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Robert Lyle

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Anatomy

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Mouse

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Robert Lyle; Frédérique Béna; Sarantis Gagos; Corinne Gehrig; Gipsy Lopez; Albert Schinzel; James Lespinasse; Armand Bottani; Sophie Dahoun; Laurence Taine; Martine Doco-Fenzy; Pascale Cornillet-Lefèbvre; Anna Pelet; Stanislas Lyonnet; Annick Toutain; Laurence Colleaux; Jürgen Horst; Ingo Kennerknecht; Nobuaki Wakamatsu; Maria Descartes; Judy C Franklin; Lina Florentin-Arar; Sophia Kitsiou-Tzeli; Emilie Aït Yahya-Graison; Maher Costantine; Pierre-Marie Sinet; Jean M Delabar; Stylianos E Antonarakis
Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21.
Marc Friedli; Sergey Nikolaev; Robert Lyle; Mélanie Arcangeli; Denis Duboule; François Spitz; Stylianos E Antonarakis
Characterization of mouse Dactylaplasia mutations: a model for human ectrodactyly SHFM3.
Catia Attanasio; Alexandre Reymond; Richard Humbert; Robert Lyle; Michael S Kuehn; Shane Neph; Peter J Sabo; Jeff Goldy; Molly Weaver; Andrew Haydock; Kristin Lee; Michael Dorschner; Emmanouil T Dermitzakis; Stylianos E Antonarakis; John A Stamatoyannopoulos
Assaying the regulatory potential of mammalian conserved non-coding sequences in human cells.

