King's College London

Research portal

Research Outputs

  1. 2015
  2. Identification and validation of biomarkers for autism spectrum disorders

    Loth, E., Spooren, W., Ham, L. M., Isaac, M. B., Auriche-Benichou, C., Banaschewski, T., Baron-Cohen, S., Broich, K., Bölte, S., Bourgeron, T., Charman, T., Collier, D., de Andres-Trelles, F., Durston, S., Ecker, C., Elferink, A., Haberkamp, M., Hemmings, R., Johnson, M. H., Jones, E. J. H. & 18 others, Khwaja, O. S., Lenton, S., Mason, L., Mantua, V., Meyer-Lindenberg, A., Lombardo, M. V., O'Dwyer, L., Okamoto, K., Pandina, G. J., Pani, L., Persico, A. M., Simonoff, E., Tauscher-Wisniewski, S., Llinares-Garcia, J., Vamvakas, S., Williams, S., Buitelaar, J. K. & Murphy, D. G. M., 31 Dec 2015, In : Nature Reviews Drug Discovery. 15, 1, p. 70-73 4 p.

    Research output: Contribution to journalArticle

  3. Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects

    Machado, R. D., Southgate, L., Eichstaedt, C. A., Aldred, M. A., Austin, E. D., Best, D. H., Chung, W. K., Benjamin, N., Elliott, C. G., Eyries, M., Fischer, C., Gräf, S., Hinderhofer, K., Humbert, M., Keiles, S. B., Loyd, J. E., Morrell, N. W., Newman, J. H., Soubrier, F., Trembath, R. C. & 2 others, Viales, R. R. & Grünig, E., Dec 2015, In : Human Mutation. 36, 12, p. 1113-27 15 p.

    Research output: Contribution to journalArticle

  4. The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis

    Robinson, P. C., Leo, P. J., Pointon, J. J., Cremin, K., Bradbury, L. A., Donnelly (chair), P., Barroso (deputy Chair), I., M Blackwell, J., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N., Plomin, R., Rautanen, A. & 59 others, Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Spencer, C. C., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Donnelly, P., Langford, C., Hunt, S. E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S. J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., Mccann, O. T., Liddle, J., Potter, S. C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Barroso, I., Deloukas, P., Mathew (chair), C. G., Blackwell, J. M., Brown, M. A., Corvin, A., Spencer, C. C. A., Mccloskey, E., Eisman, J., Jones, G., Nicholson, G., Eastell, R., Sambrook, P., Prince, R., Dennison, E., Reid, I., Wark, J., Stebbings, S., Harrison, A. A., Evans, D. M., Duncan, E. L., Wordsworth, B. P. & Brown, M. A., 26 Nov 2015, In : GENES AND IMMUNITY. 17, 1, p. 46-51

    Research output: Contribution to journalArticle

  5. Neuroimaging in autism spectrum disorder: Brain structure and function across the lifespan

    Ecker, C., Bookheimer, S. Y. & Murphy, D. G. M., 1 Nov 2015, In : Lancet Neurology. 14, 11, p. 1121-1134 14 p., 147.

    Research output: Contribution to journalArticle

  6. Family therapy for autism spectrum disorders

    Spain, D. C., Sin, P. H. J., Paliokostas, E., Furuta, M., Chalder, T., Murphy, D. G. & Happe, F. G. E., 11 Oct 2015, In : Cochrane database of systematic reviews (Online). 10CD011894

    Research output: Contribution to journalArticle

  7. Neuroanatomy of individual differences in language in adult males with autism

    Lai, M. C., Lombardo, M. V., Ecker, C., Chakrabarti, B., Suckling, J., Bullmore, E. T., Happé, F., Murphy, D. G. M. & Baron-Cohen, S., 1 Oct 2015, In : Cerebral Cortex. 25, 10, p. 3613-3628 16 p.

    Research output: Contribution to journalArticle

  8. Relationship between surface-based brain morphometric measures and intelligence in autism spectrum disorders: Influence of history of language delay

    Balardin, J. B., Sato, J. R., Vieira, G., Feng, Y., Daly, E., Murphy, C., Murphy, D., Ecker, C. & MRC AIMS consortium, 1 Oct 2015, In : Autism research. 8, 5, p. 556-566 11 p.

