King's College London

Research portal

Dr Ashley Jones

  1. Comparison of Kings clinical staging in multinational ALS cohorts

    Balendra, R., Al Khleifat, A., Jones, A., Chiwera, T., Wicks, P., Young, C. A., Shaw, P. J., Turner, M. R., Nigel Leigh, P. & Al-Chalabi, A., 18 Jun 2022, In: Amyotrophic lateral sclerosis & frontotemporal degeneration.

    Research output: Contribution to journalArticlepeer-review

  2. Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3'UTR protect against ALS

    Project MinE ALS Sequencing Consortium, NYGC ALS Consortium, Eitan, C., Siany, A., Barkan, E., Olender, T., van Eijk, K. R., Moisse, M., Farhan, S. M. K., Danino, Y. M., Yanowski, E., Marmor-Kollet, H., Rivkin, N., Yacovzada, N. S., Hung, S. T., Cooper-Knock, J., Yu, C. H., Louis, C., Masters, S. L., Kenna, K. P. & 26 others, van der Spek, R. A. A., Sproviero, W., Al Khleifat, A., Iacoangeli, A., Shatunov, A., Jones, A. R., Elbaz-Alon, Y., Cohen, Y., Chapnik, E., Rothschild, D., Weissbrod, O., Beck, G., Ainbinder, E., Ben-Dor, S., Werneburg, S., Schafer, D. P., Brown, R. H., Shaw, P. J., Van Damme, P., van den Berg, L. H., Phatnani, H., Segal, E., Ichida, J. K., Al-Chalabi, A., Veldink, J. H. & Hornstein, E., 1 Apr 2022, In: Nature Neuroscience. 25, 4, p. 433-445 13 p.

    Research output: Contribution to journalArticlepeer-review

  3. Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis

    Al Khleifat, A., Iacoangeli, A., Van Vugt, J. J. F. A., Bowles, H., Zwamborn, R. A. J., Moisse, M., Zwamborn, R. A. J., Cooper-Knock, J., Shatunov, A., Jones, A., van Rheenen, W., Opie-Martin, S., Fogh, I., Topp, S., Smith, B., Dobson, R., Shaw, C., Chiò, A., Panades, M. P., Mora, J. S. & 10 others, Shaw, P. J., Landers, J. E., Glass, J. D., Başak, A. N., Hardiman, O., Robberecht, W., Van Damme, P., van den Berg, L. H., Veldink, J. H. & Al-Chalabi, A., 19 Oct 2021, In: NPJ Genomic medicine.

