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Number of items: 24.
2014
Preston, MD;
Dudbridge, F;
(2014)
Utilising family-based designs for detecting rare variant disease associations.
Annals of human genetics, 78 (2).
pp. 129-40.
ISSN 0003-4800
DOI: https://doi.org/10.1111/ahg.12051
Sepúlveda, N;
Manjurano, A;
Drakeley, C;
Clark, TG;
(2014)
On the Performance of Multiple Imputation Based on Chained Equations in Tackling Missing Data of the African α(3.7) -Globin Deletion in a Malaria Association Study.
Annals of human genetics, 78 (4).
pp. 277-89.
ISSN 0003-4800
DOI: https://doi.org/10.1111/ahg.12065
2011
Dudbridge, F;
Holmans, PA;
Wilson, SG;
(2011)
A Flexible Model for Association Analysis in Sibships with Missing Genotype Data.
Annals of human genetics.
ISSN 0003-4800
DOI: https://doi.org/10.1111/j.1469-1809.2010.00636.x
Full text not available from this repository.
Zabaneh, D;
Gaunt, TR;
Kumari, M;
Drenos, F;
Shah, S;
Berry, D;
Power, C;
Hypponen, E;
Shah, T;
Palmen, J;
+18 more...
Pallas, J;
Talmud, PJ;
Casas, JP;
Sofat, R;
Lowe, G;
Rumley, A;
Morris, RW;
Whincup, PH;
Rodriguez, S;
Ebrahim, S;
Marmot, MG;
Smith, GD;
Lawlor, DA;
Kivimaki, M;
Whittaker, J;
Hingorani, AD;
Day, IN;
Humphries, SE;
(2011)
Genetic Variants Associated with von Willebrand Factor Levels in Healthy Men and Women Identified Using the HumanCVD BeadChip.
Annals of human genetics.
ISSN 0003-4800
DOI: https://doi.org/10.1111/j.1469-1809.2011.00654.x
Full text not available from this repository.
2009
Kulinskaya, E;
Lewin, A;
(2009)
Testing for linkage and Hardy-Weinberg disequilibrium.
Annals of human genetics, 73 (2).
pp. 253-62.
ISSN 0003-4800
DOI: https://doi.org/10.1111/j.1469-1809.2008.00501.x
2008
Chapman, JM;
Onnie, C;
Prescott, N;
Fisher, S;
Lewis, C;
Mathew, C;
Verzilli, CJ;
Whittaker, JC;
(2008)
Searching for genotype-phenotype structure: Trying to understand Crohn's disease.
Annals of human genetics, 72.
p. 688.
ISSN 0003-4800
https://researchonline.lshtm.ac.uk/id/eprint/7101
Full text not available from this repository.
Newcombe, PJ;
Verzilli, C;
Pablo-Casas, J;
Whittaker, J;
(2008)
Meta-analysis of gene/disease association studies.
Annals of human genetics, 72.
p. 689.
ISSN 0003-4800
https://researchonline.lshtm.ac.uk/id/eprint/7102
Full text not available from this repository.
Rhodes, B;
Meek, J;
Whittaker, JC;
Vyse, TJ;
(2008)
Quantification of the Genetic Component of Basal C-Reactive Protein Expression in SLE Nuclear Families.
Annals of human genetics, 72 (Pt 5).
pp. 611-20.
ISSN 0003-4800
DOI: https://doi.org/10.1111/j.1469-1809.2008.00444.x
Full text not available from this repository.
Rhodes, B;
Meek, J;
Whittaker, JC;
Vyse, TJ;
(2008)
Quantification of the genetic component of basal C-reactive protein expression in SLE nuclear families.
Annals of human genetics, 72.
pp. 611-620.
ISSN 0003-4800
https://researchonline.lshtm.ac.uk/id/eprint/7103
Full text not available from this repository.
Teo, YY;
Small, KS;
Clark, TG;
Kwiatkowski, DP;
(2008)
Perturbation analysis: a simple method for filtering SNPs with erroneous genotyping in genome-wide association studies.
Annals of human genetics, 72 (Pt 3).
pp. 368-74.
ISSN 0003-4800
DOI: https://doi.org/10.1111/j.1469-1809.2007.00422.x
Full text not available from this repository.
2007
Chapman, J;
Verzilli, C;
Whittaker, J;
(2007)
Large scale association studies: Implications for FDRs and a simple Bayesian alternative.
[Conference or Workshop Item]
https://researchonline.lshtm.ac.uk/id/eprint/8555
Full text not available from this repository.
Drenos, F;
Whittaker, JC;
Humphries, SE;
(2007)
The use of meta-analysis risk estimates for candidate genes in combination to predict coronary heart disease risk.
