Population structure, differential bias and genomic control in a large-scale, case-control association study von Clayton, David G, Todd, John A, Walker, Neil M, Smyth, Deborah J, Pask, Rebecca, Cooper, Jason D, Maier, Lisa M, Smink, Luc J, Lam, Alex C, Ovington, Nigel R, Stevens, Helen E, Nutland, Sarah, Howson, Joanna M M, Faham, Malek, Moorhead, Martin, Jones, Hywel B, Falkowski, Matthew, Hardenbol, Paul, Willis, Thomas D

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Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay von Hardenbol, Paul, Yu, Fuli, Belmont, John, Mackenzie, Jennifer, Bruckner, Carsten, Brundage, Tiffany, Boudreau, Andrew, Chow, Steve, Eberle, Jim, Erbilgin, Ayca, Falkowski, Mat, Fitzgerald, Ron, Ghose, Sy, Iartchouk, Oleg, Jain, Maneesh, Karlin-Neumann, George, Lu, Xiuhua, Miao, Xin, Moore, Bridget, Moorhead, Martin, Namsaraev, Eugeni, Pasternak, Shiran, Prakash, Eunice, Tran, Karen, Wang, Zhiyong, Jones, Hywel B, Davis, Ronald W, Willis, Thomas D, Gibbs, Richard A

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Multiplexed Variation Scanning for 1,000 Amplicons in Hundreds of Patients Using Mismatch Repair Detection (MRD) on Tag Arrays von Faham, Malek, Jianbiao Zheng, Martin Moorhead, Fakhrai-Rad, Hossein, Eugeni Namsaraev, Kee Wong, Wang, Zhiyong, Shu G. Chow, Liana Lee, Kent Suyenaga, Jennifer Reichert, Andrew Boudreau, Eberle, James, Carsten Bruckner, Maneesh Jain, George Karlin-Neumann, Jones, Hywel B., Willis, Thomas D., Buxbaum, Joseph D., Davis, Ronald W.

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A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22 von Robertson, Neil, Gray, Julia, Goodfellow, Peter N, Sawcer, Stephen, Smaldon, Niki, Feakes, Robert, Compston, Alastair, Clayton, David, Jones, Hywel B, Chataway, Jeremy

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A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders von Sakurai, Takeshi, Reichert, Jennifer, Hoffman, Ellen J., Cai, Guiqing, Jones, Hywel B., Faham, Malek, Buxbaum, Joseph D.

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Pairwise linkage disequilibrium under disease models von Schrodi, Steven J, Garcia, Veronica E, Rowland, Charley, Jones, Hywel B

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Optimal genotype determination in highly multiplexed SNP data von Moorhead, Martin, Hardenbol, Paul, Siddiqui, Farooq, Falkowski, Matthew, Bruckner, Carsten, Ireland, James, Jones, Hywel B, Jain, Maneesh, Willis, Thomas D, Faham, Malek

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Molecular and morphological evidence on the phylogeny of the Elephantidae von Thomas, Mark G., Hagelberg, Erika, Jones, Hywel B., Yang, Ziheng, Lister, Adrian M.

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Evidence and Implications for Multiplicative Interactions among Loci Predisposing to Human Common Disease von Jones, Hywel B., Faham, Malek

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Optimal genotype determination in highly multiplexed SNP data von Moorhead, Martin, Hardenbol, Paul, Siddiqui, Farooq, Falkowski, Matthew, Bruckner, Carsten, Ireland, James, Jones, Hywel B, Jain, Maneesh, Willis, Thomas D, Malek Faham

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A screen of candidates from peaks of linkage: evidence for the involvement of myeloperoxidase in multiple sclerosis von Chataway, Jeremy, Sawcer, Stephen, Feakes, Robert, Coraddu, Francesca, Broadley, Simon, Jones, Hywel B, Clayton, David, Gray, Julia, Goodfellow, Peter N, Compston, Alastair

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HLA typing in the United Kingdom multiple sclerosis genome screen von Coraddu, F, Sawcer, S, Feakes, R, Chataway, J, Broadley, S, Jones, H B, Clayton, D, Gray, J, Smith, S, Taylor, C, Goodfellow, P N, Compston, A

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No evidence for association of multiple sclerosis with the complement factors C6 and C7 von Chataway, Jeremy, Sawcer, Stephen, Sherman, David, Hobart, Michael, Fernie, Barbara, Coraddu, Francesca, Feakes, Robert, Broadley, Simon, Gray, Julia, Jones, Hywel B, Clayton, David, Goodfellow, Peter N, Compston, Alastair

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Evidence that allelic variants of the spinocerebellar ataxia type 2 gene influence susceptibility to multiple sclerosis von Chataway, J, Sawcer, S, Coraddu, F, Feakes, R, Broadley, S, Jones, H B, Clayton, D, Gray, J, Goodfellow, P N, Compston, A

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Pairwise linkage disequilibrium under disease models von Schrodi, Steven J, Garcia, Veronica E, Rowland, Charley, Jones, Hywel B

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A Review of Statistical Methods for Genome Mapping von Jones, Hywel B.

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Erratum: Optimal genotype determination in highly multiplexed SNP data von Moorhead, Martin, Hardenbol, Paul, Siddiqui, Farooq, Falkowski, Matthew, Bruckner, Carsten, Ireland, James, Jones, Hywel B, Jain, Maneesh, Willis, Thomas D, Faham, Malek

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The relative power of linkage and association studies for the detection of genes involved in hypertension von Jones, Hywel B.

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Empirical genomewide significance levels established by whole genome simulations von Sawcer, Stephen, Jones, Hywel B., Judge, David, Visser, Frank, Compston, Alastair, Goodfellow, Peter N., Clayton, David

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Response to Kruglyak von Sawcer, Stephen, Jones, Hywel B., Clayton, David

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