Zobrazeno 1 - 10
of 883
pro vyhledávání: '"J. Manni"'
Autor:
I. Jackson
Publikováno v:
European Journal of Plastic Surgery. 31:93-94
Autor:
Hayley B Gershengorn, Monisha C Bhatia, Prem Rajendra Warde, Samira S Patel, Tanira D Ferreira, Dipen J Parekh, Kymberlee J Manni, Bhavarth S Shukla
Publikováno v:
BMJ Health & Care Informatics, Vol 28, Iss 1 (2021)
Objectives We describe a hospital’s implementation of predictive models to optimise emergency response to the COVID-19 pandemic.Methods We were tasked to construct and evaluate COVID-19 driven predictive models to identify possible planning and res
Externí odkaz:
https://doaj.org/article/4b7df0facb704741a737c867966b274c
Autor:
James D. McKay, Paul Brennan, Paolo Boffetta, Richard B. Hayes, Mia Hashibe, Stefania Boccia, Leticia Fernandez, José Eluf-Neto, Victor Wünsch-Filho, Ana Menezes, Sergio Koifman, Maria Paula Curado, Vladimir Janout, Lenka Foretova, Vladimir Bencko, Alexandru Bucur, Eleonora Fabianova, Jolanta Lissowska, Neonila Szeszenia-Dabrowska, David Zaridze, Wolfgang Ahrens, Claire M. Healy, Ariana Znaor, David I. Conway, Nalin S. Thakker, Cristina Canova, Luigi Barzan, Tatiana V. Macfarlane, Xavier Castellsagué, Antonio Agudo, Kristina Kjaerheim, Lorenzo Richiardi, Ivana Holcátová, Pagona Lagiou, Simone Benhamou, Chu Chen, Stephen M. Schwartz, Renyi Wang, Shen-Chih Chang, Zuo-Feng Zhang, Erich M. Sturgis, Qingyi Wei, Philip Lazarus, Joshua E. Muscat, Marcin Lener, Joanna Trubicka, Jan Lubiński, Wilbert H. M. Peters, Johannes J. Manni, Martin Lacko, Michael D. McClean, Brock Christensen, Karl T. Kelsey, Renato Talamini, Rolando Herrero, Silvia Franceschi, Tomoko Nukui, Shama Buch, Marjorie Romkes, Jingchun Luo, Mark C. Weissler, Andrew F. Olshan, Shu-chun Chuang, Amelie Chabrier, Graham Byrnes, Valerie Gaborieau, Therese Truong, Dan Chen
Supplementary Tables 1-3 from A Sex-Specific Association between a 15q25 Variant and Upper Aerodigestive Tract Cancers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8721470dcc5e3dfc561be38e1fffa538
https://doi.org/10.1158/1055-9965.22435900.v1
https://doi.org/10.1158/1055-9965.22435900.v1
Autor:
James D. McKay, Paul Brennan, Paolo Boffetta, Richard B. Hayes, Mia Hashibe, Stefania Boccia, Leticia Fernandez, José Eluf-Neto, Victor Wünsch-Filho, Ana Menezes, Sergio Koifman, Maria Paula Curado, Vladimir Janout, Lenka Foretova, Vladimir Bencko, Alexandru Bucur, Eleonora Fabianova, Jolanta Lissowska, Neonila Szeszenia-Dabrowska, David Zaridze, Wolfgang Ahrens, Claire M. Healy, Ariana Znaor, David I. Conway, Nalin S. Thakker, Cristina Canova, Luigi Barzan, Tatiana V. Macfarlane, Xavier Castellsagué, Antonio Agudo, Kristina Kjaerheim, Lorenzo Richiardi, Ivana Holcátová, Pagona Lagiou, Simone Benhamou, Chu Chen, Stephen M. Schwartz, Renyi Wang, Shen-Chih Chang, Zuo-Feng Zhang, Erich M. Sturgis, Qingyi Wei, Philip Lazarus, Joshua E. Muscat, Marcin Lener, Joanna Trubicka, Jan Lubiński, Wilbert H. M. Peters, Johannes J. Manni, Martin Lacko, Michael D. McClean, Brock Christensen, Karl T. Kelsey, Renato Talamini, Rolando Herrero, Silvia Franceschi, Tomoko Nukui, Shama Buch, Marjorie Romkes, Jingchun Luo, Mark C. Weissler, Andrew F. Olshan, Shu-chun Chuang, Amelie Chabrier, Graham Byrnes, Valerie Gaborieau, Therese Truong, Dan Chen
