Výsledky vyhledávání - Heike Fiegler

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  1. 1
    Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays

    Array painting: a method for the rapid analysis of aberrant chromosomes using DNA microarrays Autor Heike Fiegler

    Vydáno 2003
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  2. 2
    Chromatin Architecture of the Human Genome

    Chromatin Architecture of the Human Genome Autor Nick Gilbert, Shelagh Boyle, Heike Fiegler, Kathryn Woodfine, Nigel P. Carter, Wendy A. Bickmore

    Vydáno 2004
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  3. 3
    High resolution array-CGH analysis of single cells

    High resolution array-CGH analysis of single cells Autor Heike Fiegler, Jochen B. Geigl, Sabine Langer, Diane Rigler, Keith Porter, Kristian Unger, Nigel P. Carter, Michael R. Speicher

    Vydáno 2006
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  4. 4
    Germline rates of de novo meiotic deletions and duplications causing several genomic disorders

    Germline rates of de novo meiotic deletions and duplications causing several genomic disorders Autor Daniel J. Turner, Marcos Miretti, Diana Rajan, Heike Fiegler, Nigel P. Carter, Martyn Blayney, Stephan Beck, Matthew E. Hurles

    Vydáno 2007
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  5. 5
    Spreading of mammalian DNA-damage response factors studied by ChIP-chip at damaged telomeres

    Spreading of mammalian DNA-damage response factors studied by ChIP-chip at damaged telomeres Autor Andreas Meier, Heike Fiegler, Purificacı́on Muñoz, Peter Ellis, Diane Rigler, Cordelia Langford, Marı́a A. Blasco, Nigel Carter, Stephen P. Jackson

    Vydáno 2007
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  6. 6
    Sites of Differential DNA Methylation between Placenta and Peripheral Blood

    Sites of Differential DNA Methylation between Placenta and Peripheral Blood Autor Elisavet A. Papageorgiou, Heike Fiegler, Vardhman K. Rakyan, Stephan Beck, Maj Hultén, Klea Lamnissou, Nigel P. Carter, Philippos C. Patsalis

    Vydáno 2009
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  7. 7
    Replication timing of the human genome

    Replication timing of the human genome Autor Kathryn Woodfine, Heike Fiegler, David Beare, John Collins, Owen T McCann, Bryan D. Young, Silvana Debernardi, Richard Mott, Ian Dunham, Nigel P. Carter

    Vydáno 2003
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  8. 8
    Genome-Wide Screening of Genomic Alterations and Their Clinicopathologic Implications in Non–Small Cell Lung Cancers

    Genome-Wide Screening of Genomic Alterations and Their Clinicopathologic Implications in Non–Small Cell Lung Cancers Autor Tae‐Min Kim, Seon‐Hee Yim, Jung‐Sook Lee, Miseon Kwon, Jae-Wook Ryu, Hyun Mi Kang, Heike Fiegler, Nigel P. Carter, Yeun‐Jun Chung

    Vydáno 2005
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  9. 9
    Radial chromatin positioning is shaped by local gene density, not by gene expression

    Radial chromatin positioning is shaped by local gene density, not by gene expression Autor Katrin Küpper, Alexandra C. Kölbl, Dorothee Biener, Sandra Dittrich, Johann von Hase, Tobias Thormeyer, Heike Fiegler, Nigel P. Carter, Michael R. Speicher, Thomas Cremer, Marion Cremer

    Vydáno 2007
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  10. 10
    A Whole-Genome Mouse BAC Microarray With 1-Mb Resolution for Analysis of DNA Copy Number Changes by Array Comparative Genomic Hybridization

    A Whole-Genome Mouse BAC Microarray With 1-Mb Resolution for Analysis of DNA Copy Number Changes by Array Comparative Genomic Hybridization Autor Yeun‐Jun Chung, Jos Jonkers, Hannah Kitson, Heike Fiegler, Sean Humphray, Carol Scott, Sarah Hunt, Yuejin Yu, Ichiko Nishijima, Arno Velds, Henne Holstege, Nigel Carter, Allan Bradley

    Vydáno 2004
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  11. 11
    Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization

    Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization Autor John C. Marioni, Natalie Thorne, Armand Valsesia, Tomas Fitzgerald, Richard Redon, Heike Fiegler, T. Daniel Andrews, Barbara E. Stranger, Andy G. Lynch, Emmanouil T. Dermitzakis, Nigel P. Carter, Simon Tavaré, Matthew E. Hurles

    Vydáno 2007
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  12. 12
    Diet and the evolution of human amylase gene copy number variation

    Diet and the evolution of human amylase gene copy number variation Autor George H. Perry, Nathaniel J. Dominy, Katrina G. Claw, Arthur S. Lee, Heike Fiegler, Richard Redon, John C. Werner, Fernando A. Villanea, Joanna L. Mountain, Rajeev Misra, Nigel P. Carter, Charles Lee, Anne C. Stone

    Vydáno 2007
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  13. 13
    Clinical implication of recurrent copy number alterations in hepatocellular carcinoma and putative oncogenes in recurrent gains on 1q

