Ott J - Search Results

1

Sequence variations in the collagen IX and XI genes are associated with degenerative lumbar spinal stenosis.

Noponen-Hietala N, Kyllönen E, Männikkö M, Ilkko E, Karppinen J, Ott J, Ala-Kokko L. Noponen-Hietala N, et al. Among authors: ott j. Ann Rheum Dis. 2003 Dec;62(12):1208-14. doi: 10.1136/ard.2003.008334. Ann Rheum Dis. 2003. PMID: 14644861 Free PMC article.

2

An allele of COL9A2 associated with intervertebral disc disease.

Annunen S, Paassilta P, Lohiniva J, Perälä M, Pihlajamaa T, Karppinen J, Tervonen O, Kröger H, Lähde S, Vanharanta H, Ryhänen L, Göring HH, Ott J, Prockop DJ, Ala-Kokko L. Annunen S, et al. Among authors: ott j. Science. 1999 Jul 16;285(5426):409-12. doi: 10.1126/science.285.5426.409. Science. 1999. PMID: 10411504

3

Identification of a novel common genetic risk factor for lumbar disk disease.

Paassilta P, Lohiniva J, Göring HH, Perälä M, Räinä SS, Karppinen J, Hakala M, Palm T, Kröger H, Kaitila I, Vanharanta H, Ott J, Ala-Kokko L. Paassilta P, et al. Among authors: ott j. JAMA. 2001 Apr 11;285(14):1843-9. doi: 10.1001/jama.285.14.1843. JAMA. 2001. PMID: 11308397

4

Targeted re-sequencing of linkage region on 2q21 identifies a novel functional variant for hip and knee osteoarthritis.

Taipale M, Jakkula E, Kämäräinen OP, Gao P, Skarp S, Barral S, Kiviranta I, Kröger H, Ott J, Wei GH, Ala-Kokko L, Männikkö M. Taipale M, et al. Among authors: ott j. Osteoarthritis Cartilage. 2016 Apr;24(4):655-63. doi: 10.1016/j.joca.2015.10.019. Epub 2015 Nov 19. Osteoarthritis Cartilage. 2016. PMID: 26603474 Free article.

5

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

6

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.

7

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

8

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

9

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

10

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.

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