Background: Sequence variants located at 15q25 have been associated with lung cancer and propensity to smoke. We recently reported an association between rs16969968 and risk of upper aerodigestive tract (UADT) cancers (oral cavity, oropharynx, hypoph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcba806c5c23f62a06d10c6eeed43e48
https://doi.org/10.1158/1055-9965.c.6515152
https://doi.org/10.1158/1055-9965.c.6515152
Autor:
Gretl Hendrickx, Vere M Borra, Ellen Steenackers, Timur A Yorgan, Christophe Hermans, Eveline Boudin, Jérôme J Waterval, Ineke D C Jansen, Tolunay Beker Aydemir, Niels Kamerling, Geert J Behets, Christine Plumeyer, Patrick C D'Haese, Björn Busse, Vincent Everts, Martin Lammens, Geert Mortier, Robert J Cousins, Thorsten Schinke, Robert J Stokroos, Johannes J Manni, Wim Van Hul
Publikováno v:
PLoS Genetics, Vol 14, Iss 4, p e1007321 (2018)
Hyperostosis Cranialis Interna (HCI) is a rare bone disorder characterized by progressive intracranial bone overgrowth at the skull. Here we identified by whole-exome sequencing a dominant mutation (L441R) in SLC39A14 (ZIP14). We show that L441R ZIP1
Externí odkaz:
https://doaj.org/article/3da077da62934ead948a9885d5b022b5
Autor:
Egied J. M. Hannen, Jeroen A. W. M. van der Laak, Harold M. J. Kerstens, Vincent M. J. I. Cuijpers, Antonius G. J. M. Hanselaar, Johannes J. Manni, Peter C. M. de Wilde
Publikováno v:
Analytical Cellular Pathology, Vol 22, Iss 4, Pp 183-192 (2001)
The aims of this study of head and neck tissue samples were to develop an immunohistochemical protocol based on the catalysed reporter deposition (CARD) technique to enhance staining results for use in automated true colour image analysis, to assess
Externí odkaz:
https://doaj.org/article/699ed1175eef49979a0b58169bab2549
Autor:
James D. McKay, Therese Truong, Valerie Gaborieau, Amelie Chabrier, Shu-Chun Chuang, Graham Byrnes, David Zaridze, Oxana Shangina, Neonila Szeszenia-Dabrowska, Jolanta Lissowska, Peter Rudnai, Eleonora Fabianova, Alexandru Bucur, Vladimir Bencko, Ivana Holcatova, Vladimir Janout, Lenka Foretova, Pagona Lagiou, Dimitrios Trichopoulos, Simone Benhamou, Christine Bouchardy, Wolfgang Ahrens, Franco Merletti, Lorenzo Richiardi, Renato Talamini, Luigi Barzan, Kristina Kjaerheim, Gary J. Macfarlane, Tatiana V. Macfarlane, Lorenzo Simonato, Cristina Canova, Antonio Agudo, Xavier Castellsagué, Ray Lowry, David I. Conway, Patricia A. McKinney, Claire M. Healy, Mary E. Toner, Ariana Znaor, Maria Paula Curado, Sergio Koifman, Ana Menezes, Victor Wünsch-Filho, José Eluf Neto, Leticia Fernández Garrote, Stefania Boccia, Gabriella Cadoni, Dario Arzani, Andrew F. Olshan, Mark C. Weissler, William K. Funkhouser, Jingchun Luo, Jan Lubiński, Joanna Trubicka, Marcin Lener, Dorota Oszutowska, Stephen M. Schwartz, Chu Chen, Sherianne Fish, David R. Doody, Joshua E. Muscat, Philip Lazarus, Carla J. Gallagher, Shen-Chih Chang, Zuo-Feng Zhang, Qingyi Wei, Erich M. Sturgis, Li-E Wang, Silvia Franceschi, Rolando Herrero, Karl T. Kelsey, Michael D. McClean, Carmen J. Marsit, Heather H. Nelson, Marjorie Romkes, Shama Buch, Tomoko Nukui, Shilong Zhong, Martin Lacko, Johannes J. Manni, Wilbert H. M. Peters, Rayjean J. Hung, John McLaughlin, Lars Vatten, Inger Njølstad, Gary E. Goodman, John K. Field, Triantafillos Liloglou, Paolo Vineis, Francoise