411 related articles for article (PubMed ID: 25585700)
1. Where is the causal variant? On the advantage of the family design over the case-control design in genetic association studies.
Dandine-Roulland C; Perdry H
Eur J Hum Genet; 2015 Oct; 23(10):1357-63. PubMed ID: 25585700
[TBL] [Abstract][Full Text] [Related]
2. Risk alleles for multiple sclerosis in multiplex families.
D'Netto MJ; Ward H; Morrison KM; Ramagopalan SV; Dyment DA; DeLuca GC; Handunnetthi L; Sadovnick AD; Ebers GC
Neurology; 2009 Jun; 72(23):1984-8. PubMed ID: 19506219
[TBL] [Abstract][Full Text] [Related]
3. Joint modeling of linkage and association: identifying SNPs responsible for a linkage signal.
Li M; Boehnke M; Abecasis GR
Am J Hum Genet; 2005 Jun; 76(6):934-49. PubMed ID: 15877278
[TBL] [Abstract][Full Text] [Related]
4. The expected power of genome-wide linkage disequilibrium testing using single nucleotide polymorphism markers for detecting a low-frequency disease variant.
Ohashi J; Tokunaga K
Ann Hum Genet; 2002 Jul; 66(Pt 4):297-306. PubMed ID: 12418970
[TBL] [Abstract][Full Text] [Related]
5. Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies.
Zhang K; Qin ZS; Liu JS; Chen T; Waterman MS; Sun F
Genome Res; 2004 May; 14(5):908-16. PubMed ID: 15078859
[TBL] [Abstract][Full Text] [Related]
6. Detection of inappropriate samples in association studies by an IBS-based method considering linkage disequilibrium between genetic markers.
Andoh M; Sato Y; Sakamoto H; Yoshida T; Ohtaki M
J Hum Genet; 2010 Jul; 55(7):436-40. PubMed ID: 20448652
[TBL] [Abstract][Full Text] [Related]
7. A statistical method for identification of polymorphisms that explain a linkage result.
Sun L; Cox NJ; McPeek MS
Am J Hum Genet; 2002 Feb; 70(2):399-411. PubMed ID: 11791210
[TBL] [Abstract][Full Text] [Related]
8. Contributions of linkage disequilibrium and co-segregation information to the accuracy of genomic prediction.
Sun X; Fernando R; Dekkers J
Genet Sel Evol; 2016 Oct; 48(1):77. PubMed ID: 27729012
[TBL] [Abstract][Full Text] [Related]
9. Tag SNP selection for association studies.
Stram DO
Genet Epidemiol; 2004 Dec; 27(4):365-74. PubMed ID: 15372618
[TBL] [Abstract][Full Text] [Related]
10. Evaluating the power to discriminate between highly correlated SNPs in genetic association studies.
Udler MS; Tyrer J; Easton DF
Genet Epidemiol; 2010 Jul; 34(5):463-8. PubMed ID: 20583289
[TBL] [Abstract][Full Text] [Related]
11. Analysis of single-locus tests to detect gene/disease associations.
Roeder K; Bacanu SA; Sonpar V; Zhang X; Devlin B
Genet Epidemiol; 2005 Apr; 28(3):207-19. PubMed ID: 15637715
[TBL] [Abstract][Full Text] [Related]
12. Risk alleles for multiple sclerosis identified by a genomewide study.
; Hafler DA; Compston A; Sawcer S; Lander ES; Daly MJ; De Jager PL; de Bakker PI; Gabriel SB; Mirel DB; Ivinson AJ; Pericak-Vance MA; Gregory SG; Rioux JD; McCauley JL; Haines JL; Barcellos LF; Cree B; Oksenberg JR; Hauser SL
N Engl J Med; 2007 Aug; 357(9):851-62. PubMed ID: 17660530
[TBL] [Abstract][Full Text] [Related]
13. Association of SNPs rs6498169 and rs10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease.
Al Jumah M; Al Balwi M; Hussein M; Kojan S; Al Khathaami A; Al Fawaz M; Al Muzaini B; Jawhary A; Al Abdulkareem I
Mult Scler; 2012 Oct; 18(10):1395-400. PubMed ID: 22492128
[TBL] [Abstract][Full Text] [Related]
14. Detailed analysis of the relative power of direct and indirect association studies and the implications for their interpretation.
Moskvina V; O'Donovan MC
Hum Hered; 2007; 64(1):63-73. PubMed ID: 17483598
[TBL] [Abstract][Full Text] [Related]
15. Selecting single-nucleotide polymorphisms for association studies with SNPbrowser software.
De La Vega FM
Methods Mol Biol; 2007; 376():177-93. PubMed ID: 17984546
[TBL] [Abstract][Full Text] [Related]
16. Comparative power of family-based association strategies to detect disease-causing variants under two-locus models.
Babron MC; Guilloud-Bataille M; Sahbatou M; Demenais F; Génin E; Dizier MH
Genet Epidemiol; 2012 Dec; 36(8):848-55. PubMed ID: 22887021
[TBL] [Abstract][Full Text] [Related]
17. Genetic association between polymorphisms in the ADAMTS14 gene and multiple sclerosis.
Goertsches R; Comabella M; Navarro A; Perkal H; Montalban X
J Neuroimmunol; 2005 Jul; 164(1-2):140-7. PubMed ID: 15913795
[TBL] [Abstract][Full Text] [Related]
18. Association of the FCN2 Gene Single Nucleotide Polymorphisms with Susceptibility to Pulmonary Tuberculosis.
Xu DD; Wang C; Jiang F; Wei LL; Shi LY; Yu XM; Liu CM; Liu XH; Feng XM; Ping ZP; Jiang TT; Chen ZL; Li ZJ; Li JC
PLoS One; 2015; 10(9):e0138356. PubMed ID: 26379154
[TBL] [Abstract][Full Text] [Related]
19. On selecting markers for association studies: patterns of linkage disequilibrium between two and three diallelic loci.
Garner C; Slatkin M
Genet Epidemiol; 2003 Jan; 24(1):57-67. PubMed ID: 12508256
[TBL] [Abstract][Full Text] [Related]
20. Stochastic search and joint fine-mapping increases accuracy and identifies previously unreported associations in immune-mediated diseases.
Asimit JL; Rainbow DB; Fortune MD; Grinberg NF; Wicker LS; Wallace C
Nat Commun; 2019 Jul; 10(1):3216. PubMed ID: 31324808
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
