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Dr Joanne Knight

Reader in Applied Data Science

  1. 2017
  2. E-pub ahead of print

    Genome-wide association study of a nicotine metabolism biomarker in African American smokers: impact of chromosome 19 genetic influences

    Chenoweth, M. J., Ware, J. J., Zhu, A. Z. X., Cole, C. B., Cox, L. S., Nollen, N., Ahluwalia, J. S., Benowitz, N. L., Schnoll, R. A., Hawk, L. W., Cinciripini, P. M., George, T. P., Lerman, C., Knight, J., Tyndale, R. F. & PGRN-PNAT Research Group 2/11/2017 In : Addiction. 15 p.

    Research output: Contribution to journalJournal article

  3. Published

    Genetic epistasis regulates amyloid deposition in resilient aging

    Felsky, D., Xu, J., Chibnik, L., Schneider, J., Knight, J., Kennedy, J. L., Bennett, D. A., De Jager, P. L. & Voineskos, A. N. 10/2017 In : Alzheimer's and Dementia. 13, 10, p. 1107-1116 10 p.

    Research output: Contribution to journalJournal article

  4. Published
  5. Published

    Heritability of hippocampal subfield volumes using a twin and non-twin siblings design

    Patel, S., Park, M. T. M., Devenyi, G. A., Patel, R., Masellis, M., Knight, J. & Chakravarty, M. M. 09/2017 In : Human Brain Mapping. 38, 9, p. 4337-4352 16 p.

    Research output: Contribution to journalJournal article

  6. Published

    Fine-mapping inflammatory bowel disease loci to single-variant resolution

    Knight, J. & 46 others Huang, H., Fang, M., Jostins, L., Umićević Mirkov, M., Boucher, G., Anderson, C. A., Andersen, V., Cleynen, I., Cortes, A., Crins, F., D'Amato, M., Deffontaine, V., Dmitrieva, J., Docampo, E., Elansary, M., Farh, K. K-H., Franke, A., Gori, A-S., Goyette, P., Halfvarson, J., Haritunians, T., Lawrance, I. C., Lees, C. W., Louis, E., Mariman, R., Meuwissen, T., Mni, M., Momozawa, Y., Parkes, M., Spain, S. L., Théâtre, E., Trynka, G., Satsangi, J., van Sommeren, S., Vermeire, S., Xavier, R. J., Weersma, R. K., Duerr, R. H., Mathew, C. G., Rioux, J. D., McGovern, D. P. B., Cho, J. H., Georges, M., Daly, M. J., Barrett, J. C. & International Inflammatory Bowel Disease Genetics Consortium 13/07/2017 In : Nature. 547, 7662, p. 173-178 6 p.

    Research output: Contribution to journalJournal article

  7. Published

    Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

    Knight, J., Project MinE GWAS Consortium & Schizophrenia Working Group of the Psychiatric Genomics Consortium 21/03/2017 In : Nature Communications. 8, 12 p., 14774

    Research output: Contribution to journalJournal article

  8. Published

    Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk

    Knight, J. & 63 others Warren, H. R., Evangelou, E., Cabrera, C. P., Gao, H., Ren, M., Mifsud, B., Ntalla, I., Surendran, P., Liu, C., Cook, J. P., Kraja, A. T., Drenos, F., Loh, M., Verweij, N., Marten, J., Karaman, I., Lepe, M. P. S., O'Reilly, P. F., Snieder, H., Kato, N., He, J., Tai, E. S., Said, M. A., Porteous, D., Alver, M., Poulter, N., Farrall, M., Gansevoort, R. T., Padmanabhan, S., Mägi, R., Stanton, A., Connell, J., Bakker, S. J. L., Metspalu, A., Shields, D. C., Thom, S., Brown, M., Sever, P., Esko, T., Hayward, C., van der Harst, P., Saleheen, D., Chowdhury, R., Chambers, J. C., Chasman, D. I., Chakravarti, A., Newton-Cheh, C., Lindgren, C. M., Levy, D., Kooner, J. S., Keavney, B., Tomaszewski, M., Samani, N. J., Howson, J. M. M., Tobin, M. D., Munroe, P. B., Ehret, G. B., Wain, L. V., Barnes, M. R., Tzoulaki, I., Caulfield, M. J., Elliott, P. & International Consortium of Blood Pressure (ICBP) 1000G Analyses 20/02/2017 In : Nature Genetics. 49, p. 403-415 13 p.

    Research output: Contribution to journalJournal article

  9. Published

    Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

    CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium 01/2017 In : Nature Genetics. 49, p. 27-35 9 p.

    Research output: Contribution to journalJournal article

  10. 2016
  11. Published

    Genomics implicates adaptive and innate immunity in Alzheimer’s and Parkinson’s diseases

    Gagliano, S. A., Pouget, J. G., Hardy, J., Knight, J., Barnes, M. R., Ryten, M. & Weale, M. 12/2016 In : Annals of Clinical and Translational Neurology. 3, 12, p. 924-933 10 p.

    Research output: Contribution to journalJournal article

  12. Published

    CEREBRAL PERFUSION AS AN IMAGING BIOMARKER OF PRESYMPTOMATIC GENETIC FRONTOTEMPORAL DEMENTIA: PRELIMINARY RESULTS FROM THE GENETIC FRONTOTEMPORAL DEMENTIA INITIATIVE (GENFI)

    Mutsaerts, H. J. M. M. & Knight, J. 07/2016 In : Alzheimer's and Dementia. 12, 7 Suppl., p. P409-P411 3 p.

    Research output: Contribution to journalMeeting abstract

  13. Published

    Dopamine D2 receptor gene variants and response to rasagiline in early Parkinson's disease: a pharmacogenetic study

    Masellis, M., Collinson, S., Freeman, N., Tampakeras, M., Levy, J., Tchelet, A., Eyal, E., Berkovich, E., Eliaz, R. E., Abler, V., Grossman, I., Fitzer-Attas, C., Tiwari, A., Hayden, M. R., Kennedy, J. L., Lang, A. E., Knight, J. & ADAGIO investigators 07/2016 In : Brain. 139, 7, p. 2050-2062 13 p.

