المؤلفون: Veal, CD, Reekie, KE, Lorentzen, JC, Gregersen, PK, Padyukov, L, Brookes, AJ

المصدر: Human mutation. 35(2):248-256

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:128030765

المؤلفون: Veal, CD, Reynolds, NJ, Meggitt, SJ, Allen, MH, Lindgren, CM, Kere, J, Trembath, RC, Barker, JNWN

المصدر: The Journal of investigative dermatology. 125(2):399-401

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:111283656

المؤلفون: Vermunt, L, Veal, CD, ter Meulen, L, Chrysostomou, C, van der Flier, W, Frisoni, GB, Guessous, I, Kivipelto, M, Marizzoni, M, Martinez-Lage, P, Molinuevo, JL, Porteous, D, Ritchie, K, Scheltens, P, Ousset, PJ, Ritchie, CW, Luscan, G, Brookes, AJ, Visser, PJ

المصدر: Alzheimer's & dementia : the journal of the Alzheimer's Association. 14(6):837-842

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:138430923

المؤلفون: Woolley, JP, Kirby, E, Leslie, J, Jeanson, F, Cabili, MN, Rushton, G, Hazard, JG, Ladas, V, Veal, CD, Gibson, SJ, Tassé, A-M, Dyke, SOM, Gaff, C, Thorogood, A, Knoppers, BM, Wilbanks, J, Brookes, AJ

Relation: https://www.ncbi.nlm.nih.gov/pubmed/30062047; npj Genomic Medicine, 2018, 3, 17; https://www.nature.com/articles/s41525-018-0057-4; http://hdl.handle.net/2381/43971

الاتاحة: https://www.nature.com/articles/s41525-018-0057-4
http://hdl.handle.net/2381/43971
https://doi.org/10.1038/s41525-018-0057-4

المؤلفون: Woolley, JP, Kirby, E, Leslie, J, Jeanson, F, Cahil, MN, Rushton, G, Hazard, JG, Ladas, V, Veal, CD, Gibson, SJ, Tasse, A-M, Dyke, SOM, Gaff, C, Thorogood, A, Knoppers, BM, Wilbanks, J, Brookes, AJ

Relation: pii: 57; Woolley, J. P., Kirby, E., Leslie, J., Jeanson, F., Cahil, M. N., Rushton, G., Hazard, J. G., Ladas, V., Veal, C. D., Gibson, S. J., Tasse, A. -M., Dyke, S. O. M., Gaff, C., Thorogood, A., Knoppers, B. M., Wilbanks, J. & Brookes, A. J. (2018). Responsible sharing of biomedical data and biospecimens via the "Automatable Discovery and Access Matrix" (ADA-M). NPJ GENOMIC MEDICINE, 3 (1), https://doi.org/10.1038/s41525-018-0057-4.; http://hdl.handle.net/11343/251157

الاتاحة: http://hdl.handle.net/11343/251157

المؤلفون: Tarpey, P, Thomas, S, Sarvananthan, N, Mallya, U, Lisgo, S, Talbot, CJ, Roberts, EO, Awan, M, Surendran, M, McLean, RJ, Reinecke, RD, Langmann, A, Lindner, S, Koch, M, Jain, S, Woodruff, G, Gale, RP, Degg, C, Droutsas, K, Asproudis, I, Zubcov, AA, Pieh, C, Veal, CD, MacHado, RD, Backhouse, OC, Baumber, L, Constantinescu, CS, Brodsky, MC, Hunter, DG, Hertle, RW, Read, RJ, Edkins, S, O'Meara, S, Parker, A, Stevens, C, Teague, J, Wooster, R, Futreal, PA, Trembath, RC, Stratton, MR, Raymond, FL, Gottlob, I

المصدر: Scopus ; http://www.scopus.com/home.url

وصف الملف: metadata

Relation: NATURE GENETICS, 2011, 43 (7), pp. 720-720; http://hdl.handle.net/2381/24781

الاتاحة: http://hdl.handle.net/2381/24781
https://doi.org/10.1038/ng0711-720

المؤلفون: Capon, F, Helms, C, Veal, CD, Tillman, D, Burden, AD, Barker, JN, Bowcock, AM, Trembath, RC

المصدر: Web of Science (Lite) ; http://webofknowledge.com

وصف الملف: metadata

Relation: JOURNAL OF MEDICAL GENETICS, 2004, 41 (6), pp. 459-460; http://hdl.handle.net/2381/17800

الاتاحة: http://hdl.handle.net/2381/17800
https://doi.org/10.1136/jmg.2004.018226

المؤلفون: Tarpey, P, Thomas, S, Sarvananthan, N, Mallya, U, Lisgo, S, Talbot, CJ, Roberts, EO, Awan, M, Surendran, M, McLean, RJ, Reinecke, RD, Langmann, A, Lindner, S, Koch, M, Jain, S, Woodruff, G, Gale, RP, Bastawrous, A, Degg, C, Droutsas, K, Asproudis, I, Zubcov, AA, Pieh, C, Veal, CD, Machado, RD, Backhouse, OC, Baumber, L, Constantinescu, CS, Brodsky, MC, Hunter, DG, Hertle, RW, Read, RJ, Edkins, S, O'Meara, S, Parker, A, Stevens, C, Teague, J, Wooster, R, Futreal, PA, Trembath, RC, Stratton, MR, Raymond, FL, Gottlob, I

