Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Mateja, Krajc"'
Autor:
José Garcia-Pelaez, Rita Barbosa-Matos, Silvana Lobo, Alexandre Dias, Luzia Garrido, Sérgio Castedo, Sónia Sousa, Hugo Pinheiro, Liliana Sousa, Rita Monteiro, Joaquin J Maqueda, Susana Fernandes, Fátima Carneiro, Nádia Pinto, Carolina Lemos, Carla Pinto, Manuel R Teixeira, Stefan Aretz, Svetlana Bajalica-Lagercrantz, Judith Balmaña, Ana Blatnik, Patrick R Benusiglio, Maud Blanluet, Vincent Bours, Hilde Brems, Joan Brunet, Daniele Calistri, Gabriel Capellá, Sergio Carrera, Chrystelle Colas, Karin Dahan, Robin de Putter, Camille Desseignés, Elena Domínguez-Garrido, Conceição Egas, D Gareth Evans, Damien Feret, Eleanor Fewings, Rebecca C Fitzgerald, Florence Coulet, María Garcia-Barcina, Maurizio Genuardi, Lisa Golmard, Karl Hackmann, Helen Hanson, Elke Holinski-Feder, Robert Hüneburg, Mateja Krajc, Kristina Lagerstedt-Robinson, Conxi Lázaro, Marjolijn J L Ligtenberg, Cristina Martínez-Bouzas, Sonia Merino, Geneviève Michils, Srdjan Novaković, Ana Patiño-García, Guglielmina Nadia Ranzani, Evelin Schröck, Inês Silva, Catarina Silveira, José L Soto, Isabel Spier, Verena Steinke-Lange, Gianluca Tedaldi, María-Isabel Tejada, Emma R Woodward, Marc Tischkowitz, Nicoline Hoogerbrugge, Carla Oliveira
Publikováno v:
Garcia-Pelaez, J, Barbosa-Matos, R, Lobo, S, Dias, A, Garrido, L, Castedo, S, Sousa, S, Pinheiro, H, Sousa, L, Monteiro, R, Maqueda, J J, Fernandes, S, Carneiro, F, Pinto, N, Lemos, C, Pinto, C, Teixeira, M R, Aretz, S, Bajalica-Lagercrantz, S, Balmaña, J, Blatnik, A, Benusiglio, P R, Blanluet, M, Bours, V, Brems, H, Brunet, J, Calistri, D, Capellá, G, Carrera, S, Colas, C, Dahan, K, de Putter, R, Desseignés, C, Domínguez-Garrido, E, Egas, C, Evans, D G, Feret, D, Fewings, E, Fitzgerald, R C, Coulet, F, Garcia-Barcina, M, Genuardi, M, Golmard, L, Hackmann, K, Hanson, H, Holinski-Feder, E, Hüneburg, R, Krajc, M, Lagerstedt-Robinson, K, Lázaro, C, Ligtenberg, M J L, Martínez-Bouzas, C, Merino, S, Michils, G, Novaković, S, Patiño-García, A, Ranzani, G N, Schröck, E, Silva, I, Silveira, C, Soto, J L, Spier, I, Steinke-Lange, V, Tedaldi, G, Tejada, M-I, Woodward, E R, Tischkowitz, M, Hoogerbrugge, N & Oliveira, C 2023, ' Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes : a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes ', The Lancet. Oncology, vol. 24, no. 1, pp. 91-106 . https://doi.org/10.1016/S1470-2045(22)00643-X
Lancet Oncology, 24, 1, pp. 91-106
Scientia
Lancet Oncology, 24, 91-106
Lancet Oncology, 24, 1, pp. 91-106
Scientia
Lancet Oncology, 24, 91-106
Genotype; Cancer phenotypes; Genetic tumour Genotip; Fenotips del càncer; Tumor genètic Genotipo; Fenotipos del cáncer; Tumor genético Background Truncating pathogenic or likely pathogenic variants of CDH1 cause hereditary diffuse gastric cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0135cda703c531e384ac8d463c801fde