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All Publications

2009: Robert Lyle; Frédérique Béna; Sarantis Gagos; Corinne Gehrig; Gipsy Lopez; Albert Schinzel; James Lespinasse; Armand Bottani; Sophie Dahoun; Laurence Taine; Martine Doco-Fenzy; Pascale Cornillet-Lefèbvre; Anna Pelet; Stanislas Lyonnet; Annick Toutain; Laurence Colleaux; Jürgen Horst; Ingo Kennerknecht; Nobuaki Wakamatsu; Maria Descartes; Judy C Franklin; Lina Florentin-Arar; Sophia Kitsiou-Tzeli; Emilie Aït Yahya-Graison; Maher Costantine; Pierre-Marie Sinet; Jean M Delabar; Stylianos E Antonarakis
Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21.
European journal of human genetics : EJHG 2009;17(4):454-66.
2008: Marc Friedli; Sergey Nikolaev; Robert Lyle; Mélanie Arcangeli; Denis Duboule; François Spitz; Stylianos E Antonarakis
Characterization of mouse Dactylaplasia mutations: a model for human ectrodactyly SHFM3.
Mammalian genome : official journal of the International Mammalian Genome Society 2008;19(4):272-8.
2008: Catia Attanasio; Alexandre Reymond; Richard Humbert; Robert Lyle; Michael S Kuehn; Shane Neph; Peter J Sabo; Jeff Goldy; Molly Weaver; Andrew Haydock; Kristin Lee; Michael Dorschner; Emmanouil T Dermitzakis; Stylianos E Antonarakis; John A Stamatoyannopoulos
Assaying the regulatory potential of mammalian conserved non-coding sequences in human cells.
Genome biology 2008;9(12):R168.
2007: Robert Lyle; Paola Prandini; Kazutoyo Osoegawa; Boudewijn ten Hallers; Sean Humphray; Baoli Zhu; Eduardo Eyras; Robert Castelo; Christine P Bird; Sarantis Gagos; Carol Scott; Antony Cox; Samuel Deutsch; Catherine Ucla; Marc Cruts; Sophie Dahoun; Xinwei She; Frederique Bena; Sheng-Yue Wang; Christine Van Broeckhoven; Evan E Eichler; Roderic Guigo; Jane Rogers; Pieter J de Jong; Alexandre Reymond; Stylianos E Antonarakis
Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21.
Genome research 2007;17(11):1690-6.
2007: Paola Prandini; Samuel Deutsch; Robert Lyle; Maryline Gagnebin; Celine Delucinge Vivier; Mauro Delorenzi; Corinne Gehrig; Patrick Descombes; Stephanie L Sherman; Franca Dagna Bricarelli; Chiara Baldo; Antonio Novelli; Bruno Dallapiccola; Stylianos E Antonarakis
Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance.
American journal of human genetics 2007;81(2):252-63.
2006: Giuseppe Merla; Cédric Howald; Charlotte N Henrichsen; Robert Lyle; Carine Wyss; Marie-Thérèse Zabot; Stylianos E Antonarakis; Alexandre Reymond
Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes.
American journal of human genetics 2006;79(2):332-41.
2006: David B Everman; Chad T Morgan; Robert Lyle; Mary E Laughridge; Michael Bamshad; Katie Clarkson; Randall Colby; Fiorella Gurrieri; A Micheil Innes; Jacquelyn Roberson; C T R M Schrander-Stumpel; Hans van Bokhoven; Stylianos E Antonarakis; Charles E Schwartz
Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation.
American journal of medical genetics. Part A 2006;140(13):1375-83.
2006: Robert Lyle; Uppala Radhakrishna; Jean-Louis Blouin; Sarantis Gagos; David B Everman; Corinne Gehrig; Celia Delozier-Blanchet; Jitendra V Solanki; Uday C Patel; Swapan K Nath; Fiorella Gurrieri; Giovanni Neri; Charles E Schwartz; Stylianos E Antonarakis
Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region.
American journal of medical genetics. Part A 2006;140(13):1384-95.
2006: Cédric Howald; Giuseppe Merla; M C Digilio; Styliani Amenta; Robert Lyle; Samuel Deutsch; Urmila Choudhury; Armand Bottani; Stylianos E Antonarakis; Helen Fryssira; B Dallapiccola; Alexandre Reymond
Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletions.
Journal of medical genetics 2006;43(3):266-73.
2005: Barbara E Stranger; Matthew Forrest; andrew clark; Mark J Minichiello; Samuel Deutsch; Robert Lyle; Sarah Hunt; Brenda Kahl; Stylianos E Antonarakis; Simon Tavaré; Panos Deloukas; Emmanouil T Dermitzakis
Genome-wide associations of gene expression variation in humans.
PLoS genetics 2005;1(6):e78.
2005: Samuel Deutsch; Robert Lyle; Emmanouil T Dermitzakis; Homa Attar; Lakshman Subrahmanyan; Corinne Gehrig; Leila Parand; Maryline Gagnebin; Jacques Rougemont; Victor Jongeneel; Stylianos E Antonarakis
Gene expression variation and expression quantitative trait mapping of human chromosome 21 genes.
Human molecular genetics 2005;14(23):3741-9.
2005: Marie Wattenhofer; Alexandre Reymond; Véronique Falciola; Anne Charollais; Dorothée Caille; Christelle Borel; Robert Lyle; Xavier Estivill; Michael B Petersen; Paolo Meda; Stylianos E Antonarakis
Different mechanisms preclude mutant CLDN14 proteins from forming tight junctions in vitro.
Human mutation 2005;25(6):543-9.
