-
2
-
-
0032706080
-
Twins and the genetic architecture of osteoarthritis
-
MacGregor AJ, Spector TD. Twins and the genetic architecture of osteoarthritis. Rheumatology 1999;38:583-90.
-
(1999)
Rheumatology
, vol.38
, pp. 583-590
-
-
MacGregor, A.J.1
Spector, T.D.2
-
3
-
-
0030786608
-
Genetic influences in end-stage osteoarthritis. Sibling risks of hip and knee replacement for idiopathic osteoarthritis
-
Chitnavis J, Sinsheimer JS, Clipsham K et al. Genetic influences in end-stage osteoarthritis. Sibling risks of hip and knee replacement for idiopathic osteoarthritis. J Bone Joint Surg 1997;79B:660-4.
-
(1997)
J Bone Joint Surg
, vol.79 B
, pp. 660-664
-
-
Chitnavis, J.1
Sinsheimer, J.S.2
Clipsham, K.3
-
4
-
-
0029997864
-
Genetic liability to osteoarthritis may be greater in women than men
-
Kaprio J, Kujala UM, Peltonen L, Koskenvuo M. Genetic liability to osteoarthritis may be greater in women than men. Br Med J 1996;313:232.
-
(1996)
Br Med J
, vol.313
, pp. 232
-
-
Kaprio, J.1
Kujala, U.M.2
Peltonen, L.3
Koskenvuo, M.4
-
5
-
-
0031748678
-
Evidence for a Mendelian gene in a segregation analysis of generalized radiographic osteoarthritis
-
Felson DT, Couropmitree NN, Chaisson CE et al. Evidence for a Mendelian gene in a segregation analysis of generalized radiographic osteoarthritis. Arthritis Rheum 1998;41:1064-71.
-
(1998)
Arthritis Rheum
, vol.41
, pp. 1064-1071
-
-
Felson, D.T.1
Couropmitree, N.N.2
Chaisson, C.E.3
-
6
-
-
0022621476
-
Prevalence of primary coxarthrosis in siblings of patients with primary coxarthrosis
-
Lindberg H. Prevalence of primary coxarthrosis in siblings of patients with primary coxarthrosis. Clin Orthop 1986;203:273-5.
-
(1986)
Clin Orthop
, vol.203
, pp. 273-275
-
-
Lindberg, H.1
-
7
-
-
0028334826
-
Mechanical and constitutional risk factors for symptomatic knee osteoarthritis: Differences between medial tibio-femoral and patello-femoral disease
-
Cooper C, McAlindon T, Snow S et al. Mechanical and constitutional risk factors for symptomatic knee osteoarthritis: differences between medial tibio-femoral and patello-femoral disease. J Rheumatol 1994;21:307-13.
-
(1994)
J Rheumatol
, vol.21
, pp. 307-313
-
-
Cooper, C.1
McAlindon, T.2
Snow, S.3
-
8
-
-
0029665141
-
A-2→G transition at the 3′ acceptor splice site of IVSI7 characterizes the COL2A1 gene mutation in the original Stickler syndrome kindred
-
Williams CJ, Ganguly A, Considine E et al. A-2→G transition at the 3′ acceptor splice site of IVSI7 characterizes the COL2A1 gene mutation in the original Stickler syndrome kindred. Am J Med Genet 1996;63:461-7.
-
(1996)
Am J Med Genet
, vol.63
, pp. 461-467
-
-
Williams, C.J.1
Ganguly, A.2
Considine, E.3
-
9
-
-
0027466854
-
Early-onset osteoarthritis linked to the type II procollagen gene
-
Vikkula M, Palotie A, Ritvaniemi P et al. Early-onset osteoarthritis linked to the type II procollagen gene. Arthritis Rheum 1993;36:401-9.