    Research output: Contribution to journalArticle

  9. Decreased centrality of cortical volume covariance networks in autism spectrum disorders

    Balardin, J. B., Comfort, W. E., Daly, E., Murphy, C., Andrews, D., Murphy, D. G. M., Ecker, C., MRC AIMS consortium & Sato, J. R., Oct 2015, In : Journal of psychiatric research. 69, p. 142-149 8 p.

    Research output: Contribution to journalArticle

  10. Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome

    Meester, J. A. N., Southgate, L., Stittrich, A-B., Venselaar, H., Beekmans, S. J. A., den Hollander, N., Bijlsma, E. K., Helderman-van den Enden, A., Verheij, J. B. G. M., Glusman, G., Roach, J. C., Lehman, A., Patel, M. S., de Vries, B. B. A., Ruivenkamp, C., Itin, P., Prescott, K., Clarke, S., Trembath, R., Zenker, M. & 4 others, Sukalo, M., Van Laer, L., Loeys, B. & Wuyts, W., 3 Sep 2015, In : American Journal of Human Genetics. 97, 3, p. 475-82 8 p.

    Research output: Contribution to journalArticle

  11. Activating CARD14 Mutations are Associated with Generalised Pustular Psoriasis but Rarely Account for Familial Recurrence in Psoriasis Vulgaris

    Berki, D. M., Liu, L., Choon, S-E., David Burden, A., Griffiths, C. E., Navarini, A. A., Tan, E. S., Irvine, A. D., Ranki, A., Ogo, T., Petrof, G., Mahil, S. K., Duckworth, M., Allen, M. H., Vito, P., Trembath, R., McGrath, J., Smith, C. H., Capon, F. & Barker, J. N., 13 Aug 2015, In : Journal of Investigative Dermatology. 135, p. 2964–297

    Research output: Contribution to journalArticle

  12. Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies

    Southgate, L., Sukalo, M., Karountzos, A. S. V., Taylor, E. J., Collinson, C. S., Ruddy, D., Snape, K. M., Dallapiccola, B., Tolmie, J. L., Joss, S., Brancati, F., Digilio, M. C., Graul-Neumann, L. M., Salviati, L., Coerdt, W., Jacquemin, E., Wuyts, W., Zenker, M., Machado, R. D. & Trembath, R. C., Aug 2015, In : Circulation-Cardiovascular Genetics. 8, 4, p. 572-81 10 p.

    Research output: Contribution to journalArticle

  13. Germline Mutations in the CDKN2B Tumor Suppressor Gene Predispose to Renal Cell Carcinoma

    Jafri, M., Wake, N. C., Ascher, D. B., Pires, D. E. V., Gentle, D., Morris, M. R., Rattenberry, E., Simpson, M. A., Trembath, R. C., Weber, A., Woodward, E. R., Donaldson, A., Blundell, T. L., Latif, F. & Maher, E. R., Jul 2015, In : Cancer discovery. 5, 7, p. 723-9 7 p.

    Research output: Contribution to journalArticle

  14. Episodic Recollection Difficulties in ASD Result from Atypical Relational Encoding: Behavioral and Neural Evidence

    Gaigg, S. B., Bowler, D. M., Ecker, C., Calvo-Merino, B. & Murphy, D. G., 1 Jun 2015, In : Autism research. 8, 3, p. 317-327 11 p.

    Research output: Contribution to journalArticle

  15. DOCK6 mutations are responsible for a distinct autosomal-recessive variant of Adams-Oliver syndrome associated with brain and eye anomalies

    Sukalo, M., Tilsen, F., Kayserili, H., Müller, D., Tüysüz, B., Ruddy, D. M., Wakeling, E., Ørstavik, K. H., Snape, K. M., Trembath, R., De Smedt, M., van der Aa, N., Skalej, M., Mundlos, S., Wuyts, W., Southgate, L. & Zenker, M., Jun 2015, In : Human Mutation. 36, 6, p. 593-8 6 p.