    Research output: Contribution to journalJournal article

  14. Published

    Investigating the causal relationship of C-reactive protein with 32 complex somatic and psychiatric outcomes: a large-scale cross-consortium Mendelian randomization study

    Knight, J. & 47 others Prins, B. P., Abbasi, A., Wong, A., Vaez, A., Nolte, I., Franceschini, N., Stuart, P. E., Guterriez Achury, J., Mistry, V., Bradfield, J. P., Valdes, A. M., Bras, J., Shatunov, A., Lu, C., Han, B., Raychaudhuri, S., Bevan, S., Mayes, M. D., Tsoi, L. C., Evangelou, E., Nair, R. P., Grant, S. F. A., Polychronakos, C., Radstake, T. R. D., van Heel, D. A., Dunstan, M. L., Wood, N. W., Al-Chalabi, A., Dehghan, A., Hakonarson, H., Markus, H. S., Elder, J. T., Arking, D. E., Spector, T. D., Koeleman, B. P. C., van Duijn, C. M., Martin, J., Morris, A. P., Weersma, R. K., Wijmenga, C., Munroe, P. B., Perry, J. R. B., Pouget, J. G., Jamshidi, Y., Snieder, H., Alizadeh, B. Z. & PAGE Consortium 21/06/2016 In : PLoS Medicine. 13, 6, 29 p., e1001976

    Research output: Contribution to journalJournal article

  15. E-pub ahead of print

    Genome-wide association studies suggest limited immune gene enrichment in schizophrenia compared to 5 autoimmune diseases

    Pouget, J. G., Gonçalves, V. F., Spain, S. L., Finucane, H. K., Raychaudhuri, S., Kennedy, J. L., Knight, J. & Schizophrenia Working Group of the Psychiatric Genomics Consortium 30/05/2016 In : Schizophrenia Bulletin. 42, 5, p. 1176-1184 9 p.

    Research output: Contribution to journalJournal article

  16. Published

    Allele-skewed DNA modification in the brain: relevance to a schizophrenia GWAS

    Gagliano, S. A., Ptak, C., Mak, D. Y. F., Shamsi, M., Oh, G., Knight, J., Boutros, P. C. & Petronis, A. 5/05/2016 In : American Journal of Human Genetics. 98, 5, p. 956-962 7 p.

    Research output: Contribution to journalJournal article

  17. Published

    Gene prioritization for imaging genetics studies using gene ontology and a stratified false discovery rate approach

    Patel, S., Park, M. T. M., Chakravarty, M. M., Knight, J. & Alzheimer's Disease Neuroimaging Initiative 7/04/2016 In : Frontiers in Neuroinformatics. 10, 13 p., 14

    Research output: Contribution to journalJournal article

  18. Published

    Genetic association analysis of N-methyl-d-aspartate receptor subunit gene GRIN2B and clinical response to clozapine

    Taylor, D. L., Tiwari, A. K., Lieberman, J. A., Potkin, S. G., Meltzer, H. Y., Knight, J., Remington, G., Müller, D. J. & Kennedy, J. L. 03/2016 In : Human Psychopharmacology: Clinical and Experimental. 31, 2, p. 121-134 14 p.

    Research output: Contribution to journalJournal article

  19. Published

    Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

    Knight, J. & 35 others Franke, B., Stein, J. L., Ripke, S., Anttila, V., Hibar, D. P., van Hulzen, K. J. E., Arias-Vasquez, A., Smoller, J. W., Nichols, T. E., Neale, M. C., McIntosh, A. M., Lee, P., McMahon, F. J., Meyer-Lindenberg, A., Mattheisen, M., Andreassen, O. A., Gruber, O., Sachdev, P. S., Roiz-Santiañez, R., Saykin, A. J., Ehrlich, S., Mather, K. A., Turner, J. A., Schwarz, E., Thalamuthu, A., Yao, Y., Ho, Y. Y. W., Martin, N. G., Wright, M. J., O'Donovan, M. C., Thompson, P. M., Neale, B. M., Medland, S. E., Sullivan, P. F. & Schizophrenia Working Group of the Psychiatric Genomics Consortium 03/2016 In : Nature Reviews Neuroscience. 19, 3, p. 420-431 12 p.

    Research output: Contribution to journalJournal article

  20. Published

    Schizophrenia risk from complex variation of complement component 4

    Sekar, A., Bialas, A. R., de Rivera, H., Davis, A., Hammond, T. R., Kamitaki, N., Tooley, K., Presumey, J., Baum, M., Van Doren, V., Genovese, G., Rose, S. A., Handsaker, R. E., Daly, M. J., Carroll, M. C., Stevens, B., McCarroll, S. A., Knight, J. & Schizophrenia Working Group of the Psychiatric Genomics Consortium 11/02/2016 In : Nature. 530, 7589, p. 177-183 7 p.

    Research output: Contribution to journalJournal article

  21. Published

    IBD genetic risk profile in healthy first-degree relatives of Crohn's disease patients

    Kevans, D., Silverberg, M. S., Borowski, K., Griffiths, A., Xu, W., Onay, V., Paterson, A. D., Knight, J., Croitoru, K. & GEM Project 02/2016 In : Journal of Crohn's and Colitis. 10, 2, p. 209-215 7 p.

    Research output: Contribution to journalJournal article

  22. 2015
  23. Published

    Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

    Loh, P-R., Bhatia, G., Gusev, A., Finucane, H. K., Bulik-Sullivan, B. K., Pollack, S. J., de Candia, T. R., Lee, S. H., Wray, N. R., Kendler, K. S., O'Donovan, M. C., Neale, B. M., Patterson, N., Price, A. L., Knight, J. & Schizophrenia Working Group of Psychiatric Genomics Consortium 12/2015 In : Nature Genetics. 47, 12, p. 1385-1392 8 p.

    Research output: Contribution to journalJournal article

  24. Published

    Modeling linkage disequilibrium increases accuracy of polygenic risk scores

    Knight, J. & 35 others Vilhjálmsson, B. J., Yang, J., Finucane, H. K., Gusev, A., Lindström, S., Ripke, S., Genovese, G., Loh, P-R., Bhatia, G., Do, R., Hayeck, T., Won, H-H., Kathiresan, S., Pato, M., Pato, C., Tamimi, R., Stahl, E., Zaitlen, N., Pasaniuc, B., Belbin, G., Kenny, E. E., Schierup, M. H., De Jager, P., Patsopoulos, N. A., McCarroll, S., Daly, M., Purcell, S., Chasman, D., Neale, B., Goddard, M., Visscher, P. M., Kraft, P., Patterson, N., Price, A. L. & Schizophrenia Working Group of the Psychiatric Genomics Consortium, Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) study 1/10/2015 In : American Journal of Human Genetics. 97, 4, p. 576-592 17 p.