-
(1993)
Arthritis Rheum
, vol.36
, pp. 401-409
-
-
Vikkula, M.1
Palotie, A.2
Ritvaniemi, P.3
-
10
-
-
0028952248
-
Differential allelic expression of the type II collagen gene (COL2A1) in osleoarthritic cartilage
-
Loughlin J, Irven C, Athanosou N, Carr A, Sykes B. Differential allelic expression of the type II collagen gene (COL2A1) in osleoarthritic cartilage. Am J Hum Genet 1995;56:1186-93.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1186-1193
-
-
Loughlin, J.1
Irven, C.2
Athanosou, N.3
Carr, A.4
Sykes, B.5
-
11
-
-
0030886744
-
Association of early osteoarthritis of the knee with a Taq I polymorphism of the vitamin D receptor gene
-
Keen RW, Hart DJ, Lanchbury JS, Spector TD. Association of early osteoarthritis of the knee with a Taq I polymorphism of the vitamin D receptor gene. Arthritis Rheum 1997;40:1444-9.
-
(1997)
Arthritis Rheum
, vol.40
, pp. 1444-1449
-
-
Keen, R.W.1
Hart, D.J.2
Lanchbury, J.S.3
Spector, T.D.4
-
12
-
-
0030742584
-
Vitamin D receptor genotype is associated with radiographic osteoarthritis at the knee
-
Uittcrlinden AG, Burger H, Huang Q et al. Vitamin D receptor genotype is associated with radiographic osteoarthritis at the knee. J Clin Invest 1997;100:259-63.
-
(1997)
J Clin Invest
, vol.100
, pp. 259-263
-
-
Uittcrlinden, A.G.1
Burger, H.2
Huang, Q.3
-
13
-
-
0028606374
-
Sibling pair analysis shows no linkage of generalized osteoarthritis to the loci encoding type II collagen, cartilage link protein or cartilage matrix protein
-
Loughlin J, Irven C, Fergusson C, Sykes B. Sibling pair analysis shows no linkage of generalized osteoarthritis to the loci encoding type II collagen, cartilage link protein or cartilage matrix protein. Br J Rheumatol 1994; 33:1103-6.
-
(1994)
Br J Rheumatol
, vol.33
, pp. 1103-1106
-
-
Loughlin, J.1
Irven, C.2
Fergusson, C.3
Sykes, B.4
-
14
-
-
0029833063
-
A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valinc in α1(XI) collagen
-
Richards AJ, Yates JR, Williams R et al. A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valinc in α1(XI) collagen. Hum Mol Genet 1996;5:1339-43.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1339-1343
-
-
Richards, A.J.1
Yates, J.R.2
Williams, R.3
-
15
-
-
0028815298
-
Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus
-
Vikkula M, Mariman ECM, Lui VCH et al. Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus. Cell 1995;80:431-7.
-
(1995)
Cell
, vol.80
, pp. 431-437
-
-
Vikkula, M.1
Mariman, E.C.M.2
Lui, V.C.H.3
-
16
-
-
0033358606
-
Identification of novel pro-α2 (IX) collagen gene mutations in two families with distinctive oligo-epiphyseal forms of multiple epiphyseal dysplasia
-
Holden P, Canty EG, Mortier GR et al. Identification of novel pro-α2 (IX) collagen gene mutations in two families with distinctive oligo-epiphyseal forms of multiple epiphyseal dysplasia. Am J Hum Genet 1999;65:31-8.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 31-38
-
-
Holden, P.1
Canty, E.2
Mortier, G.R.3
-
17
-
-
0031963913
-
Identification of live novel mutations in the cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasia
-
Loughlin J, Irven C, Mustafa Z et al. Identification of live novel mutations in the cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasia. Hum Mutat 1998;suppl.1:S10-17.
-
(1998)
Hum Mutat
, Issue.1 SUPPL.
-
-
Loughlin, J.1
Irven, C.2
Mustafa, Z.3
-
18
-
-
0024313371
-
HLA-A, B antigens and α1-antitrypsin phenotypes in nodal generalised osteoarthritis and erosive osteoarthritis
-
Pattrick M, Manhire A, Ward AM, Doherty M. HLA-A, B antigens and α1-antitrypsin phenotypes in nodal generalised osteoarthritis and erosive osteoarthritis. Ann Rheum Dis 1989;48:470-5.
