نتائج البحث - "Jennifer H. Barrett"

1

Associations of pigmentary and naevus phenotype with melanoma risk in two populations with comparable ancestry but contrasting levels of ambient sun exposure

المؤلفون: Florence Demenais, Helen Schmid, G.G. Giles, Mark A. Jenkins, Julia Newton-Bishop, Alisa M. Goldstein, Lamiae Azizi, Bruce K. Armstrong, Martin Drummond, P.A. Kanetsky, Richard F. Kefford, Jennifer H. Barrett, Anne E. Cust, John L. Hopper, David E. Elder, D T Bishop, Graham J. Mann, Joanne F. Aitken

المصدر: Journal of the European Academy of Dermatology and Venereology
Journal of the European Academy of Dermatology and Venereology : JEADV, vol 33, iss 10

مصطلحات موضوعية: Male, Skin Neoplasms, genetic structures, Skin Pigmentation, 030207 dermatology & venereal diseases, 0302 clinical medicine, Risk Factors, Medicine, skin and connective tissue diseases, 10. No inequality, Melanoma, Cancer, Nevus, Pigmented, Confounding, Environmental exposure, Middle Aged, Tumor Burden, 3. Good health, Phenotype, Infectious Diseases, 030220 oncology & carcinogenesis, Sunlight, Original Article, Female, Risk assessment, Adult, medicine.medical_specialty, Adolescent, Original Articles and Short Reports Oncology, Clinical Sciences, Dermatology, Risk Assessment, White People, Young Adult, 03 medical and health sciences, Sex Factors, Pigmented, Clinical Research, Humans, Climate-Related Exposures and Conditions, Hair Color, Nevus, Aged, Whites, business.industry, Dermatology & Venereal Diseases, Australia, Case-control study, Extremities, Environmental Exposure, Odds ratio, United Kingdom, Case-Control Studies, Relative risk, Cutaneous melanoma, Attributable risk, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80dfcf3a5712e4931de322d9cca31b62Test
https://doi.org/10.1111/jdv.15680Test

2

Development and external validation study of a melanoma risk prediction model incorporating clinically assessed naevi and solar lentigines

المؤلفون: Anne E. Cust, Julia Newton-Bishop, John R. Davies, Jennifer H. Barrett, Mark A. Jenkins, G.G. Giles, John L. Hopper, Kylie Vuong, Martin Drummond, H. Schmid, Kevin McGeechan, Joanne F. Aitken, Graham J. Mann, D T Bishop, Bruce K. Armstrong

المصدر: Br J Dermatol

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c23682d9c17d611c43fa128841434dfTest
https://pubmed.ncbi.nlm.nih.gov/31608432Test

3

Evidence of NLRP3-inflammasome activation in rheumatoid arthritis (RA); genetic variants within the NLRP3-inflammasome complex in relation to susceptibility to RA and response to anti-TNF treatment

المؤلفون: Sinisa Savic, C. Wong, Kimme L. Hyrich, Anne Barton, Anthony G. Wilson, Sarah M Churchman, Darren Plant, Michael F. McDermott, Steve Eyre, Jennifer H. Barrett, Piercarlo Sarzi-Puttini, Rebeccah J. Mathews, James I. Robinson, John D. Isaacs, John C. Taylor, Ann W. Morgan, M. Battellino, Graham P. Cook, Paul Emery

المصدر: Annals of the Rheumatic Diseases; Vol 73

مصطلحات موضوعية: Male, Inflammasomes, Etanercept, Arthritis, Rheumatoid, 0302 clinical medicine, Immunology and Allergy, Medicine, skin and connective tissue diseases, 0303 health sciences, integumentary system, Caspase 1, Middle Aged, MEFV, 3. Good health, Neoplasm Proteins, Rheumatoid arthritis, Antirheumatic Agents, Tumor necrosis factor alpha, Female, medicine.drug, musculoskeletal diseases, Adult, Genotype, Immunology, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, Rheumatology, NLR Family, Pyrin Domain-Containing 3 Protein, Adalimumab, Humans, Genetic Predisposition to Disease, RNA, Messenger, 030304 developmental biology, Aged, 030203 arthritis & rheumatology, business.industry, Tumor Necrosis Factor-alpha, Gene Expression Profiling, Pyrin, medicine.disease, Infliximab, CARD Signaling Adaptor Proteins, Cytoskeletal Proteins, Case-Control Studies, Expression quantitative trait loci, Multivariate Analysis, Linear Models, business, Carrier Proteins

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20b508b8f4830786156631147b5633e8Test

4

Reevaluation of the interaction between HLA-DRB1 shared epitope alleles, PTPN22, and smoking in determining susceptibility to autoantibody-positive and autoantibody-negative rheumatoid arthritis in a large UK Caucasian population

المؤلفون: Ann W. Morgan, Henry A. Erlich, Angela M. Carter, Paul Wordsworth, Paul Emery, David M. Reid, Wendy Thomson, Pille Harrison, Anne Barton, Lynne J. Hocking, Jane Worthington, Jennifer H. Barrett, Stephen G. Martin, Sophia Steer, Anthony G. Wilson

مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, Immunology, Population, Peptides, Cyclic, White People, PTPN22, Arthritis, Rheumatoid, Epitopes, Young Adult, Rheumatology, Rheumatoid Factor, immune system diseases, medicine, Immunology and Allergy, Rheumatoid factor, Humans, Pharmacology (medical), Genetic Predisposition to Disease, education, skin and connective tissue diseases, HLA-DRB1, Alleles, Aged, Autoantibodies, Aged, 80 and over, education.field_of_study, Models, Genetic, business.industry, Smoking, Autoantibody, Case-control study, Protein Tyrosine Phosphatase, Non-Receptor Type 22, Odds ratio, HLA-DR Antigens, Middle Aged, medicine.disease, United Kingdom, Logistic Models, Rheumatoid arthritis, Case-Control Studies, Female, business, HLA-DRB1 Chains

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fc707331e5c7674186b0f1c2c7945f6Test
https://doi.org/10.1002/art.24752Test

5

Confirmation of association ofFCGR3Bbut notFCGR3Acopy number with susceptibility to autoantibody positive rheumatoid arthritis

المؤلفون: James I. Robinson, Ian M. Carr, Dawn L. Cooper, John D. Isaacs, Lubna Haroon Rashid, Paul Emery, Anthony G. Wilson, Braggss, Anne Barton, Ann W. Morgan, Jennifer H. Barrett, Stephen G. Martin

المصدر: Human Mutation. 33:741-749

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d71e0636a6c0cb2dc1f82e393709e2dTest
https://doi.org/10.1002/humu.22031Test

6

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer

المؤلفون: Frederik J. Hes, Richard S. Houlston, Ceres Fernandez-Rozadilla, Maggie Gorman, Harry Campbell, Ben Kinnersley, Albert Tenesa, Carli M. J. Tops, Melanie Schrumpf, Nicola Whiffin, Asta Försti, D. Timothy Bishop, Ella Barclay, Robert M.W. Hofstra, Fay J. Hosking, L. Y. Ooi, Claire Smillie, Graeme R. Grimes, Caroline Hayward, Arnoud Boot, Amy Lloyd, Stephan Buch, Manuela Pinheiro, Sara E. Dobbins, Clemens Schafmayer, Jennifer H. Barrett, Kari Hemminki, Helga Westers, Tom van Wezel, David J. Porteous, Archie Campbell, Sergi Castellví-Bel, Carla M. A. Pinto, Evropi Theodoratou, Lina Zgaga, Antoni Castells, Roland Wolf, Juul T. Wijnen, Hans Morreau, Peter Broderick, Susan M. Farrington, Victoria Svinti, Sarah E. Harris, Emma Northwood, Angel Carracedo, Andre Franke, Lynn Martin, Gillian Smith, Peter Propping, David Forman, Hans F. A. Vasen, Malcolm G. Dunlop, Ian Tomlinson, Dina Ruano, Wolgang Lieb, Claire Palles, Manuel R. Teixeira, Ian J. Deary, Clara Ruiz-Ponte, Maria Timofeeva, Jochen Hampe

المساهمون: Neurology, Internal Medicine, Medical Genetics

المصدر: Scientific Reports, 5
Scientific Reports
Scientific Reports, 5:16286. Nature Publishing Group
Scientific Reports, 5. Nature Publishing Group
Timofeeva, M N, Kinnersley, B, Farrington, S M, Whiffin, N, Palles, C, Svinti, V, Lloyd, A, Gorman, M, Ooi, L, Hosking, F, Barclay, E, Zgaga, L, Dobbins, S, Martin, L, Theodoratou, E, Broderick, P, Tenesa, A, Smillie, C, Grimes, G, Hayward, C, Campbell, A, Porteous, D, Deary, I J, Harris, S E, Northwood, E L, Barrett, J H, Smith, G, Wolf, R, Forman, D, Morreau, H, Ruano, D, Tops, C, Wijnen, J, Schrumpf, M, Boot, A, Vasen, H F A, Hes, F J, Van Wezel, T, Franke, A, Lieb, W, Schafmayer, C, Hampe, J, Buch, S, Propping, P, Hemminki, K, F??rsti, A, Westers, H, Hofstra, R, Pinheiro, M, Pinto, C, Teixeira, M, Ruiz-ponte, C, Fern??ndez-rozadilla, C, Carracedo, A, Castells, A, Castellv??-bel, S, Campbell, H, Bishop, D T, Tomlinson, I P M, Dunlop, M G & Houlston, R S 2015, ' Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer ', Scientific Reports, vol. 5, pp. 16286 . https://doi.org/10.1038/srep16286Test