    Research output: Contribution to journalArticlepeer-review

  4. Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

    Johnson, J. O., Chia, R., Miller, D. E., Li, R., Kumaran, R., Abramzon, Y., Alahmady, N., Renton, A. E., Topp, S. D., Gibbs, J. R., Cookson, M. R., Sabir, M. S., Dalgard, C. L., Troakes, C., Jones, A. R., Shatunov, A., Iacoangeli, A., Al Khleifat, A., Ticozzi, N., Silani, V. & 277 others, Gellera, C., Blair, I. P., Dobson-Stone, C., Kwok, J. B., Bonkowski, E. S., Palvadeau, R., Tienari, P. J., Morrison, K. E., Shaw, P. J., Al-Chalabi, A., Brown, R. H., Calvo, A., Mora, G., Al-Saif, H., Gotkine, M., Leigh, F., Chang, I. J., Perlman, S. J., Glass, I., Scott, A. I., Shaw, C. E., Basak, A. N., Landers, J. E., Chiò, A., Crawford, T. O., Smith, B. N., Traynor, B. J., Smith, B. N., Ticozzi, N., Fallini, C., Gkazi, A. S., Topp, S. D., Scotter, E. L., Kenna, K. P., Keagle, P., Tiloca, C., Vance, C., Troakes, C., Colombrita, C., King, A., Pensato, V., Castellotti, B., Baas, F., Ten Asbroek, A. L. M. A., McKenna-Yasek, D., McLaughlin, R. L., Polak, M., Asress, S., Esteban-Pérez, J., Stevic, Z., D'Alfonso, S., Mazzini, L., Comi, G. P., Del Bo, R., Ceroni, M., Gagliardi, S., Querin, G., Bertolin, C., Van Rheenen, W., Rademakers, R., Van Blitterswijk, M., Lauria, G., Duga, S., Corti, S., Cereda, C., Corrado, L., Sorarù, G., Williams, K. L., Nicholson, G. A., Blair, I. P., Leblond-Manry, C., Rouleau, G. A., Hardiman, O., Morrison, K. E., Veldink, J. H., Van Den Berg, L. H., Al-Chalabi, A., Pall, H., Shaw, P. J., Turner, M. R., Talbot, K., Taroni, F., García-Redondo, A., Wu, Z., Glass, J. D., Gellera, C., Ratti, A., Brown, R. H., Silani, V., Shaw, C. E., Landers, J. E., Dalgard, C. L., Adeleye, A., Soltis, A. R., Alba, C., Viollet, C., Bacikova, D., Hupalo, D. N., Sukumar, G., Pollard, H. B., Wilkerson, M. D., Martinez, E. M. G., Abramzon, Y., Ahmed, S., Arepalli, S., Baloh, R. H., Bowser, R., Brady, C. B., Brice, A., Broach, J., Campbell, R. H., Camu, W., Chia, R., Cooper-Knock, J., Ding, J., Drepper, C., Drory, V. E., Dunckley, T. L., Eicher, J. D., England, B. K., Faghri, F., Feldman, E., Floeter, M. K., Fratta, P., Geiger, J. T., Gerhard, G., Gibbs, J. R., Gibson, S. B., Glass, J. D., Hardy, J., Harms, M. B., Heiman-Patterson, T. D., Hernandez, D. G., Jansson, L., Kirby, J., Kowall, N. W., Laaksovirta, H., Landeck, N., Landi, F., Le Ber, I., Lumbroso, S., Macgowan, D. J. L., Maragakis, N. J., Mora, G., Mouzat, K., Murphy, N. A., Myllykangas, L., Nalls, M. A., Orrell, R. W., Ostrow, L. W., Pamphlett, R., Pickering-Brown, S., Pioro, E. P., Pletnikova, O., Pliner, H. A., Pulst, S. M., Ravits, J. M., Renton, A. E., Rivera, A., Robberecht, W., Rogaeva, E., Rollinson, S., Rothstein, J. D., Scholz, S. W., Sendtner, M., Sidle, K. C., Simmons, Z., Singleton, A. B., Smith, N., Stone, D. J., Tienari, P. J., Troncoso, J. C., Valori, M., Van Damme, P., Van Deerlin, V. M., Van Den Bosch, L., Zinman, L., Landers, J. E., Chiò, A., Traynor, B. J., Angelocola, S. M., Ausiello, F. P., Barberis, M., Bartolomei, I., Battistini, S., Bersano, E., Bisogni, G., Borghero, G., Brunetti, M., Cabona, C., Calvo, A., Canale, F., Canosa, A., Cantisani, T. A., Capasso, M., Caponnetto, C., Cardinali, P., Carrera, P., Casale, F., Chiò, A., Colletti, T., Conforti, F. L., Conte, A., Conti, E., Corbo, M., Cuccu, S., Dalla Bella, E., D'Errico, E., Demarco, G., Dubbioso, R., Ferrarese, C., Ferraro, P. M., Filippi, M., Fini, N., Floris, G., Fuda, G., Gallone, S., Gianferrari, G., Giannini, F., Grassano, M., Greco, L., Iazzolino, B., Introna, A., La Bella, V., Lattante, S., Lauria, G., Liguori, R., Logroscino, G., Logullo, F. O., Lunetta, C., Mandich, P., Mandrioli, J., Manera, U., Manganelli, F., Marangi, G., Marinou, K., Marrosu, M. G., Martinelli, I., Messina, S., Moglia, C., Mora, G., Mosca, L., Murru, M. R., Origone, P., Passaniti, C., Petrelli, C., Petrucci, A., Pozzi, S., Pugliatti, M., Quattrini, A., Ricci, C., Riolo, G., Riva, N., Russo, M., Sabatelli, M., Salamone, P., Salivetto, M., Salvi, F., Santarelli, M., Sbaiz, L., Sideri, R., Simone, I., Simonini, C., Spataro, R., Tanel, R., Tedeschi, G., Ticca, A., Torriello, A., Tranquilli, S., Tremolizzo, L., Trojsi, F., Vasta, R., Vacchiano, V., Vita, G., Volanti, P., Zollino, M. & Zucchi, E., Oct 2021, In: JAMA Neurology. 78, 10, p. 1236-1248 13 p.