-
(1989)
Ann Rheum Dis
, vol.48
, pp. 470-475
-
-
Pattrick, M.1
Manhire, A.2
Ward, A.M.3
Doherty, M.4
-
19
-
-
0033358527
-
Osteoarthritis-susceptibility locus on chromosome 11q, detected by linkage
-
Chapman K, Mustafa Z, Irven C et al. Osteoarthritis-susceptibility locus on chromosome 11q, detected by linkage. Am J Hum Genet 1999;65:167-74.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 167-174
-
-
Chapman, K.1
Mustafa, Z.2
Irven, C.3
-
20
-
-
0025001452
-
Amplification of the COL2A1 3′ variable region used for segregation analysis in a family with the Stickler syndrome
-
Priestley L, Kumar D, Sykes B. Amplification of the COL2A1 3′ variable region used for segregation analysis in a family with the Stickler syndrome. Hum Genet 1990;85:525-6.
-
(1990)
Hum Genet
, vol.85
, pp. 525-526
-
-
Priestley, L.1
Kumar, D.2
Sykes, B.3
-
21
-
-
0027234925
-
Physical and linkage mapping of the human and murine genes for the α1 chain of type IX collagen (COL9A1)
-
Warman ML, Tiller GE, Polumbo PA et al. Physical and linkage mapping of the human and murine genes for the α1 chain of type IX collagen (COL9A1). Genomics 1993;17:694-8.
-
(1993)
Genomics
, vol.17
, pp. 694-698
-
-
Warman, M.L.1
Tiller, G.E.2
Polumbo, P.A.3
-
22
-
-
0026879815
-
An Alu variable polyA repeat polymorphism upstream of L-myc at 1p32
-
Makela TP, Hellsten E, Vesa J, Alitalo K, Peltonen L. An Alu variable polyA repeat polymorphism upstream of L-myc at 1p32. Hum Mol Genet 1992;1:217.
-
(1992)
Hum Mol Genet
, vol.1
, pp. 217
-
-
Makela, T.P.1
Hellsten, E.2
Vesa, J.3
Alitalo, K.4
Peltonen, L.5
-
23
-
-
0031949272
-
Marshall syndrome associated with a splicing defect at the COL1lA1 locus
-
Griffith AJ, Sprunger LK, SirkoOsadsa DA, Tiller GE, Meisler MH, Warman ML. Marshall syndrome associated with a splicing defect at the COL1lA1 locus. Am J Hum Genet 1998;62:816-23.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 816-823
-
-
Griffith, A.J.1
Sprunger, L.K.2
SirkoOsadsa, D.A.3
Tiller, G.E.4
Meisler, M.H.5
Warman, M.L.6
-
24
-
-
0029070079
-
Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene
-
Briggs MD, Huffman SM, King LM et al. Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene. Nat Genet 1995;10:330-6.
-
(1995)
Nat Genet
, vol.10
, pp. 330-336
-
-
Briggs, M.D.1
Huffman, S.M.2
King, L.M.3
-
25
-
-
0026409253
-
GT repeat polymorphism in the human proteoglycan link gene (CRTL1) promoter region
-
Hecht JT, Wang Y, Rhodes C, Yamada Y. GT repeat polymorphism in the human proteoglycan link gene (CRTL1) promoter region. Nucleic Acids Res 1991; 19:6666.
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 6666
-
-
Hecht, J.T.1
Wang, Y.2
Rhodes, C.3
Yamada, Y.4
-
26
-
-
0027425636
-
A (CA)n repeat polymorphism at the 5′ end of the α1-antitrypsin gene (P1)
-
Byth BC, Cox DW. A (CA)n repeat polymorphism at the 5′ end of the α1-antitrypsin gene (P1). Hum Mol Genet 1993;2:1752.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1752
-
-
Byth, B.C.1
Cox, D.W.2
-
27
-
-
0027978110
-
The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure disequilibrium mapping
-
Hastbacka J, de la Chapelle A, Mahtani MM et al. The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure disequilibrium mapping. Cell 1994;78:1073-87.
