King's College London

Research portal

Dr Peter Green

  1. 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, BH., 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 Feb 2015, In : PL o S Genetics. 11, 2, 19 p., e1004955.

    Research output: Contribution to journalArticle

  2. Exome Sequencing in Brown-Vialetto-Van Laere Syndrome Response

    Josifova, D., Wiseman, M. & Green, P., 8 Oct 2010, In : American Journal of Human Genetics. 87, 4, p. 569 - 570 2 p.

    Research output: Contribution to journalLetter

  3. Multiple common variants for celiac disease influencing immune gene expression

    Dubois, P. C. A., Trynka, G., Franke, L., Hunt, K. A., Romanos, J., Curtotti, A., Zhernakova, A., Heap, G. A. R., Adany, R., Aromaa, A., Bardella, M. T., van den Berg, L. H., Bockett, N. A., de la Concha, E. G., Dema, B., Fehrmann, R. S. N., Fernandez-Arquero, M., Fiatal, S., Grandone, E., Green, P. M. & 47 others, Groen, H. J. M., Gwilliam, R., Houwen, R. H. J., Hunt, S. E., Kaukinen, K., Kelleher, D., Korponay-Szabo, I., Kurppa, K., MacMathuna, P., Maki, M., Mazzilli, M. C., McCann, O. T., Mearin, M. L., Mein, C. A., Mirza, M. M., Mistry, V., Mora, B., Morley, K., Mulder, C. J., Murray, J. A., Nunez, C., Oosterom, E., Ophoff, R. A., Polanco, I., Peltonen, L., Platteel, M., Rybak, A., Salomaa, V., Schweizer, J. J., Sperandeo, M. P., Tack, G. J., Turner, G., Veldink, J. H., Verbeek, W. H. M., Weersma, R. K., Wolters, V. M., Urcelay, E., Cukrowska, B., Greco, L., Neuhausen, S. L., McManus, R., Barisani, D., Deloukas, P., Barrett, J. C., Saavalainen, P., Wijmenga, C. & van Heel, D. A., Apr 2010, In : Nature Genetics. 42, 4, p. 295 - U42 8 p.

    Research output: Contribution to journalArticle

  4. Brown-Vialetto-Van Laere Syndrome, a Ponto-Bulbar Palsy with Deafness, Is Caused by Mutations in C20orf54

    Green, P., Wiseman, M., Crow, Y. J., Houlden, H., Riphagen, S., Lin, J-P., Raymond, F. L., Childs, A-M., Sheridan, E., Edwards, S. & Josifova, D., 2010, In : American Journal of Human Genetics. 86, 3, p. 485 - 489 5 p.

    Research output: Contribution to journalArticle

  5. Genetic linkage of a new autosomal dominant poikiloderma-upper oesophageal cancer syndrome to a 21-cM interval on 3q21-24

    Tanaka, A., Lai-Cheong, J. E., Weinel, S., Fisher, S. A., Green, P., Kulp-Shorten, C. L., Callen, J. P. & McGrath, A., 2009, In : British Journal of Dermatology. 160, 4, p. 921 - 922 2 p.

    Research output: Contribution to journalMeeting abstract

  6. Unique heterozygous intron 22 inversion band pattern in a haemophilic male detected by long polymerase chain reaction (PCR)

    Theophilus, B. D. M., Enayat, M. S., Green, P. M., Wilde, J. T. & Hill, F. G. H., Apr 2008, In : Thrombosis and Haemostasis. 99, 4, p. 774 - 775 2 p.

    Research output: Contribution to journalArticle

  7. Duplications involving int22h-1 of the factor VIII gene: a cause for concern in genetic testing for hemophilia A?

    Green, P., Hill, M. & Bowen, D. J., Oct 2007, In : JOURNAL OF THROMBOSIS AND HAEMOSTASIS. 5, 10, p. 2155 - 2156 2 p.

    Research output: Contribution to journalLetter

  8. Investigation of association of the DLG5 gene with phenotypes of inflammatory bowel disease in the British population

    Pearce, A. V., Fisher, S. A., Prescott, N. J., Onnie, C. M., Pattni, R., Green, P. M., Forbes, A., Mansfield, J., Sanderson, J., Schreiber, S., Lewis, C. M. & Mathew, C. G., Apr 2007, In : International Journal of Colorectal Disease. 22, 4, p. 419 - 424 6 p.

    Research output: Contribution to journalArticle

  9. Molecular genetics of hemophilia.

    Giannelli, F. & Green, PM., 2007, Genomics and genetics: from molecular details to analysis and techniques.. Meyers, RA. (ed.). Weinheim: Wiley-VCH Verlag GmbH & Co. KGaA, p. 1057 - 1083 27 p.

    Research output: Chapter in Book/Report/Conference proceedingChapter

  10. Assaying chromosomal inversions by single-molecular haplotyping

    Turner, D. J., Shendure, J., Porreca, G., Church, G., Green, P., Tyler-Smith, C. & Hurles, M. E., Jun 2006, In : NATURE METHODS. 3, 6, p. 439 - 445 7 p.