Clavel-Chapelon, Domenico Palli, Rosario Tumino, Vittorio Krogh, Salvatore Panico, Carlos A. González, J. Ramón Quirós, Carmen Martínez, Carmen Navarro, Eva Ardanaz, Nerea Larrañaga, Kay-Tee Khaw, Timothy Key, H. Bas Bueno-de-Mesquita, Petra H. M. Peeters, Antonia Trichopoulou, Jakob Linseisen, Heiner Boeing, Göran Hallmans, Kim Overvad, Anne Tjønneland, Merethe Kumle, Elio Riboli, Kristjan Välk, Tõnu Voodern, Andres Metspalu, Diana Zelenika, Anne Boland, Marc Delepine, Mario Foglio, Doris Lechner, Hélène Blanché, Ivo G. Gut, Pilar Galan, Simon Heath, Mia Hashibe, Richard B. Hayes, Paolo Boffetta, Mark Lathrop, Paul Brennan
Publikováno v:
PLoS Genetics, Vol 7, Iss 4 (2011)
Externí odkaz:
https://doaj.org/article/bd42d7968470441ea3a04a60c4ec4b2e
Autor:
James D McKay, Therese Truong, Valerie Gaborieau, Amelie Chabrier, Shu-Chun Chuang, Graham Byrnes, David Zaridze, Oxana Shangina, Neonila Szeszenia-Dabrowska, Jolanta Lissowska, Peter Rudnai, Eleonora Fabianova, Alexandru Bucur, Vladimir Bencko, Ivana Holcatova, Vladimir Janout, Lenka Foretova, Pagona Lagiou, Dimitrios Trichopoulos, Simone Benhamou, Christine Bouchardy, Wolfgang Ahrens, Franco Merletti, Lorenzo Richiardi, Renato Talamini, Luigi Barzan, Kristina Kjaerheim, Gary J Macfarlane, Tatiana V Macfarlane, Lorenzo Simonato, Cristina Canova, Antonio Agudo, Xavier Castellsagué, Ray Lowry, David I Conway, Patricia A McKinney, Claire M Healy, Mary E Toner, Ariana Znaor, Maria Paula Curado, Sergio Koifman, Ana Menezes, Victor Wünsch-Filho, José Eluf Neto, Leticia Fernández Garrote, Stefania Boccia, Gabriella Cadoni, Dario Arzani, Andrew F Olshan, Mark C Weissler, William K Funkhouser, Jingchun Luo, Jan Lubiński, Joanna Trubicka, Marcin Lener, Dorota Oszutowska, Stephen M Schwartz, Chu Chen, Sherianne Fish, David R Doody, Joshua E Muscat, Philip Lazarus, Carla J Gallagher, Shen-Chih Chang, Zuo-Feng Zhang, Qingyi Wei, Erich M Sturgis, Li-E Wang, Silvia Franceschi, Rolando Herrero, Karl T Kelsey, Michael D McClean, Carmen J Marsit, Heather H Nelson, Marjorie Romkes, Shama Buch, Tomoko Nukui, Shilong Zhong, Martin Lacko, Johannes J Manni, Wilbert H M Peters, Rayjean J Hung, John McLaughlin, Lars Vatten, Inger Njølstad, Gary E Goodman, John K Field, Triantafillos Liloglou, Paolo Vineis, Francoise Clavel-Chapelon, Domenico Palli, Rosario Tumino, Vittorio Krogh, Salvatore Panico, Carlos A González, J Ramón Quirós, Carmen Martínez, Carmen Navarro, Eva Ardanaz, Nerea Larrañaga, Kay-Tee Khaw, Timothy Key, H Bas Bueno-de-Mesquita, Petra H M Peeters, Antonia Trichopoulou, Jakob Linseisen, Heiner Boeing, Göran Hallmans, Kim Overvad, Anne Tjønneland, Merethe Kumle, Elio Riboli, Kristjan Välk, Tõnu Vooder, Andres Metspalu, Diana Zelenika, Anne Boland, Marc Delepine, Mario Foglio, Doris Lechner, Hélène Blanché, Ivo G Gut, Pilar Galan, Simon Heath, Mia Hashibe, Richard B Hayes, Paolo Boffetta, Mark Lathrop, Paul Brennan
Publikováno v:
PLoS Genetics, Vol 7, Iss 3, p e1001333 (2011)
Genome-wide association studies (GWAS) have been successful in identifying common genetic variation involved in susceptibility to etiologically complex disease. We conducted a GWAS to identify common genetic variation involved in susceptibility to up
Externí odkaz:
https://doaj.org/article/846c8a4060ef41a19a022b13df570b81
Autor:
