Lennon A - Search Results

1

A genome-wide search for linkage in a large bipolar family: comparison of genotyping accuracy using di- and tetranucleotide repeat microsatellite markers.

He L, Morris S, Lennon A, St Clair DM, Porteous DJ, Wright AF, Muir WJ, Blackwood DH. He L, et al. Among authors: lennon a. Psychiatr Genet. 1996 Fall;6(3):123-9. doi: 10.1097/00041444-199623000-00004. Psychiatr Genet. 1996. PMID: 8902888

2

Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa.

Vervoort R, Lennon A, Bird AC, Tulloch B, Axton R, Miano MG, Meindl A, Meitinger T, Ciccodicola A, Wright AF. Vervoort R, et al. Among authors: lennon a. Nat Genet. 2000 Aug;25(4):462-6. doi: 10.1038/78182. Nat Genet. 2000. PMID: 10932196

3

Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration.

Hayward C, Shu X, Cideciyan AV, Lennon A, Barran P, Zareparsi S, Sawyer L, Hendry G, Dhillon B, Milam AH, Luthert PJ, Swaroop A, Hastie ND, Jacobson SG, Wright AF. Hayward C, et al. Among authors: lennon a. Hum Mol Genet. 2003 Oct 15;12(20):2657-67. doi: 10.1093/hmg/ddg289. Epub 2003 Aug 27. Hum Mol Genet. 2003. PMID: 12944416

4

Identification of a 5' splice site mutation in the RPGR gene in a family with X-linked retinitis pigmentosa (RP3).

Dry KL, Manson FD, Lennon A, Bergen AA, Van Dorp DB, Wright AF. Dry KL, et al. Among authors: lennon a. Hum Mutat. 1999;13(2):141-5. doi: 10.1002/(SICI)1098-1004(1999)13:2<141::AID-HUMU6>3.0.CO;2-Q. Hum Mutat. 1999. PMID: 10094550

5

Disease mechanisms in late-onset retinal macular degeneration associated with mutation in C1QTNF5.

Shu X, Tulloch B, Lennon A, Vlachantoni D, Zhou X, Hayward C, Wright AF. Shu X, et al. Among authors: lennon a. Hum Mol Genet. 2006 May 15;15(10):1680-9. doi: 10.1093/hmg/ddl091. Epub 2006 Apr 6. Hum Mol Genet. 2006. PMID: 16600989

6

Zebrafish Rpgr is required for normal retinal development and plays a role in dynein-based retrograde transport processes.

Shu X, Zeng Z, Gautier P, Lennon A, Gakovic M, Patton EE, Wright AF. Shu X, et al. Among authors: lennon a. Hum Mol Genet. 2010 Feb 15;19(4):657-70. doi: 10.1093/hmg/ddp533. Epub 2009 Dec 1. Hum Mol Genet. 2010. PMID: 19955120

7

RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosmin.

Shu X, Fry AM, Tulloch B, Manson FD, Crabb JW, Khanna H, Faragher AJ, Lennon A, He S, Trojan P, Giessl A, Wolfrum U, Vervoort R, Swaroop A, Wright AF. Shu X, et al. Among authors: lennon a. Hum Mol Genet. 2005 May 1;14(9):1183-97. doi: 10.1093/hmg/ddi129. Epub 2005 Mar 16. Hum Mol Genet. 2005. PMID: 15772089

8

Biochemical characterisation of the C1QTNF5 gene associated with late-onset retinal degeneration. A genetic model of age-related macular degeneration.

Shu X, Tulloch B, Lennon A, Hayward C, O'Connell M, Cideciyan AV, Jacobson SG, Wright AF. Shu X, et al. Among authors: lennon a. Adv Exp Med Biol. 2006;572:41-8. doi: 10.1007/0-387-32442-9_7. Adv Exp Med Biol. 2006. PMID: 17249553 No abstract available.

9

Characterisation of a C1qtnf5 Ser163Arg knock-in mouse model of late-onset retinal macular degeneration.

Shu X, Luhmann UF, Aleman TS, Barker SE, Lennon A, Tulloch B, Chen M, Xu H, Jacobson SG, Ali R, Wright AF. Shu X, et al. Among authors: lennon a. PLoS One. 2011;6(11):e27433. doi: 10.1371/journal.pone.0027433. Epub 2011 Nov 16. PLoS One. 2011. PMID: 22110650 Free PMC article.

10

Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome.

Wright AF, Reddick AC, Schwartz SB, Ferguson JS, Aleman TS, Kellner U, Jurklies B, Schuster A, Zrenner E, Wissinger B, Lennon A, Shu X, Cideciyan AV, Stone EM, Jacobson SG, Swaroop A. Wright AF, et al. Among authors: lennon a. Hum Mutat. 2004 Nov;24(5):439. doi: 10.1002/humu.9285. Hum Mutat. 2004. PMID: 15459973

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