2005: Siv Fokstuen; Jean-Louis Blouin; Robert Lyle; René Lerch; M Beghetti; François Mach; Juan Sztajzel; Stylianos E Antonarakis; U Sigwart
[The contribution of molecular genetics to clinical cardiology: the example of hypertrophic cardiomyopathy].
Revue médicale suisse 2005;1(21):1448, 1450, 1452-3.
2004: Stylianos E Antonarakis; Robert Lyle; Emmanouil T Dermitzakis; Alexandre Reymond; Samuel Deutsch
Chromosome 21 and down syndrome: from genomics to pathophysiology.
Nature reviews. Genetics 2004;5(10):725-38.
2004: Robert Lyle; Corinne Gehrig; Charlotte Neergaard-Henrichsen; Samuel Deutsch; Stylianos E Antonarakis
Gene expression from the aneuploid chromosome in a trisomy mouse model of down syndrome.
Genome research 2004;14(7):1268-74.
2003: Caroline Tapparel; Alexandre Reymond; Christophe Girardet; Louis Guillou; Robert Lyle; Christine Lamon; Pierre Hutter; Stylianos E Antonarakis
The TPTE gene family: cellular expression, subcellular localization and alternative splicing.
Gene 2003;323():189-99.
2003: Xavier de Mollerat du Jeu; Fiorella Gurrieri; Chad T Morgan; Eugenio Sangiorgi; David B Everman; Paola Gaspari; Jeanne Amiel; Michael Bamshad; Robert Lyle; Jean-Louis Blouin; Judith E Allanson; Bernard Le Marec; Melba Wilson; Nancy E Braverman; Uppala Radhakrishna; Celia Delozier-Blanchet; Albert G Abbott; Vincent Elghouzzi; Stylianos E Antonarakis; Roger E Stevenson; Arnold Munnich; Giovanni Neri; Charles E Schwartz
A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24.
Human molecular genetics 2003;12(16):1959-71.
2003: Roderic Guigo; Emmanouil T Dermitzakis; Pankaj Agarwal; Chris P Ponting; Genís Parra; Alexandre Reymond; Josep F Abril; Evan Keibler; Robert Lyle; Catherine Ucla; Stylianos E Antonarakis; Michael R Brent
Comparison of mouse and human genomes followed by experimental verification yields an estimated 1,019 additional genes.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(3):1140-5.
2003: Stylianos Antonarakis; Alexandre Reymond; Robert Lyle; Samuel Deutsch; Emmanouil T Dermitzakis
Chromosome 21 and Down syndrome: the post-sequence era.
Cold Spring Harbor symposia on quantitative biology 2003;68():425-30.
2002: Alexandre Reymond; Valeria Marigo; Murat B Yaylaoglu; Antonio Leoni; Catherine Ucla; Nathalie Scamuffa; Cristina Caccioppoli; Emmanouil T Dermitzakis; Robert Lyle; Sandro Banfi; Gregor Eichele; Stylianos E Antonarakis; Andrea Ballabio
Human chromosome 21 gene expression atlas in the mouse.
Nature 2002;420(6915):582-6.
2002: Emmanouil T Dermitzakis; Alexandre Reymond; Robert Lyle; Nathalie Scamuffa; Catherine Ucla; Samuel Deutsch; Brian J Stevenson; Volker Flegel; Philipp Bucher; Victor Jongeneel; Stylianos E Antonarakis
Numerous potentially functional but non-genic conserved sequences on human chromosome 21.
Nature 2002;420(6915):578-82.
2002: Alexandre Reymond; Anamaria A Camargo; Samuel Deutsch; Brian J Stevenson; Raphael B Parmigiani; Catherine Ucla; Fabiana Bettoni; Colette Rossier; Robert Lyle; Michel Guipponi; Sandro de Souza; Christian Iseli; Victor Jongeneel; Philipp Bucher; Andrew J G Simpson; Stylianos E Antonarakis
Nineteen additional unpredicted transcripts from human chromosome 21.
Genomics 2002;79(6):824-32.
2002: Stylianos E Antonarakis; Robert Lyle; Samuel Deutsch; Alexandre Reymond
Chromosome 21: a small land of fascinating disorders with unknown pathophysiology.
The International journal of developmental biology 2002;46(1):89-96.
2001: Michel Guipponi; Caroline Tapparel; O Jousson; Nathalie Scamuffa; Christophe Mas; Colette Rossier; Pierre Hutter; Paolo Meda; Robert Lyle; Alexandre Reymond; Stylianos E Antonarakis
The murine orthologue of the Golgi-localized TPTE protein provides clues to the evolutionary history of the human TPTE gene family.
Human genetics 2001;109(6):569-75.
2001: Alexandre Reymond; Marc Friedli; Charlotte N Henrichsen; F Chapot; Samuel Deutsch; Catherine Ucla; Colette Rossier; Robert Lyle; Michel Guipponi; Stylianos E Antonarakis
From PREDs and open reading frames to cDNA isolation: revisiting the human chromosome 21 transcription map.
Genomics 2001;78(1-2):46-54.
2001: Stylianos E Antonarakis; Robert Lyle; R Chrast; Hamish Scott
Differential gene expression studies to explore the molecular pathophysiology of Down syndrome.
Brain research. Brain research reviews 2001;36(2-3):265-74.
2001: Marie Wattenhofer; Kazunori Shibuya; Jun Kudoh; Robert Lyle; Joäelle Michaud; Colette Rossier; K Kawasaki; Shuichi Asakawa; Shinsei Minoshima; A Berry; Batsheva Bonne-Tamir; Nobuyoshi Shimizu; Stylianos E Antonarakis; Hamish Scott
Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domains.
Human genetics 2001;108(2):140-7.