Ott J - Search Results

1

A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27.

Gieser L, Fujita R, Göring HH, Ott J, Hoffman DR, Cideciyan AV, Birch DG, Jacobson SG, Swaroop A. Gieser L, et al. Among authors: ott j. Am J Hum Genet. 1998 Nov;63(5):1439-47. doi: 10.1086/302121. Am J Hum Genet. 1998. PMID: 9792872 Free PMC article.

2

A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.

Fujita R, Bingham E, Forsythe P, McHenry C, Aita V, Navia BA, Dry K, Segal M, Devoto M, Bruns G, Wright AF, Ott J, Sieving PA, Swaroop A. Fujita R, et al. Among authors: ott j. Am J Hum Genet. 1996 Jul;59(1):152-8. Am J Hum Genet. 1996. PMID: 8659520 Free PMC article.

3

Relationship estimation in affected sib pair analysis of late-onset diseases.

Göring HH, Ott J. Göring HH, et al. Among authors: ott j. Eur J Hum Genet. 1997 Mar-Apr;5(2):69-77. Eur J Hum Genet. 1997. PMID: 9195155

4

TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa.

Banerjee P, Kleyn PW, Knowles JA, Lewis CA, Ross BM, Parano E, Kovats SG, Lee JJ, Penchaszadeh GK, Ott J, Jacobson SG, Gilliam TC. Banerjee P, et al. Among authors: ott j. Nat Genet. 1998 Feb;18(2):177-9. doi: 10.1038/ng0298-177. Nat Genet. 1998. PMID: 9462751

5

Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3.

Banerjee P, Lewis CA, Kleyn PW, Shugart YY, Ross BM, Penchaszadeh GK, Ott J, Jacobson SG, Gilliam TC, Knowles JA. Banerjee P, et al. Among authors: ott j. Genomics. 1998 Mar 1;48(2):171-7. doi: 10.1006/geno.1997.5174. Genomics. 1998. PMID: 9521870 Free article.

6

Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21.

Shugart YY, Banerjee P, Knowles JA, Lewis CA, Jacobson SG, Matise TC, Penchaszadeh G, Gilliam TC, Ott J. Shugart YY, et al. Among authors: ott j. Am J Hum Genet. 1995 Aug;57(2):499-502. Am J Hum Genet. 1995. PMID: 7668276 Free PMC article. No abstract available.

7

Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p.

Knowles JA, Shugart Y, Banerjee P, Gilliam TC, Lewis CA, Jacobson SG, Ott J. Knowles JA, et al. Among authors: ott j. Hum Mol Genet. 1994 Aug;3(8):1401-3. doi: 10.1093/hmg/3.8.1401. Hum Mol Genet. 1994. PMID: 7987322

8

Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele.

McGee TL, Devoto M, Ott J, Berson EL, Dryja TP. McGee TL, et al. Among authors: ott j. Am J Hum Genet. 1997 Nov;61(5):1059-66. doi: 10.1086/301614. Am J Hum Genet. 1997. PMID: 9345108 Free PMC article.

9

Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits.

Schork NJ, Boehnke M, Terwilliger JD, Ott J. Schork NJ, et al. Among authors: ott j. Am J Hum Genet. 1993 Nov;53(5):1127-36. Am J Hum Genet. 1993. PMID: 8213836 Free PMC article.

10

Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration.

Lewis CA, Batlle IR, Batlle KG, Banerjee P, Cideciyan AV, Huang J, Alemán TS, Huang Y, Ott J, Gilliam TC, Knowles JA, Jacobson SG. Lewis CA, et al. Among authors: ott j. Invest Ophthalmol Vis Sci. 1999 Aug;40(9):2106-14. Invest Ophthalmol Vis Sci. 1999. PMID: 10440267

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