    Research output: Contribution to journalArticle

  11. A single nucleotide polymorphism in the promoter region of the stomelysin-1 gene is assoicated with aortic aneurysm formation.

    Degurara, J., Burmand, K. G., Taylor, P. R., Stern, R. F., Green, P., Mirza, M., Lewis, C., Berg, J. & Smith, A., 2005, In : British Journal of Surgery. 92, 10, p. 1322 - 1323 2 p.

    Research output: Contribution to journalMeeting abstract

  12. Gene conversion and evolution of Xq28 duplicons involved in recurring inversions causing severe hemophilia A

    Bagnall, R. D., Ayres, K. L., Green, P. M. & Giannelli, F., 2005, In : Genome Research. 15, 2, p. 214 - 223 10 p.

    Research output: Contribution to journalArticle

  13. Hemophilia B - molecular basis

    Green, P. M., Berntorp, E. E. (ed.) & Hoots, W. K. (ed.), 2005, Textbook of Hemophilia. Lee, C. A. & Berntorp, W. K. (eds.). Malden: Blackwell Publishing, p. 91 - 96 6 p.

    Research output: Chapter in Book/Report/Conference proceedingChapter

  14. Hemophilia, molecular genetics of

    Giannelli, F. & Green, P. M., 2005, Growth factors and oncogenes in gastrointestinal cancers to informatics (computational biology). Meyers, R. A. (ed.). Weinheim: Wiley-VCH Verlag GmbH & Co, p. 109 - 135 27 p. (Encyclopedia of molecular cell biology and molecular medicine. Volume 6.).

    Research output: Chapter in Book/Report/Conference proceedingChapter

  15. Radiosensitivity in breast cancer susceptibility.

    Barwell, J., Georgiou, A., Kesterton, I., Pangon, L., Langman, C., Berg, J., Kote-Jarai, Z., Green, P., Sodha, N., Morris, J., Solomon, E., Docherty, Z., Camplejohn, R., Eeles, R. & Hodgson, S., 2005, In : Journal of Medical Genetics. 42, p. S21 - S21

    Research output: Contribution to journalMeeting abstract

  16. The 5A-allele of the matrix metalloproteinase-3 (MMP-3) gene may be important in the pathogenesis of aortic aneurysm formation.

    Deguara, J., Burnand, K. G., Taylor, P. R., Stern, R. F., Green, P., Mirza, M., Lewis, C., Berg, J. & Smith, A., 2005, In : British Journal of Haematology. 92, 4, p. 499 - 500 2 p.

    Research output: Contribution to journalMeeting abstract

  17. A case of allele drop-out and preferential amplification in NPC1.

    Ward, C., Fensom, A., Green, P., Yau, S., Bussoli, T. & Heptinstall, L., 2004, In : Journal of Medical Genetics. 41, p. S76 - S76

    Research output: Contribution to journalMeeting abstract

  18. DNA variation in a 13-Mb region including the F9gene: inferring the genealogical history and causal role of a hemophilia B mutation (IVS 5+13 A -> G)

    Anagnostopoulos, T., Morris, A. P., Ayres, K. L., Giannelli, F. & Green, P. M., Dec 2003, In : JOURNAL OF THROMBOSIS AND HAEMOSTASIS. 1, 12, p. 2609 - 2614 6 p.

    Research output: Contribution to journalArticle

  19. Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome

    King, K., Flinter, F. A., Nihalani, V. & Green, P. M., Dec 2002, In : Human Genetics. 111, 6, p. 548 - 554 7 p.

    Research output: Contribution to journalArticle

  20. Haemophilia. This bad blood

    Green, P. M., Dec 2001, In : The Lancet. 358, p. S34 - S34

    Research output: Contribution to journalArticle

  21. Hair roots as the ideal source of mRNA for genetic testing

    King, K., Flinter, F. A. & Green, P. M., Jun 2001, In : Journal of Medical Genetics. 38, 6, p. E20

    Research output: Contribution to journalLetter

  22. Somatic mosaicism associated with a mild Alport syndrome phenotype

    Plant, K. E., Boye, E., Green, P. M., Vetrie, D. & Flinter, F. A., 2000, In : Journal of Medical Genetics. 37, 3, p. 238 - 239 2 p.

    Research output: Contribution to journalLetter

  23. The X chromosome and the rate of deleterious mutations in humans

    Giannelli, F. & Green, P. M., 2000, In : American Journal of Human Genetics. 67, 2, p. 515 - 517 3 p.

    Research output: Contribution to journalArticle

  24. Towards a comprehensive mutation screening strategy for Alport syndrome

    King, K., Flinter, F. A. & Green, P. M., 2000, In : Journal of Medical Genetics. 37, p. S77 - S77

    Research output: Contribution to journalMeeting abstract

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