94 related articles for article (PubMed ID: 12523047)
1. [Icelandic genealogical registry sheds light on the significance of heredity in osteoarthritis].
Ingvarsson T; Lohmander S
Lakartidningen; 2002 Nov; 99(47):4724-8. PubMed ID: 12523047
[TBL] [Abstract][Full Text] [Related]
2. Prevalence and inheritance of hip osteoarthritis in Iceland.
Ingvarsson T
Acta Orthop Scand Suppl; 2000 Dec; 298():1-46. PubMed ID: 11338422
[TBL] [Abstract][Full Text] [Related]
3. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
4. Strong linkage on 2q33.3 to familial early-onset generalized osteoarthritis and a consideration of two positional candidate genes.
Meulenbelt I; Min JL; van Duijn CM; Kloppenburg M; Breedveld FC; Slagboom PE
Eur J Hum Genet; 2006 Dec; 14(12):1280-7. PubMed ID: 16912703
[TBL] [Abstract][Full Text] [Related]
5. Heredity, genes and osteoarthritis.
Williams CJ; Jimenez SA
Rheum Dis Clin North Am; 1993 Aug; 19(3):523-43. PubMed ID: 8210573
[TBL] [Abstract][Full Text] [Related]
6. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
Jensen HK
Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167
[TBL] [Abstract][Full Text] [Related]
7. The genetic epidemiology of human primary osteoarthritis: current status.
Loughlin J
Expert Rev Mol Med; 2005 May; 7(9):1-12. PubMed ID: 15910695
[TBL] [Abstract][Full Text] [Related]
8. Recent advances in the genetic investigation of osteoarthritis.
Peach CA; Carr AJ; Loughlin J
Trends Mol Med; 2005 Apr; 11(4):186-91. PubMed ID: 15823757
[TBL] [Abstract][Full Text] [Related]
9. Genetic epidemiology of primary osteoarthritis.
Loughlin J
Curr Opin Rheumatol; 2001 Mar; 13(2):111-6. PubMed ID: 11224735
[TBL] [Abstract][Full Text] [Related]
10. Quantitative genetics of secondary hip joint osteoarthritis in a Labrador Retriever-Greyhound pedigree.
Hays L; Zhang Z; Mateescu RG; Lust G; Burton-Wurster NI; Todhunter RJ
Am J Vet Res; 2007 Jan; 68(1):35-41. PubMed ID: 17199416
[TBL] [Abstract][Full Text] [Related]
11. Identification of quantitative trait loci for osteoarthritis of hip joints in dogs.
Mateescu RG; Burton-Wurster NI; Tsai K; Phavaphutanon J; Zhang Z; Murphy KE; Lust G; Todhunter RJ
Am J Vet Res; 2008 Oct; 69(10):1294-300. PubMed ID: 18828685
[TBL] [Abstract][Full Text] [Related]
12. Lack of support for the presence of an osteoarthritis susceptibility locus on chromosome 6p.
Meenagh GK; McGibbon D; Nixon J; Wright GD; Doherty M; Hughes AE
Arthritis Rheum; 2005 Jul; 52(7):2040-3. PubMed ID: 15986344
[TBL] [Abstract][Full Text] [Related]
13. Is osteoarthritis a genetic disease?
Newman B; Wallis GA
Clin Invest Med; 2002 Aug; 25(4):139-49. PubMed ID: 12220042
[TBL] [Abstract][Full Text] [Related]
14. Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals.
Michaelides M; Johnson S; Simunovic MP; Bradshaw K; Holder G; Mollon JD; Moore AT; Hunt DM
Eye (Lond); 2005 Jan; 19(1):2-10. PubMed ID: 15094734
[TBL] [Abstract][Full Text] [Related]
15. Exclusion of an extracolonic disease modifier locus on chromosome 1p33-36 in a large Swiss familial adenomatous polyposis kindred.
Plasilova M; Russell AM; Wanner A; Wolf A; Dobbie Z; Müller HJ; Heinimann K
Eur J Hum Genet; 2004 May; 12(5):365-71. PubMed ID: 14735163
[TBL] [Abstract][Full Text] [Related]
16. The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants.
van Heel DA; Dechairo BM; Dawson G; McGovern DP; Negoro K; Carey AH; Cardon LR; Mackay I; Jewell DP; Lench NJ
Hum Mol Genet; 2003 Oct; 12(20):2569-75. PubMed ID: 12928481
[TBL] [Abstract][Full Text] [Related]
17. Lumbar disc disease shows linkage to chromosome 19 overlapping with a QTL for hand OA.
Williams FM; Kato BS; Livshits G; Sambrook PN; Spector TD; MacGregor AJ
Ann Rheum Dis; 2008 Jan; 67(1):117-9. PubMed ID: 17660224
[TBL] [Abstract][Full Text] [Related]
18. Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome.
Stalmans I
Verh K Acad Geneeskd Belg; 2005; 67(4):229-76. PubMed ID: 16334858
[TBL] [Abstract][Full Text] [Related]
19. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
Le Ber I; Camuzat A; Berger E; Hannequin D; Laquerrière A; Golfier V; Seilhean D; Viennet G; Couratier P; Verpillat P; Heath S; Camu W; Martinaud O; Lacomblez L; Vercelletto M; Salachas F; Sellal F; Didic M; Thomas-Anterion C; Puel M; Michel BF; Besse C; Duyckaerts C; Meininger V; Campion D; Dubois B; Brice A;
Neurology; 2009 May; 72(19):1669-76. PubMed ID: 19433740
[TBL] [Abstract][Full Text] [Related]
20. A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.
Lee H; Jen JC; Wang H; Chen Z; Mamsa H; Sabatti C; Baloh RW; Nelson SF
Hum Mol Genet; 2006 Jan; 15(2):251-8. PubMed ID: 16330481
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