مصطلحات موضوعية: Activating Transcription Factor 1/genetics, EXPRESSION, Linkage disequilibrium, SUSCEPTIBILITY LOCI, Genotype, VARIANT, European Continental Ancestry Group, IDENTIFIES 6, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Article, Linkage Disequilibrium, White People, SDG 3 - Good Health and Well-being, Gene Frequency, Genetic variation, Odds Ratio, Coding region, Humans, HETEROGENEITY, European Continental Ancestry Group/genetics, Allele, GENOME-WIDE ASSOCIATION, Allele frequency, Gene, METAANALYSIS, Alleles, Adaptor Proteins, Signal Transducing, Medicine(all), Genetics, RISK, Activating Transcription Factor 1, Multidisciplinary, Cadherins/genetics, Intracellular Signaling Peptides and Proteins, Genetic Variation, Proteins, Cadherins, Colorectal Neoplasms/genetics, 3. Good health, DISCOVERY, Case-Control Studies, Proteins/genetics, Colorectal Neoplasms, SCAN, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9238dafb31e9af55e1a3a42fc1fdfb4Test

7

Genome-wide association study identifies three new melanoma susceptibility loci

المؤلفون: Eitan Friedman, Shenying Fang, Jeffrey E. Lee, Esther Azizi, Marie-Françoise Avril, Douglas F. Easton, Julia A. Newton Bishop, Julie Lang, Elizabeth M. Gillanders, Juliette Randerson-Moor, Jan Lubinski, D. Timothy Bishop, Bruce K. Armstrong, Donato Calista, Florence Demenais, Joan Anton Puig-Butille, Anne E. Cust, Tadeusz Dȩbniak, Graham G. Giles, Grant W. Montgomery, Lorenza Pastorino, David C. Whiteman, Kevin M. Brown, Nicholas G. Martin, Diana Zelenika, Maria Teresa Landi, Jennifer H. Barrett, Veronica Höiom, Pilar Galan, Qingyi Wei, Johan Hansson, Lars A. Akslen, Bert Bakker, Brigitte Bressac-de Paillerets, Josep Malvehy, Rainer Tuominen, Wilma Bergman, Mark M. Iles, Stuart MacGregor, Jiali Han, Rona M. MacKie, Nicholas K. Hayward, Richard F. Kefford, Mark A. Jenkins, Christian Ingvar, Anders Molven, Graham J. Mann, Lisa A. Cannon-Albright, David E. Elder, Göran Jönsson, Joanne F. Aitken, Mark Harland, John L. Hopper, David L. Duffy, Eve Corda, Helen Snowden, Peter A. Kanetsky, Alisa M. Goldstein, Alison M. Dunning, John C. Taylor, Giorgio Landi, Håkan Olsson, Paola Ghiorzo, Nienke van der Stoep, Bart Janssen, Per Arne Andresen, Susana Puig, Nelleke A. Gruis, Marko Hočevar, Frans A. van Nieuwpoort, Srdjan Novaković, G. Mark Lathrop, Patricia Van Belle, Giovanna Bianchi-Scarrà, Christopher I. Amos

المساهمون: St. James's University Hospital, Cancer Council, Partenaires INRAE, Oslo University Hospital [Oslo], University of Bergen (UiB), Haukeland University Hospital, The Westmead Institute for Medical Research, Université Paris Descartes - Paris 5 (UPD5), Sheba Med Ctr, Tel Aviv University [Tel Aviv], Leiden University, University of Genoa (UNIGE), Fdn Jean Daussel CEPH, Institut Gustave Roussy (IGR), Département de biologie et pathologie médicales [Gustave Roussy], Maurizio Bufalini Hosp, University of Utah, University of Melbourne, University of Sydney, Pomeranian Med Univ, Unité de Recherche en Epidémiologie Nutritionnelle (UREN), Université Paris 13 (UP13)-Institut National de la Recherche Agronomique (INRA)-Conservatoire National des Arts et Métiers [CNAM] (CNAM)-Université Sorbonne Paris Cité (USPC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Wellcome Trust [076113], European Commission [LSHC-CT-2006-018702], Cancer Research UK [C588/A4994, C588/A10589, C8216/A6129], US National Institutes of Health (NIH) [CA83115], NIH, National Cancer Institute (NCI), Division of Cancer Epidemiology and Genetics

المصدر: Nature genetics
Nature Genetics, 43(11), 1108-U98
Nature Genetics
Nature Genetics, Nature Publishing Group, 2011, 43 (11), pp.1108-U98. ⟨10.1038/ng.959⟩
Dipòsit Digital de la UB
Universidad de Barcelona

مصطلحات موضوعية: Skin Neoplasms, NEVI, [SDV]Life Sciences [q-bio], PHENOTYPIC CHARACTERISTICS, Genome-wide association study, Single-nucleotide polymorphism, Locus (genetics), Biology, Polymorphism, Single Nucleotide, Article, Genètica mèdica, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, SEQUENCE VARIANTS, Skin cancer, Nevus, SNP, Humans, Genetic Predisposition to Disease, Gene, Melanoma, Càncer de pell, METAANALYSIS, POPULATION, 030304 developmental biology, RISK, 0303 health sciences, CUTANEOUS MALIGNANT-MELANOMA, Medical genetics, Case-control study, WOMEN, medicine.disease, GENE, CANCER, 030220 oncology & carcinogenesis, Case-Control Studies, Cutaneous melanoma, Genome-Wide Association Study