    Research output: Contribution to journalJournal article

  25. Published

    Predictors of outcome in ulcerative colitis

    Waterman, M., Knight, J., Dinani, A., Xu, W., Stempak, J. M., Croitoru, K., Nguyen, G. C., Cohen, Z., McLeod, R. S., Greenberg, G. R., Steinhart, A. H. & Silverberg, M. S. 09/2015 In : Inflammatory Bowel Diseases. 21, 9, p. 2097-2105 9 p.

    Research output: Contribution to journalJournal article

  26. Published

    Smoking gun or circumstantial evidence?: comparison of statistical learning methods using functional annotations for prioritizing risk variants

    Gagliano, S. A., Ravji, R., Barnes, M. R., Weale, M. E. & Knight, J. 24/08/2015 In : Scientific Reports. 5, 11 p., 13373

    Research output: Contribution to journalJournal article

  27. Published

    Addiction-related genes in gambling disorders: new insights from parallel human and pre-clinical models

    Lobo, D. S. S., Aleksandrova, L., Knight, J., Casey, D. M., el-Guebaly, N., Nobrega, J. N. & Kennedy, J. L. 08/2015 In : Molecular Psychiatry. 20, 8, p. 1002-1010 9 p.

    Research output: Contribution to journalJournal article

  28. Published

    A genome-wide association study of suicide severity scores in bipolar disorder

    Zai, C. C., Gonçalves, V. F., Tiwari, A. K., Gagliano, S. A., Hosang, G., de Luca, V., Shaikh, S. A., King, N., Chen, Q., Xu, W., Strauss, J., Breen, G., Lewis, C. M., Farmer, A. E., McGuffin, P., Knight, J., Vincent, J. B. & Kennedy, J. L. 06/2015 In : Journal of Psychiatric Research. 65, p. 23-29 7 p.

    Research output: Contribution to journalJournal article

  29. Published

    Assessing models for genetic prediction of complex traits: a comparison of visualization and quantitative methods

    Gagliano, S. A., Paterson, A. D., Weale, M. E. & Knight, J. 22/05/2015 In : BMC Genomics. 16, 11 p., 405

    Research output: Contribution to journalJournal article

  30. Published

    Enhanced meta-analysis and replication studies identify five new psoriasis susceptibility loci

    Knight, J. & 32 others Tsoi, L. C., Spain, S. L., Ellinghaus, E., Stuart, P. E., Capon, F., Tejasvi, T., Kang, H. M., Allen, M. H., Lambert, S., Stoll, S. W., Weidinger, S., Gudjonsson, J. E., Koks, S., Kingo, K., Esko, T., Das, S., Metspalu, A., Weichenthal, M., Enerback, C., Krueger, G. G., Voorhees, J. J., Chandran, V., Rosen, C. F., Rahman, P., Gladman, D. D., Reis, A., Nair, R. P., Franke, A., Barker, J. N. W. N., Abecasis, G. R., Trembath, R. C. & Elder, J. T. 5/05/2015 In : Nature Communications. 6, 8 p., 7001

    Research output: Contribution to journalJournal article

  31. Published

    LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

    Bulik-Sullivan, B. K., Loh, P-R., Finucane, H. K., Ripke, S., Yang, J., Patterson, N., Daly, M. J., Price, A. L., Neale, B. M., Knight, J. & Schizophrenia Working Group of the Psychiatric Genomics Consortium 03/2015 In : Nature Genetics. 47, 3, p. 291-295 5 p.

    Research output: Contribution to journalJournal article

  32. Published

    Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes

    Knight, J. & 29 others Prescott, N. J., Lehne, B., Stone, K., Lee, J. C., Taylor, K., Papouli, E., Mirza, M. M., Simpson, M. A., Spain, S. L., Lu, G., Fraternali, F., Bumpstead, S. J., Gray, E., Amar, A., Bye, H., Green, P., Chung-Faye, G., Hayee, B. H., Pollok, R., Satsangi, J., Parkes, M., Barrett, J. C., Mansfield, J. C., Sanderson, J., Lewis, C. M., Weale, M. E., Schlitt, T., Mathew, C. G. & UK IBD Genetics Consortium 11/02/2015 In : PLOS Genetics. 11, 2, e1004955

    Research output: Contribution to journalJournal article

  33. Published

    CYP2A6 reduced activity gene variants confer reduction in lung cancer risk in African American smokers: findings from two independent populations

    Wassenaar, C. A., Ye, Y., Cai, Q., Aldrich, M. C., Knight, J., Spitz, M. R., Wu, X., Blot, W. J. & Tyndale, R. F. 01/2015 In : Carcinogenesis. 36, 1, p. 99-103 5 p.

    Research output: Contribution to journalJournal article

  34. Published

    Investigation of TSPO variants in schizophrenia and antipsychotic treatment outcomes

    Knight, J. & 23 others Pouget, J. G., Gonçalves, V. F., Nurmi, E. L., Laughlin, C. P., Mallya, K. S., McCracken, J. T., Aman, M. G., McDougle, C. J., Scahill, L., Misener, V. L., Tiwari, A. K., Zai, C. C., Brandl, E. J., Felsky, D., Leung, A. Q., Lieberman, J. A., Meltzer, H. Y., Potkin, S. G., Niedling, C., Steimer, W., Leucht, S., Müller, D. J. & Kennedy, J. L. 01/2015 In : Pharmacogenomics. 16, 1, p. 5-22 18 p.

