Lehmann OJ - Search Results

1

Axenfeld-Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome.

Maclean K, Smith J, St Heaps L, Chia N, Williams R, Peters GB, Onikul E, McCrossin T, Lehmann OJ, Adès LC. Maclean K, et al. Among authors: lehmann oj. Am J Med Genet A. 2005 Feb 1;132A(4):381-5. doi: 10.1002/ajmg.a.30274. Am J Med Genet A. 2005. PMID: 15654696 Review.

2

FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation.

Aldinger KA, Lehmann OJ, Hudgins L, Chizhikov VV, Bassuk AG, Ades LC, Krantz ID, Dobyns WB, Millen KJ. Aldinger KA, et al. Among authors: lehmann oj. Nat Genet. 2009 Sep;41(9):1037-42. doi: 10.1038/ng.422. Epub 2009 Aug 9. Nat Genet. 2009. PMID: 19668217 Free PMC article.

3

Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions.

Lehmann OJ, Ebenezer ND, Ekong R, Ocaka L, Mungall AJ, Fraser S, McGill JI, Hitchings RA, Khaw PT, Sowden JC, Povey S, Walter MA, Bhattacharya SS, Jordan T. Lehmann OJ, et al. Invest Ophthalmol Vis Sci. 2002 Jun;43(6):1843-9. Invest Ophthalmol Vis Sci. 2002. PMID: 12036988

4

Chromosomal anomalies on 6p25 in iris hypoplasia and Axenfeld-Rieger syndrome patients defined on a purpose-built genomic microarray.

Ekong R, Jeremiah S, Judah D, Lehmann O, Mirzayans F, Hung YC, Walter MA, Bhattacharya S, Gant TW, Povey S, Wolfe J. Ekong R, et al. Hum Mutat. 2004 Jul;24(1):76-85. doi: 10.1002/humu.20059. Hum Mutat. 2004. PMID: 15221791

5

Identification of the gene for Nance-Horan syndrome (NHS).

Brooks SP, Ebenezer ND, Poopalasundaram S, Lehmann OJ, Moore AT, Hardcastle AJ. Brooks SP, et al. Among authors: lehmann oj. J Med Genet. 2004 Oct;41(10):768-71. doi: 10.1136/jmg.2004.022517. J Med Genet. 2004. PMID: 15466011 Free PMC article.

6

GDF6, a novel locus for a spectrum of ocular developmental anomalies.

Asai-Coakwell M, French CR, Berry KM, Ye M, Koss R, Somerville M, Mueller R, van Heyningen V, Waskiewicz AJ, Lehmann OJ. Asai-Coakwell M, et al. Among authors: lehmann oj. Am J Hum Genet. 2007 Feb;80(2):306-15. doi: 10.1086/511280. Epub 2006 Dec 29. Am J Hum Genet. 2007. PMID: 17236135 Free PMC article.

7

Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma.

Lehmann OJ, Ebenezer ND, Jordan T, Fox M, Ocaka L, Payne A, Leroy BP, Clark BJ, Hitchings RA, Povey S, Khaw PT, Bhattacharya SS. Lehmann OJ, et al. Am J Hum Genet. 2000 Nov;67(5):1129-35. doi: 10.1016/S0002-9297(07)62943-7. Epub 2000 Sep 27. Am J Hum Genet. 2000. PMID: 11007653 Free PMC article.

8

The Axenfeld-Rieger Syndrome Gene FOXC1 Contributes to Left-Right Patterning.

Chrystal PW, French CR, Jean F, Havrylov S, van Baarle S, Peturson AM, Xu P, Crump JG, Pilgrim DB, Lehmann OJ, Waskiewicz AJ. Chrystal PW, et al. Among authors: lehmann oj. Genes (Basel). 2021 Jan 26;12(2):170. doi: 10.3390/genes12020170. Genes (Basel). 2021. PMID: 33530637 Free PMC article.

9

Reduced human and murine corneal thickness in an Axenfeld-Rieger syndrome subtype.

Asai-Coakwell M, Backhouse C, Casey RJ, Gage PJ, Lehmann OJ. Asai-Coakwell M, et al. Among authors: lehmann oj. Invest Ophthalmol Vis Sci. 2006 Nov;47(11):4905-9. doi: 10.1167/iovs.06-0457. Invest Ophthalmol Vis Sci. 2006. PMID: 17065505

10

Ocular coloboma: Genetic variants reveal a dynamic model of eye development.

Yoon KH, Fox SC, Dicipulo R, Lehmann OJ, Waskiewicz AJ. Yoon KH, et al. Among authors: lehmann oj. Am J Med Genet C Semin Med Genet. 2020 Sep;184(3):590-610. doi: 10.1002/ajmg.c.31831. Epub 2020 Aug 27. Am J Med Genet C Semin Med Genet. 2020. PMID: 32852110 Review.

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