    Research output: Contribution to journalArticlepeer-review

  5. Cross-reactive probes on Illumina DNA methylation arrays: A large study on ALS shows that a cautionary approach is warranted in interpreting epigenome-wide association studies

    Hop, P. J., Zwamborn, R. A. J., Hannon, E. J., Dekker, A. M., van Eijk, K. R., Walker, E. M., Iacoangeli, A., Jones, A. R., Shatunov, A., Khleifat, A. A., Opie-Martin, S., Shaw, C. E., Morrison, K. E., Shaw, P. J., McLaughlin, R. L., Hardiman, O., Al-Chalabi, A., van Den Berg, L. H., Mill, J. & Veldink, J. H., 1 Dec 2020, In: NAR Genomics and Bioinformatics. 2, 4, lqaa105.

    Research output: Contribution to journalArticlepeer-review

  6. Relationship between smoking and ALS: Mendelian randomisation interrogation of causality

    Opie-Martin, S., Wootton, R. E., Budu-Aggrey, A., Shatunov, A., Jones, A. R., Iacoangeli, A., Al Khleifat, A., Davey-Smith, G. & Al-Chalabi, A., 1 Dec 2020, In: Journal of Neurology, Neurosurgery and Psychiatry. 91, 12, p. 1312-1315 4 p.

    Research output: Contribution to journalArticlepeer-review

  7. Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics

    Iacoangeli, A., Lin, T., Al Khleifat, A., Jones, A. R., Opie-Martin, S., Coleman, J. R. I., Shatunov, A., Sproviero, W., Williams, K. L., Garton, F., Restuadi, R., Henders, A. K., Mather, K. A., Needham, M., Mathers, S., Nicholson, G. A., Rowe, D. B., Henderson, R., McCombe, P. A., Pamphlett, R. & 11 others, Blair, I. P., Schultz, D., Sachdev, P. S., Newhouse, S. J., Proitsi, P., Fogh, I., Ngo, S. T., Dobson, R. J. B., Wray, N. R., Steyn, F. J. & Al-Chalabi, A., 27 Oct 2020, In: Cell Reports. 33, 4, p. 108323

    Research output: Contribution to journalArticlepeer-review

  8. UK Case control study of smoking and risk of Amyotrophic Lateral Sclerosis

    Martin, S. C., Jones, A. R., Iacoangeli, A., Al Khleifat, A., Oumar, M., Shaw, P. J., Shaw, C. E. D., Morrison, K. E., Wootton, R. E., Smith, G. D., Pearce, N. & Al-Chalabi, A., 17 Apr 2020, In: Amyotrophic lateral sclerosis & frontotemporal degeneration. 21, 3-4, p. 222-227 6 p.

    Research output: Contribution to journalArticlepeer-review

  9. C9orf72 intermediate expansions of 24–30 repeats are associated with ALS

    Alzheimer’s Disease Neuroimaging Initiative, Iacoangeli, A., Al Khleifat, A., Jones, A. R., Sproviero, W., Shatunov, A., Opie-Martin, S., Morrison, K. E., Shaw, P. J., Shaw, C. E., Fogh, I., Dobson, R. J., Newhouse, S. J. & Al-Chalabi, A., 17 Jul 2019, In: Acta Neuropathologica Communications. 7, 1, 7 p., 115.

    Research output: Contribution to journalArticlepeer-review

  10. Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy

    NNIPPS and BBBIPPS Study Groups, 1 Jul 2019, In: Movement Disorders. 34, 7, p. 1049-1059 11 p.

    Research output: Contribution to journalArticlepeer-review

  11. DNAscan: Personal computer compatible NGS analysis, annotation and visualisation

    Iacoangeli, A., Al Khleifat, A., Sproviero, W., Shatunov, A., Jones, A. R., Morgan, S. L., Pittman, A., Dobson, R. J., Newhouse, S. J. & Al-Chalabi, A., 27 Apr 2019, In: BMC Bioinformatics. 20, 1, 213.