    Research output: Contribution to journalJournal article

  35. 2014
  36. Published

    Complex host genetics influence the microbiome in inflammatory bowel disease

    Knights, D., Silverberg, M. S., Weersma, R. K., Gevers, D., Dijkstra, G., Huang, H., Tyler, A. D., van Sommeren, S., Imhann, F., Stempak, J. M., Huang, H., Vangay, P., Al-Ghalith, G. A., Russell, C., Sauk, J., Knight, J., Daly, M. J., Huttenhower, C. & Xavier, R. J. 2/12/2014 In : Genome Biology. 6, 12, 11 p., 107

    Research output: Contribution to journalJournal article

  37. Published

    Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

    Knight, J. & 22 others Gusev, A., Lee, S. H., Trynka, G., Finucane, H., Vilhjálmsson, B. J., Xu, H., Zang, C., Ripke, S., Bulik-Sullivan, B., Stahl, E., Kähler, A. K., Hultman, C. M., Purcell, S. M., McCarroll, S. A., Daly, M., Pasaniuc, B., Sullivan, P. F., Neale, B. M., Wray, N. R., Raychaudhuri, S., Price, A. L. & Schizophrenia Working Group of the Psychiatric Genomics Consortium 6/11/2014 In : American Journal of Human Genetics. 95, 5, p. 535-552 18 p.

    Research output: Contribution to journalJournal article

  38. Published

    The role of leptin, melanocortin, and neurotrophin system genes on body weight in anorexia nervosa and bulimia nervosa

    Knight, J. & 26 others Yilmaz, Z., Kaplan, A. S., Tiwari, A. K., Levitan, R. D., Piran, S., Bergen, A. W., Kaye, W. H., Hakonarson, H., Wang, K., Berrettini, W. H., Brandt, H. A., Bulik, C. M., Crawford, S., Crow, S., Fichter, M. M., Halmi, K. A., Johnson, C. L., Keel, P. K., Klump, K. L., Magistretti, P., Mitchell, J., Strober, M., Thornton, L. M., Treasure, J., Woodside, D. B. & Kennedy, J. L. 08/2014 In : Journal of Psychiatric Research. 55, p. 77-86 10 p.

    Research output: Contribution to journalJournal article

  39. Published

    Biological insights from 108 schizophrenia-associated genetic loci

    Knight, J. & Schizophrenia Working Group of the Psychiatric Genomics Consortium 24/07/2014 In : Nature. 511, 7510, p. 421-427 7 p.

    Research output: Contribution to journalJournal article

  40. Published

    Protein kinase cAMP-dependent regulatory type II beta (PRKAR2B) gene variants in antipsychotic-induced weight gain

    Gagliano, S. A., Tiwari, A. K., Freeman, N., Lieberman, J. A., Meltzer, H. Y., Kennedy, J. L., Knight, J. & Müller, D. J. 07/2014 In : Human Psychopharmacology: Clinical and Experimental. 29, 4, p. 330-335 6 p.

    Research output: Contribution to journalJournal article

  41. Published

    Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris

    Knight, J. & 23 others Navarini, A. A., Simpson, M. A., Weale, M., Carlavan, I., Reiniche, P., Burden, D. A., Layton, A., Bataille, V., Allen, M., Pleass, R., Pink, A., Creamer, D., English, J., Munn, S., Walton, S., Willis, C., Déret, S., Voegel, J. J., Spector, T., Smith, C. H., Trembath, R. C., Barker, J. N. W. N. & Acne Genetic Study Group 13/06/2014 In : Nature Communications. 5, 6 p., 4020

    Research output: Contribution to journalJournal article

  42. Published

    A Bayesian method to incorporate hundreds of functional characteristics with association evidence to improve variant prioritization

    Gagliano, S. A., Barnes, M. R., Weale, M. E. & Knight, J. 20/05/2014 In : PLoS ONE. 9, 5, 14 p., e98122

    Research output: Contribution to journalJournal article

  43. Published

    Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1

    Xu, W., Cohen-Woods, S., Chen, Q., Noor, A., Knight, J., Hosang, G., Parikh, S. V., De Luca, V., Tozzi, F., Muglia, P., Forte, J., McQuillin, A., Hu, P., Gurling, H. M. D., Kennedy, J. L., McGuffin, P., Farmer, A., Strauss, J. & Vincent, J. B. 4/01/2014 In : Journal of Medical Genetics. 15, 13 p., 2

    Research output: Contribution to journalJournal article

  44. 2012
  45. Published

    Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis

    Knight, J., Spain, S. L., Capon, F., Hayday, A., Nestle, F. O., Clop, A., Barker, J. N. W. N., Weale, M. E., Trembath, R. C. & Wellcome Trust Case Control Consortium 1/12/2012 In : Human Molecular Genetics. 21, 23, p. 5185-5192 8 p.

    Research output: Contribution to journalJournal article

  46. Published

    Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

    Knight, J. & 65 others Tsoi, L. C., Spain, S. L., Ellinghaus, E., Stuart, P. E., Capon, F., Ding, J., Li, Y., Tejasvi, T., Gudjonsson, J. E., Kang, H. M., Allen, M. H., McManus, R., Novelli, G., Samuelsson, L., Schalkwijk, J., Ståhle, M., Burden, A. D., Smith, C. H., Cork, M. J., Estivill, X., Bowcock, A. M., Krueger, G. G., Weger, W., Worthington, J., Tazi-Ahnini, R., Nestle, F. O., Hayday, A., Hoffmann, P., Winkelmann, J., Wijmenga, C., Langford, C., Edkins, S., Andrews, R., Blackburn, H., Strange, A., Band, G., Pearson, R. D., Vukcevic, D., Spencer, C. C. A., Deloukas, P., Mrowietz, U., Schreiber, S., Weidinger, S., Koks, S., Kingo, K., Esko, T., Metspalu, A., Lim, H. W., Voorhees, J. J., Weichenthal, M., Wichmann, H. E., Chandran, V., Rosen, C. F., Rahman, P., Gladman, D. D., Griffiths, C. E. M., Reis, A., Kere, J., Nair, R. P., Franke, A., Barker, J. N. W. N., Abecasis, G. R., Elder, J. T., Trembath, R. C. & Collaborative Association Study of Psoriasis (CASP) 12/2012 In : Nature Genetics. 44, 12, p. 1341-1348 8 p.

    Research output: Contribution to journalLetter

  47. Published

    Introduction to genetic association studies

    Lewis, C. M. & Knight, J. 03/2012 In : Cold Spring Harbor Protocols. 2012, 3, p. 297-306 10 p.