    Research output: Contribution to journalArticle

  16. Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants

    Malik, R., Freilinger, T., Winsvold, B. S., Anttila, V., Vander Heiden, J., Traylor, M., De Vries, B., Holliday, E. G., Terwindt, G. M., Sturm, J., Bis, J. C., Hopewell, J. C., Ferrari, M. D., Rannikmae, K., Wessman, M., Kallela, M., Kubisch, C., Fornage, M., Meschia, J. F., Lehtimaki, T. & 105 others, Sudlow, C., Clarke, R., Chasman, D. I., Mitchell, B. D., Maguire, J., Kaprio, J., Farrall, M., Raitakari, O. T., Kurth, T., Ikram, M. A., Reiner, A. P., Longstreth, W. T., Rothwell, P. M., Strachan, D. P., Sharma, P., Seshadri, S., Quaye, L., Cherkas, L., Schurks, M., Rosand, J., Ligthart, L., Boncoraglio, G. B., Davey Smith, G., Van Duijn, C. M., Stefansson, K., Worrall, B. B., Nyholt, D. R., Markus, H. S., Van Den Maagdenberg, A. M. J. M., Cotsapas, C., Zwart, J. A., Palotie, A., Dichgans, M., Thorsteinsdottir, U., Destefano, A. L., Levi, C., Gretarsdottir, S., Donnelly, P., Barroso, I., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. NA., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath F, R. C., Viswanathan, A. C., Wood, N. W., Spencer, C. CA., Band, G., Bellengues, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Langford, C., Hunt, S. E., Edkind, S., Gwilliam, R., Blackburn, H., Bumpstead, S. J., Dronv, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., Mccann, O. T., Liddle, J., Potter, S. C., Ravindrarajah, R., Rickette, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Gormley, P., Bettella, F., Mcmahon, G., Todt, U., Palta, P., Hamalainen, E., Steinberg, S., Stefansson, H., Farkkila, M., Artto, V., Kaunisto, M. A., Schoenen, J., Frants, R. R., Borck, G., Gobel, H., Heinze, A., Heinze-kuhn, K. & Muller-myhsok, B., 26 May 2015, In : Neurology. 84, 21, p. 2132-2145 14 p., 21 .

    Research output: Contribution to journalArticle

  17. Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome

    Vorstman, J. A. S., Breetvelt, E. J., Duijff, S. N., Eliez, S., Schneider, M., Jalbrzikowski, M., Armando, M., Vicari, S., Shashi, V., Hooper, S. R., Chow, E. W. C., Fung, W. L. A., Butcher, N. J., Young, D. A., McDonald-McGinn, D. M., Vogels, A., Van Amelsvoort, T., Gothelf, D., Weinberger, R., Weizman, A. & 33 others, Klaassen, P. W. J., Koops, S., Kates, W. R., Antshel, K. M., Simon, T. J., Ousley, O. Y., Swillen, A., Gur, R. E., Bearden, C. E., Kahn, R. S., Bassett, A. S., Emanuel, B. S., Zackai, E. H., Kushan, L., Fremont, W., Schoch, K., Stoddard, J., Cubells, J., Fu, F., Campbell, L. E., Fritsch, R., Vergaelen, E., Neeleman, M., Boot, E., Debbané, M., Philip, N., Green, T., Van DenBree, M. B. M., Murphy, D., Canyelles, J. M., Arango, C., Murphy, K. C. & Pontillo, M., 1 Apr 2015, In : JAMA Psychiatry. 72, 4, p. 377-385 9 p.

    Research output: Contribution to journalArticle

  18. IL36RN mutations define a severe autoinflammatory phenotype of generalized pustular psoriasis

    Hussain, S., Berki, D. M., Choon, S-E., Burden, A. D., Allen, M. H., Arostegui, J. I., Chaves, A., Duckworth, M., Irvine, A. D., Mockenhaupt, M., Navarini, A. A., Seyger, M. M. B., Soler-Palacin, P., Prins, C., Valeyrie-Allanore, L., Vicente, M. A., Trembath, R. C., Smith, C. H., Barker, J. N. & Capon, F., Apr 2015, In : Journal of Allergy and Clinical Immunology. 135, 4, p. 1067-1070.e9 12 p.

