SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Yongjun Luo, Yuxiao Wang, Hongxiang Lu, Yuqi Gao, ‘Ome’ on the range: update on high-altitude acclimatization/adaptation and disease, Mol. BioSyst., 2014, 10, 11, 2748

    CrossRef

  2. 2
    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, Association of FCGR3A and FCGR3B Copy Number Variations With Systemic Lupus Erythematosus and Rheumatoid Arthritis in Taiwanese Patients, Arthritis & Rheumatology, 2014, 66, 11
  3. 3
    Ryosuke Kaneko, Manabu Abe, Takahiro Hirabayashi, Arikuni Uchimura, Kenji Sakimura, Yuchio Yanagawa, Takeshi Yagi, Expansion of stochastic expression repertoire by tandem duplication in mouse Protocadherin-α cluster, Scientific Reports, 2014, 4, 6263

    CrossRef

  4. 4
    Tomasz K. Wojdacz, Matteo Bottai, Marie Vahter, Karin Broberg, Exposure to arsenic and intra-chromosomal instability in blood, Metallomics, 2014, 6, 8, 1387

    CrossRef

  5. 5
    Rachael Thomas, Luke Borst, Daniel Rotroff, Alison Motsinger-Reif, Kerstin Lindblad-Toh, Jaime F. Modiano, Matthew Breen, Genomic profiling reveals extensive heterogeneity in somatic DNA copy number aberrations of canine hemangiosarcoma, Chromosome Research, 2014, 22, 3, 305

    CrossRef

  6. 6
    Zsolt Ronai, Reka Kovacs-Nagy, Eszter Szantai, Zsuzsanna Elek, Maria Sasvari-Szekely, Gabor Faludi, Judit Benkovits, Janos M. Rethelyi, Anna Szekely, Glycogen synthase kinase 3 beta gene structural variants as possible risk factors of bipolar depression, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 2014, 165, 3
  7. 7
    James R. Iben, Richard J. Maraia, tRNA gene copy number variation in humans, Gene, 2014, 536, 2, 376

    CrossRef

  8. 8
    Satoko Yamamoto, Mutsuko Yamamoto-Ibusuki, Yutaka Yamamoto, Saori Fujiwara, Hirotaka Iwase, A comprehensive analysis of Aurora A; transcript levels are the most reliable in association with proliferation and prognosis in breast cancer, BMC Cancer, 2013, 13, 1, 217

    CrossRef

  9. 9
    Xiao-Yun Hu, Xu-Ming Bai, Xue Qiao, Ya-Qun Zhu, Copy number variation at 6q13 is associated with lung cancer risk in a Han Chinese population, Experimental Lung Research, 2013, 39, 10, 427

    CrossRef

  10. 10
    Wei Shen, Yi Gu, Rui Zhu, Lan Zhang, Jiwei Zhang, Chunmei Ying, Copy number variations of the F8 gene are associated with venous thromboembolism, Blood Cells, Molecules, and Diseases, 2013, 50, 4, 259

    CrossRef

  11. 11
    Yutaka Suehiro, Takae Okada, Naoya Shikamoto, Yibo Zhan, Kohei Sakai, Naoko Okayama, Mitsuaki Nishioka, Tomoko Furuya, Atsunori Oga, Shigeto Kawauchi, Noriko Maeda, Michiko Tamesa, Yukiko Nagashima, Shigeru Yamamoto, Masaaki Oka, Yuji Hinoda, Kohsuke Sasaki, Germline copy number variations associated with breast cancer susceptibility in a Japanese population, Tumor Biology, 2013, 34, 2, 947

    CrossRef

  12. 12
    Maria Poptsova, Samprit Banerjee, Omer Gokcumen, Mark A Rubin, Francesca Demichelis, Impact of constitutional copy number variants on biological pathway evolution, BMC Evolutionary Biology, 2013, 13, 1, 19

    CrossRef

  13. 13
    Anne Marie Minihane, The genetic contribution to disease risk and variability in response to diet: where is the hidden heritability?, Proceedings of the Nutrition Society, 2013, 72, 01, 40

    CrossRef

  14. 14
    Hoh BoonPeng, Khalid Yusoff, The utility of copy number variation (CNV) in studies of hypertension-related left ventricular hypertrophy (LVH): rationale, potential and challenges, Molecular Cytogenetics, 2013, 6, 1, 8

    CrossRef

  15. 15
    Lisa J. Martin, D. Woodrow Benson, Genomic and Personalized Medicine, 2013,

    CrossRef

  16. 16
    Stylianos E. Antonarakis, David N. Cooper, Emery and Rimoin's Principles and Practice of Medical Genetics, 2013,

    CrossRef

  17. 17
    Tie-Lin Yang, Yan Guo, Christopher J. Papasian, Hong-Wen Deng, Genetics of Bone Biology and Skeletal Disease, 2013,

    CrossRef

  18. 18
    HE Yu, K Hawash, J Picker, J Stoler, D Urion, B-L Wu, Y Shen, A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism, Clinical Genetics, 2012, 81, 3
  19. 19
    Xinmin Li, Jian Zhou, Shareef A. Nahas, Haolei Wan, Hailiang Hu, Richard A. Gatti, Common copy number variations in fifty radiosensitive cell lines, Genomics, 2012, 99, 2, 96