https://lirias.kuleuven.be/handle/20.500.12942/714811
https://lirias.kuleuven.be/handle/20.500.12942/714811
Autor:
Miranda P. Steenbeek, Majke H.D. van Bommel, Johan Bulten, Julia A. Hulsmann, Joep Bogaerts, Christine Garcia, Han T. Cun, Karen H. Lu, Heleen J. van Beekhuizen, Lucas Minig, Katja N. Gaarenstroom, Marielle Nobbenhuis, Mateja Krajc, Vilius Rudaitis, Barbara M. Norquist, Elizabeth M. Swisher, Marian J.E. Mourits, Leon F.A.G. Massuger, Nicoline Hoogerbrugge, Rosella P.M.G. Hermens, Joanna IntHout, Joanne A. de Hullu
Publikováno v:
J Clin Oncol
Journal of Clinical Oncology, 40(17), 1879-1891. American Society of Clinical Oncology
Journal of Clinical Oncology, 40(17), 1879-+. LIPPINCOTT WILLIAMS & WILKINS
Journal of Clinical Oncology, 40, 17, pp. 1879-1891
Journal of Clinical Oncology, 40(17), 1879-1891. AMER SOC CLINICAL ONCOLOGY
Journal of Clinical Oncology, 40, 1879-1891
Journal of Clinical Oncology, 40(17), 1879-1891. American Society of Clinical Oncology
Journal of Clinical Oncology, 40(17), 1879-+. LIPPINCOTT WILLIAMS & WILKINS
Journal of Clinical Oncology, 40, 17, pp. 1879-1891
Journal of Clinical Oncology, 40(17), 1879-1891. AMER SOC CLINICAL ONCOLOGY
Journal of Clinical Oncology, 40, 1879-1891
PURPOSE After risk-reducing salpingo-oophorectomy (RRSO), BRCA1/ 2 pathogenic variant (PV) carriers have a residual risk to develop peritoneal carcinomatosis (PC). The etiology of PC is not yet clarified, but may be related to serous tubal intraepith
Autor:
Ksenija Strojnik, Vita Setrajcic Dragos, Srdjan Novaković, Vida Stegel, Ana Blatnik, Mateja Krajc
Publikováno v:
Breast Cancer Research and Treatment
Purpose To analyze the prevalence of pathogenic/likely pathogenic variants (P/LPVs) in BRCA1 and BRCA2 genes in the largest cohort of Slovenian male breast cancer (MBC) patients to date and to explore a possible correlation between the Slovenian foun
Autor:
Barbara Gazic, Tea Nizic-Kos, Vida Stegel, Nikola Besic, Srdjan Novaković, Ana Blatnik, Petra Škerl, Mateja Krajc
Publikováno v:
Annals of Surgical Oncology. 28:2561-2570
Currently, data on pathogenic variants in the CHEK2 gene and their impact on cancer risk are lacking. This study aimed to explore the characteristics of breast cancer (BC) patients from families with CHEK2 pathogenic variants in Slovenia. In the year
Autor:
Ana Blatnik, Domen Ribnikar, Vita Šetrajčič Dragoš, Srdjan Novaković, Vida Stegel, Biljana Grčar Kuzmanov, Nina Boc, Barbara Perić, Petra Škerl, Gašper Klančar, Mateja Krajc
Publikováno v:
Breast cancer, str. 921–927, Vol. 29, 2022
COBISS-ID: 514824473
Breast cancer, vol. 29, 2022.
COBISS-ID: 514824473
Breast cancer, vol. 29, 2022.