    Research output: Contribution to journalJournal article

  48. 2011
  49. Published

    Mutations in IL36RN/IL1F5 are associated with the severe episodic inflammatory skin disease known as generalized pustular psoriasis

    Onoufriadis, A., Simpson, M. A., Pink, A. E., Di Meglio, P., Smith, C. H., Pullabhatla, V., Knight, J., Spain, S. L., Nestle, F. O., Burden, A. D., Capon, F., Trembath, R. C. & Barker, J. N. W. N. 9/09/2011 In : American Journal of Human Genetics. 89, 3, p. 432-437 6 p.

    Research output: Contribution to journalJournal article

  50. Published

    A genome-wide significant linkage for severe depression on chromosome 3: the depression network study

    Knight, J. & 27 others Breen, G., Webb, B. T., Butler, A. W., van den Oord, E. J. C. G., Tozzi, F., Craddock, N., Gill, M., Korszun, A., Maier, W., Middleton, L., Mors, O., Owen, M. J., Cohen-Woods, S., Perry, J., Galwey, N. W., Upmanyu, R., Craig, I., Lewis, C. M., Ng, M., Brewster, S., Preisig, M., Rietschel, M., Jones, L., Rice, J., Muglia, P., Farmer, A. E. & McGuffin, P. 08/2011 In : American Journal of Psychiatry. 168, 8, p. 840-847 8 p.

    Research output: Contribution to journalJournal article

  51. Published

    Using functional annotation for the empirical determination of Bayes Factors for genome-wide association study analysis

    Knight, J., Barnes, M. R., Breen, G. & Weale, M. E. 27/04/2011 In : PLoS ONE. 6, 4, 8 p., e14808

    Research output: Contribution to journalJournal article

  52. Published

    Common variants in DGKK are strongly associated with risk of hypospadias

    van der Zanden, L. F. M., van Rooij, I. A. L. M., Feitz, W. F. J., Knight, J., Donders, A. R. T., Renkema, K. Y., Bongers, E. M. H. F., Vermeulen, S. H. H. M., Kiemeney, L. A. L. M., Veltman, J. A., Arias-Vásquez, A., Zhang, X., Markljung, E., Qiao, L., Baskin, L. S., Nordenskjöld, A., Roeleveld, N., Franke, B. & Knoers, N. V. A. M. 01/2011 In : Nature Genetics. 43, 1, p. 48-50 3 p.

    Research output: Contribution to journalLetter

  53. 2010
  54. Published

    A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1

    Knight, J. & 84 others Strange, A., Capon, F., Spencer, C. C. A., Weale, M. E., Allen, M. H., Barton, A., Band, G., Bellenguez, C., Bergboer, J. G. M., Blackwell, J. M., Bramon, E., Bumpstead, S. J., Casas, J. P., Cork, M. J., Corvin, A., Deloukas, P., Dilthey, A., Duncanson, A., Edkins, S., Estivill, X., Fitzgerald, O., Freeman, C., Giardina, E., Gray, E., Hofer, A., Hüffmeier, U., Hunt, S. E., Irvine, A. D., Jankowski, J., Kirby, B., Langford, C., Lascorz, J., Leman, J., Leslie, S., Mallbris, L., Markus, H. S., Mathew, C. G., McLean, W. H. I., McManus, R., Mössner, R., Moutsianas, L., Naluai, A. T., Nestle, F. O., Novelli, G., Onoufriadis, A., Palmer, C. N. A., Perricone, C., Pirinen, M., Plomin, R., Potter, S. C., Pujol, R. M., Rautanen, A., Riveira-Munoz, E., Ryan, A. W., Salmhofer, W., Samuelsson, L., Sawcer, S. J., Schalkwijk, J., Smith, C. H., Ståhle, M., Su, Z., Tazi-Ahnini, R., Traupe, H., Viswanathan, A. C., Warren, R. B., Weger, W., Wolk, K., Wood, N., Worthington, J., Young, H. S., Zeeuwen, P. L. J. M., Hayday, A., Burden, A. D., Griffiths, C. E. M., Kere, J., Reis, A., McVean, G., Evans, D. M., Brown, M. A., Barker, J. N., Peltonen, L., Donnelly, P., Trembath, R. C. & Genetic Analysis of Psoriasis Consortium & the Wellcome Trust Case Control Consortium 2 11/2010 In : Nature Genetics. 42, 11, p. 985-990 6 p.

    Research output: Contribution to journalLetter

  55. Published

    An investigation of candidate regions for association with bipolar disorder

    Knight, J., Rochberg, N. S., Saccone, S. F., Nurnberger, J. I., Rice, J. P. & NIMH Genetics Initiative Bipolar Disorder Consortium 5/10/2010 In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics . 153B, 7, p. 1292-1297 6 p.

    Research output: Contribution to journalJournal article

  56. Published

    The Bipolar Association Case-Control Study (BACCS) and meta-analysis: no association with the 5,10-Methylenetetrahydrofolate reductase gene and bipolar disorder

    Knight, J. & 21 others Cohen-Woods, S., Craig, I., Gaysina, D., Gray, J., Gunasinghe, C., Craddock, N., Elkin, A., Jones, L., Kennedy, J., King, N., Korszun, A., Owen, M., Parikh, S., Strauss, J., Sterne, A., Tozzi, F., Perry, J., Muglia, P., Vincent, J., McGuffin, P. & Farmer, A. 5/10/2010 In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics . 153B, 7, p. 1298-1304 7 p.

    Research output: Contribution to journalJournal article

  57. Published

    Natural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlanders

    Knight, J. & 28 others Beall, C. M., Cavalleri, G. L., Deng, L., Elston, R. C., Gao, Y., Li, C., Li, J. C., Liang, Y., McCormack, M., Montgomery, H. E., Pan, H., Robbins, P. A., Shianna, K. V., Tam, S. C., Tsering, N., Veeramah, K. R., Wang, W., Wangdui, P., Weale, M. E., Xu, Y., Xu, Z., Yang, L., Zaman, M. J., Zeng, C., Zhang, L., Zhang, X., Zhaxi, P. & Zheng, Y. T. 22/06/2010 In : Proceedings of the National Academy of Sciences. 107, 25, p. 11459-11464 6 p.