    CrossRef

  20. 20
    Janusz Blasiak, Ewelina Synowiec, Antero Salminen, Kai Kaarniranta, Genetic Variability in DNA Repair Proteins in Age-Related Macular Degeneration, International Journal of Molecular Sciences, 2012, 13, 12, 13378

    CrossRef

  21. 21
    Linlu Zhao, Elizabeth W Triche, Kyle M Walsh, Michael B Bracken, Audrey F Saftlas, Josephine Hoh, Andrew T Dewan, Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients, BMC Pregnancy and Childbirth, 2012, 12, 1, 61

    CrossRef

  22. 22
    Sung-Wook Jang, Camila Lopez-Anido, Ryan MacArthur, John Svaren, James Inglese, Identification of Drug Modulators Targeting Gene-Dosage Disease CMT1A, ACS Chemical Biology, 2012, 7, 7, 1205

    CrossRef

  23. 23
    Suhani H Almal, Harish Padh, Implications of gene copy-number variation in health and diseases, Journal of Human Genetics, 2012, 57, 1, 6

    CrossRef

  24. 24
    Christoph Standfuß, Heike Pospisil, Andreas Klein, SNP microarray analyses reveal copy number alterations and progressive genome reorganization during tumor development in SVT/t driven mice breast cancer, BMC Cancer, 2012, 12, 1, 380

    CrossRef

  25. 25
    Gerhard Meisenberg, William H. Simmons, Principles of Medical Biochemistry, 2012,

    CrossRef

  26. 26
    Brent L. Fogel, Daniel H. Geschwind, Neurology in Clinical Practice, 2012,

    CrossRef

  27. 27
    Jinho Yoo, In Cheol Ha, Gyu Tae Chang, Kwang Su Jung, Kiejung Park, Yangseok Kim, CNVAS: Copy Number Variation Analysis System — The analysis tool for genomic alteration with a powerful visualization module, BioChip Journal, 2011, 5, 3, 265

    CrossRef

  28. 28
    Ke-Da Yu, Qi Fang, Zhi-Ming Shao, Combining accurate genetic and clinical information in breast cancer risk model, Breast Cancer Research and Treatment, 2011, 128, 1, 283

    CrossRef

  29. 29
    Minhyeok Lee, Yeiwon Lee, Hyun-Jung Cho, Jeeyoung Hong, Sun-Jung Kwon, Chang-Gyo Park, Hoi-Young Lee, Ji-Woong Son, Jaeku Kang, Copy number variations of chromosome 17p13.1 might be linked to high risk of lung cancer in heavy smokers, Molecular Biology Reports, 2011, 38, 8, 5211

    CrossRef

  30. 30
    Kosuke Yoshihara, Atsushi Tajima, Sosuke Adachi, Jinhua Quan, Masayuki Sekine, Hiroaki Kase, Tetsuro Yahata, Ituro Inoue, Kenichi Tanaka, Germline copy number variations in BRCA1-associated ovarian cancer patients, Genes, Chromosomes and Cancer, 2011, 50, 3
  31. 31
    Peifen Fu, Mutsuko Ibusuki, Yutaka Yamamoto, Mitsuhiro Hayashi, Keiichi Murakami, Shusen Zheng, Hirotaka Iwase, Insulin-like growth factor-1 receptor gene expression is associated with survival in breast cancer: a comprehensive analysis of gene copy number, mRNA and protein expression, Breast Cancer Research and Treatment, 2011, 130, 1, 307

    CrossRef

  32. 32
    Evan Charney, Biology and Politics, 2011,

    CrossRef

  33. 33
    Tesfaye M. Baye, Lisa J. Martin, Gurjit K. Khurana Hershey, Application of genetic/genomic approaches to allergic disorders, Journal of Allergy and Clinical Immunology, 2010, 126, 3, 425

    CrossRef

  34. You have free access to this content34
    Vijayalakshmi Varma, Carolyn Wise, Jim Kaput, Carbohydrate metabolic pathway genes associated with quantitative trait loci (QTL) for obesity and type 2 diabetes: Identification by data mining, Biotechnology Journal, 2010, 5, 9
  35. 35
    Christine Schwienbacher, Alessandro De Grandi, Christian Fuchsberger, Maurizio F. Facheris, Mirija Svaldi, Matthias Wjst, Peter P. Pramstaller, Andrew A. Hicks, Copy number variation and association over T-cell receptor genes—influence of DNA source, Immunogenetics, 2010, 62, 8, 561

    CrossRef

  36. You have free access to this content36
    David N. Cooper, Jian-Min Chen, Edward V. Ball, Katy Howells, Matthew Mort, Andrew D. Phillips, Nadia Chuzhanova, Michael Krawczak, Hildegard Kehrer-Sawatzki, Peter D. Stenson, Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics, Human Mutation, 2010, 31, 6
  37. 37
    Richarda M Voer, Ramprasath Venkatachalam, Ad Geurts Kessel, Roland P Kuiper, Germline Copy Number Variation and Cancer Risk, eLS,
  38. 38
    Amanda Gonçalves Silva, Tatiane Cristina Rodrigues, Peter Lees Pearson, Carla Rosenberg, Ana Cristina Victorino Krepischi, Germline Genomic Copy Number Variation Contribution to Cancer Predisposition, eLS,