    Clinical implication of recurrent copy number alterations in hepatocellular carcinoma and putative oncogenes in recurrent gains on 1q Autor Tae‐Min Kim, Seon‐Hee Yim, Seung–Hun Shin, Haidong Xu, Yuchae Jung, C. K. Park, Jong‐Young Choi, Won‐Sang Park, Miseon Kwon, Heike Fiegler, Nigel P. Carter, Mun‐Gan Rhyu, Yeun‐Jun Chung

    Vydáno 2008
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  14. 14
    Guidelines for molecular karyotyping in constitutional genetic diagnosis

    Guidelines for molecular karyotyping in constitutional genetic diagnosis Autor Joris Vermeesch, Heike Fiegler, Nicole de Leeuw, Károly Szuhai, Jacqueline Schoumans, Roberto Ciccone, Frank Speleman, Anita Rauch, Jill Clayton‐Smith, Conny van Ravenswaaij, Damien Sanlaville, Philippos C. Patsalis, Helen V. Firth, Koenraad Devriendt, Orsetta Zuffardi

    Vydáno 2007
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    Revisão
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  15. 15
    Genomic Profiling Identifies Discrete Deletions Associated with Translocations in Glioblastoma Multiforme

    Genomic Profiling Identifies Discrete Deletions Associated with Translocations in Glioblastoma Multiforme Autor Paul Mulholland, Heike Fiegler, Chiara Maria Mazzanti, P.A. Gorman, Peter Sasieni, Julian Adams, T. Alwyn Jones, J. W. Babbage, R Vatcheva, Kouichi Ichimura, Philip East, C. Poullikas, V. Peter Collins, N.P. Carter, Ian Tomlinson, Denise Sheer

    Vydáno 2006
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  16. 16
    A comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGH

    A comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGH Autor Rebecca Roylance, Patricia Gorman, T Papior, Y. Louise Wan, Megan L. Ives, J. E. Vivienne Watson, Collin C. Collins, Noel C. Wortham, Cordelia Langford, Heike Fiegler, N Carter, Cheryl Gillett, Peter Sasieni, S Pinder, A M Hanby, Ian Tomlinson

    Vydáno 2006
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  17. 17
    Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

    Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents Autor Carla Rosenberg, Jeroen Knijnenburg, Egbert Bakker, Angela Maria Vianna‐Morgante, Willem C.R. Sloos, Paulo Alberto Otto, Marjolein Kriek, Kerstin Hansson, Ana Cristina Victorino Krepischi, Heike Fiegler, Nigel P. Carter, Emilia K. Bijlsma, Arie van Haeringen, Károly Szuhai, Hans J. Tanke

    Vydáno 2005
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  18. 18
    An integrated resource for genome-wide identification and analysis of human tissue-specific differentially methylated regions (tDMRs)

    An integrated resource for genome-wide identification and analysis of human tissue-specific differentially methylated regions (tDMRs) Autor Vardhman K. Rakyan, Thomas A. Down, Natalie Thorne, Paul Flicek, Eugene Kulesha, Stefan Gräf, Eleni M. Tomazou, Liselotte Bäckdahl, Nathan Johnson, Marlis Herberth, Kevin Howe, David K. Jackson, Marcos Miretti, Heike Fiegler, John C. Marioni, Ewan Birney, Tim Hubbard, Nigel P. Carter, Simon Tavaré, Stephan Beck

    Vydáno 2008
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  19. 19
    Accurate and reliable high-throughput detection of copy number variation in the human genome

    Accurate and reliable high-throughput detection of copy number variation in the human genome Autor Heike Fiegler, Richard Redon, Dan Andrews, Clare L. Scott, Robert Andrews, C. Carder, Richard Clark, Oliver M. Dovey, Peter J. I. Ellis, Lars Feuk, Lisa French, Paul Hunt, Dimitrios Rafail Kalaitzopoulos, James R. Larkin, Lyndal Montgomery, George H. Perry, Bob Plumb, Keith Porter, Rachel E. Rigby, Diane Rigler, Armand Valsesia, Cordelia Langford, Sean Humphray, Stephen W. Scherer, Charles Lee, Matthew E. Hurles, Nigel P. Carter

    Vydáno 2006
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  20. 20
    Global variation in copy number in the human genome

    Global variation in copy number in the human genome Autor Richard Redon, Shumpei Ishikawa, Karen Fitch, Lars Feuk, George H. Perry, T. Daniel Andrews, Heike Fiegler, Michael H. Shapero, Andrew R. Carson, Wei‐Wen Chen, Eun Kyung Cho, Stephanie Dallaire, Jennifer L. Freeman, Juan R. González, Mónica Gratacòs, Jing Huang, Dimitrios Rafail Kalaitzopoulos, Daisuke Komura, Jeffrey R. MacDonald, Christian R. Marshall, Rui Mei, Lyndal Montgomery, Kunihiro Nishimura, K. Okamura, Fan Shen, Martin J. Somerville, Joëlle Tchinda, Armand Valsesia, Cara Woodwark, Fengtang Yang, Junjun Zhang, Tatiana Zerjal, Jane Zhang, Lluı́s Armengol, Donald F. Conrad, Xavier Estivill, Chris Tyler‐Smith, Nigel P. Carter, Hiroyuki Aburatani, Charles Lee, Keith Jones, Stephen W. Scherer, Matthew E. Hurles

    Vydáno 2006
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