Mansfield DC - Search Results

1

Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.

Bruford EA, Riise R, Teague PW, Porter K, Thomson KL, Moore AT, Jay M, Warburg M, Schinzel A, Tommerup N, Tornqvist K, Rosenberg T, Patton M, Mansfield DC, Wright AF. Bruford EA, et al. Among authors: mansfield dc. Genomics. 1997 Apr 1;41(1):93-9. doi: 10.1006/geno.1997.4613. Genomics. 1997. PMID: 9126487

2

Automation of genetic linkage analysis using fluorescent microsatellite markers.

Mansfield DC, Brown AF, Green DK, Carothers AD, Morris SW, Evans HJ, Wright AF. Mansfield DC, et al. Genomics. 1994 Nov 15;24(2):225-33. doi: 10.1006/geno.1994.1610. Genomics. 1994. PMID: 7698743

3

Automated linkage analysis in psychiatric disorders.

He L, Mansfield DC, Brown AF, Green DK, Morris SW, St Clair DM, Muir WJ, Maclean A, Wright AF, Blackwood DH. He L, et al. Among authors: mansfield dc. Am J Med Genet. 1995 Jun 19;60(3):192-8. doi: 10.1002/ajmg.1320600305. Am J Med Genet. 1995. PMID: 7573170

4

Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa.

Keen TJ, Hims MM, McKie AB, Moore AT, Doran RM, Mackey DA, Mansfield DC, Mueller RF, Bhattacharya SS, Bird AC, Markham AF, Inglehearn CF. Keen TJ, et al. Among authors: mansfield dc. Eur J Hum Genet. 2002 Apr;10(4):245-9. doi: 10.1038/sj.ejhg.5200797. Eur J Hum Genet. 2002. PMID: 12032732

5

Unusual Retinal Vascular Proliferation in von Hippel-Lindau Disease.

Islam F, Hull S, Mansfield DC, Moore AT, Bird A. Islam F, et al. Among authors: mansfield dc. JAMA Ophthalmol. 2016 Sep 1;134(9):1073-4. doi: 10.1001/jamaophthalmol.2016.2046. JAMA Ophthalmol. 2016. PMID: 27366993 No abstract available.

6

A new locus for autosomal dominant familial exudative vitreoretinopathy maps to chromosome 11p12-13.

Downey LM, Keen TJ, Roberts E, Mansfield DC, Bamashmus M, Inglehearn CF. Downey LM, et al. Among authors: mansfield dc. Am J Hum Genet. 2001 Mar;68(3):778-81. doi: 10.1086/318790. Epub 2001 Jan 19. Am J Hum Genet. 2001. PMID: 11179025 Free PMC article.

7

Genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of the EVR1 locus on chromosome 11q in a large autosomal dominant pedigree.

Bamashmus MA, Downey LM, Inglehearn CF, Gupta SR, Mansfield DC. Bamashmus MA, et al. Among authors: mansfield dc. Br J Ophthalmol. 2000 Apr;84(4):358-63. doi: 10.1136/bjo.84.4.358. Br J Ophthalmol. 2000. PMID: 10729291 Free PMC article.

8

Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta.

Parry DA, Mighell AJ, El-Sayed W, Shore RC, Jalili IK, Dollfus H, Bloch-Zupan A, Carlos R, Carr IM, Downey LM, Blain KM, Mansfield DC, Shahrabi M, Heidari M, Aref P, Abbasi M, Michaelides M, Moore AT, Kirkham J, Inglehearn CF. Parry DA, et al. Among authors: mansfield dc. Am J Hum Genet. 2009 Feb;84(2):266-73. doi: 10.1016/j.ajhg.2009.01.009. Epub 2009 Feb 5. Am J Hum Genet. 2009. PMID: 19200525 Free PMC article.

9

The Role of RPGR and Its Interacting Proteins in Ciliopathies.

Patnaik SR, Raghupathy RK, Zhang X, Mansfield D, Shu X. Patnaik SR, et al. J Ophthalmol. 2015;2015:414781. doi: 10.1155/2015/414781. Epub 2015 Jun 1. J Ophthalmol. 2015. PMID: 26124960 Free PMC article. Review.

10

Retinitis Pigmentosa: Disease Mechanisms, Diagnosis, and Therapies.

Shu X, Pang JJ, Zhang H, Mansfield D. Shu X, et al. J Ophthalmol. 2015;2015:819452. doi: 10.1155/2015/819452. Epub 2015 Jun 11. J Ophthalmol. 2015. PMID: 26171242 Free PMC article. No abstract available.

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