Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Katerina P Kypreou"'
Autor:
Irene Stefanaki, Orestis A Panagiotou, Elisavet Kodela, Helen Gogas, Katerina P Kypreou, Foteini Chatzinasiou, Vasiliki Nikolaou, Michaela Plaka, Iro Kalfa, Christina Antoniou, John P A Ioannidis, Evangelos Evangelou, Alexander J Stratigos
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e55712 (2013)
BACKGROUND: Genetic association studies have revealed numerous polymorphisms conferring susceptibility to melanoma. We aimed to replicate previously discovered melanoma-associated single-nucleotide polymorphisms (SNPs) in a Greek case-control populat
Externí odkaz:
https://doaj.org/article/befb663a37a74372bc963a7bd93a2d95
Autor:
Fani Karagianni, Ching-Ni Njauw, Katerina P. Kypreou, Aravela Stergiopoulou, Michaela Plaka, Dorothea Polydorou, Vasiliki Chasapi, Leontios Pappas, Ioannis A. Stratigos, Gregory Champsas, Peter Panagiotou, Helen Gogas, Evangelos Evangelou, Hensin Tsao, Alexander J. Stratigos, Irene Stefanaki
Publikováno v:
Acta Dermato-Venereologica, Vol 98, Iss 9, Pp 862-866 (2018)
Approximately 5–10% of melanoma cases occur in a familial context. CDKN2A/CDK4 were the first high-penetrance melanoma genes identified. The aims of this study were to evaluate CDKN2A/CDK4 variants in Greek familial melanoma patients and to correla
Externí odkaz:
https://doaj.org/article/a4a434b325354ada9b03910e61a6bf55
Autor:
M C Fargnoli, Hongmei Nan, Sara Gandini, Evangelos Evangelou, Francesco Sera, José C. García-Borrón, A. De Nicolo, Alexandros Stratigos, Nelleke A. Gruis, Patrick Maisonneuve, David Polsky, DeAnn Lazovich, Cristina Pellegrini, Sara Raimondi, Julia Newton-Bishop, Julian Little, Paola Ghiorzo, I. Stefanaki, Gabriella Guida, Gloria Ribas, Peter A. Kanetsky, Maria Teresa Landi, Katerina P. Kypreou, S. Puig
Publikováno v:
J Eur Acad Dermatol Venereol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33790ac2d7a4b90752b889bbecee6663
https://hdl.handle.net/1887/3280198
https://hdl.handle.net/1887/3280198
Autor:
Eduardo Nagore, Caroline Hayward, Christopher I. Amos, Douglas F. Easton, Zaida García-Casado, Julie Lang, Anjali K. Henders, Veronica Höiom, Lisa Bowdler, Kathryn P. Burdon, Laura Del Regno, Nick Orr, Per Arne Andresen, Tongwu Zhang, Rose Yang, Myriam Brossard, Eric K. Moses, Dirk Schadendorf, Laura Cattaneo, Casey Rowe, Essen-Heidelberg Investigators, Hans-Joachim Schulze, Jamie E Craig, D. Timothy Bishop, Anne E. Cust, Johan Hansson, David E. Elder, Nelleke A. Gruis, Donato Calista, Wei V. Chen, Abrar A. Qureshi, Amy Hutchinson, Pilar Galan, Leanne Wallace, Jennifer H. Barrett, Nilesh J. Samani, Maria Teresa Landi, Per Helsing, Andreas Hadjisavvas, Fengju Song, Celia Requena, Elizabeth M. Gillanders, Arantxa Rodriguez, Joan Anton Puig-Butille, Blair H. Smith, Mark Smithers, Michael Malasky, Marianna Sanna, Miriam Potrony, Maria A. Loizidou, Evangelos Evangelou, Richard A. Scolyer, Karen A. Pooley, Rachel E. Neale, Mario Falchi, Adèle C. Green, Monica Rodolfo, Ketty Peris, Licia Rivoltini, Mark M. Iles, Catherine M. Olsen, Alexander J. Stratigos, Tadeusz Dębniak, Weiyin Zhou, H. Peter Soyer, Xin Li, Margaret A. Tucker, Rajesh Kumar, Håkan Olsson, Anders Molven, Nicholas G. Martin, Anthony J. Swerdlow, Aurelie Vogt, Lars A. Akslen, Stuart MacGregor, Sarah V. Ward, Hamida Mohamdi, Bruna Dalmasso, Grant W. Montgomery, Rona M. MacKie, Esther Azizi, Gonçalo R. Abecasis, Chiara Menin, Alison M. Dunning, Ibd investigators, Kevin M. Brown, Jiali Han, Veryan Codd, Graham J. Mann, Nicholas K. Hayward, Marko Hočevar, Eitan Friedman, Richard A. Sturm, Paola Queirolo, Qtwin Investigators, Lawrie Wheeler, Lars G. Fritsche, Shenying Fang, Kiarash Khosrotehrani, Nicole A Kukutsch, Pol Gimenez-Xavier, Belynda Hicks, Matthew Zawistowski, Alessia Visconti, Jessica Harris, Chad M. Brummett, Paola Ghiorzo, andMe, David G. Hunter, Veronique Bataille, Julia Newton-Bishop, Srdjan Novaković, Amfs Investigators, Siranoush Manoukian, Jianxin Shi, Mitchell J. Machiela, G. Mark Lathrop, Josep Malvehy, Katerina P. Kypreou, Susana Puig, Dale R. Nyholt, I. Stefanaki, Maria Concetta Fargnoli, Lisa A. Simms, Kerrie McAloney, M. Malt, Adam J. Trower, Matthew Law, Lei Song, Paul D.P. Pharoah, Christian Ingvar, Jiyeon Choi, Alisa M. Goldstein, Jeffrey E. Lee, Mark Harland, Cristina Pellegrini, Daniela Massi, Sarah Simi, Scott D. Gordon, Jacobo Martinez, Florence Demenais, Kristine Jones, Graham L. Radford-Smith, David C. Whiteman, Lorenza Pastorino, Lisa Elefanti, Arcangela De Nicolo, Mario Mandalà, Juliette Randerson-Moor, Q-Mega, Jan Lubinski, Stephen J. Chanock, Marie-Françoise Avril, David L. Duffy, Helen Gogas, Nienke van der Stoep, Peter A. Kanetsky, Georgina V. Long
