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  1. 1
    Genetics in schizophrenia: where are we and what next?

    Genetics in schizophrenia: where are we and what next? by Arun K. Tiwari, Clement C. Zai, Daniel J. Müller, James L. Kennedy

    Published 2010
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  2. 2
    Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome

    Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome by Julien Barc, François Briec, Sébastien Schmitt, Florence Kyndt, Martine Le Cunff, Estelle Baron, C Vieyres, Frédéric Sacher, Richard Redon, Cédric Le Caignec, Hervé Le Marec, Vincent Probst, Jean‐Jacques Schott

    Published 2010
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  3. 3
    Circulating free DNA as non-invasive diagnostic biomarker for childhood solid tumors

    Circulating free DNA as non-invasive diagnostic biomarker for childhood solid tumors by Sho Kurihara, Yuka Ueda, Yoshiyuki Onitake, Taijiro Sueda, Emi Ohta, Nagisa Morihara, Shoko Hirano, Fumiko Irisuna, Eiso Hiyama

    Published 2015
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  4. 4
    Recurrent RECQL4 Imbalance and Increased Gene Expression Levels Are Associated with Structural Chromosomal Instability in Sporadic Osteosarcoma

    Recurrent RECQL4 Imbalance and Increased Gene Expression Levels Are Associated with Structural Chromosomal Instability in Sporadic Osteosarcoma by Georges Maire, Maisa Yoshimoto, Susan Chilton‐MacNeill, Paul S. Thorner, Maria Zieleńska, Jeremy A. Squire

    Published 2009
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  5. 5
    Capsulation and gene copy number at the cap locus of Haemophilus influenzae type b

    Capsulation and gene copy number at the cap locus of Haemophilus influenzae type b by J. Simon Kroll, E. Richard Moxon

    Published 1988
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  6. 6
    Copy‐number variation in the pathogenesis of autism spectrum disorder

    Copy‐number variation in the pathogenesis of autism spectrum disorder by Emiko Shishido, Branko Aleksić, Norio Ozaki

    Published 2013
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    Revisão
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  7. 7
    Association of <i>FCGR3A</i> and <i>FCGR3B</i> Copy Number Variations With Systemic Lupus Erythematosus and Rheumatoid Arthritis in Taiwanese Patients

    Association of <i>FCGR3A</i> and <i>FCGR3B</i> Copy Number Variations With Systemic Lupus Erythematosus and Rheumatoid Arthritis in Taiwanese Patients by Ji‐Yih Chen, Chin‐Man Wang, Su‐Wei Chang, Ching‐Hui Cheng, Yeong‐Jian Jan Wu, Jing‐Chi Lin, Bing Yang, Huei‐Huang Ho, Jianming Wu

    Published 2014
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  8. 8
    The prognostic value of EGFR overexpression and amplification in Esophageal squamous cell Carcinoma

    The prognostic value of EGFR overexpression and amplification in Esophageal squamous cell Carcinoma by Dongxian Jiang, Xiaojing Li, Hai Wang, Yuan Shi, Chen Xu, Shaohua Lu, Jie Huang, Yifan Xu, Haiying Zeng, Jieakesu Su, Yingyong Hou, Lijie Tan

    Published 2015
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  9. 9
    Concurrent Whole-Genome Haplotyping and Copy-Number Profiling of Single Cells

    Concurrent Whole-Genome Haplotyping and Copy-Number Profiling of Single Cells by Masoud Zamani Esteki, Eftychia Dimitriadou, Ligia Mateiu, Cindy Melotte, Niels van der Aa, Parveen Kumar, Rakhi Das, Koen Theunis, Jie Cheng, Eric Legius, Yves Moreau, Sophie Debrock, Thomas D’Hooghe, Pieter Verdyck, Martine De Rycke, Karen Sermon, Joris Vermeesch, Thierry Voet

    Published 2015
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  10. 10
    Assessment of copy number variations in the brain genome of schizophrenia patients

    Assessment of copy number variations in the brain genome of schizophrenia patients by Miwako Sakai, Yuichiro Watanabe, Toshiyuki Someya, Kazuaki Araki, Masako Shibuya, Kazuhiro Niizato, Kenichi Oshima, Yasuto Kunii, Hirooki Yabe, Junya Matsumoto, Akira Wada, Mizuki Hino, Takeshi Hashimoto, Akitoyo Hishimoto, Noboru Kitamura, Shuji Iritani, Osamu Shirakawa, Kiyoshi Maeda, Akinori Miyashita, Shin‐ichi Niwa, Hitoshi Takahashi, Akiyoshi Kakita, Ryozo Kuwano, Hiroyuki Nawa

    Published 2015
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  11. 11
    The UBC-40 Urothelial Bladder Cancer cell line index: a genomic resource for functional studies