-
(1994)
Cell
, vol.78
, pp. 1073-1087
-
-
Hastbacka, J.1
De La Chapelle, A.2
Mahtani, M.M.3
-
28
-
-
0022423476
-
A highly polymorphic region 3′ to the human type II collagen gene
-
Stoker NG, Cheah KSE, Griffin JR, Pope FM, Solomon E. A highly polymorphic region 3′ to the human type II collagen gene. Nucleic Acids Res 1985;13:4613-22.
-
(1985)
Nucleic Acids Res
, vol.13
, pp. 4613-4622
-
-
Stoker, N.G.1
Cheah, K.S.E.2
Griffin, J.R.3
Pope, F.M.4
Solomon, E.5
-
29
-
-
0028240980
-
Chromosome-specific microsatellite sets for fluorescence-based, semiautomated genome mapping
-
Reed PW, Davies JL, Copeman JB et al. Chromosome-specific microsatellite sets for fluorescence-based, semiautomated genome mapping. Nat Genet 1994;7:390-5.
-
(1994)
Nat Genet
, vol.7
, pp. 390-395
-
-
Reed, P.W.1
Davies, J.2
Copeman, J.B.3
-
30
-
-
0031831322
-
Sometimes it's hot, sometimes it's not
-
Lernmark A, Ott J. Sometimes it's hot, sometimes it's not. Nat Genet 1998;19:213-4.
-
(1998)
Nat Genet
, vol.19
, pp. 213-214
-
-
Lernmark, A.1
Ott, J.2
-
31
-
-
0002710362
-
-
Gershon ES, Cloninger CR, eds. Washington, DC: American Psychiatric Press
-
Suarez B, Hampe C, Van Eerdewegh P. In: Gershon ES, Cloninger CR, eds. Genetic approaches to mental disorders. Washington, DC: American Psychiatric Press, 1994:23-46.
-
(1994)
Genetic Approaches to Mental Disorders
, pp. 23-46
-
-
Suarez, B.1
Hampe, C.2
Van Eerdewegh, P.3
-
32
-
-
0031729735
-
Hormone replacement therapy, other reproductive variables and symptomatic hip osteoarthritis in elderly white women: A case-control study
-
Dennison EM, Arden NK, Kellingray S, Croft P, Coggon D, Cooper C. Hormone replacement therapy, other reproductive variables and symptomatic hip osteoarthritis in elderly white women: a case-control study. Br J Rheumatol 1998;37:1198-1202.
-
(1998)
Br J Rheumatol
, vol.37
, pp. 1198-1202
-
-
Dennison, E.M.1
Arden, N.K.2
Kellingray, S.3
Croft, P.4
Coggon, D.5
Cooper, C.6
-
33
-
-
0027509678
-
Osteoarthritis associated with mild chondrodysplasia in transgenic mice expressing α1(IX) collagen chains with a central deletion
-
Nakata K, Ono K, Miyazaki J-I et al. Osteoarthritis associated with mild chondrodysplasia in transgenic mice expressing α1(IX) collagen chains with a central deletion. Proc Natl Acad Sci USA 1993;90:2870-4.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 2870-2874
-
-
Nakata, K.1
Ono, K.2
Miyazaki, J.-I.3
-
34
-
-
0028290671
-
Mice lacking α1(IX) collagen develop noninflammatory degenerative joint disease
-
Fassler R, Schnegelsberg PNJ, Dausman J et al. Mice lacking α1(IX) collagen develop noninflammatory degenerative joint disease. Proc Natl Acad Sci USA 1994; 91:5070-4.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 5070-5074
-
-
Fassler, R.1
Schnegelsberg, P.N.J.2
Dausman, J.3
|