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Professor Joanne Knight

Chair in Applied Data Science

  1. 2015
  2. Published

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

    Prescott, N. J., Lehne, B., Stone, K., Lee, J. C., Taylor, K., Knight, J., 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. & Pollok, R. & 10 others, 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 Journal/MagazineJournal articlepeer-review

  3. 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 Journal/MagazineJournal articlepeer-review

  4. Published

    Investigation of TSPO variants in schizophrenia and antipsychotic treatment outcomes

    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. & 4 others, Leucht, S., Knight, J., Müller, D. J. & Kennedy, J. L., 01/2015, In: Pharmacogenomics. 16, 1, p. 5-22 18 p.

    Research output: Contribution to Journal/MagazineJournal articlepeer-review

  5. 2014
  6. 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 Journal/MagazineJournal articlepeer-review

  7. Published

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

    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 Journal/MagazineJournal articlepeer-review

  8. Published

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

    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. & 7 others, Mitchell, J., Strober, M., Thornton, L. M., Treasure, J., Woodside, D. B., Knight, J. & Kennedy, J. L., 08/2014, In: Journal of Psychiatric Research. 55, p. 77-86 10 p.

    Research output: Contribution to Journal/MagazineJournal articlepeer-review

  9. Published

    Biological insights from 108 schizophrenia-associated genetic loci

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

    Research output: Contribution to Journal/MagazineJournal articlepeer-review

  10. 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 Journal/MagazineJournal articlepeer-review

  11. Published

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

    Navarini, A. A., Simpson, M. A., Weale, M., Knight, J., 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. & 4 others, 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 Journal/MagazineJournal articlepeer-review

  12. 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 Journal/MagazineJournal articlepeer-review

  13. 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 Journal/MagazineJournal articlepeer-review

  14. 2012
  15. 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 Journal/MagazineJournal articlepeer-review

  16. Published

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

    Tsoi, L. C., Spain, S. L., Knight, J., 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. & 31 others, 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. & Collaborative Association Study of Psoriasis (CASP), 12/2012, In: Nature Genetics. 44, 12, p. 1341-1348 8 p.

    Research output: Contribution to Journal/MagazineLetterpeer-review

  17. 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 Journal/MagazineJournal articlepeer-review

  18. 2011
  19. 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 Journal/MagazineJournal articlepeer-review

  20. Published

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

    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. & 8 others, Preisig, M., Rietschel, M., Jones, L., Knight, J., 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 Journal/MagazineJournal articlepeer-review

  21. 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 Journal/MagazineJournal articlepeer-review

  22. 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 Journal/MagazineLetterpeer-review

  23. 2010
  24. Published

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

    Strange, A., Capon, F., Spencer, C. C. A., Knight, J., 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. & 31 others, 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. & 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 Journal/MagazineLetterpeer-review

  25. 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 Journal/MagazineJournal articlepeer-review

  26. Published

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

    Cohen-Woods, S., Craig, I., Gaysina, D., Gray, J., Gunasinghe, C., Craddock, N., Elkin, A., Jones, L., Kennedy, J., King, N., Korszun, A., Knight, J., Owen, M., Parikh, S., Strauss, J., Sterne, A., Tozzi, F., Perry, J., Muglia, P. & Vincent, J. & 2 others, 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 Journal/MagazineJournal articlepeer-review

  27. Published

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

    Beall, C. M., Cavalleri, G. L., Deng, L., Elston, R. C., Gao, Y., Knight, J., 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. & 9 others, 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 of the United States of America. 107, 25, p. 11459-11464 6 p.

    Research output: Contribution to Journal/MagazineJournal articlepeer-review

  28. 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 Journal/MagazineJournal articlepeer-review

  29. 2009
  30. 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 Journal/MagazineJournal articlepeer-review

  31. 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 Journal/MagazineJournal articlepeer-review

  32. Published

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

    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., Knight, J., 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. & 10 others, 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 Journal/MagazineJournal articlepeer-review

  33. 2008
  34. Published

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

    Chen, W., Zhou, K., Sham, P., Franke, B., Kuntsi, J., Campbell, D., Fleischman, K., Knight, J., 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. & 30 others, 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 Journal/MagazineJournal articlepeer-review

  35. 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 Journal/MagazineJournal articlepeer-review

  36. 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 Journal/MagazineJournal articlepeer-review

  37. 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 Journal/MagazineJournal articlepeer-review

  38. 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 Journal/MagazineJournal articlepeer-review

  39. 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 Journal/MagazineJournal articlepeer-review

  40. 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 Journal/MagazineJournal articlepeer-review

  41. 2007
  42. 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 Journal/MagazineJournal articlepeer-review

  43. 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 Journal/MagazineJournal articlepeer-review

  44. 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 Journal/MagazineLetterpeer-review

  45. 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 Journal/MagazineJournal articlepeer-review

  46. 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 Journal/MagazineEditorialpeer-review

  47. 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/Proceedings - With ISBN/ISSNChapter

  48. 2006
  49. 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 Journal/MagazineJournal articlepeer-review

  50. Published

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

    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., Knight, J., Andreou, P., Altink, M., Arnold, R., Boer, F., Buschgens, C. & Butler, L. & 42 others, 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 Journal/MagazineJournal articlepeer-review

  51. 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 Journal/MagazineJournal articlepeer-review

  52. 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 Journal/MagazineJournal articlepeer-review

  53. 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 Journal/MagazineJournal articlepeer-review

  54. 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 Journal/MagazineJournal articlepeer-review

  55. 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 Journal/MagazineJournal articlepeer-review

  56. 2005
  57. 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 Journal/MagazineJournal articlepeer-review

  58. 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 Journal/MagazineJournal articlepeer-review

  59. 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 Journal/MagazineJournal articlepeer-review

  60. 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 Journal/MagazineJournal articlepeer-review

  61. 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 Journal/MagazineJournal articlepeer-review

  62. 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 Journal/MagazineJournal articlepeer-review

  63. 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 Journal/MagazineJournal articlepeer-review

  64. 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 Journal/MagazineJournal articlepeer-review

  65. 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 Journal/MagazineJournal articlepeer-review

  66. 2004
  67. 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 Journal/MagazineJournal articlepeer-review

  68. 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 Journal/MagazineJournal articlepeer-review

  69. 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 Journal/MagazineJournal articlepeer-review

  70. 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 Journal/MagazineJournal articlepeer-review

  71. 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 Journal/MagazineJournal articlepeer-review

  72. 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 Journal/MagazineJournal articlepeer-review

  73. 2003
  74. 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 Journal/MagazineJournal articlepeer-review

  75. Published

    Genome-wide mapping of human loci for essential hypertension

    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., Knight, J., Newhouse, S., Hooper, J., Lee, W., Brain, N., Clayton, D. & Lathrop, G. M. & 3 others, 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 Journal/MagazineJournal articlepeer-review

  76. 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 Journal/MagazineJournal articlepeer-review

  77. 2002
  78. 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 Journal/MagazineJournal articlepeer-review

  79. 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/Proceedings - With ISBN/ISSNChapter

  80. 2000
  81. 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 Journal/MagazineJournal articlepeer-review

  82. 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 Journal/MagazineJournal articlepeer-review

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