    Research output: Contribution to journalJournal article

  58. Published

    Software for generating liability distributions for pedigrees conditional on their observed disease states and covariates

    Campbell, D. D., Sham, P. C., Knight, J., Wickham, H. & Landau, S. 02/2010 In : Genetic Epidemiology. 34, 2, p. 159-170 12 p.

    Research output: Contribution to journalJournal article

  59. 2009
  60. Published

    Depression Case Control (DeCC) study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder

    Cohen-Woods, S., Gaysina, D., Craddock, N., Farmer, A., Gray, J., Gunasinghe, C., Hoda, F., Jones, L., Knight, J., Korszun, A., Owen, M. J., Sterne, A., Craig, I. W. & McGuffin, P. 15/04/2009 In : Human Molecular Genetics. 18, 8, p. 1504-1509 6 p.

    Research output: Contribution to journalJournal article

  61. Published

    A comparison of association statistics between pooled and individual genotypes

    Knight, J., Saccone, S. F., Zhang, Z., Ballinger, D. G. & Rice, J. P. 03/2009 In : Human Heredity. 67, 4, p. 219-225 7 p.

    Research output: Contribution to journalJournal article

  62. Published

    Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration

    Knight, J. & 29 others Simpson, C. L., Lemmens, R., Miskiewicz, K., Broom, W. J., Hansen, V. K., van Vught, P. W. J., Landers, J. E., Sapp, P., Van Den Bosch, L., Neale, B. M., Turner, M. R., Veldink, J. H., Ophoff, R. A., Tripathi, V. B., Beleza, A., Shah, M. N., Proitsi, P., Van Hoecke, A., Carmeliet, P., Horvitz, H. R., Leigh, P. N., Shaw, C. E., van den Berg, L. H., Sham, P. C., Powell, J. F., Verstreken, P., Brown, R. H., Robberecht, W. & Al-Chalabi, A. 1/02/2009 In : Human Molecular Genetics. 18, 3, p. 472-481 10 p.

    Research output: Contribution to journalJournal article

  63. 2008
  64. Published

    DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage

    Knight, J. & 49 others Chen, W., Zhou, K., Sham, P., Franke, B., Kuntsi, J., Campbell, D., Fleischman, K., Andreou, P., Arnold, R., Altink, M., Boer, F., Boholst, M. J., Buschgens, C., Butler, L., Christiansen, H., Fliers, E., Howe-Forbes, R., Gabriëls, I., Heise, A., Korn-Lubetzki, I., Marco, R., Medad, S., Minderaa, R., Müller, U. C., Mulligan, A., Psychogiou, L., Rommelse, N., Sethna, V., Uebel, H., McGuffin, P., Plomin, R., Banaschewski, T., Buitelaar, J., Ebstein, R., Eisenberg, J., Gill, M., Manor, I., Miranda, A., Mulas, F., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E., Steinhausen, H-C., Taylor, E., Thompson, M., Faraone, S. V. & Asherson, P. 5/12/2008 In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics . 147B, 8, p. 1450-1460 11 p.

    Research output: Contribution to journalJournal article

  65. Published

    A simple method for assessing the strength of evidence for association at the level of the whole gene

    Curtis, D., Vine, A. E. & Knight, J. 17/11/2008 In : Advances and Applications in Bioinformatics and Chemistry : AABC. 1, p. 115-120 6 p.

    Research output: Contribution to journalJournal article

  66. Published

    CLUMPHAP: a simple tool for performing haplotype-based association analysis

    Knight, J., Curtis, D. & Sham, P. C. 09/2008 In : Genetic Epidemiology. 32, 6, p. 539-545 7 p.

    Research output: Contribution to journalJournal article

  67. Published

    Investigation into the ability of SNP chipsets and microsatellites to detect association with a disease locus

    Curtis, D., Vine, A. E. & Knight, J. 07/2008 In : Annals of Human Genetics. 72, 4, p. 547-556 10 p.

    Research output: Contribution to journalJournal article

  68. Published

    Differential methylation of the X-chromosome is a possible source of discordance for bipolar disorder female monozygotic twins

    Rosa, A., Picchioni, M. M., Kalidindi, S., Loat, C. S., Knight, J., Toulopoulou, T., Vonk, R., van der Schot, A. C., Nolen, W., Kahn, R. S., McGuffin, P., Murray, R. M. & Craig, I. W. 5/06/2008 In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics . 147B, 4, p. 459-462 4 p.

    Research output: Contribution to journalJournal article

  69. Published

    Study of regions of extended homozygosity provides a powerful method to explore haplotype structure of human populations

    Curtis, D., Vine, A. E. & Knight, J. 03/2008 In : Annals of Human Genetics. 72, 2, p. 261-278 18 p.

    Research output: Contribution to journalJournal article

  70. Published

    Association of the serotonin transporter gene, neuroticism and smoking behaviours

    O'Gara, C., Knight, J., Stapleton, J., Luty, J., Neale, B., Nash, M., Heuzo-Diaz, P., Hoda, F., Cohen, S., Sutherland, G., Collier, D., Sham, P., Ball, D., McGuffin, P. & Craig, I. 2008 In : Journal of Human Genetics . 53, 3, p. 239-246 8 p.

    Research output: Contribution to journalJournal article

  71. 2007
  72. Published

    Dopamine genes and pathological gambling in discordant sib-pairs

    da Silva Lobo, D. S., Vallada, H. P., Knight, J., Martins, S. S., Tavares, H., Gentil, V. & Kennedy, J. L. 12/2007 In : Journal of Gambling Studies. 23, 4, p. 421-433 13 p.

    Research output: Contribution to journalJournal article

  73. Published

    Application of multi-locus analytical methods to identify interacting loci in case-control studies

    Vermeulen, S. H. H. M., Den Heijer, M., Sham, P. C. & Knight, J. 09/2007 In : Annals of Human Genetics. 71, 5, p. 689-700 12 p.

    Research output: Contribution to journalJournal article

  74. Published

    Age at onset in sod1-mediated amyotrophic lateral sclerosis shows familiality

    Fogh, I., Rijsdijk, F., Andersen, P. M., Sham, P. C., Knight, J., Neale, B., McKenna-Yasek, D., Silani, V., Brown, R. H., Powell, J. F. & Al-Chalabi, A. 08/2007 In : Neurogenetics. 8, 3, p. 235-236 2 p.

