Papers authored by Richard Redon
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Marc Hulsman ,
Camille Charbonnier,
Benjamin Grenier-Boley,
Olivier Quenez ,
Detelina Grozeva ,
Jeroen G. J. van Rooij,
Rebecca Sims ,
Shahzad Ahmad ,
Najaf Amin ,
Penny J. Norsworthy ,
Oriol Dols-Icardo ,
Holger Hummerich,
Amit Kawalia,
Philippe Amouyel
and 92 other authors
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Todor Arsov,
David A. Wallace,
Helene Halkjær Jensen ,
Mette Nyegaard ,
Lia Crotti ,
Marcin Adamski,
Yafei Zhang,
Matt A. Field ,
Vicki Athanasopoulos ,
Isabelle Baró ,
Bárbara B. Ribeiro de Oliveira-Mendes ,
Richard Redon ,
Flavien Charpentier ,
Hariharan Raju
and 12 other authors
Infanticide vs. inherited cardiac arrhythmias
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Gasnat Shaboodien,
Darren T. Houniet,
Nonhlanhla P. Khumalo,
Chantal Bou-Hanna,
Nathalie Bodak,
S. Kuery,
Valérie Cormier-Daire ,
Albert David,
Elise Glen,
Dominique Figarella-Branger,
Laurence Faivre ,
Arnold Munnich,
Antoine Hamel
and 17 other authors
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Martien Am Groenen
Large scale variation in DNA copy number in chicken breeds
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Pascal Chavernac,
Juan E. Sandoval,
Philippe Mabo,
Richard Redon ,
Jean-Jacques Schott,
Hervé Le Marec,
Hervé Le Marec,
Michel Haissaguerre
and 1 other authors
Identification of Large Families in Early Repolarization Syndrome
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Richard Redon
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Richard Redon
and 2 other authors
Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis
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aCGH.Spline--an R package for aCGH dye bias normalization
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Cédric Le Caignec,
Cédric Le Caignec,
Hervé Le Marec,
Vincent Probst,
Jean-Jacques Schott
Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome
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Debra Day-Salvatore,
Antoine Hamel,
Karolina A. Siwicka,
Maria Bitner-Glindzicz,
Dominique Heymann,
Lena Kjellén,
Cornelia Kraus,
Jules G. Leroy,
Geert R. Mortier ,
Anita Rauch,
Alain Verloes,
Albert David
and 3 other authors
Mesomelia-Synostoses Syndrome Results from Deletion of SULF1 and SLCO5A1 Genes at 8q13
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Karen E. Strathdee,
Mike D. R. Croning,
Mary P. Malloy,
Walter J. Muir,
Ben S. Pickard,
Ian J. Deary,
Douglas H. R. Blackwood,
Nigel P. Carter,
Seth G. N. Grant
Confirmed rare copy number variants implicate novel genes in schizophrenia
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Katherine M. Dominy,
Michiaki Kubo,
Cathryn M. Lewis,
Sheila A. Fisher,
Richard Redon ,
Ni Huang,
Barbara E. Stranger,
Katarzyna Blaszczyk,
Barry Hudspith,
Gareth Parkes,
Naoya Hosono,
Keiko Yamazaki,
Clive M. Onnie,
Alastair Forbes
and 7 other authors
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Chris Yau,
McArdle Wl,
Mark Walker,
Neil M. Walker,
Chris Wallace,
Margaret Warren-Perry,
Nicholas A. Watkins,
John Webster,
Michael N. Weedon,
Anthony G. Wilson,
Matthew Woodburn,
Bp Paul Wordsworth,
Allan H. Young,
Eleftheria Zeggini
and 302 other authors
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Nigel P. Carter,
Seth G. N. Grant
The Role of DNA Copy Number Variation in Schizophrenia
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Lars Feuk,
Omer Gokcumen,
Yujun Zhang,
T. Daniel Andrews,
Jan Aerts,
T. Daniel Andrews,
Chris Barnes,
Peter Campbell,
Tomas Fitzgerald,
Min Hu,
Chun Hwa Ihm,
Kati Kristiansson
and 17 other authors
Origins and functional impact of copy number variation in the human genome
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Nigel P. Carter
Comparative genomic hybridization: microarray design and data interpretation.
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Tomas Fitzgerald,
Nigel P. Carter
Comparative genomic hybridization: DNA labeling, hybridization and detection.
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Diane Rigler,
Nigel P. Carter
Comparative genomic hybridization: DNA preparation for microarray fabrication.
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