    The UBC-40 Urothelial Bladder Cancer cell line index: a genomic resource for functional studies by Julie Earl, Daniel Rico, Enrique Carrillo de Santa Pau, Benjamín Rodríguez‐Santiago, Marinela Méndez‐Pertuz, Herbert Auer, Gonzalo Goméz-López, H. Barton Grossman, David G. Pisano, Wolfgang A. Schulz, Luis A. Pérez‐Jurado, Alfredo Carrato, Dan Theodorescu, Stephen J. Chanock, Alfonso Valencia, Francisco X. Real

    Published 2015
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  12. 12
    Febrile infection‐related epilepsy syndrome (FIRES) is not caused by <i>SCN1A, POLG, PCDH19</i> mutations or rare copy number variations

    Febrile infection‐related epilepsy syndrome (FIRES) is not caused by <i>SCN1A, POLG, PCDH19</i> mutations or rare copy number variations by Silke Appenzeller, Ingo Helbig, Ulrich Stephani, Martin Häusler, Gerhard Kluger, May Bungeroth, Stefanie H. Müller, Gregor Kuhlenbäumer, Andreas van Baalen

    Published 2012
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  13. 13
    Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes

    Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes by Kacie N. Riley, Lisa M. Catalano, John Bernat, Stacie D. Adams, Donna M. Martin, Seema R. Lalani, Ankita Patel, Rachel D. Burnside, Jeffrey W. Innis, M. Katharine Rudd

    Published 2015
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  14. 14
    A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease

    A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease by Xiaoqing Zhang, Yuejuan Xu, Deyuan Liu, Juan Geng, Chen Sun, Zhengwen Jiang, Qihua Fu, Kun Sun

    Published 2015
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  15. 15
    CONSERTING: integrating copy-number analysis with structural-variation detection

    CONSERTING: integrating copy-number analysis with structural-variation detection by Xiang Chen, Pankaj Gupta, Jianmin Wang, Joy Nakitandwe, Kathryn G. Roberts, James Dalton, Matthew Parker, Samir Patel, Linda Holmfeldt, Debbie Payne, John Easton, Jing Ma, Michael Rusch, Gang Wu, Aman Patel, Suzanne J. Baker, Michael A. Dyer, Sheila Shurtleff, Stephen Espy, Stanley Pounds, James R. Downing, David W. Ellison, Charles G. Mullighan, Jinghui Zhang

    Published 2015
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  16. 16
    Whole‐genome copy number variation analysis in anophthalmia and microphthalmia

    Whole‐genome copy number variation analysis in anophthalmia and microphthalmia by KF Schilter, Linda M. Reis, Adele Schneider, TM Bardakjian, Omar Abdul‐Rahman, BA Kozel, HH Zimmerman, Ulrich Broeckel, EV Semina

    Published 2013
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  17. 17
    Combined Analysis of SNP Array Data Identifies Novel CNV Candidates and Pathways in Ependymoma and Mesothelioma

    Combined Analysis of SNP Array Data Identifies Novel CNV Candidates and Pathways in Ependymoma and Mesothelioma by Gabriel Wajnberg, Benilton S. Carvalho, Carlos Gil Ferreira, Fábio Passetti

    Published 2015
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  18. 18
    Mutational profiles in triple-negative breast cancer defined by ultradeep multigene sequencing show high rates of PI3K pathway alterations and clinically relevant entity subgroup specific differences

    Mutational profiles in triple-negative breast cancer defined by ultradeep multigene sequencing show high rates of PI3K pathway alterations and clinically relevant entity subgroup s... by Mark Kriegsmann, Volker Endris, Thomas Wolf, Nicole Pfarr, Albrecht Stenzinger, Sibylle Loibl, Carsten Denkert, Andreas Schneeweiß, Jan Budczies, Hans‐Peter Sinn, Wilko Weichert

    Published 2014
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  19. 19
    Genomic Copy Number Variations of the Complement Component<i>C4B</i>Gene Are Associated With Chronic Central Serous Chorioretinopathy

    Genomic Copy Number Variations of the Complement Component<i>C4B</i>Gene Are Associated With Chronic Central Serous Chorioretinopathy by Myrte B. Breukink, Rosa L. Schellevis, Camiel J. F. Boon, Sascha Fauser, Carel B. Hoyng, Anneke I. den Hollander, Eiko K. de Jong

    Published 2015
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  20. 20
    Copy number and the stability of 2-micron circle-based artificial plasmids of Saccharomyces cerevisiae

    Copy number and the stability of 2-micron circle-based artificial plasmids of Saccharomyces cerevisiae by A. B. Futcher, B. S. Cox

    Published 1984
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