    Research output: Contribution to journalArticle

  19. White-matter relaxation time and myelin water fraction differences in young adults with autism

    Zinkstok, J. R., Daly, E., Ecker, C., Williams, S. C. R., Murphy, D. G. M., Bailey, A. J., Baron-Cohen, S., Bolton, P. F., Bullmore, E. T., Carrington, S., Chakrabarti, B., Daly, E. M., Deoni, S. C. L., Ecker, C., Happe, F., Henty, J., Jezzard, P., Johnston, P., Jones, D. K., Lombardo, M. V. & 11 others, Madden, A., Mullins, D., Murphy, C., Murphy, D. G., Pasco, G., Sadek, S. A., Spain, D., Steward, R., Suckling, J., Wheelwright, S. & Williams, S., 12 Mar 2015, In : Psychological Medicine. 45, 4, p. 795-805 11 p.

    Research output: Contribution to journalArticle

  20. Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms

    Baurecht, H., Hotze, M., Brand, S., Büning, C., Cormican, P., Corvin, A., Ellinghaus, D., Ellinghaus, E., Esparza-Gordillo, J., Fölster-Holst, R., Franke, A., Gieger, C., Hubner, N., Illig, T., Irvine, A. D., Kabesch, M., Lee, Y. A. E., Lieb, W., Marenholz, I., McLean, W. H. I. & 18 others, Morris, D. W., Mrowietz, U., Nair, R., Nöthen, M. M., Novak, N., O'Regan, G. M., Schreiber, S., Smith, C., Strauch, K., Stuart, P. E., Trembath, R., Tsoi, L. C., Weichenthal, M., Barker, J., Elder, J. T., Weidinger, S., Cordell, H. J. & Brown, S. J., 8 Jan 2015, In : American Journal of Human Genetics. 96, 1, p. 104-120 17 p.

    Research output: Contribution to journalArticle

  21. Emotional detachment in psychopathy: Involvement of dorsal default-mode connections

    Arjun, S., Gregory, S. L., Dell' Acqua, F., Thomas, E., Simmons, A., Murphy, D. G., Hodgins, S. M., Blackwood, N. & Craig, M. C., Jan 2015, In : Cortex. 62, p. 11-19 9 p.

    Research output: Contribution to journalArticle

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

    Tsoi, L. C., Spain, S. L., Ellinghaus, E., Stuart, P. E., Capon, F., Knight, J., 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. & 13 others, 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., 2015, In : Nature Communications. 6, 7001.

    Research output: Contribution to journalArticle

  23. GABA(A) Receptors in Autism - a Multicenter Positron Emission Tomography Study

    Mendez Hernandez, M. A., Borg, J., Horder, J., Veronese, M., Lundberg, J., Myers, J., Andersson, M., Mick, I., Tangen, A., Farde, L., Halldin, C., Selvaraj, S., Lingford-Hughes, A., Howes, O. D., Nutt, D. J. & Murphy, D. G., 2015, 14th International Meeting for Autism Research (IMFAR), 2015.

    Research output: Chapter in Book/Report/Conference proceedingMeeting abstract

  24. 2014
  25. European clinical network: autism spectrum disorder assessments and patient characterisation

    Ashwood, K. L., Buitelaar, J., Murphy, D., Spooren, W. & Charman, T., 4 Dec 2014, In : European Child and Adolescent Psychiatry. 24, 8, p. 985-995 11 p.

    Research output: Contribution to journalArticle

  26. Public-private partnership: A new engine for translational research in neurosciences

    Murphy, D. G. M., Goldman, M., Loth, E. & Spooren, W., 5 Nov 2014, In : Neuron. 84, 3, p. 533-536 4 p.