Christine Plumeyer, Jérôme Waterval, Ellen Steenackers, Tolunay Beker Aydemir, Robert Cousins, Wim Van Hul, Geert Mortier, Vincent Everts, Timur A. Yorgan, Bjoern Busse, Thorsten Schinke, Vere Borra, Martin Lammens, Gretl Hendrickx, Christophe Hermans, Patrick C. D'Haese, Niels Kamerling, Ineke D. C. Jansen, Johannes J. Manni, Eveline Boudin, Robert J. Stokroos, Geert J. Behets
Publikováno v:
PLoS Genetics, Vol 14, Iss 4, p e1007321 (2018)
Plos Genetics, 14,
PLoS genetics
Hendrickx, G, Borra, V M, Steenackers, E, Yorgan, T A, Hermans, C, Boudin, E, Waterval, J J, Jansen, I D C, Aydemir, T B, Kamerling, N, Behets, G J, Plumeyer, C, D'Haese, P C, Busse, B, Everts, V, Lammens, M, Mortier, G, Cousins, R J, Schinke, T, Stokroos, R J, Manni, J J & van Hul, W 2018, ' Conditional mouse models support the role of SLC39A14 (ZIP14) in Hyperostosis Cranialis Interna and in bone homeostasis ', PLoS Genetics, vol. 14, no. 4, e1007321, pp. e1007321 . https://doi.org/10.1371/journal.pgen.1007321
PLoS Genetics, 14(4):e1007321. Public Library of Science
PLOS Genetics, 14(4):e1007321. Public Library of Science
PLoS Genetics
Plos Genetics, 14, 4, pp.
Plos Genetics, 14,
PLoS genetics
Hendrickx, G, Borra, V M, Steenackers, E, Yorgan, T A, Hermans, C, Boudin, E, Waterval, J J, Jansen, I D C, Aydemir, T B, Kamerling, N, Behets, G J, Plumeyer, C, D'Haese, P C, Busse, B, Everts, V, Lammens, M, Mortier, G, Cousins, R J, Schinke, T, Stokroos, R J, Manni, J J & van Hul, W 2018, ' Conditional mouse models support the role of SLC39A14 (ZIP14) in Hyperostosis Cranialis Interna and in bone homeostasis ', PLoS Genetics, vol. 14, no. 4, e1007321, pp. e1007321 . https://doi.org/10.1371/journal.pgen.1007321
PLoS Genetics, 14(4):e1007321. Public Library of Science
PLOS Genetics, 14(4):e1007321. Public Library of Science
PLoS Genetics
Plos Genetics, 14, 4, pp.
Hyperostosis Cranialis Interna (HCI) is a rare bone disorder characterized by progressive intracranial bone overgrowth at the skull. Here we identified by whole-exome sequencing a dominant mutation (L441R) in SLC39A14 (ZIP14). We show that L441R ZIP1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::409f65a85f3b0eb34d37e44418518809
https://dare.uva.nl/personal/pure/en/publications/conditional-mouse-models-support-the-role-of-slc39a14-zip14-in-hyperostosis-cranialis-interna-and-in-bone-homeostasis(2e23ef49-ad8c-49f9-b496-c1f29746300e).html
https://dare.uva.nl/personal/pure/en/publications/conditional-mouse-models-support-the-role-of-slc39a14-zip14-in-hyperostosis-cranialis-interna-and-in-bone-homeostasis(2e23ef49-ad8c-49f9-b496-c1f29746300e).html
Autor:
Ernst-Jan M. Speel, Michelene N. Chenault, Sophie G.H. Litjens, Jacqueline M. Van der Wal, Adri C. Voogd, Verona E. Bergshoeff, Fredrik J. Bot, Ed Schuuring, Frans C. S. Ramaekers, Annick Haesevoets, Stijn J.A. Van der Heijden, Johannes J. Manni, Bernd Kremer, Anton H. N. Hopman
Publikováno v:
Pathology, 46(3), 216-224
Pathology, 46(3), 216-224. LIPPINCOTT WILLIAMS & WILKINS
Pathology, 46(3), 216-224. LIPPINCOTT WILLIAMS & WILKINS
Summary The histopathology of premalignant laryngeal lesions does not provide reliable information on the risk of malignant transformation, hence we examined new molecular markers which can easily be implemented in clinical practice. Dual-target fluo