Annals of human genetics, 71 (Pt 5).
pp. 611-9.
ISSN 0003-4800
DOI: https://doi.org/10.1111/j.1469-1809.2007.00359.x
Full text not available from this repository.
Hoggart, C;
de Iorio, M;
Whittaker, J;
Balding, D;
(2007)
Bayesian shrinkage priors for detecting multiple causal variants from genome-wide association studies.
Annals of human genetics, 71.
p. 557.
ISSN 0003-4800
https://researchonline.lshtm.ac.uk/id/eprint/8558
Full text not available from this repository.
Monaco, A;
Falcaro, M;
Consortium, ATS;
(2007)
Multivariate linkage analysis of Specific Language Impairment (SLI).
Annals of human genetics, 71.
pp. 660-673.
ISSN 0003-4800
https://researchonline.lshtm.ac.uk/id/eprint/1654
Full text not available from this repository.
Palla, L;
Siegmund, D;
(2007)
The effect of assortative mating on the power of transmission disequilibrium test.
[Conference or Workshop Item]
https://researchonline.lshtm.ac.uk/id/eprint/1924821
Full text not available from this repository.
Teo, YY;
Fry, AE;
Clark, TG;
Tai, ES;
Seielstad, M;
(2007)
On the usage of HWE for identifying genotyping errors.
Annals of human genetics, 71 (Pt 5).
701-3; author reply 704.
ISSN 0003-4800
DOI: https://doi.org/10.1111/j.1469-1809.2007.00356.x
Full text not available from this repository.
Verzilli, C;
Chapman, J;
Hingorani, A;
Pablo-Casas, J;
Shah, T;
Smeeth, L;
Whittaker, J;
(2007)
Bayesian meta analysis of genetic association studies with different sets of markers.
Annals of human genetics, 71.
pp. 552-553.
ISSN 0003-4800
https://researchonline.lshtm.ac.uk/id/eprint/8490
Full text not available from this repository.
2006
Baksh, MF;
Balding, DJ;
Vyse, TJ;
Whittaker, JC;
(2006)
A likelihood ratio approach to family-based association studies with covariates.
Annals of human genetics, 70 (Pt 1).
pp. 131-9.
ISSN 0003-4800
DOI: https://doi.org/10.1111/j.1529-8817.2005.00189.x
Full text not available from this repository.
Casas, JP;
Cooper, J;
Miller, GJ;
Hingorani, AD;
Humphries, SE;
(2006)
Investigating the genetic determinants of cardiovascular disease using candidate genes and meta-analysis of association studies.
Annals of human genetics, 70.
pp. 145-169.
ISSN 0003-4800
https://researchonline.lshtm.ac.uk/id/eprint/12818
Full text not available from this repository.
2005
Pardi, F;
Lewis, CM;
Whittaker, JC;
(2005)
SNP selection for association studies: Maximizing power across SNP choice and study size.
Annals of human genetics, 69.
pp. 733-746.
ISSN 0003-4800
DOI: https://doi.org/10.1111/j.1529-8817.2005.00202.x
Full text not available from this repository.
2004
Bonilla, C;
Parra, EJ;
Pfaff, CL;
Dios, S;
Marshall, JA;
Hamman, RF;
Ferrell, RE;
Hoggart, CL;
McKeigue, PM;
Shriver, MD;
(2004)
Admixture in the Hispanics of the San Luis Valley, Colorado, and its implications for complex trait gene mapping.
Annals of human genetics, 68 (2).
pp. 139-153.
ISSN 0003-4800
DOI: https://doi.org/10.1046/j.1529-8817.2003.00084.x
Full text not available from this repository.
2003
Byng, MC;
Whittaker, JC;
Cuthbert, AP;
Mathew, CG;
Lewis, CM;
(2003)
SNP subset selection for genetic association studies.
Annals of human genetics, 67 (Pt 6).
pp. 543-56.
ISSN 0003-4800
DOI: https://doi.org/10.1046/j.1529-8817.2003.00055.x
Full text not available from this repository.
2001
Whittaker, JC;
Morris, AP;
(2001)
Family-based tests of association and/or linkage.
Annals of human genetics, 65 (Pt 5).
pp. 407-19.
ISSN 0003-4800
DOI: https://doi.org/10.1017/S0003480001008818
Full text not available from this repository.
2000
McKeigue, P M;
Carpenter, J R;
Parra, E J;
Shriver, M D;
(2000)
Estimation of admixture and detection of linkage in admixed populations by a Bayesian approach: application to African-American populations.
Annals of human genetics, 64 (Pt 2).
pp. 171-86.
ISSN 0003-4800
https://researchonline.lshtm.ac.uk/id/eprint/19869
Full text not available from this repository.