    Research output: Contribution to journalArticlepeer-review

  12. Telomere length is greater in ALS than in controls: A whole genome sequencing study

    Al Khleifat, A., Iacoangeli, A., Shatunov, A., Fang, T., Sproviero, W., Jones, A. R., Opie-Martin, S., Morrison, K. E., Shaw, P. J., Shaw, C. E. D., Powell, J. F., Dobson, R. J. B., Newhouse, S. & Al-Chalabi, A., 3 Apr 2019, In: Amyotrophic lateral sclerosis & frontotemporal degeneration. 20, 3-4, p. 229-234 6 p., IAFD 1586951.

    Research output: Contribution to journalArticlepeer-review

  13. Younger age of onset in familial amyotrophic lateral sclerosis is a result of pathogenic gene variants, rather than ascertainment bias

    Mehta, P. R., Jones, A. R., Opie-Martin, S., Shatunov, A., Iacoangeli, A., Al Khleifat, A., Smith, B. N., Topp, S., Morrison, K. E., Shaw, P. J., Shaw, C. E., Morgan, S., Pittman, A. & Al-Chalabi, A., 30 Sep 2018, (E-pub ahead of print) In: Journal of Neurology, Neurosurgery and Psychiatry.

    Research output: Contribution to journalArticlepeer-review

  14. Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases

    Chen, J. A., Chen, Z., Won, H., Huang, A. Y., Lowe, J. K., Wojta, K., Yokoyama, J. S., Bensimon, G., Leigh, P. N., Payan, C., Shatunov, A., Jones, A. R., Lewis, C. M., Deloukas, P., Amouyel, P., Tzourio, C., Dartigues, J. F., Ludolph, A., Boxer, A. L., Bronstein, J. M. & 3 others, Al-Chalabi, A., Geschwind, D. H. & Coppola, G., 8 Aug 2018, In: Molecular Neurodegeneration. 13, 1, 41.

    Research output: Contribution to journalArticlepeer-review

  15. Stage of prolonged survival in ALS –: Author's reply

    Al-Chalabi, A., Fang, T., Khleifat, A. A., Meurgey, J-H., Jones, A., Leigh, P. N. & Bensimon, G., Jul 2018, In: The Lancet Neurology. 17, 7, p. 579-580 2 p.

    Research output: Contribution to journalArticlepeer-review

  16. Stage at which riluzole treatment prolongs survival in patients with amyotrophic lateral sclerosis: a retrospective analysis of data from a dose-ranging study

    Fang, T., Al Khleifat, A., Meurgey, J-H., Jones, A., Leigh, P. N., Bensimon, G. & Al-Chalabi, A., 1 May 2018, In: Lancet Neurology. 17, 5, p. 416-422 7 p.

    Research output: Contribution to journalArticlepeer-review

  17. Elongator subunit 3 (ELP3) modifies ALS through tRNA modification

    Bento-Abreu, A., Jager, G., Swinnen, B., Rué, L., Hendrickx, S., Jones, A., Staats, K. A., Taes, I., Eykens, C., Nonneman, A., Nuyts, R., Timmers, M., Silva, L., Chariot, A., Nguyen, L., Ravits, J., Lemmens, R., Cabooter, D., Van Den Bosch, L., Van Damme, P. & 3 others, Al-Chalabi, A., Bystrom, A. & Robberecht, W., 1 Apr 2018, In: Human Molecular Genetics. 27, 7, p. 1276-1289 14 p.

    Research output: Contribution to journalArticlepeer-review

  18. Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials

    van Eijk, R. P. A., Jones, A., Sproviero, W., Shatunov, A., Shaw, P. J., Leigh, P. N., Young, C. A., Shaw, C. E., Mora, G., Mandrioli, J., Borghero, G., Volanti, P., Diekstra, F. P., van Rheenen, W., Verstraete, E., Eijkemans, M. J. C., Veldink, J. H., Chio, A., Al-Chalabi, A., van den Berg, L. H. & 2 others, van Es, M. A. & For UKMND-LiCALS and LITALS Study Group, 31 Oct 2017, In: Neurology. 89, 18, p. 1915-1922 8 p.

    Research output: Contribution to journalArticlepeer-review

  19. Plasma REST: a novel candidate biomarker of Alzheimer’s disease is modified by psychological intervention in an at-risk population

    Ashton, N. J., Hye, A., Leckey, C. A., Jones, A. R., Gardner, A., Elliott, C., Wetherell, J. L., Lenze, E. J., Killick, R. & Marchant, N. L., 6 Jun 2017, (E-pub ahead of print) In: Translational psychiatry. 7, 6, e1148.

