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There are 7969 results for: content related to: Effect of homozygous deletions at 22q13.1 on alcohol dependence severity and cue-elicited BOLD response in the precuneus

  1. You have free access to this content
    Deletion Variants of RABGAP1L, 10q21.3, and C4 Are Associated With the Risk of Systemic Lupus Erythematosus in Korean Women

    Arthritis & Rheumatism

    Volume 65, Issue 4, April 2013, Pages: 1055–1063, Ji-Hong Kim, Seung-Huyn Jung, Joon Seol Bae, Hye-Soon Lee, Seon-Hee Yim, So-Yeon Park, So-Young Bang, Hae-Jin Hu, Hyoung Doo Shin, Sang-Cheol Bae and Yeun-Jun Chung

    Version of Record online : 28 MAR 2013, DOI: 10.1002/art.37854

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    Genome-Wide Copy Number Variation Analysis Identifies Deletion Variants Associated With Ankylosing Spondylitis

    Arthritis & Rheumatology

    Volume 66, Issue 8, August 2014, Pages: 2103–2112, Seung-Hyun Jung, Seon-Hee Yim, Hae-Jin Hu, Kyu Hoon Lee, Joo-Hyun Lee, Dong-Hyuk Sheen, Mi-Kyoung Lim, Soon-Young Kim, Sung-Won Park, So-Hee Kim, Kyudong Han, Tae-Hwan Kim, Seung-Cheol Shim and Yeun-Jun Chung

    Version of Record online : 28 JUL 2014, DOI: 10.1002/art.38650

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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

    Version of Record online : 6 SEP 2012, DOI: 10.1038/oby.2010.323

  4. 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

  5. The Genetic Effect of Copy Number Variations on the Risk of Alcoholism in a Korean Population

    Alcoholism: Clinical and Experimental Research

    Volume 36, Issue 1, January 2012, Pages: 35–42, Joon Seol Bae, Myung Hun Jung, Boung Chul Lee, Hyun Sub Cheong, Byung Lae Park, Lyoung Hyo Kim, Jeong-Hyun Kim, Charisse Flerida A. Pasaje, Jin Sol Lee, Kyoung Hwa Jung, Young Gyu Chai, Hyoung Doo Shin and Ihn-Geun Choi

    Version of Record online : 25 JUL 2011, DOI: 10.1111/j.1530-0277.2011.01578.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

  7. 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

  8. Association Between Copy Number Variation Losses and Alcohol Dependence Across African American and European American Ethnic Groups

    Alcoholism: Clinical and Experimental Research

    Volume 38, Issue 5, May 2014, Pages: 1266–1274, Alvaro E. Ulloa, Jiayu Chen, Victor M. Vergara, Vince Calhoun and Jingyu Liu

    Version of Record online : 11 FEB 2014, DOI: 10.1111/acer.12364

  9. 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

  10. 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

  11. Association between copy number variants in 16p11.2 and major depressive disorder in a German case–control sample

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 3, April 2012, Pages: 263–273, Franziska Degenhardt, Lutz Priebe, Stefan Herms, Manuel Mattheisen, Thomas W. Mühleisen, Sandra Meier, Susanne Moebus, Jana Strohmaier, Magdalena Groß, René Breuer, Christoph Lange, Per Hoffmann, Andreas Meyer-Lindenberg, Andreas Heinz, Henrik Walter, Susanne Lucae, Christiane Wolf, Bertram Müller-Myhsok, Florian Holsboer, Wolfgang Maier, Marcella Rietschel, Markus M. Nöthen and Sven Cichon

    Version of Record online : 17 FEB 2012, DOI: 10.1002/ajmg.b.32034

  12. Germline copy number variations in BRCA1-associated ovarian cancer patients

    Genes, Chromosomes and Cancer

    Volume 50, Issue 3, March 2011, Pages: 167–177, Kosuke Yoshihara, Atsushi Tajima, Sosuke Adachi, Jinhua Quan, Masayuki Sekine, Hiroaki Kase, Tetsuro Yahata, Ituro Inoue and Kenichi Tanaka

    Version of Record online : 7 DEC 2010, DOI: 10.1002/gcc.20841

  13. An Integrative Segmentation Method for Detecting Germline Copy Number Variations in SNP Arrays

    Genetic Epidemiology

    Volume 36, Issue 4, May 2012, Pages: 373–383, Jianxin Shi and Peng Li

    Version of Record online : 26 APR 2012, DOI: 10.1002/gepi.21631

  14. 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

    Version of Record online : 30 AUG 2013, DOI: 10.1002/humu.22387

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    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

  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. 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

  18. 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

    Version of Record online : 6 FEB 2015, DOI: 10.1111/age.12267

  19. Copy Number Variations in 6q14.1 and 5q13.2 are Associated with Alcohol Dependence

    Alcoholism: Clinical and Experimental Research

    Volume 36, Issue 9, September 2012, Pages: 1512–1518, Peng Lin, Sarah M. Hartz, Jen-Chyong Wang, Arpana Agrawal, Tian-Xiao Zhang, Nicholas McKenna, Kathleen Bucholz, Andrew I. Brooks, Jay A. Tischfield, Howard J. Edenberg, Victor M. Hesselbrock, John R. Kramer, Samuel Kuperman, Marc A. Schuckit, Alison M. Goate, Laura J. Bierut and John P. Rice, COGA Collaborators, COGEND Collaborators, GENEVA

    Version of Record online : 15 JUN 2012, DOI: 10.1111/j.1530-0277.2012.01758.x

  20. 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

    Version of Record online : 11 MAR 2015, DOI: 10.1111/apa.12969