Search Results - Nigel P. Carter

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  1. 1
    Methods and strategies for analyzing copy number variation using DNA microarrays

    Methods and strategies for analyzing copy number variation using DNA microarrays by Nigel P. Carter

    Published 2007
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  2. 2
    The Role of DNA Copy Number Variation in Schizophrenia

    The Role of DNA Copy Number Variation in Schizophrenia by Gloria W.C. Tam, Richard Redon, Nigel P. Carter, Seth G. N. Grant

    Published 2009
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  3. 3
    Chromatin Architecture of the Human Genome

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

    Published 2004
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  4. 4
    Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21

    Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21 by Elisavet A. Papageorgiou, Alex Karagrigoriou, Evdokia Tsaliki, Voula Velissariou, Nigel P. Carter, Philippos C. Patsalis

    Published 2011
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  5. 5
    High resolution array-CGH analysis of single cells

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

    Published 2006
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  6. 6
    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 by Daniel J. Turner, Marcos Miretti, Diana Rajan, Heike Fiegler, Nigel P. Carter, Martyn Blayney, Stephan Beck, Matthew E. Hurles

    Published 2007
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  7. 7
    Challenges and standards in integrating surveys of structural variation

    Challenges and standards in integrating surveys of structural variation by Stephen W. Scherer, Charles Lee, Ewan Birney, David Altshuler, Evan E. Eichler, Nigel P. Carter, Matthew E. Hurles, Lars Feuk

    Published 2007
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  8. 8
    Sites of Differential DNA Methylation between Placenta and Peripheral Blood

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

    Published 2009
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  9. 9
    Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndrome

    Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndrome by Richard Redon, Geneviève Baujat, Damien Sanlaville, Martine Le Merrer, Michel Vekemans, Arnold Münnich, Nigel P. Carter, Valérie Cormier‐Daire, Laurence Colleaux

    Published 2006
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  10. 10
    Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal Cohort

    Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal Cohort by Júlia Baptista, Catherine Mercer, Elena Prigmore, Susan Gribble, Nigel P. Carter, Viv Maloney, N. Simon Thomas, Patricia A. Jacobs, John A. Crolla

    Published 2008
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  11. 11
    Replication timing of the human genome

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

    Published 2003
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  12. 12
    Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.

    Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics. by Nigel P. Carter, M.A. Ferguson‐Smith, M T Perryman, H. Telenius, Adele Pelmear, M. Leversha, Mary Glancy, Stephen Wood, K Cook, H M Dyson

    Published 1992
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  13. 13
    Mutations in TCF4, Encoding a Class I Basic Helix-Loop-Helix Transcription Factor, Are Responsible for Pitt-Hopkins Syndrome, a Severe Epileptic Encephalopathy Associated with Autonomic Dysfunction

    Mutations in TCF4, Encoding a Class I Basic Helix-Loop-Helix Transcription Factor, Are Responsible for Pitt-Hopkins Syndrome, a Severe Epileptic Encephalopathy Associated with Auto... by Jeanne Amiel, Marlène Rio, Loïc de Pontual, Richard Redon, Valérie Malan, Nathalie Boddaert, Perrine Plouin, Nigel P. Carter, Stanislas Lyonnet, Arnold Münnich, Laurence Colleaux

    Published 2007
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  14. 14
    DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

    DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources by Helen V. Firth, Shola M. Richards, A. Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, Roger Pettett, Nigel P. Carter

    Published 2009
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  15. 15
    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 by 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

    Published 2005
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  16. 16
    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 by 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

    Published 2007
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  17. 17
    Adaptive Evolution of UGT2B17 Copy-Number Variation

    Adaptive Evolution of UGT2B17 Copy-Number Variation by Yali Xue, Donglin Sun, Allan Daly, Fengtang Yang, Xue Zhou, Mengyao Zhao, Ni Huang, Tatiana Zerjal, Charles Lee, Nigel P. Carter, Matthew E. Hurles, Chris Tyler‐Smith

    Published 2008
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  18. 18
    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 by 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

    Published 2007
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  19. 19
    Copy number variation: New insights in genome diversity

    Copy number variation: New insights in genome diversity by Jennifer L. Freeman, George H. Perry, Lars Feuk, Richard Redon, Steven A. McCarroll, David Altshuler, Hiroyuki Aburatani, Keith Jones, Chris Tyler‐Smith, Matthew E. Hurles, Nigel P. Carter, Stephen W. Scherer, Charles Lee

    Published 2006
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  20. 20
    Diet and the evolution of human amylase gene copy number variation

    Diet and the evolution of human amylase gene copy number variation by 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

    Published 2007
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