    Research output: Contribution to journalArticlepeer-review

  20. A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK

    Morgan, S., Shatunov, A., Sproviero, W., Jones, A. R., Shoai, M., Hughes, D., Al Khleifat, A., Malaspina, A., Morrison, K. E., Shaw, P. J., Shaw, C. E., Sidle, K., Orrell, R. W., Fratta, P., Hardy, J., Pittman, A. & Al-Chalabi, A., 1 Jun 2017, In: Brain : a journal of neurology. 140, 6, p. 1611-1618 8 p.

    Research output: Contribution to journalArticlepeer-review

  21. C9orf72 expansion differentially affects males with spinal onset amyotrophic lateral sclerosis

    Rooney, J., Fogh, I., Westeneng, H-J., Vajda, A., McLaughlin, R., Heverin, M., Jones, A., van Eijk, R., Calvo, A., Mazzini, L., Shaw, C., Morrison, K., Shaw, P. J., Robberecht, W., Van Damme, P., Al-Chalabi, A., van den Berg, L., Chiò, A., Veldink, J. & Hardiman, O., 23 Sep 2016, (E-pub ahead of print) In: Journal of neurology, neurosurgery, and psychiatry. 7 p.

    Research output: Contribution to journalArticlepeer-review

  22. Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis

    Gaastra, B., Shatunov, A., Pulit, S., Jones, A. R., Sproviero, W., Gillett, A., Chen, Z., Kirby, J., Fogh, I., Powell, J. F., Leigh, P. N., Morrison, K. E., Shaw, P. J., Shaw, C. E., van den Berg, L. H., Veldink, J. H., Lewis, C. M. & Al-Chalabi, A., 2 Sep 2016, In: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration . 17, 7-8, p. 593-599 7 p.

    Research output: Contribution to journalArticlepeer-review

  23. NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

    Kenna, K. P., van Doormaal, P. T. C., Dekker, A. M., Ticozzi, N., Kenna, B. J., Diekstra, F. P., van Rheenen, W., van Eijk, K. R., Jones, A. R., Keagle, P., Shatunov, A., Sproviero, W., Smith, B. N., van Es, M. A., Topp, S. D., Kenna, A., Miller, J. W., Fallini, C., Tiloca, C., McLaughlin, R. L. & 31 others, Vance, C., Troakes, C., Colombrita, C., Mora, G., Calvo, A., Verde, F., Al-Sarraj, S., King, A., Calini, D., de Belleroche, J., Baas, F., van der Kooi, A. J., de Visser, M., Ten Asbroek, A. L. M. A., Sapp, P. C., McKenna-Yasek, D., Polak, M., Asress, S., Muñoz-Blanco, J. L., Strom, T. M., Meitinger, T., Morrison, K. E., Lauria, G., Williams, K. L., Leigh, P. N., Nicholson, G. A., Turner, M. R., Glass, J. D., Al-Chalabi, A., Shaw, C. E. & SLAGEN Consortium, 1 Sep 2016, In: Nature Genetics. 48, 9, p. 1037-42 6 p.

    Research output: Contribution to journalLetterpeer-review

  24. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

    van Rheenen, W., Shatunov, A., Dekker, A. M., McLaughlin, R. L., Diekstra, F. P., Pulit, S. L., van der Spek, R. A. A., Võsa, U., de Jong, S., Robinson, M. R., Yang, J., Fogh, I., van Doormaal, P. T., Tazelaar, G. H. P., Koppers, M., Blokhuis, A. M., Sproviero, W., Jones, A. R., Kenna, K. P., van Eijk, K. R. & 31 others, Harschnitz, O., Schellevis, R. D., Brands, W. J., Medic, J., Menelaou, A., Vajda, A., Ticozzi, N., Lin, K., Rogelj, B., Vrabec, K., Ravnik-Glavač, M., Koritnik, B., Zidar, J., Leonardis, L., Grošelj, L. D., Millecamps, S., Salachas, F., Meininger, V., de Carvalho, M., Pinto, S., Fratta, P., Topp, S., Curtis, C., Shaw, C. E., Smith, B. N., Leigh, P. N., Powell, J., Lewis, C. M., Breen, G., Al-Chalabi, A. & PARALS Registry, Sep 2016, In: Nature Genetics. 48, p. 1043–1048

