Lyle R - Search Results

1

The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elements.

van Geel M, Heather LJ, Lyle R, Hewitt JE, Frants RR, de Jong PJ. van Geel M, et al. Among authors: lyle r. Genomics. 1999 Oct 1;61(1):55-65. doi: 10.1006/geno.1999.5942. Genomics. 1999. PMID: 10512680

2

The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes.

Lyle R, Wright TJ, Clark LN, Hewitt JE. Lyle R, et al. Genomics. 1995 Aug 10;28(3):389-97. doi: 10.1006/geno.1995.1166. Genomics. 1995. PMID: 7490072

3

Diagnosis by sequencing: correction of misdiagnosis from FSHD2 to LGMD2A by whole-exome analysis.

Leidenroth A, Sorte HS, Gilfillan G, Ehrlich M, Lyle R, Hewitt JE. Leidenroth A, et al. Among authors: lyle r. Eur J Hum Genet. 2012 Sep;20(9):999-1003. doi: 10.1038/ejhg.2012.42. Epub 2012 Feb 29. Eur J Hum Genet. 2012. PMID: 22378277 Free PMC article.

4

An alternatively spliced transcript, p65 delta 2, of the gene encoding the p65 subunit of the transcription factor NF-kappa B.

Lyle R, Valleley EM, Sharpe PT, Hewitt JE. Lyle R, et al. Gene. 1994 Jan 28;138(1-2):265-6. doi: 10.1016/0378-1119(94)90823-0. Gene. 1994. PMID: 7907305

5

Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy.

Hewitt JE, Lyle R, Clark LN, Valleley EM, Wright TJ, Wijmenga C, van Deutekom JC, Francis F, Sharpe PT, Hofker M, et al. Hewitt JE, et al. Among authors: lyle r. Hum Mol Genet. 1994 Aug;3(8):1287-95. doi: 10.1093/hmg/3.8.1287. Hum Mol Genet. 1994. PMID: 7987304

6

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

7

From PREDs and open reading frames to cDNA isolation: revisiting the human chromosome 21 transcription map.

Reymond A, Friedli M, Henrichsen CN, Chapot F, Deutsch S, Ucla C, Rossier C, Lyle R, Guipponi M, Antonarakis SE. Reymond A, et al. Among authors: lyle r. Genomics. 2001 Nov;78(1-2):46-54. doi: 10.1006/geno.2001.6640. Genomics. 2001. PMID: 11707072

8

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.

9

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

10

Identification of copy number variants from exome sequence data.

Samarakoon PS, Sorte HS, Kristiansen BE, Skodje T, Sheng Y, Tjønnfjord GE, Stadheim B, Stray-Pedersen A, Rødningen OK, Lyle R. Samarakoon PS, et al. Among authors: lyle r. BMC Genomics. 2014 Aug 7;15(1):661. doi: 10.1186/1471-2164-15-661. BMC Genomics. 2014. PMID: 25102989 Free PMC article.

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