    Research output: Contribution to journalArticle

  27. New treatment targets for autism spectrum disorders: EU-AIMS

    Loth, E., Spooren, W. & Murphy, D. G., 1 Nov 2014, In : The Lancet Psychiatry. 1, 6, p. 413-415 3 p.

    Research output: Contribution to journalArticle

  28. Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

    Postmus, I., Trompet, S., Deshmukh, H. A., Barnes, M. R., Li, X., Warren, H. R., Chasman, D. I., Zhou, K., Arsenault, B. J., Donnelly, L. A., Wiggins, K. L., Avery, C. L., Griffin, P., Feng, Q., Taylor, K. D., Li, G., Evans, D. S., Smith, A. V., De Keyser, C. E., Johnson, A. D. & 142 others, De Craen, A. J. M., Stott, D. J., Buckley, B. M., Ford, I., Westendorp, R. G. J., Eline Slagboom, P., Sattar, N., Munroe, P. B., Sever, P., Poulter, N., Stanton, A., Shields, D. C., O???brien, E., Shaw-hawkins, S., Ida Chen, Y., Nickerson, D. A., Smith, J. D., Pierre Dub??, M., Matthijs Boekholdt, S., Kees Hovingh, G., Kastelein, J. J. P., Mckeigue, P. M., Betteridge, J., Neil, A., Durrington, P. N., Doney, A., Carr, F., Morris, A., Mccarthy, M. I., Groop, L., Ahlqvist, E., Bis, J. C., Rice, K., Smith, N. L., Lumley, T., Whitsel, E. A., St??rmer, T., Boerwinkle, E., Ngwa, J. S., O???donnell, C. J., Vasan, R. S., Wei, W., Wilke, R. A., Liu, C., Sun, F., Guo, X., Heckbert, S. R., Post, W., Sotoodehnia, N., Arnold, A. M., Stafford, J. M., Ding, J., Herrington, D. M., Kritchevsky, S. B., Eiriksdottir, G., Launer, L. J., Harris, T. B., Chu, A. Y., Giulianini, F., Macfadyen, J. G., Barratt, B. J., Nyberg, F., Stricker, B. H., Uitterlinden, A. G., Hofman, A., Rivadeneira, F., Emilsson, V., Franco, O. H., Ridker, P. M., Gudnason, V., Liu, Y., Denny, J. C., Ballantyne, C. M., Rotter, J. I., Adrienne Cupples, L., Psaty, B. M., Palmer, C. N. A., Tardif, J., Colhoun, H. M., Hitman, G., Krauss, R. M., Wouter Jukema, J., Caulfield, M. J., Donnelly, P., Barroso, I., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R., Viswanathan, A. C., Wood, N. W., Spencer, C. C. A., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Donnelly, P., Langford, C., Hunt, S. E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S. J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., Mccann, O. T., Liddle, J., Potter, S. C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Barroso, I., Deloukas, P., Mathew, C. G., Blackwell, J. M., Brown, M. A., Corvin, A., Mccarthy, M. I. & Spencer, C. C. A., 28 Oct 2014, In : Nature Communications. 5, 5068.

    Research output: Contribution to journalArticle

  29. Coregistering functional near-infrared spectroscopy with underlying cortical areas in infants

    Lloyd-Fox, S., Richards, J. E., Blasi, A., Murphy, D. G. M., Elwell, C. E. & Johnson, M. H., 1 Oct 2014, In : Neurophotonics. 1, 2, 14007RR.

    Research output: Contribution to journalArticle

  30. Germline FH mutations presenting with pheochromocytoma

    Clark, G. R., Sciacovelli, M., Gaude, E., Walsh, D. M., Kirby, G., Simpson, M. A., Trembath, R. C., Berg, J. N., Woodward, E. R., Kinning, E., Morrison, P. J., Frezza, C. & Maher, E. R., 1 Oct 2014, In : The Journal of clinical endocrinology and metabolism. 99, 10, p. E2046-E2050 5 p.

