Sullivan LS - Search Results

1

Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies.

Sohocki MM, Daiger SP, Bowne SJ, Rodriquez JA, Northrup H, Heckenlively JR, Birch DG, Mintz-Hittner H, Ruiz RS, Lewis RA, Saperstein DA, Sullivan LS. Sohocki MM, et al. Among authors: sullivan ls. Hum Mutat. 2001;17(1):42-51. doi: 10.1002/1098-1004(2001)17:1<42::AID-HUMU5>3.0.CO;2-K. Hum Mutat. 2001. PMID: 11139241 Free PMC article.

2

X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11.

McGuire RE, Sullivan LS, Blanton SH, Church MW, Heckenlively JR, Daiger SP. McGuire RE, et al. Among authors: sullivan ls. Am J Hum Genet. 1995 Jul;57(1):87-94. Am J Hum Genet. 1995. PMID: 7611300 Free PMC article.

3

Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated family.

McGuire RE, Gannon AM, Sullivan LS, Rodriguez JA, Daiger SP. McGuire RE, et al. Among authors: sullivan ls. Hum Genet. 1995 Jan;95(1):71-4. doi: 10.1007/BF00225078. Hum Genet. 1995. PMID: 7814030

4

Tetranucleotide repeat polymorphism (D8S582) for human EST00680 (D8S340E).

Sullivan LS, Parrish J, Wagner MJ, Wells D, Blanton SH, Daiger SP. Sullivan LS, et al. Hum Mol Genet. 1994 Feb;3(2):386. doi: 10.1093/hmg/3.2.386-a. Hum Mol Genet. 1994. PMID: 8004122 No abstract available.

5

Inherited retinal degeneration: exceptional genetic and clinical heterogeneity.

Sullivan LS, Daiger SP. Sullivan LS, et al. Mol Med Today. 1996 Sep;2(9):380-6. doi: 10.1016/s1357-4310(96)10037-x. Mol Med Today. 1996. PMID: 8885257 Review.

6

Genetic mapping of RP1 on 8q11-q21 in an Australian family with autosomal dominant retinitis pigmentosa reduces the critical region to 4 cM between D8S601 and D8S285.

Xu SY, Denton M, Sullivan L, Daiger SP, Gal A. Xu SY, et al. Hum Genet. 1996 Dec;98(6):741-3. doi: 10.1007/s004390050296. Hum Genet. 1996. PMID: 8931712

7

Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sites.

Sohocki MM, Sullivan LS, Harrison WR, Sodergren EJ, Elder FF, Weinstock G, Tanase S, Daiger SP. Sohocki MM, et al. Among authors: sullivan ls. Genomics. 1997 Mar 1;40(2):247-52. doi: 10.1006/geno.1996.4604. Genomics. 1997. PMID: 9119391

8

Exclusion of atypical vitelliform macular dystrophy from 8q24.3 and from other known macular degenerative loci.

Sohocki MM, Sullivan LS, Mintz-Hittner HA, Small K, Ferrell RE, Daiger SP. Sohocki MM, et al. Among authors: sullivan ls. Am J Hum Genet. 1997 Jul;61(1):239-41. doi: 10.1016/S0002-9297(07)64299-2. Am J Hum Genet. 1997. PMID: 9246008 Free PMC article. No abstract available.

9

Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24.

Yee RW, Sullivan LS, Lai HT, Stock EL, Lu Y, Khan MN, Blanton SH, Daiger SP. Yee RW, et al. Among authors: sullivan ls. Genomics. 1997 Nov 15;46(1):152-4. doi: 10.1006/geno.1997.5028. Genomics. 1997. PMID: 9403072

10

A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.

Sohocki MM, Sullivan LS, Mintz-Hittner HA, Birch D, Heckenlively JR, Freund CL, McInnes RR, Daiger SP. Sohocki MM, et al. Among authors: sullivan ls. Am J Hum Genet. 1998 Nov;63(5):1307-15. doi: 10.1086/302101. Am J Hum Genet. 1998. PMID: 9792858 Free PMC article.

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