Publikováno v:
Nature Genetics
Nature Genetics, Nature Publishing Group, 2020, 52 (5), pp.494-504. ⟨10.1038/s41588-020-0611-8⟩
Nature genetics
Nature Genetics, 52(5), 494-504. NATURE PUBLISHING GROUP
Nature Genetics, Nature Publishing Group, 2020, 52 (5), pp.494-504. ⟨10.1038/s41588-020-0611-8⟩
Nature genetics
Nature Genetics, 52(5), 494-504. NATURE PUBLISHING GROUP
Meta-analysis of 36,760 cases and 375,188 controls identifies 54 loci associated with susceptibility to cutaneous melanoma. Further analysis combining nevus count and hair color GWAS results provide insights into the genetic architecture of melanoma.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0663ba533ad6d0d069e8827e0d374241
https://discovery.dundee.ac.uk/files/49101915/Landi_2019_main_text_NG_A52232R2_15012020_2_.pdf
https://discovery.dundee.ac.uk/files/49101915/Landi_2019_main_text_NG_A52232R2_15012020_2_.pdf
Autor:
Vasiliki Chasapi, Katerina P. Kypreou, Peter Panagiotou, I. Stefanaki, Evangelos Evangelou, Fani Karagianni, Dorothea Polydorou, Helen Gogas, Alexander J. Stratigos, Gregory Champsas, Hensin Tsao, Michaela Plaka, Ioannis A. Stratigos, Leontios Pappas, Aravela Stergiopoulou, Ching-Ni Njauw
Publikováno v:
Acta Dermato-Venereologica, Vol 98, Iss 9, Pp 862-866 (2018)
Acta dermato-venereologica
Acta dermato-venereologica
Approximately 5–10% of melanoma cases occur in a familial context. CDKN2A/CDK4 were the first high- penetrance melanoma genes identified. The aims of this study were to evaluate CDKN2A/CDK4 variants in Greek familial melanoma patients and to correl
Autor:
Mark M. Iles, Maria A. Loizidou, Evangelos Evangelou, Kyriacos Kyriacou, Andreas Hadjisavvas, Niki Dimou, Stuart MacGregor, I. Stefanaki, Matthew Law, Georgios Ntritsos, Alexandros Stratigos, Katerina P. Kypreou
Publikováno v:
e370
e369
Journal of the European Academy of Dermatology and Venereology
e369
Journal of the European Academy of Dermatology and Venereology
Autor:
Christina Antoniou, Evangelos Evangelou, I. Stefanaki, E. Drakaki, Electra Nicolaidou, Alexandros Stratigos, Katerina P. Kypreou, Giorgos Ntritsos, Sofia Masouri
Publikováno v:
Molecular Diagnosis & Therapy. 20:221-225
Psoriasis is a highly divergent disease with many disease phenotypes, but there are currently no established biomarkers to predict the therapeutic outcomes of systemic treatments. With the introduction of biologic therapies during the last decade and
Autor:
Alexander J. Stratigos, Kyriaki Antonopoulou, George M. Spyrou, Katerina P. Kypreou, Fani Karagianni, Evangelos Evangelou, John P. A. Ioannidis, I. Stefanaki, Foteini Chatzinasiou, Emmanouil Athanasiadis, Lars Bertram, Christina M. Lill
Publikováno v:
Journal of Investigative Dermatology. 135(4):1074-1079
We updated a field synopsis of genetic associations of cutaneous melanoma (CM) by systematically retrieving and combining data from all studies in the field published as of August 31, 2013. Data were available from 197 studies, which included 83,343
Autor:
Elisavet Kodela, Alexandros Stratigos, I. Stefanaki, Sofia Masouri, Evangelos Evangelou, Ch. Antoniou, Katerina P. Kypreou, G. Bethimoutis, Georgios Ntritsos
Publikováno v:
British Journal of Dermatology. 173:552-554
Autor:
Christina Antoniou, Alexander J. Stratigos, Clio Dessinioti, Vasiliki Nikolaou, Vana Sypsa, Gerasimos Dimisianos, Elisavet Kodela, Katerina P. Kypreou
Publikováno v:
Experimental Dermatology. 24:476-478
Melanocortin 1 receptor (MC1R) gene variants are a major contributor to pigmentation characteristics and the modulation of sporadic basal cell carcinoma (BCC) risk. This is a hospital-based, case-control study to investigate the association of MC1R v