Lyle R - Search Results

1

Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of events.

Dahoun S, Gagos S, Gagnebin M, Gehrig C, Burgi C, Simon F, Vieux C, Extermann P, Lyle R, Morris MA, Antonarakis SE, Béna F, Blouin JL. Dahoun S, et al. Among authors: lyle r. Am J Med Genet A. 2008 Aug 15;146A(16):2086-93. doi: 10.1002/ajmg.a.32431. Am J Med Genet A. 2008. PMID: 18627064

2

Chromosome 21: a small land of fascinating disorders with unknown pathophysiology.

Antonarakis SE, Lyle R, Deutsch S, Reymond A. Antonarakis SE, et al. Among authors: lyle r. Int J Dev Biol. 2002 Jan;46(1):89-96. Int J Dev Biol. 2002. PMID: 11902692 Review.

3

Gene expression from the aneuploid chromosome in a trisomy mouse model of down syndrome.

Lyle R, Gehrig C, Neergaard-Henrichsen C, Deutsch S, Antonarakis SE. Lyle R, et al. Genome Res. 2004 Jul;14(7):1268-74. doi: 10.1101/gr.2090904. Genome Res. 2004. PMID: 15231743 Free PMC article.

4

Gene expression variation and expression quantitative trait mapping of human chromosome 21 genes.

Deutsch S, Lyle R, Dermitzakis ET, Attar H, Subrahmanyan L, Gehrig C, Parand L, Gagnebin M, Rougemont J, Jongeneel CV, Antonarakis SE. Deutsch S, et al. Among authors: lyle r. Hum Mol Genet. 2005 Dec 1;14(23):3741-9. doi: 10.1093/hmg/ddi404. Epub 2005 Oct 26. Hum Mol Genet. 2005. PMID: 16251198

5

Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region.

Lyle R, Radhakrishna U, Blouin JL, Gagos S, Everman DB, Gehrig C, Delozier-Blanchet C, Solanki JV, Patel UC, Nath SK, Gurrieri F, Neri G, Schwartz CE, Antonarakis SE. Lyle R, et al. Am J Med Genet A. 2006 Jul 1;140(13):1384-95. doi: 10.1002/ajmg.a.31247. Am J Med Genet A. 2006. PMID: 16691619

6

Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance.

Prandini P, Deutsch S, Lyle R, Gagnebin M, Delucinge Vivier C, Delorenzi M, Gehrig C, Descombes P, Sherman S, Dagna Bricarelli F, Baldo C, Novelli A, Dallapiccola B, Antonarakis SE. Prandini P, et al. Among authors: lyle r. Am J Hum Genet. 2007 Aug;81(2):252-63. doi: 10.1086/519248. Epub 2007 Jun 20. Am J Hum Genet. 2007. PMID: 17668376 Free PMC article.

7

Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21.

Lyle R, Béna F, Gagos S, Gehrig C, Lopez G, Schinzel A, Lespinasse J, Bottani A, Dahoun S, Taine L, Doco-Fenzy M, Cornillet-Lefèbvre P, Pelet A, Lyonnet S, Toutain A, Colleaux L, Horst J, Kennerknecht I, Wakamatsu N, Descartes M, Franklin JC, Florentin-Arar L, Kitsiou S, Aït Yahya-Graison E, Costantine M, Sinet PM, Delabar JM, Antonarakis SE. Lyle R, et al. Eur J Hum Genet. 2009 Apr;17(4):454-66. doi: 10.1038/ejhg.2008.214. Epub 2008 Nov 12. Eur J Hum Genet. 2009. PMID: 19002211 Free PMC article.

8

Chromosome 21 and down syndrome: from genomics to pathophysiology.

Antonarakis SE, Lyle R, Dermitzakis ET, Reymond A, Deutsch S. Antonarakis SE, et al. Among authors: lyle r. Nat Rev Genet. 2004 Oct;5(10):725-38. doi: 10.1038/nrg1448. Nat Rev Genet. 2004. PMID: 15510164 Review.

9

Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21.

Lyle R, Prandini P, Osoegawa K, ten Hallers B, Humphray S, Zhu B, Eyras E, Castelo R, Bird CP, Gagos S, Scott C, Cox A, Deutsch S, Ucla C, Cruts M, Dahoun S, She X, Bena F, Wang SY, Van Broeckhoven C, Eichler EE, Guigo R, Rogers J, de Jong PJ, Reymond A, Antonarakis SE. Lyle R, et al. Genome Res. 2007 Nov;17(11):1690-6. doi: 10.1101/gr.6675307. Epub 2007 Sep 25. Genome Res. 2007. PMID: 17895424 Free PMC article.

10

Chromosome 21 and Down syndrome: the post-sequence era.

Antonarakis SE, Reymond A, Lyle R, Deutsch S, Dermitzakis ET. Antonarakis SE, et al. Among authors: lyle r. Cold Spring Harb Symp Quant Biol. 2003;68:425-30. doi: 10.1101/sqb.2003.68.425. Cold Spring Harb Symp Quant Biol. 2003. PMID: 15338645 No abstract available.

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