BAP1 cancer syndrome is a rare and highly penetrant hereditary cancer predisposition. Uveal melanoma, mesothelioma, renal cell carcinoma (RCC) and cutaneous melanoma are considered BAP1 cancer syndrome core cancers, whereas association with breast ca
Autor:
Vida Stegel, Barbara Gazic, Mateja Krajc, Ana Blatnik, Andraz Perhavec, Srdjan Novaković, Sebastijan Merlo, Andreja Gornjec
Publikováno v:
Radiology and Oncology, Vol 54, Iss 2, Pp 180-186 (2020)
Radiology and Oncology
Radiology and Oncology
Background We assessed the prevalence, localization, type and outcome of occult cancer at risk-reducing salpingo-oophorectomy or salpingectomy (RRSO) in asymptomatic carriers of pathogenic or likely pathogenic BRCA1/2 variants and high-risk BRCA1/2 n
Publikováno v:
European journal of surgical oncology, vol. 47, no. 8, pp. 1900-1906, 2021.
European journal of surgical oncology, str. 1900-1906, Vol. 47, no. 8, Aug. 2021
COBISS-ID: 6045447
European journal of surgical oncology, str. 1900-1906, Vol. 47, no. 8, Aug. 2021
COBISS-ID: 6045447
Objectives. Risk-reducing mastectomy (RRM) is one of key prevention strategies in female carriers of germline BRCA pathogenic/likely pathogenic variants (PV/LPV). We retrospectively investigated the rate, timing and longitudinal trends of bilateral R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a845e751a5beae9844a5fe6078e91c44
https://dirros.openscience.si/Dokument.php?id=20594&dn=
https://dirros.openscience.si/Dokument.php?id=20594&dn=
Autor:
Vesna Zadnik, Kristijana Hertl, Peter B. Dean, Katja Jarm, Maja Primic Žakelj, Cveto Šval, Lawrence von Karsa, Maksimiljan Kadivec, Urban Zdešar, Barbara Gazic, Igor Josipović, Mateja Krajc, Veronika Kutnar, Mateja Kurir Borovčić, Janez Žgajnar
Publikováno v:
PLoS ONE, Vol 16, Iss 10, p e0258343 (2021)
PLoS ONE
PLoS ONE
Setting The organised, population-based breast cancer screening programme in Slovenia began providing biennial mammography screening for women aged 50–69 in 2008. The programme has taken a comprehensive approach to quality assurance as recommended
Autor:
David Humberto Marmolejo, Mark Yu Zheng Wong, Svetlana Bajalica-Lagercrantz, Marc Tischkowitz, Judith Balmaña, Attila Balázs Patócs, Pierre Chappuis, Chrystelle Colas, Maurizio Genuardi, Maria Haanpää, Hildegunn Hoberg Vetti, Nicoline Hoogerbrugge, Arvids Irmejs, Tiina Kahre, Barbara Klink, Mateja Krajc, Tamara Hussong Milagre, Robin de Putter, Verena Steinke-Lange, Karin Wadt, Katharina Wimmer
Publikováno v:
European Journal of Medical Genetics, 64, 12
European Journal of Medical Genetics, 64
European Journal of Medical Genetics, 64
Item does not contain fulltext Hereditary breast and ovarian cancer (HBOC) is a syndrome defined by an increased risk of developing breast and/or ovarian cancer most commonly due to germline disease-causing variants in the BRCA1 and BRCA2 genes, but
Autor:
Giovanna Masala, Susan L. Neuhausen, Montserrat Garcia Closas, Vasilios Georgoulias, Paul D.P. Pharoah, Katarzyna Tomczyk, Henrik Flyger, Håkan Olsson, D. Timothy Bishop, Alison M. Dunning, Eitan Friedman, Matthew Pugh, Michael Jones, Johanna Mattson, Sarah Maguire, Richard S. Houlston, Paul A. James, Douglas F. Easton, Valentina Silvestri, Srdjan Novaković, Rosie Cooke, Maartje J. Hooning, Eleni Perraki, Manuela Gago-Dominguez, Domenico Palli, Laura Ottini, Nick Orr, Kyle Thompson, Heli Nevanlinna, Yael Laitman, Antoinette Hollestelle, Stig E. Bojesen, Timothy Winter, Alison H. Trainer, Ines Zanna, Mateja Krajc, Linda Steele, Jose E. Castelao, Emmanouil Saloustros, Olivia Fletcher, Ingrid Hedenfalk, Alan Ashworth, Anthony J. Swerdlow