    Research output: Contribution to journalLetter

  75. Published

    A pragmatic suggestion for dealing with results for candidate genes obtained from genome wide association studies

    Curtis, D., Vine, A. E. & Knight, J. 10/05/2007 In : Genetics. 8, 6 p., 20

    Research output: Contribution to journalJournal article

  76. Published

    Homing in on depression genes

    McGuffin, P., Cohen, S. & Knight, J. 02/2007 In : American Journal of Psychiatry. 164, 2, p. 195-197 3 p.

    Research output: Contribution to journalEditorial

  77. Published

    Regional multi-locus association models

    Knight, J., Sham, P., Shaun, P. & Neale, B. 2007 Statistical genetics: gene mapping through linkage and association. Neale, B., Ferreira, M., Medland, S. & Posthuma, D. (eds.). London: Taylor and Francis

    Research output: Contribution in Book/Report/ProceedingsChapter

  78. 2006
  79. Published

    Investigation of the ability of haplotype association and logistic regression to identify associated susceptibility loci

    North, B. V., Sham, P. C., Knight, J., Martin, E. R. & Curtis, D. 11/2006 In : Annals of Human Genetics. 70, 6, p. 893-906 14 p.

    Research output: Contribution to journalJournal article

  80. Published

    The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

    Knight, J. & 61 others Brookes, K., Xu, X., Chen, W., Zhou, K., Neale, B., Lowe, N., Anney, R., Franke, B., Gill, M., Ebstein, R., Buitelaar, J., Sham, P., Campbell, D., Andreou, P., Altink, M., Arnold, R., Boer, F., Buschgens, C., Butler, L., Christiansen, H., Feldman, L., Fleischman, K., Fliers, E., Howe-Forbes, R., Goldfarb, A., Heise, A., Gabriëls, I., Korn-Lubetzki, I., Johansson, L., Marco, R., Medad, S., Minderaa, R., Mulas, F., Müller, U., Mulligan, A., Rabin, K., Rommelse, N., Sethna, V., Sorohan, J., Uebel, H., Psychogiou, L., Weeks, A., Barrett, R., Craig, I., Banaschewski, T., Sonuga-Barke, E., Eisenberg, J., Kuntsi, J., Manor, I., McGuffin, P., Miranda, A., Oades, R. D., Plomin, R., Roeyers, H., Rothenberger, A., Sergeant, J., Steinhausen, H-C., Taylor, E., Thompson, M., Faraone, S. V. & Asherson, P. 10/2006 In : Molecular Psychiatry. 11, 10, p. 934-953 20 p.

    Research output: Contribution to journalJournal article

  81. Published

    Design and analysis of association studies using pooled DNA from large twin samples

    Knight, J. & Sham, P. 09/2006 In : Behavior Genetics. 36, 5, p. 665-677 13 p.

    Research output: Contribution to journalJournal article

  82. Published

    NADPH oxidase (CYBA) and FcgammaR polymorphisms as risk factors for aggressive periodontitis: a case-control association study

    Nibali, L., Parkar, M., Brett, P., Knight, J., Tonetti, M. S. & Griffiths, G. S. 08/2006 In : Journal of Clinical Periodontology. 33, 8, p. 529-539 11 p.

    Research output: Contribution to journalJournal article

  83. Published

    Polymorphisms in the phosphate and tensin homolog gene are not associated with late-onset Alzheimer's disease

    Hamilton, G., Samedi, F., Knight, J., Archer, N., Foy, C., Walter, S., Turic, D., Jehu, L., Moore, P., Hollingworth, P., O'Donovan, M. C., Williams, J., Owen, M. J., Lovestone, S. & Powell, J. F. 19/06/2006 In : Neuroscience Letters. 401, 1-2, p. 77-80 4 p.

    Research output: Contribution to journalJournal article

  84. Published

    Program report: GENECOUNTING support programs

    Curtis, D., Knight, J. & Sham, P. C. 03/2006 In : Annals of Human Genetics. 70, Pt 2, p. 277-279 3 p.

    Research output: Contribution to journalJournal article

  85. Published

    A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during pregnancy

    Brookes, K-J., Mill, J., Guindalini, C., Curran, S., Xu, X., Knight, J., Chen, C-K., Huang, Y-S., Sethna, V., Taylor, E., Chen, W., Breen, G. & Asherson, P. 01/2006 In : Archives of General Psychiatry. 63, 1, p. 74-81 8 p.

    Research output: Contribution to journalJournal article

  86. 2005
  87. Published

    Whole genome linkage scan of recurrent depressive disorder from the depression network study

    McGuffin, P., Knight, J., Breen, G., Brewster, S., Boyd, P. R., Craddock, N., Gill, M., Korszun, A., Maier, W., Middleton, L., Mors, O., Owen, M. J., Perry, J., Preisig, M., Reich, T., Rice, J., Rietschel, M., Jones, L., Sham, P. & Farmer, A. E. 15/11/2005 In : Human Molecular Genetics. 14, 22, p. 3337-3345 9 p.

    Research output: Contribution to journalJournal article

  88. Published

    DNA pooling analysis of ADHD and genes regulating vesicle release of neurotransmitters

    Brookes, K. J., Knight, J., Xu, X. & Asherson, P. 5/11/2005 In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics . 139B, 1, p. 33-37 5 p.

    Research output: Contribution to journalJournal article

  89. Published

    A new method of linkage analysis using LOD scores for quantitative traits supports linkage of monoamine oxidase activity to D17S250 in the Collaborative Study on the Genetics of Alcoholism pedigrees

    Curtis, D., Knight, J. & Sham, P. C. 09/2005 In : Psychiatric Genetics. 15, 3, p. 181-187 7 p.

    Research output: Contribution to journalJournal article

  90. Published

    SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children

    Butcher, L. M., Meaburn, E., Knight, J., Sham, P. C., Schalkwyk, L. C., Craig, I. W. & Plomin, R. 15/05/2005 In : Human Molecular Genetics. 14, 10, p. 1315-1325 11 p.

