572 related articles for article (PubMed ID: 17785532)
1. Prediction of individual genetic risk to disease from genome-wide association studies.
Wray NR; Goddard ME; Visscher PM
Genome Res; 2007 Oct; 17(10):1520-8. PubMed ID: 17785532
[TBL] [Abstract][Full Text] [Related]
2. Genome-wide strategies for detecting multiple loci that influence complex diseases.
Marchini J; Donnelly P; Cardon LR
Nat Genet; 2005 Apr; 37(4):413-7. PubMed ID: 15793588
[TBL] [Abstract][Full Text] [Related]
3. Identification of susceptibility loci contributing to a complex disease using conventional segregation, linkage, and association methods.
Falk CT; Ashley A; Lamb N; Sherman SL
Genet Epidemiol; 1995; 12(6):601-6. PubMed ID: 8787980
[TBL] [Abstract][Full Text] [Related]
4. Evaluation of genome-wide power of genetic association studies based on empirical data from the HapMap project.
Nannya Y; Taura K; Kurokawa M; Chiba S; Ogawa S
Hum Mol Genet; 2007 Oct; 16(20):2494-505. PubMed ID: 17666406
[TBL] [Abstract][Full Text] [Related]
5. Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.
Weiss LA
Expert Rev Mol Diagn; 2009 Nov; 9(8):795-803. PubMed ID: 19895225
[TBL] [Abstract][Full Text] [Related]
6. Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies.
Lin S; Chakravarti A; Cutler DJ
Nat Genet; 2004 Nov; 36(11):1181-8. PubMed ID: 15502828
[TBL] [Abstract][Full Text] [Related]
7. How many genes underlie the occurrence of common complex diseases in the population?
Yang Q; Khoury MJ; Friedman J; Little J; Flanders WD
Int J Epidemiol; 2005 Oct; 34(5):1129-37. PubMed ID: 16043441
[TBL] [Abstract][Full Text] [Related]
8. Analysis of HLA and non-HLA alleles can identify individuals at high risk for celiac disease.
Romanos J; van Diemen CC; Nolte IM; Trynka G; Zhernakova A; Fu J; Bardella MT; Barisani D; McManus R; van Heel DA; Wijmenga C
Gastroenterology; 2009 Sep; 137(3):834-40, 840.e1-3. PubMed ID: 19454285
[TBL] [Abstract][Full Text] [Related]
9. Optimal two-stage strategy for detecting interacting genes in complex diseases.
Ionita I; Man M
BMC Genet; 2006 Jun; 7():39. PubMed ID: 16776843
[TBL] [Abstract][Full Text] [Related]
10. A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST).
Morgenthaler S; Thilly WG
Mutat Res; 2007 Feb; 615(1-2):28-56. PubMed ID: 17101154
[TBL] [Abstract][Full Text] [Related]
11. Using genome-wide pathway analysis to unravel the etiology of complex diseases.
Elbers CC; van Eijk KR; Franke L; Mulder F; van der Schouw YT; Wijmenga C; Onland-Moret NC
Genet Epidemiol; 2009 Jul; 33(5):419-31. PubMed ID: 19235186
[TBL] [Abstract][Full Text] [Related]
12. Implications of small effect sizes of individual genetic variants on the design and interpretation of genetic association studies of complex diseases.
Ioannidis JP; Trikalinos TA; Khoury MJ
Am J Epidemiol; 2006 Oct; 164(7):609-14. PubMed ID: 16893921
[TBL] [Abstract][Full Text] [Related]
13. Association mapping of complex diseases in linked regions: estimation of genetic effects and feasibility of testing rare variants.
Wang WY; Cordell HJ; Todd JA
Genet Epidemiol; 2003 Jan; 24(1):36-43. PubMed ID: 12508254
[TBL] [Abstract][Full Text] [Related]
14. The allelic spectra of common diseases may resemble the allelic spectrum of the full genome.
Wang WY; Pike N
Med Hypotheses; 2004; 63(4):748-51. PubMed ID: 15325027
[TBL] [Abstract][Full Text] [Related]
15. Risk estimation for multifactorial diseases. A report of the International Commission on Radiological Protection.
Ann ICRP; 1999; 29(3-4):1-144. PubMed ID: 11108911
[TBL] [Abstract][Full Text] [Related]
16. Screening large-scale association study data: exploiting interactions using random forests.
Lunetta KL; Hayward LB; Segal J; Van Eerdewegh P
BMC Genet; 2004 Dec; 5():32. PubMed ID: 15588316
[TBL] [Abstract][Full Text] [Related]
17. Simultaneous estimation of gene-gene and gene-environment interactions for numerous loci using double penalized log-likelihood.
Tanck MW; Jukema JW; Zwinderman AH
Genet Epidemiol; 2006 Dec; 30(8):645-51. PubMed ID: 16917921
[TBL] [Abstract][Full Text] [Related]
18. Schizophrenia genetics: advancing on two fronts.
Owen MJ; Williams HJ; O'Donovan MC
Curr Opin Genet Dev; 2009 Jun; 19(3):266-70. PubMed ID: 19345090
[TBL] [Abstract][Full Text] [Related]
19. Genome-wide SNP association: identification of susceptibility alleles for osteoarthritis.
Abel K; Reneland R; Kammerer S; Mah S; Hoyal C; Cantor CR; Nelson MR; Braun A
Autoimmun Rev; 2006 Apr; 5(4):258-63. PubMed ID: 16697966
[TBL] [Abstract][Full Text] [Related]
20. Recent progress in rheumatoid arthritis genetics: one step towards improved patient care.
Plenge RM
Curr Opin Rheumatol; 2009 May; 21(3):262-71. PubMed ID: 19365266
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