Publikováno v:
Maguire, S, Perrakis, E, Tomczyk, K, Jones, M, Fletcher, O, Pugh, M, Winter, T, Thompson, K, Cooke, R, Trainer, A H, Paul, J, Bojesen, S E, Flyger, H, Nevanlinna, H, Mattson, J, Friedman, E, Laitman, Y, Palli, D, Masala, G, Zanna, I, Ottini, L, Silvestri, V, Hollestelle, A, Hooning, M J, Novaković, S, Krajc, M, Gago-Dominguez, M, Castelao, J E, Olsson, H, Hedenfalk, I, Saloustros, E, Georgoulias, V, Easton, D F, Pharoah, P, Dunning, A M, Timothy Bishop, D, Neuhausen, S L, Steele, L, Ashworth, A, García-Closas, M, Houlston, R, Swerdlow, A J & Orr, N 2020, ' Common susceptibility loci for male breast cancer ', Journal of the National Cancer Institute, vol. 2020, dja101 . https://doi.org/10.1093/jnci/djaa101
Journal of the National Cancer Institute, 113(4), 453-461. Oxford University Press
JNCI Journal of the National Cancer Institute
Maguire, S, Perraki, E, Tomczyk, K, Jones, M E, Fletcher, O, Pugh, M, Winter, T, Thompson, K, Cooke, R, Trainer, A, James, P, Bojesen, S, Flyger, H, Nevanlinna, H, Mattson, J, Friedman, E, Laitman, Y, Palli, D, Masala, G, Zanna, I, Ottini, L, Silvestri, V, Hollestelle, A, Hooning, M J, Novaković, S, Krajc, M, Gago-dominguez, M, Castelao, J E, Olsson, H, Hedenfalk, I, Saloustros, E, Georgoulias, V, Easton, D F, Pharoah, P, Dunning, A M, Bishop, D T, Neuhausen, S L, Steele, L, Ashworth, A, Garcia Closas, M, Houlston, R, Swerdlow, A & Orr, N 2021, ' Common Susceptibility Loci for Male Breast Cancer ', National Cancer Institute. Journal (Online), vol. 113, no. 4, pp. 453-461 . https://doi.org/10.1093/jnci/djaa101
Journal of the National Cancer Institute, 113(4), 453-461. Oxford University Press
JNCI Journal of the National Cancer Institute
Maguire, S, Perraki, E, Tomczyk, K, Jones, M E, Fletcher, O, Pugh, M, Winter, T, Thompson, K, Cooke, R, Trainer, A, James, P, Bojesen, S, Flyger, H, Nevanlinna, H, Mattson, J, Friedman, E, Laitman, Y, Palli, D, Masala, G, Zanna, I, Ottini, L, Silvestri, V, Hollestelle, A, Hooning, M J, Novaković, S, Krajc, M, Gago-dominguez, M, Castelao, J E, Olsson, H, Hedenfalk, I, Saloustros, E, Georgoulias, V, Easton, D F, Pharoah, P, Dunning, A M, Bishop, D T, Neuhausen, S L, Steele, L, Ashworth, A, Garcia Closas, M, Houlston, R, Swerdlow, A & Orr, N 2021, ' Common Susceptibility Loci for Male Breast Cancer ', National Cancer Institute. Journal (Online), vol. 113, no. 4, pp. 453-461 . https://doi.org/10.1093/jnci/djaa101
BackgroundThe aetiology of male breast cancer (MBC) is poorly understood. In particular, the extent to which the genetic basis of MBC differs from female breast cancer (FBC) is unknown. A previous genome-wide association study (GWAS) of MBC identifie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99cf7e99c539a55981e4d31bff3d1fde
https://pure.qub.ac.uk/en/publications/549ad521-1148-4008-b767-1a9f0ecf4a66
https://pure.qub.ac.uk/en/publications/549ad521-1148-4008-b767-1a9f0ecf4a66