    Research output: Contribution to journalJournal article

  91. Published

    DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: no evidence for association

    Xu, X., Knight, J., Brookes, K., Mill, J., Sham, P., Craig, I., Taylor, E. & Asherson, P. 5/04/2005 In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics . 134B, 1, p. 115-118 4 p.

    Research output: Contribution to journalJournal article

  92. Published

    Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1B

    Mill, J., Xu, X., Ronald, A., Curran, S., Price, T., Knight, J., Craig, I., Sham, P., Plomin, R. & Asherson, P. 5/02/2005 In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics . 133B, 1, p. 68-73 6 p.

    Research output: Contribution to journalJournal article

  93. Published

    TTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's disease

    Garcia-Barcelo, M., Ganster, R. W., Lui, V. C. H., Leon, T. Y. Y., So, M-T., Lau, A. M. F., Fu, M., Sham, M-H., Knight, J., Zannini, M. S., Sham, P. C. & Tam, P. K. H. 15/01/2005 In : Human Molecular Genetics. 14, 2, p. 191-204 14 p.

    Research output: Contribution to journalJournal article

  94. Published

    The effect of haplotype-block definitions on inference of haplotype-block structure and htSNPs selection

    Ding, K., Zhou, K., Zhang, J., Knight, J., Zhang, X. & Shen, Y. 01/2005 In : Molecular Biology and Evolution. 22, 1, p. 148-159 12 p.

    Research output: Contribution to journalJournal article

  95. Published

    A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays

    Simpson, C. L., Knight, J., Butcher, L. M., Hansen, V. K., Meaburn, E., Schalkwyk, L. C., Craig, I. W., Powell, J. F., Sham, P. C. & Al-Chalabi, A. 2005 In : Nucleic Acids Research. 33, 3, e25

    Research output: Contribution to journalJournal article

  96. 2004
  97. Published

    Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD

    Mill, J., Richards, S., Knight, J., Curran, S., Taylor, E. & Asherson, P. 08/2004 In : Molecular Psychiatry. 9, 8, p. 801-810 10 p.

    Research output: Contribution to journalJournal article

  98. Published

    Attention-Deficit Hyperactivity Disorder in the post-genomic era

    Asherson, P., Knight, J. & IMAGE Consortium 07/2004 In : European Child and Adolescent Psychiatry. 13 , Suppl 1, p. I50-70 21 p.

    Research output: Contribution to journalJournal article

  99. Published

    Evidence that RNA editing modulates splice site selection in the 5-HT2C receptor gene

    Flomen, R., Knight, J., Sham, P., Kerwin, R. & Makoff, A. 1/04/2004 In : Nucleic Acids Research. 32, 7, p. 2113-2122 10 p.

    Research output: Contribution to journalJournal article

  100. Published

    A survey of current software for genetic power calculations

    Knight, J. 2/03/2004 In : BMC Genomics. 1, 3, p. 225-227 3 p.

    Research output: Contribution to journalJournal article

  101. Published

    Endothelial nitric oxide gene haplotypes and risk of cerebral small-vessel disease

    Hassan, A. E. M., Gormley, K., O'Sullivan, M., Knight, J., Sham, P. C., Vallance, P., Bamford, J. & Markus, H. S. 03/2004 In : Stroke; a journal of cerebral circulation. 35, 3, p. 654-659 6 p.

    Research output: Contribution to journalJournal article

  102. Published

    Haplotype association analysis of discrete and continuous traits using mixture of regression models

    Sham, P. C., Rijsdijk, F. V., Knight, J., Makoff, A., North, B. & Curtis, D. 03/2004 In : Behavior Genetics. 34, 2, p. 207-214 8 p.

    Research output: Contribution to journalJournal article

  103. 2003
  104. Published

    Mapping loci influencing blood pressure in the Framingham pedigrees using model-free LOD score analysis of a quantitative trait

    Knight, J., North, B. V., Sham, P. C. & Curtis, D. 31/12/2003 In : Genetics. 4 , Suppl. 1, 4 p., S74

    Research output: Contribution to journalJournal article

  105. Published

    Genome-wide mapping of human loci for essential hypertension

    Knight, J. & 22 others Caulfield, M., Munroe, P., Pembroke, J., Samani, N., Dominiczak, A., Brown, M., Benjamin, N., Webster, J., Ratcliffe, P., O'Shea, S., Papp, J., Taylor, E., Dobson, R., Newhouse, S., Hooper, J., Lee, W., Brain, N., Clayton, D., Lathrop, G. M., Farrall, M., Connell, J. & MRC British Genetics of Hypertension Study 21/06/2003 In : The Lancet. 361, 9375, p. 2118-2123 6 p.

    Research output: Contribution to journalJournal article

  106. Published

    Human chromosome 17 in essential hypertension

    Knight, J., Munroe, P. B., Pembroke, J. C. & Caulfield, M. J. 03/2003 In : Annals of Human Genetics. 67, 2, p. 193-206 14 p.

    Research output: Contribution to journalJournal article

  107. 2002
  108. Published

    Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy

    Chioza, B., Osei-Lah, A., Nashef, L., Suarez-Merino, B., Wilkie, H., Sham, P., Knight, J., Asherson, P. & Makoff, A. J. 12/2002 In : European Journal of Human Genetics. 10, 12, p. 857-864 8 p.

    Research output: Contribution to journalJournal article

  109. Published

    Genes for hypertension

    Caulfield, M., Knight, J., Gardener, G., O’Shea, S. & Monroe, P. 2002 An introduction to vascular biology: from basic science to clinical practice. Hunt, B. J. (ed.). 2nd ed ed. Cambridge: Cambridge University Press

    Research output: Contribution in Book/Report/ProceedingsChapter

  110. 2000
  111. Published

    Investigation of chromosome 17q as a locus for human essential hypertension in African Caribbeans

    Knight, J., Gardner, G. T., Clark, A. J. & Caulfield, M. J. 06/2000 In : Journal of Human Hypertension. 14, 6, p. 385-387 3 p.

    Research output: Contribution to journalJournal article

  112. Published

    1990-2000: progress in determining high blood pressure genes

    Munroe, P. B., Knight, J. & Caulfield, M. J. 05/2000 In : Annals of the Academy of Medicine, Singapore. 29, 3, p. 357-363 7 p.

    Research output: Contribution to journalJournal article

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