Ott J - Search Results

1

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.

2

Two-locus linkage analysis in multiple sclerosis (MS).

Tienari PJ, Terwilliger JD, Ott J, Palo J, Peltonen L. Tienari PJ, et al. Among authors: ott j. Genomics. 1994 Jan 15;19(2):320-5. doi: 10.1006/geno.1994.1064. Genomics. 1994. PMID: 7514567 Free article.

3

Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32: incorporation of linkage disequilibrium in multipoint analysis.

Hellsten E, Vesa J, Speer MC, Mäkelä TP, Järvelä I, Alitalo K, Ott J, Peltonen L. Hellsten E, et al. Among authors: ott j. Genomics. 1993 Jun;16(3):720-5. doi: 10.1006/geno.1993.1253. Genomics. 1993. PMID: 8325646

4

Early-onset osteoarthritis linked to the type II procollagen gene. Detailed clinical phenotype and further analyses of the gene.

Vikkula M, Palotie A, Ritvaniemi P, Ott J, Ala-Kokko L, Sievers U, Aho K, Peltonen L. Vikkula M, et al. Among authors: ott j. Arthritis Rheum. 1993 Mar;36(3):401-9. doi: 10.1002/art.1780360317. Arthritis Rheum. 1993. PMID: 8452585

5

Predisposition to familial osteoarthrosis linked to type II collagen gene.

Palotie A, Väisänen P, Ott J, Ryhänen L, Elima K, Vikkula M, Cheah K, Vuorio E, Peltonen L. Palotie A, et al. Among authors: ott j. Lancet. 1989 Apr 29;1(8644):924-7. doi: 10.1016/s0140-6736(89)92507-5. Lancet. 1989. PMID: 2565419

6

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.

7

Haplotype and multipoint linkage analysis in Finnish choroideremia families.

Sankila EM, Lehner T, Eriksson AW, Forsius H, Kärnä J, Page D, Ott J, de la Chapelle A. Sankila EM, et al. Among authors: ott j. Hum Genet. 1989 Dec;84(1):66-70. doi: 10.1007/BF00210674. Hum Genet. 1989. PMID: 2575071

8

Lack of association between the apolipoprotein B gene 3' hypervariable region alleles and coronary artery disease in Finnish patients with angiographically documented coronary artery disease.

Heliö T, Palotie A, Tötterman KJ, Ott J, Kauppinen-Mäkelin R, Tikkanen MJ. Heliö T, et al. Among authors: ott j. J Intern Med. 1992 Jan;231(1):49-57. doi: 10.1111/j.1365-2796.1992.tb00498.x. J Intern Med. 1992. PMID: 1732399

9

The effect of marker heterozygosity on the power to detect linkage disequilibrium.

Ott J, Rabinowitz D. Ott J, et al. Genetics. 1997 Oct;147(2):927-30. doi: 10.1093/genetics/147.2.927. Genetics. 1997. PMID: 9335624 Free PMC article.

10

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.

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