Ott J - Search Results

1

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.

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

First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q.

Devoto M, Shimoya K, Caminis J, Ott J, Tenenhouse A, Whyte MP, Sereda L, Hall S, Considine E, Williams CJ, Tromp G, Kuivaniemi H, Ala-Kokko L, Prockop DJ, Spotila LD. Devoto M, et al. Among authors: ott j. Eur J Hum Genet. 1998 Mar-Apr;6(2):151-7. doi: 10.1038/sj.ejhg.5200169. Eur J Hum Genet. 1998. PMID: 9781060

4

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.

5

Osteopenia in 37 members of seven families: analysis based on a model of dominant inheritance.

Spotila LD, Caminis J, Devoto M, Shimoya K, Sereda L, Ott J, Whyte MP, Tenenhouse A, Prockop DJ. Spotila LD, et al. Among authors: ott j. Mol Med. 1996 May;2(3):313-24. Mol Med. 1996. PMID: 8784784 Free PMC article.

6

Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus.

Ikonen E, Palo J, Ott J, Gusella J, Somer H, Karila L, Palotie A, Peltonen L. Ikonen E, et al. Among authors: ott j. Am J Hum Genet. 1990 Jan;46(1):5-11. Am J Hum Genet. 1990. PMID: 1967208 Free PMC article.

7

Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis.

Ellison KA, Fill CP, Terwilliger J, DeGennaro LJ, Martin-Gallardo A, Anvret M, Percy AK, Ott J, Zoghbi H. Ellison KA, et al. Among authors: ott j. Am J Hum Genet. 1992 Feb;50(2):278-87. Am J Hum Genet. 1992. PMID: 1734712 Free PMC article.

8

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

9

Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7.

Vilkki J, Ott J, Savontaus ML, Aula P, Nikoskelainen EK. Vilkki J, et al. Among authors: ott j. Am J Hum Genet. 1991 Mar;48(3):486-91. Am J Hum Genet. 1991. PMID: 1998335 Free PMC article.

10

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.

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