المصدر: PubMed ; http://www.ncbi.nlm.nih.gov/pubmed/

مصطلحات موضوعية: Brain, Chromosome Mapping, Chromosomes, Human, Cytoskeletal Proteins, Eye Movements, Female, Gene Expression Regulation, Developmental, Genes, X-Linked, Genetic Linkage, Humans, Male, Membrane Proteins, Mutation, Nystagmus, Congenital, Pedigree, Retina

وصف الملف: metadata

Relation: NAT GENET, 2006, 38 (11), pp. 1242-1244; http://hdl.handle.net/2381/15523; ng1893

الاتاحة: http://hdl.handle.net/2381/15523
https://doi.org/10.1038/ng1893

المؤلفون: Veal, CD, Clough, RL, Barber, RC, Mason, S, Tillman, D, Ferry, B, Jones, AB, Ameen, M, Balendran, N, Powis, SH, Burden, AD, Barker, JNWN, Trembath, RC

المصدر: Web of Science (Lite) ; http://webofknowledge.com

مصطلحات موضوعية: psoriasis, PSORS1, epistasis

وصف الملف: metadata

Relation: JOURNAL OF MEDICAL GENETICS, 2001, 38 (1), pp. 7-13; http://hdl.handle.net/2381/15488

الاتاحة: http://hdl.handle.net/2381/15488
https://doi.org/10.1136/jmg.38.1.7

المؤلفون: Veal, CD, Capon, F, Allen, MH, Heath, EK, Evans, JC, Jones, A, Patel, S, Burden, D, Tillman, D, Barker, JN, Trembath, RC

المصدر: PubMed ; http://www.ncbi.nlm.nih.gov/pubmed/

مصطلحات موضوعية: Case-Control Studies, Chromosome Mapping, Chromosomes, Human, Pair 6, Genetic Predisposition to Disease, Genetic Variation, Haplotypes, Humans, Linkage Disequilibrium, Molecular Sequence Data, Polymorphism, Single Nucleotide, Psoriasis

وصف الملف: metadata

Relation: AM J HUM GENET, 2002, 71 (3), pp. 554-564; http://hdl.handle.net/2381/15361; S0002-9297(07)60335-8

الاتاحة: http://hdl.handle.net/2381/15361
https://doi.org/10.1086/342289

المؤلفون: Epstein, MP, Veal, CD, Trembath, RC, Barker, JNWN, Li, C, Satten, GA

المصدر: Web of Science (Lite) ; http://webofknowledge.com

وصف الملف: metadata

Relation: AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 76 (4), pp. 592-608; http://hdl.handle.net/2381/15362

الاتاحة: http://hdl.handle.net/2381/15362
https://doi.org/10.1086/429225

المؤلفون: Tarpey P, Thomas S, Sarvananthan N, Mallya U, Lisgo S, Talbot CJ, Roberts EO, Awan M, Surendran M, McLean RJ, Reinecke RD, Langmann A, Lindner S, Koch M, Jain S, Woodruff G, Gale RP, Degg C, Droutsas K, Asproudis I, Zubcov AA, Pieh C, Veal CD, MacHado RD, Backhouse OC, Baumber L, Constantinescu CS, Brodsky MC, Hunter DG, Hertle RW, Read RJ, Edkins S, O'Meara S, Parker A, Stevens C, Teague J, Wooster R, Futreal PA, Trembath RC, Stratton MR, Raymond FL, Gottlob I

المصدر: Nature Genetics, 01-10-2006

Relation: https://eprints.ncl.ac.uk/72554

الاتاحة: https://eprints.ncl.ac.uk/72554

المؤلفون: Barker, JN, Bowcock, AM, Burden, AD, Capon, F, Helms, C, Tillman, D, Trembath, RC, Veal, CD

Relation: Barker, J., Bowcock, A., Burden, A., Capon, F., Helms, C., Tillman, D. , Trembath, R. and Veal, C. (2004) Genetic analysis of PSORS2 markers in a UK dataset supports the association between RAPTOR SNPs and familial psoriasis. Journal of Medical Genetics , 41, pp. 459-460. (doi:10.1136/jmg.2004.018226 )

الاتاحة: https://eprints.gla.ac.uk/18731/

المؤلفون: Tarpey, P, Thomas, S, Sarvananthan, N, Mallya, U, Lisgo, S, Talbot, CJ, Roberts, EO, Awan, M, Surendran, M, McLean, RJ, Reinecke, RD, Langmann, A, Lindner, S, Koch, M, Woodruff, G, Gale, R, Degg, C, Droutsas, K, Asproudis, I, Zubcov, AA, Pieh, C, Veal, CD, Machado, RD, Backhouse, OC, Baumber, L, Jain, S, Constantinescu, CS, Brodsky, MC, Hunter, DG, Hertle, RW, Read, RJ, Edkins, S, O’Meara, S, Parker, A, Stevens, C, Teague, J, Wooster, R, Futreal, PA, Trembath, RC, Stratton, MR, Raymond, FL, Gottlob, I

