 10.1002/14651858.CD004763.pub2

  20. Photoreceptor synapses degenerate early in experimental choroidal neovascularization

    Journal of Comparative Neurology

    Volume 483, Issue 3, 14 March 2005, Pages: 263–277, Alejandro Caicedo, Diego G. Espinosa-Heidmann, Duco Hamasaki, Yolanda Piña and Scott W. Cousins

    Article first published online : 28 JAN 2005, DOI: 10.1002/cne.20413