    Research output: Contribution to journalArticle

  31. Response inhibition and serotonin in autism: a functional MRI study using acute tryptophan depletion

    Daly, E., Ecker, C., Hallahan, B., Deeley, Q., Craig, M., Murphy, C., Johnston, P., Spain, D., Gillan, N., Gudbrandsen, M., Brammer, M., Giampietro, V., Lamar, M., Page, L., Toal, F., Schmitz, N., Cleare, A., Robertson, D., Rubia, K. & Murphy, D. G. M., 1 Sep 2014, In : Brain. 137, 9, p. 2600-2610 11 p.

    Research output: Contribution to journalArticle

  32. Are power calculations useful? A multicentre neuroimaging study

    Suckling, J., Henty, J., Ecker, C., Deoni, S. C., Lombardo, M. V., Baron-Cohen, S., Jezzard, P., Barnes, A., Chakrabarti, B., Ooi, C., Lai, M-C., Williams, S. C., Murphy, D. G. M., Bullmore, E. & for the MRC AIMS Consortium, Aug 2014, In : Human Brain Mapping. 35, 8, p. 3569-3577 9 p.

    Research output: Contribution to journalArticle

  33. The correlation between reading and mathematics ability at age twelve has a substantial genetic component

    Davis, O. S. P., Band, G., Pirinen, M., Haworth, C. M. A., Meaburn, E. L., Kovas, Y., Harlaar, N., Docherty, S. J., Hanscombe, K. B., Trzaskowski, M., Curtis, C. J. C., Strange, A., Freeman, C., Bellenguez, C., Su, Z., Pearson, R., Vukcevic, D., Langford, C., Deloukas, P., Hunt, S. & 31 others, Gray, E., Dronov, S., Potter, S. C., Tashakkori-Ghanbaria, A., Edkins, S., Bumpstead, S. J., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Duncanson, A., Jankowski, J. A. Z., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Rautanen, A., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Barroso, I., Peltonen, L., Dale, P. S., Petrill, S. A., Schalkwyk, L. S., Craig, I. W., Lewis, C. M., Price, T. S., Plomin, R. & Wellcome Trust Case Control Consortium, 8 Jul 2014, In : Nature Communications. 5, 6 p., 4204.

    Research output: Contribution to journalArticle

  34. 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., Deret, S., Voegel, J. J., Spector, T. & 4 others, Smith, C. H., Trembath, R. C., Barker, J. N. & Acne Genetic Study Grp, Jun 2014, In : Nature Communications. 5, 6 p., 4020.

    Research output: Contribution to journalArticle

  35. Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

    Schneider, M., Debbane, M., Bassett, A. S., Chow, E. W. C., Fung, W. L. A., van den Bree, M. B. M., Owen, M., Murphy, K. C., Niarchou, M., Kates, W. R., Antshel, K. M., Fremont, W., McDonald-McGinn, D. M., Gur, R. E., Zackai, E. H., Vorstman, J., Duijff, S. N., Klaassen, P. W. J., Swillen, A., Gothelf, D. & 17 others, Green, T., Weizman, A., Van Amelsvoort, T., Evers, L., Boot, E., Shashi, V., Hooper, S. R., Bearden, C. E., Jalbrzikowski, M., Armando, M., Vicari, S., Murphy, D. G., Ousley, O., Campbell, L. E., Simon, T. J., Eliez, S. & Int Consortium Brain Behav 22q11 2, Jun 2014, In : The American Journal of Psychiatry. 171, 6, p. 627-639 13 p.

    Research output: Contribution to journalLiterature review

  36. AP1S3 Mutations Are Associated with Pustular Psoriasis and Impaired Toll-like Receptor 3 Trafficking

    Setta-Kaffetzi, N., Simpson, M. A., Navarini, A. A., Patel, V. M., Lu, H-C., Allen, M. H., Duckworth, M., Bachelez, H., Burden, A. D., Choon, S-E., Griffiths, C. E. M., Kirby, B., Kolios, A., Seyger, M. M. B., Prins, C., Smahi, A., Trembath, R. C., Fraternali, F., Smith, C. H., Barker, J. N. & 1 others, Capon, F., 1 May 2014, In : American Journal of Human Genetics. 94, 5, p. 790-797 8 p.

    Research output: Contribution to journalArticle

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