مصطلحات موضوعية: Male, Chromosomes, Human, X, genetic structures, Eye Movements, Genetic Linkage, Brain, Chromosome Mapping, Gene Expression Regulation, Developmental, Membrane Proteins, eye diseases, Article, Retina, Pedigree, Cytoskeletal Proteins, Genes, X-Linked, Mutation, Humans, Female, Nystagmus, Congenital

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::b3385dae51b2eba053bb011e8c2508cc
https://europepmc.org/articles/PMC2592600/

المؤلفون: Allen, MH, Barker, JNWN, Burden, D, Capon, F, Evans, JC, Heath, EK, Jones, A, Patel, S, Tillman, D, Trembath, RC, Veal, CD

Relation: Allen, M. et al. (2002) Family-based analysis using a dense single-nucleotide polymorphism-based map defines genetic variation at PSORS1, the major psoriasis-susceptibility locus. American Journal of Human Genetics , 71, pp. 554-564.

الاتاحة: https://eprints.gla.ac.uk/18841/

المؤلفون: Veal, CD, Capon, F, Allen, MH, Heath, EK, Burden, D, Tillman, D, Barker, JNWN, Trembath, RC

المصدر: Veal , CD , Capon , F , Allen , MH , Heath , EK , Burden , D , Tillman , D , Barker , JNWN & Trembath , RC 2002 , ' Family-based analysis using a dense single nucleotide polymorphism based map defines genetic variation at PSORS1, the major psoriasis susceptibility locus. ' , British Journal of Dermatology , vol. 147 , no. 5 , pp. 1052 .

Relation: https://kclpure.kcl.ac.uk/portal/en/publications/f294d00e-1e5d-40e7-b04a-3079f2f8fd4f

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/f294d00e-1e5d-40e7-b04a-3079f2f8fd4f
http://www.scopus.com/inward/record.url?scp=18544383722&partnerID=8YFLogxK

المؤلفون: Ameen, M, Balendran, N, Barber, RC, Barker, JNWN, Burden, AD, Clough, RL, Ferry, B, Jones, AB, Mason, S, Powis, SH, Tillman, D, Trembath, RC, Veal, CD

Relation: Ameen, M. et al. (2001) Identification of a novel psoriasis susceptibility locus at 1p and evidence of epistasis between PSORS1 and candidate loci. Journal of Medical Genetics , 38, pp. 7-13.

الاتاحة: https://eprints.gla.ac.uk/18967/

المؤلفون: Jandu, Harkeran, Veal, Colin, Fachal, Laura, Luccarini, Craig, Altabas González, Manuel, Aguado-Barrera, Miguel E, Gutiérrez-Enríquez, Sara, Reyes López, Victoria

المساهمون: Institut Català de la Salut, Jandu HK, Veal CD Department of Genetics and Genome Biology, University of Leicester, Leicester, United Kingdom. Fachal L Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom. Luccarini C Centre for Cancer Genetic Epidemiology, Strangeways Research Laboratory, University of Cambridge, Cambridge, United Kingdom. Aguado-Barrera ME Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), Santiago de Compostela, Spain. Fundación Pública Galega de Medicina Xenómica, Santiago de Compostela, Spain. Altabas M, Reyes V Servei d’Oncologia Radioteràpica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Gutiérrez-Enríquez S Hereditary Cancer Genetics Group, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

المصدر: Scientia

مصطلحات موضوعية: Mama - Càncer - Radioteràpia - Complicacions, Mama - Càncer - Aspectes genètics, DISEASES::Neoplasms::Neoplasms by Site::Breast Neoplasms, Other subheadings::Other subheadings::Other subheadings::/radiotherapy, ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Radiotherapy, Other subheadings::Other subheadings::Other subheadings::/adverse effects, AND EQUIPMENT::Investigative Techniques::Epidemiologic Methods::Epidemiologic Research Design::Genome-Wide Association Study, ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de la mama, Otros calificadores::Otros calificadores::Otros calificadores::/radioterapia, TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::radioterapia, Otros calificadores::Otros calificadores::Otros calificadores::/efectos adversos, DIAGNÓSTICOS Y TERAPÉUTICOS::técnicas de investigación::métodos epidemiológicos::diseño de la investigación epidemiológica::estudio de asociación genómica completa

وصف الملف: application/pdf

Relation: Radiotherapy and Oncology;187; https://doi.org/10.1016/j.radonc.2023.109806; Jandu HK, Veal CD, Fachal L, Luccarini C, Aguado-Barrera ME, Altabas M, et al. Genome-wide association study of treatment-related toxicity two years following radiotherapy for breast cancer. Radiother Oncol. 2023 Oct;187:109806.; https://hdl.handle.net/11351/10339

الاتاحة: https://hdl.handle.net/11351/10339
https://doi.org/10.1016/j.radonc.2023.109806