Lyle R - Search Results

1

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

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

Human chromosome 21 gene expression atlas in the mouse.

Reymond A, Marigo V, Yaylaoglu MB, Leoni A, Ucla C, Scamuffa N, Caccioppoli C, Dermitzakis ET, Lyle R, Banfi S, Eichele G, Antonarakis SE, Ballabio A. Reymond A, et al. Among authors: lyle r. Nature. 2002 Dec 5;420(6915):582-6. doi: 10.1038/nature01178. Nature. 2002. PMID: 12466854

4

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.

5

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.

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

Nineteen additional unpredicted transcripts from human chromosome 21.

Reymond A, Camargo AA, Deutsch S, Stevenson BJ, Parmigiani RB, Ucla C, Bettoni F, Rossier C, Lyle R, Guipponi M, de Souza S, Iseli C, Jongeneel CV, Bucher P, Simpson AJ, Antonarakis SE. Reymond A, et al. Among authors: lyle r. Genomics. 2002 Jun;79(6):824-32. doi: 10.1006/geno.2002.6781. Genomics. 2002. PMID: 12036297

8

Numerous potentially functional but non-genic conserved sequences on human chromosome 21.

Dermitzakis ET, Reymond A, Lyle R, Scamuffa N, Ucla C, Deutsch S, Stevenson BJ, Flegel V, Bucher P, Jongeneel CV, Antonarakis SE. Dermitzakis ET, et al. Among authors: lyle r. Nature. 2002 Dec 5;420(6915):578-82. doi: 10.1038/nature01251. Nature. 2002. PMID: 12466853

9

Genome-wide associations of gene expression variation in humans.

Stranger BE, Forrest MS, Clark AG, Minichiello MJ, Deutsch S, Lyle R, Hunt S, Kahl B, Antonarakis SE, Tavaré S, Deloukas P, Dermitzakis ET. Stranger BE, et al. Among authors: lyle r. PLoS Genet. 2005 Dec;1(6):e78. doi: 10.1371/journal.pgen.0010078. Epub 2005 Dec 16. PLoS Genet. 2005. PMID: 16362079 Free PMC article.

10

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

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