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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
Published in Nature genetics (01.11.2005)
Published in Nature genetics (01.11.2005)
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Multiplexed Variation Scanning for 1,000 Amplicons in Hundreds of Patients Using Mismatch Repair Detection (MRD) on Tag Arrays
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.
Published in Proceedings of the National Academy of Sciences - PNAS (11.10.2005)
Published in Proceedings of the National Academy of Sciences - PNAS (11.10.2005)
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Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay
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Published in Genome research (01.02.2005)
Published in Genome research (01.02.2005)
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A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22
Robertson, Neil, Gray, Julia, Goodfellow, Peter N, Sawcer, Stephen, Smaldon, Niki, Feakes, Robert, Compston, Alastair, Clayton, David, Jones, Hywel B, Chataway, Jeremy
Published in Nature genetics (01.08.1996)
Published in Nature genetics (01.08.1996)
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A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders
Sakurai, Takeshi, Reichert, Jennifer, Hoffman, Ellen J, Cai, Guiqing, Jones, Hywel B, Faham, Malek, Buxbaum, Joseph D
Published in Autism research (01.08.2008)
Published in Autism research (01.08.2008)
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Pairwise linkage disequilibrium under disease models
SCHRODI, Steven J, GARCIA, Veronica E, ROWLAND, Charley, JONES, Hywel B
Published in European journal of human genetics : EJHG (01.02.2007)
Published in European journal of human genetics : EJHG (01.02.2007)
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Optimal genotype determination in highly multiplexed SNP data
MOORHEAD, Martin, HARDENBOL, Paul, SIDDIQUI, Farooq, FALKOWSKI, Matthew, BRUCKNER, Carsten, IRELAND, James, JONES, Hywel B, JAIN, Maneesh, WILLIS, Thomas D, FAHAM, Malek
Published in European journal of human genetics : EJHG (01.02.2006)
Published in European journal of human genetics : EJHG (01.02.2006)
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Optimal genotype determination in highly multiplexed SNP data
Moorhead, Martin, Hardenbol, Paul, Siddiqui, Farooq, Falkowski, Matthew, Bruckner, Carsten, Ireland, James, Jones, Hywel B, Jain, Maneesh, Willis, Thomas D, Malek Faham
Published in European journal of human genetics : EJHG (01.08.2006)
Published in European journal of human genetics : EJHG (01.08.2006)
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A screen of candidates from peaks of linkage: evidence for the involvement of myeloperoxidase in multiple sclerosis
Chataway, Jeremy, Sawcer, Stephen, Feakes, Robert, Coraddu, Francesca, Broadley, Simon, Jones, Hywel B, Clayton, David, Gray, Julia, Goodfellow, Peter N, Compston, Alastair
Published in Journal of neuroimmunology (03.08.1999)
Published in Journal of neuroimmunology (03.08.1999)
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HLA typing in the United Kingdom multiple sclerosis genome screen
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
Published in Neurogenetics (01.12.1998)
Published in Neurogenetics (01.12.1998)
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No evidence for association of multiple sclerosis with the complement factors C6 and C7
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
Published in Journal of neuroimmunology (01.09.1999)
Published in Journal of neuroimmunology (01.09.1999)
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Evidence that allelic variants of the spinocerebellar ataxia type 2 gene influence susceptibility to multiple sclerosis
Chataway, J, Sawcer, S, Coraddu, F, Feakes, R, Broadley, S, Jones, H B, Clayton, D, Gray, J, Goodfellow, P N, Compston, A
Published in Neurogenetics (01.04.1999)
Published in Neurogenetics (01.04.1999)
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Pairwise linkage disequilibrium under disease models
Schrodi, Steven J, Garcia, Veronica E, Rowland, Charley, Jones, Hywel B
Published in European journal of human genetics : EJHG (01.02.2007)
Published in European journal of human genetics : EJHG (01.02.2007)
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Erratum: Optimal genotype determination in highly multiplexed SNP data
Moorhead, Martin, Hardenbol, Paul, Siddiqui, Farooq, Falkowski, Matthew, Bruckner, Carsten, Ireland, James, Jones, Hywel B, Jain, Maneesh, Willis, Thomas D, Faham, Malek
Published in European journal of human genetics : EJHG (25.07.2006)
Published in European journal of human genetics : EJHG (25.07.2006)
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Response to Kruglyak
Sawcer, Stephen, Jones, Hywel B., Clayton, David
Published in American journal of human genetics (01.04.1998)
Published in American journal of human genetics (01.04.1998)
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The relative power of linkage and association studies for the detection of genes involved in hypertension
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