    Research output: Contribution to journalArticlepeer-review

  25. Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis

    Fogh, I., Lin, K., Tiloca, C., Rooney, J., Gellera, C., Diekstra, F. P., Ratti, A., Shatunov, A., Van Es, M. A., Proitsi, P., Jones, A., Sproviero, W., Chiò, A., McLaughlin, R. L., Sorarù, G., Corrado, L., Stahl, D., Del Bo, R., Cereda, C., Castellotti, B. & 29 others, Glass, J. D., Newhouse, S., Dobson, R., Smith, B. N., Topp, S., Van Rheenen, W., Meininger, V., Melki, J., Morrison, K. E., Shaw, P. J., Leigh, P. N., Andersen, P. M., Comi, G. P., Ticozzi, N., Mazzini, L., D'Alfonso, S., Traynor, B. J., Van Damme, P., Robberecht, W., Brown, R. H., Landers, J. E., Hardiman, O., Lewis, C. M., Van Den Berg, L. H., Shaw, C. E., Veldink, J. H., Silani, V., Al-Chalabi, A. & Powell, J., 1 Jul 2016, In: JAMA Neurology. 73, 7, p. 812-820 9 p.

    Research output: Contribution to journalArticlepeer-review

  26. The ALSFRS as an outcome measure in therapeutic trials and its relationship to symptom onset

    Proudfoot, M., Jones, A., Talbot, K., Al-Chalabi, A. & Turner, M. R., 11 Feb 2016, (E-pub ahead of print) In: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration . p. 1-12 12 p.

    Research output: Contribution to journalArticlepeer-review

  27. Regionality of disease progression predicts prognosis in amyotrophic lateral sclerosis

    Van Der Kleij, L. A., Jones, A. R., Steen, I. N., Young, C. A., Shaw, P. J., Shaw, C. E., Leigh, P. N., Turner, M. R. & Al-Chalabi, A., 27 Nov 2015, In: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration . 16, 7-8, p. 442-447 6 p.

    Research output: Contribution to journalArticlepeer-review

  28. Investigation of next-generation sequencing technologies as a diagnostic tool for amyotrophic lateral sclerosis

    Morgan, S., Shoai, M., Fratta, P., Sidle, K., Orrell, R., Sweeney, M. G., Shatunov, A., Sproviero, W., Jones, A., Al-Chalabi, A., Malaspina, A., Houlden, H., Hardy, J. & Pittman, A., Mar 2015, In: Neurobiology of Aging. 36, 3, p. 1600.e5-1600.e8 3 p.

    Research output: Contribution to journalArticlepeer-review

  29. Stratified gene expression analysis identifies major amyotrophic lateral sclerosis genes

    Jones, A. R., Troakes, C., King, A., Sahni, V., De Jong, S., Bossers, K., Papouli, E., Mirza, M., Al-Sarraj, S., Shaw, C. E., Shaw, P. J., Kirby, J., Veldink, J. H., Macklis, J. D., Powell, J. F. & Al-Chalabi, A., 19 Feb 2015, (E-pub ahead of print) In: Neurobiology of Aging. p. 2006.e1-2006.e9 9 p.

    Research output: Contribution to journalArticlepeer-review

  30. Intermediate length C9orf72 expansion in an ALS patient without classical C9orf72 neuropathology

    Beer, A. M., Cooper-Knock, J., Higginbottom, A., Highley, J. R., Wharton, S. B., Ince, P. G., Milano, A., Jones, A. A., Al-Chalabi, A., Kirby, J. & Shaw, P. J., 2014, (E-pub ahead of print) In: Amyotrophic lateral sclerosis & frontotemporal degeneration. p. 1-3 3 p.

    Research output: Contribution to journalArticlepeer-review

  31. Neuroendocrine Merkel Cell Carcinoma is Associated with Mutations in Key DNA Repair, Epigenetic and Apoptosis Pathways: A Case-Based Study using Targeted Massively Parallel Sequencing

    Graves, C. A., Jones, A., Reynolds, J., Stuart, J., Pirisi, L., Botrous, P. & Wells, J., 2014, (E-pub ahead of print) In: Neuroendocrinology.

    Research output: Contribution to journalArticlepeer-review

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