114 related articles for article (PubMed ID: 17549761)
1. Testing association for markers on the X chromosome.
Zheng G; Joo J; Zhang C; Geller NL
Genet Epidemiol; 2007 Dec; 31(8):834-43. PubMed ID: 17549761
[TBL] [Abstract][Full Text] [Related]
2. A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus.
Oldenburg RA; van Dooren MF; de Graaf B; Simons E; Govaerts L; Swagemakers S; Verkerk JM; Oostra BA; Bertoli-Avella AM
Hum Reprod; 2008 Dec; 23(12):2835-41. PubMed ID: 18689850
[TBL] [Abstract][Full Text] [Related]
3. Parathyroid hormone-responsive B1 gene is associated with premature ovarian failure.
Kang H; Lee SK; Kim MH; Song J; Bae SJ; Kim NK; Lee SH; Kwack K
Hum Reprod; 2008 Jun; 23(6):1457-65. PubMed ID: 18349106
[TBL] [Abstract][Full Text] [Related]
4. Acyl-CoA synthetase long-chain family member 6 is associated with premature ovarian failure.
Kang H; Lee SK; Kim MH; Choi H; Lee SH; Kwack K
Fertil Steril; 2009 Apr; 91(4 Suppl):1339-43. PubMed ID: 18555221
[TBL] [Abstract][Full Text] [Related]
5. A tag-single nucleotide polymorphisms approach to the vascular endothelial growth factor-A gene in age-related macular degeneration.
Richardson AJ; Islam FM; Guymer RH; Cain M; Baird PN
Mol Vis; 2007 Nov; 13():2148-52. PubMed ID: 18079689
[TBL] [Abstract][Full Text] [Related]
6. Genome-wide selection of tag SNPs using multiple-marker correlation.
Hao K
Bioinformatics; 2007 Dec; 23(23):3178-84. PubMed ID: 18006555
[TBL] [Abstract][Full Text] [Related]
7. Efficacy assessment of SNP sets for genome-wide disease association studies.
Wollstein A; Herrmann A; Wittig M; Nothnagel M; Franke A; Nürnberg P; Schreiber S; Krawczak M; Hampe J
Nucleic Acids Res; 2007; 35(17):e113. PubMed ID: 17726055
[TBL] [Abstract][Full Text] [Related]
8. Bayesian variable and model selection methods for genetic association studies.
Fridley BL
Genet Epidemiol; 2009 Jan; 33(1):27-37. PubMed ID: 18618760
[TBL] [Abstract][Full Text] [Related]
9. A 100K genome-wide association scan for diabetes and related traits in the Framingham Heart Study: replication and integration with other genome-wide datasets.
Florez JC; Manning AK; Dupuis J; McAteer J; Irenze K; Gianniny L; Mirel DB; Fox CS; Cupples LA; Meigs JB
Diabetes; 2007 Dec; 56(12):3063-74. PubMed ID: 17848626
[TBL] [Abstract][Full Text] [Related]
10. Protective effect of complement factor B and complement component 2 variants in age-related macular degeneration.
Spencer KL; Hauser MA; Olson LM; Schmidt S; Scott WK; Gallins P; Agarwal A; Postel EA; Pericak-Vance MA; Haines JL
Hum Mol Genet; 2007 Aug; 16(16):1986-92. PubMed ID: 17576744
[TBL] [Abstract][Full Text] [Related]
11. Effect of linkage disequilibrium between markers in linkage and association analyses.
Dupuis J; Albers K; Allen-Brady K; Cho K; Elston RC; Kappen HJ; Tang H; Thomas A; Thomson G; Tsung E; Yang Q; Zhang W; Zhao K; Zheng G; Ziegler JT
Genet Epidemiol; 2007; 31 Suppl 1():S139-48. PubMed ID: 18046770
[TBL] [Abstract][Full Text] [Related]
12. Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations.
Rampersaud E; Damcott CM; Fu M; Shen H; McArdle P; Shi X; Shelton J; Yin J; Chang YP; Ott SH; Zhang L; Zhao Y; Mitchell BD; O'Connell J; Shuldiner AR
Diabetes; 2007 Dec; 56(12):3053-62. PubMed ID: 17846126
[TBL] [Abstract][Full Text] [Related]
13. A general method for linkage disequilibrium correction for multipoint linkage and association.
Kurbasic A; Hössjer O
Genet Epidemiol; 2008 Nov; 32(7):647-57. PubMed ID: 18481794
[TBL] [Abstract][Full Text] [Related]
14. [Proceeding of research on X chromosome genetic markers].
Zhang WJ; Zhou XP; Jia ZJ
Fa Yi Xue Za Zhi; 2003; 19(4):249-52. PubMed ID: 14671805
[TBL] [Abstract][Full Text] [Related]
15. An efficient family-based association test using multiple markers.
Xu X; Rakovski C; Xu X; Laird N
Genet Epidemiol; 2006 Nov; 30(7):620-6. PubMed ID: 16868964
[TBL] [Abstract][Full Text] [Related]
16. Novel X-chromosomal defect associated with abnormal ovarian function.
Rao L; Babu A; Padmalatha V; Kanakavalli M; Deenadayal M; Singh L
J Obstet Gynaecol Res; 2005 Feb; 31(1):12-5. PubMed ID: 15669985
[TBL] [Abstract][Full Text] [Related]
17. Simple strategies for haplotype analysis of the X chromosome with application to age-related macular degeneration.
Jiang R; Dong J; Joo J; Geller NL; Zheng G
Eur J Hum Genet; 2011 Jul; 19(7):801-6. PubMed ID: 21386871
[TBL] [Abstract][Full Text] [Related]
18. Selection of single-nucleotide polymorphisms in disease association data.
Joo J; Tian X; Zheng G; Lin JP; Geller NL
BMC Genet; 2005 Dec; 6 Suppl 1(Suppl 1):S93. PubMed ID: 16451709
[TBL] [Abstract][Full Text] [Related]
19. Study of 25 X-chromosome SNPs in the Portuguese.
Pereira V; Tomas C; Amorim A; Morling N; Gusmão L; Prata MJ
Forensic Sci Int Genet; 2011 Aug; 5(4):336-8. PubMed ID: 21036684
[TBL] [Abstract][Full Text] [Related]
20. X chromosome association testing in genome wide association studies.
Hickey PF; Bahlo M
Genet Epidemiol; 2011 Nov; 35(7):664-70. PubMed ID: 21818774
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]