Search Results

There are 51267 results for: content related to: Multiple correspondence discriminant analysis: An application to detect stratification in copy number variation

  1. 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

    Version of Record online : 8 MAR 2013, DOI: 10.1002/humu.22288

  2. You have free access to this content
    Investigation of the HIN200 Locus in UK SLE Families Identifies Novel Copy Number Variants

    Annals of Human Genetics

    Volume 75, Issue 3, May 2011, Pages: 383–397, Michelle M. A. Fernando, Adam J. de Smith, Lachlan Coin, David L. Morris, Philippe Froguel, Jonathan Mangion, Alexandra I. F. Blakemore, Robert R. Graham, Timothy W. Behrens and Timothy J. Vyse

    Version of Record online : 14 MAR 2011, DOI: 10.1111/j.1469-1809.2011.00641.x

  3. 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

  4. 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

  5. Looking for differences in copy number between blood and brain in sporadic amyotrophic lateral sclerosis

    Muscle & Nerve

    Volume 44, Issue 4, October 2011, Pages: 492–498, Roger Pamphlett, Julia M. Morahan, Natasha Luquin and Bing Yu

    Version of Record online : 8 AUG 2011, DOI: 10.1002/mus.22095

  6. MCDA Twins with Discordant Malformations: Submicroscopic Chromosomal Anomalies Detected by Chromosomal Microarray Analysis and Clinical Outcomes

    Prenatal Diagnosis

    Accepted manuscript online: 17 JUN 2016, Ruan Peng, Yi Zhou, Hong-Ning Xie, Ju Zheng, Ying-Jun Xie and Jian-Bo Yang

    DOI: 10.1002/pd.4859

  7. Segmentation and Estimation for SNP Microarrays: A Bayesian Multiple Change-Point Approach


    Volume 66, Issue 3, September 2010, Pages: 675–683, Yu Chuan Tai, Mark N. Kvale and John S. Witte

    Version of Record online : 17 SEP 2009, DOI: 10.1111/j.1541-0420.2009.01328.x

  8. Discovery and Functional Assessment of Gene Variants in the Vascular Endothelial Growth Factor Pathway

    Human Mutation

    Volume 35, Issue 2, February 2014, Pages: 227–235, Laia Paré-Brunet, Dylan Glubb, Patrick Evans, Antoni Berenguer-Llergo, Amy S. Etheridge, Andrew D. Skol, Anna Di Rienzo, Shiwei Duan, Eric R. Gamazon and Federico Innocenti

    Version of Record online : 27 NOV 2013, DOI: 10.1002/humu.22475

  9. Abstracts from the Eighteenth Annual Meeting of the International Genetic Epidemiology Society

    Genetic Epidemiology

    Volume 33, Issue 8, December 2009, Pages: 752–835,

    Version of Record online : 23 NOV 2009, DOI: 10.1002/gepi.20463

  10. Searching genetic risk factors for schizophrenia and bipolar disorder: learn from the past and back to the future

    Human Mutation

    Volume 30, Issue 8, August 2009, Pages: 1139–1152, Maaike Alaerts and Jurgen Del-Favero

    Version of Record online : 28 APR 2009, DOI: 10.1002/humu.21042

  11. 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

  12. Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization

    Human Mutation

    Volume 28, Issue 11, November 2007, Pages: 1124–1132, Yao-Shan Fan, Parul Jayakar, Hongbo Zhu, Deborah Barbouth, Stephanie Sacharow, Ana Morales, Virginia Carver, Paul Benke, Peter Mundy and Louis J. Elsas

    Version of Record online : 9 JUL 2007, DOI: 10.1002/humu.20581

  13. You have free access to this content
    Diagnostic interpretation of array data using public databases and internet sources

    Human Mutation

    Volume 33, Issue 6, June 2012, Pages: 930–940, Nicole de Leeuw, Trijnie Dijkhuizen, Jayne Y. Hehir-Kwa, Nigel P. Carter, Lars Feuk, Helen V. Firth, Robert M. Kuhn, David H. Ledbetter, Christa Lese Martin, Conny M. A. van Ravenswaaij-Arts, Steven W. Scherer, Soheil Shams, Steven Van Vooren, Rolf Sijmons, Morris Swertz and Ros Hastings

    Version of Record online : 7 MAY 2012, DOI: 10.1002/humu.22049

  14. Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array

    Human Mutation

    Volume 29, Issue 3, March 2008, Pages: 398–408, Teresita Díaz de Ståhl, Johanna Sandgren, Arkadiusz Piotrowski, Helena Nord, Robin Andersson, Uwe Menzel, Adam Bogdan, Ann-Charlotte Thuresson, Andrzej Poplawski, Desiree von Tell, Caisa M. Hansson, Amir I. Elshafie, Gehad ElGhazali, Stephan Imreh, Magnus Nordenskjöld, Meena Upadhyaya, Jan Komorowski, Carl E.G. Bruder and Jan P. Dumanski

    Version of Record online : 30 NOV 2007, DOI: 10.1002/humu.20659

  15. You have free access to this content
    Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: Genomic dissection makes the link with autism


    Volume 53, Issue 9, September 2012, Pages: 1526–1538, Gaetan Lesca, Gabrielle Rudolf, Audrey Labalme, Edouard Hirsch, Alexis Arzimanoglou, Pierre Genton, Jacques Motte, Anne de Saint Martin, Maria-Paola Valenti, Clotilde Boulay, Julitta De Bellescize, Pascale Kéo-Kosal, Nadia Boutry-Kryza, Patrick Edery, Damien Sanlaville and Pierre Szepetowski

    Version of Record online : 27 JUN 2012, DOI: 10.1111/j.1528-1167.2012.03559.x

  16. Gene copy number variation and common human disease

    Clinical Genetics

    Volume 77, Issue 3, March 2010, Pages: 201–213, M Fanciulli, E Petretto and TJ Aitman

    Version of Record online : 10 DEC 2009, DOI: 10.1111/j.1399-0004.2009.01342.x

  17. 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

  18. Identification of rare copy number variants in high burden schizophrenia families

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 3, April 2013, Pages: 273–282, Maarten J. Van Den Bossche, Mojca Strazisar, Sophia Cammaerts, Anthony M. Liekens, Geert Vandeweyer, Veerle Depreeuw, Maria Mattheijssens, An-Sofie Lenaerts, Sonia De Zutter, Peter De Rijk, Bernard Sabbe and Jurgen Del-Favero

    Version of Record online : 15 MAR 2013, DOI: 10.1002/ajmg.b.32146

  19. Copy Number Variations

    Next Generation Sequencing and Whole Genome Selection in Aquaculture

    Jianguo Lu, Zhanjiang (John) Liu, Pages: 21–33, 2010

    Published Online : 10 DEC 2010, DOI: 10.1002/9780470958964.ch2

  20. You have free access to this content
    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