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There are 8654 results for: content related to: Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths

  1. 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

  2. Application of chromosomal microarray in the evaluation of abnormal prenatal findings

    Clinical Genetics

    Volume 84, Issue 1, July 2013, Pages: 47–54, SA Yatsenko, S Davis, NW Hendrix, U Surti, S Emery, T Canavan, P Speer, L Hill, M Clemens and A Rajkovic

    Article first published online : 4 NOV 2012, DOI: 10.1111/cge.12027

  3. 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

    Article first published online : 27 JUN 2012, DOI: 10.1111/j.1528-1167.2012.03559.x

  4. 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

    Article first published online : 10 DEC 2009, DOI: 10.1111/j.1399-0004.2009.01342.x

  5. You have full text access to this OnlineOpen article
    Duplications in ADHD patients harbour neurobehavioural genes that are co-expressed with genes associated with hyperactivity in the mouse

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 168, Issue 2, March 2015, Pages: 97–107, Avigail Taylor, Julia Steinberg and Caleb Webber

    Article first published online : 5 FEB 2015, DOI: 10.1002/ajmg.b.32285

  6. 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

  7. Implementation of high-resolution SNP arrays in the investigation of fetuses with ultrasound malformations: 5 years of clinical experience

    Clinical Genetics

    Volume 86, Issue 3, September 2014, Pages: 264–269, C. Liao, F. Fu, R. Li, G.-e. Xie, Y.-l. Zhang, J. Li and D.-z. Li

    Article first published online : 31 OCT 2013, DOI: 10.1111/cge.12271

  8. 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

  9. 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

    Article first published online : 28 APR 2010, DOI: 10.1002/jso.21585

  10. You have full text access to this OnlineOpen article
    Copy number variant analysis from exome data in 349 patients with epileptic encephalopathy

    Annals of Neurology

    Volume 78, Issue 2, August 2015, Pages: 323–328, Epilepsy Phenome/Genome Project & Epi4K Consortium

    Article first published online : 1 JUL 2015, DOI: 10.1002/ana.24457

  11. Copy number variation characteristics in subpopulations of patients with autism spectrum disorders

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 156, Issue 2, March 2011, Pages: 115–124, Anna Bremer, MaiBritt Giacobini, Mats Eriksson, Peter Gustavsson, Viviann Nordin, Elisabeth Fernell, Christopher Gillberg, Ann Nordgren, Åsa Uppströmer, Britt-Marie Anderlid, Magnus Nordenskjöld and Jacqueline Schoumans

    Article first published online : 8 DEC 2010, DOI: 10.1002/ajmg.b.31142

  12. Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis

    International Journal of Cancer

    Volume 136, Issue 6, 15 March 2015, Pages: E578–E589, Sukanya Horpaopan, Isabel Spier, Alexander M. Zink, Janine Altmüller, Stefanie Holzapfel, Andreas Laner, Stefanie Vogt, Siegfried Uhlhaas, Stefanie Heilmann, Dietlinde Stienen, Sandra M. Pasternack, Kathleen Keppler, Ronja Adam, Katrin Kayser, Susanne Moebus, Markus Draaken, Franziska Degenhardt, Hartmut Engels, Andrea Hofmann, Markus M. Nöthen, Verena Steinke, Alberto Perez-Bouza, Stefan Herms, Elke Holinski-Feder, Holger Fröhlich, Holger Thiele, Per Hoffmann and Stefan Aretz

    Article first published online : 30 SEP 2014, DOI: 10.1002/ijc.29215

  13. 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

    Article first published online : 8 AUG 2011, DOI: 10.1002/mus.22095

  14. A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 165, Issue 8, December 2014, Pages: 619–626, Danielle S. Rudd, Michael Axelsen, Eric A. Epping, Nancy C. Andreasen and Thomas H. Wassink

    Article first published online : 16 SEP 2014, DOI: 10.1002/ajmg.b.32266

  15. Copy number variation plays an important role in clinical epilepsy

    Annals of Neurology

    Volume 75, Issue 6, June 2014, Pages: 943–958, Heather Olson, Yiping Shen, Jennifer Avallone, Beth R. Sheidley, Rebecca Pinsky, Ann M. Bergin, Gerard T. Berry, Frank H. Duffy, Yaman Eksioglu, David J. Harris, Fuki M. Hisama, Eugenia Ho, Mira Irons, Christina M. Jacobsen, Philip James, Sanjeev Kothare, Omar Khwaja, Jonathan Lipton, Tobias Loddenkemper, Jennifer Markowitz, Kiran Maski, J. Thomas Megerian, Edward Neilan, Peter C. Raffalli, Michael Robbins, Amy Roberts, Eugene Roe, Caitlin Rollins, Mustafa Sahin, Dean Sarco, Alison Schonwald, Sharon E. Smith, Janet Soul, Joan M. Stoler, Masanori Takeoka, Wen-Han Tan, Alcy R. Torres, Peter Tsai, David K. Urion, Laura Weissman, Robert Wolff, Bai-Lin Wu, David T. Miller and Annapurna Poduri

    Article first published online : 13 JUN 2014, DOI: 10.1002/ana.24178

  16. You have free access to this content
    Genetic susceptibility to male infertility: news from genome-wide association studies


    Volume 2, Issue 3, May 2014, Pages: 315–321, K. I. Aston

    Article first published online : 19 FEB 2014, DOI: 10.1111/j.2047-2927.2014.00188.x

  17. Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability

    Clinical Genetics

    Volume 83, Issue 2, February 2013, Pages: 145–154, Y Qiao, C Tyson, M Hrynchak, E Lopez-Rangel, J Hildebrand, S Martell, C Fawcett, L Kasmara, K Calli, C Harvard, X Liu, JJA Holden, SME Lewis and E Rajcan-Separovic

    Article first published online : 9 APR 2012, DOI: 10.1111/j.1399-0004.2012.01860.x

  18. Rare copy number variants are common in young children with autism spectrum disorder

    Acta Paediatrica

    Volume 104, Issue 6, June 2015, Pages: 610–618, Mats Anders Eriksson, Agne Liedén, Joakim Westerlund, Anna Bremer, Josephine Wincent, Ellika Sahlin, Christopher Gillberg, Elisabeth Fernell and Britt-Marie Anderlid

    Article first published online : 11 MAR 2015, DOI: 10.1111/apa.12969

  19. Copy number variations in multiple sclerosis and neuromyelitis optica

    Annals of Neurology

    Volume 78, Issue 5, November 2015, Pages: 762–774, Shinya Sato, Ken Yamamoto, Takuya Matsushita, Noriko Isobe, Yuji Kawano, Kyoko Iinuma, Masaaki Niino, Toshiyuki Fukazawa, Yuri Nakamura, Mitsuru Watanabe, Tomomi Yonekawa, Katsuhisa Masaki, Satoshi Yoshimura, Hiroyuki Murai, Ryo Yamasaki, Jun-ichi Kira and and the Japan Multiple Sclerosis Genetics Consortium

    Article first published online : 18 SEP 2015, DOI: 10.1002/ana.24511

  20. You have free access to this content
    Copy number variations and susceptibility to lateral temporal epilepsy: A study of 21 pedigrees


    Volume 55, Issue 10, October 2014, Pages: 1651–1658, Manuela Fanciulli, Elena Pasini, Sandro Malacrida, Pasquale Striano, Salvatore Striano, Roberto Michelucci, Ruth Ottman and Carlo Nobile

    Article first published online : 19 SEP 2014, DOI: 10.1111/epi.12767