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There are 15482 results for: content related to: Bayesian hierarchical mixture modeling to assign copy number from a targeted CNV array

  1. You have free access to this content
    Copy number variation in autoimmunity — importance hidden in complexity?

    European Journal of Immunology

    Volume 42, Issue 8, August 2012, Pages: 1969–1976, Lina M. Olsson and Rikard Holmdahl

    Version of Record online : 3 AUG 2012, DOI: 10.1002/eji.201242601

  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

    Version of Record online : 6 MAR 2012, DOI: 10.1111/j.1365-2052.2012.02317.x

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    Copy number variants are produced in response to low-dose ionizing radiation in cultured cells

    Environmental and Molecular Mutagenesis

    Volume 55, Issue 2, March 2014, Pages: 103–113, Martin F. Arlt, Sountharia Rajendran, Shanda R. Birkeland, Thomas E. Wilson and Thomas W. Glover

    Version of Record online : 10 DEC 2013, DOI: 10.1002/em.21840

  4. 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

    Version of Record online : 7 JUN 2013, DOI: 10.1002/mgg3.18

  5. Identification of novel gastric cancer-associated CNVs by integrated analysis of microarray

    Journal of Surgical Oncology

    Volume 102, Issue 5, 1 October 2010, Pages: 454–461, Chan-Hee Park, Sun-Young Rha, Hei-Cheul Jeung, Seung-Hui Kang, Dong-Hyuk Ki, Won-Suk Lee, Sung-Hoon Noh and Hyun-Cheol Chung

    Version of Record online : 28 APR 2010, DOI: 10.1002/jso.21585

  6. The XVth World Congress of Psychiatric Genetics, October 7–11, 2007: Rapporteur summaries of oral presentations

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 2, 5 March 2008, Pages: 233–277, Anna Alkelai, Amber Baum, Melanie Carless, James Crowley, Tania DasBanerjee, Emma Dempster, Sophia Docherty, Elizabeth Hare, Michael J Galsworthy, Deepak Grover, Dylan Glubb, Robert Karlsson, Jonathan Mill, Srijan Sen, Marlon P. Quinones, Eric J. Vallender, Ranjana Verma, Neetha.N. Vijayan, Sandra Villafuerte, Aristotle N. Voineskos, Heather Volk, Lan Yu, Petra Zimmermann and Lynn E. DeLisi

    Version of Record online : 22 FEB 2008, DOI: 10.1002/ajmg.b.30711

  7. Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 4, June 2014, Pages: 303–313, Abdul Noor, Anath C. Lionel, Sarah Cohen-Woods, Narges Moghimi, James Rucker, Alanna Fennell, Bhooma Thiruvahindrapuram, Liana Kaufman, Bryan Degagne, John Wei, Sagar V. Parikh, Pierandrea Muglia, Julia Forte, Stephen W. Scherer, James L. Kennedy, Wei Xu, Peter McGuffin, Anne Farmer, John Strauss and John B. Vincent

    Version of Record online : 3 APR 2014, DOI: 10.1002/ajmg.b.32232

  8. Reduced burden of very large and rare CNVs in bipolar affective disorder

    Bipolar Disorders

    Volume 15, Issue 8, December 2013, Pages: 893–898, Detelina Grozeva, George Kirov, Donald F Conrad, Chris P Barnes, Matthew Hurles, Michael J Owen, Michael C O'Donovan and Nick Craddock

    Version of Record online : 16 OCT 2013, DOI: 10.1111/bdi.12125

  9. The genetic variability and commonality of neurodevelopmental disease

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 160C, Issue 2, 15 May 2012, Pages: 118–129, Bradley P. Coe, Santhosh Girirajan and Evan E. Eichler

    Version of Record online : 12 APR 2012, DOI: 10.1002/ajmg.c.31327

  10. 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

    Version of Record online : 21 AUG 2013, DOI: 10.1111/cge.12242

  11. Correlating Multiallelic Copy Number Polymorphisms with Disease Susceptibility

    Human Mutation

    Volume 34, Issue 1, January 2013, Pages: 1–13, Stuart Cantsilieris and Stefan J. White

    Version of Record online : 23 AUG 2012, DOI: 10.1002/humu.22172

  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

    Version of Record online : 26 JUL 2014, DOI: 10.1002/bdra.23279

  13. Independent replication of an association of CNVR7113.6 with Crohn's disease in caucasians

    Inflammatory Bowel Diseases

    Volume 18, Issue 2, February 2012, Pages: 305–311, Rebecca L. Roberts, Lina-Marcela Diaz-Gallo, Murray L. Barclay, María Gómez-García, Carlos Cardeña, Tony R. Merriman, Richard B. Gearry and Javier Martin

    Version of Record online : 10 MAY 2011, DOI: 10.1002/ibd.21752

  14. 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

    Version of Record online : 24 MAY 2012, DOI: 10.1002/gepi.21643

  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

    Version of Record online : 24 APR 2012, DOI: 10.1002/gepi.21618

  16. 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

    Version of Record online : 27 APR 2015, DOI: 10.1111/age.12288

  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

    Version of Record online : 30 SEP 2011, DOI: 10.1002/humu.21601

  18. The impact of array genomic hybridization on mental retardation research: a review of current technologies and their clinical utility

    Clinical Genetics

    Volume 72, Issue 4, October 2007, Pages: 271–287, F Zahir and JM Friedman

    Version of Record online : 28 AUG 2007, DOI: 10.1111/j.1399-0004.2007.00847.x

  19. Clinical Significance of De Novo and Inherited Copy-Number Variation

    Human Mutation

    Volume 34, Issue 12, December 2013, Pages: 1679–1687, Anneke T. Vulto-van Silfhout, Jayne Y. Hehir-Kwa, Bregje W.M. van Bon, Janneke H.M. Schuurs-Hoeijmakers, Stephen Meader, Claudia J.M. Hellebrekers, Ilse J.M. Thoonen, Arjan P.M. de Brouwer, Han G. Brunner, Caleb Webber, Rolph Pfundt, Nicole de Leeuw and Bert B.A. de Vries

    Version of Record online : 10 OCT 2013, DOI: 10.1002/humu.22442

  20. Genome-wide copy number variation in the bovine genome detected using low coverage sequence of popular beef breeds,

    Animal Genetics

    B. N. Keel, J. W. Keele and W. M. Snelling

    Version of Record online : 24 OCT 2016, DOI: 10.1111/age.12519