Bilaketaren emaitzak - Veronica Höiom

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  1. 1
    The genetics of uveal melanoma: current insights

    The genetics of uveal melanoma: current insights nork Veronica Höiom, Hildur Helgadóttir

    Argitaratua 2016
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  2. 2
    Germline<i>CDKN2A</i>Mutation Status and Survival in Familial Melanoma Cases

    Germline<i>CDKN2A</i>Mutation Status and Survival in Familial Melanoma Cases nork Hildur Helgadóttir, Veronica Höiom, Rainer Tuominen, K. Nielsen, Göran Jönsson, Håkan Olsson, Johan Hansson

    Argitaratua 2016
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  3. 3
    High risk of tobacco-related cancers in<i>CDKN2A</i>mutation-positive melanoma families

    High risk of tobacco-related cancers in<i>CDKN2A</i>mutation-positive melanoma families nork Hildur Helgadóttir, Veronica Höiom, Göran Jönsson, Rainer Tuominen, Christian Ingvar, Åke Borg, Håkan Olsson, Johan Hansson

    Argitaratua 2014
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  4. 4
    Efficacy of novel immunotherapy regimens in patients with metastatic melanoma with germline <i>CDKN2A</i> mutations

    Efficacy of novel immunotherapy regimens in patients with metastatic melanoma with germline <i>CDKN2A</i> mutations nork Hildur Helgadóttir, Paola Ghiorzo, Remco van Doorn, Susana Puig, Max Levin, Richard Kefford, Martin Lauss, Paola Queirolo, Lorenza Pastorino, Ellen Kapiteijn, Míriam Potrony, Cristina Carrera, Håkan Olsson, Veronica Höiom, Göran Jönsson

    Argitaratua 2018
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  5. 5
    IRF4 Variants Have Age-Specific Effects on Nevus Count and Predispose to Melanoma

    IRF4 Variants Have Age-Specific Effects on Nevus Count and Predispose to Melanoma nork David L. Duffy, Mark M. Iles, Dan Glass, Gu Zhu, Jennifer H. Barrett, Veronica Höiom, Zhen Zhao, Richard A. Sturm, Nicole Soranzo, Christopher J. Hammond, Marina Kvaskoff, David C. Whiteman, Massimo Mangino, Johan Hansson, Julia Newton‐Bishop, Veronique Bataille, Nicholas K. Hayward, Nicholas G. Martin, D. Timothy Bishop, Timothy D. Spector, Grant W. Montgomery

    Argitaratua 2010
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  6. 6
    Inherited variants in the <i>MC1R</i> gene and survival from cutaneous melanoma: a BioGenoMEL study

    Inherited variants in the <i>MC1R</i> gene and survival from cutaneous melanoma: a BioGenoMEL study nork John R. Davies, Juliette A. Randerson‐Moor, Kairen Kukalizch, Mark Harland, Rajiv Kumar, Srinivasan Madhusudan, Eduardo Nagore, Johan Hansson, Veronica Höiom, Paola Ghiorzo, Nelleke A. Gruis, Peter A. Kanetsky, Judith Wendt, Dace Pjanova, Susana Puig, Philippe Saïag, Dirk Schadendorf, Nadem Soufir, Ichiro Okamoto, Paul Affleck, Zaida García‐Casado, Zighereda Ogbah, Aija Ozola, Paola Queirolo, Antje Sucker, Jennifer H. Barrett, Remco van Doorn, D. Timothy Bishop, Julia Newton‐Bishop

    Argitaratua 2012
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  7. 7
    Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families

    Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families nork John Charles A. Lacson, Shahriar A. Zamani, Luis Alberto Ribeiro Fróes, Nandita Mitra, Qian Lü, Scarlet H. Doyle, Esther Azizi, Claudia Balestrini, D. Timothy Bishop, William Bruno, Blanca Carlos‐Ortega, Francisco Cuéllar, Anne Ε. Cust, David E. Elder, Anne‐Marie Gerdes, Paola Ghiorzo, Thaís Corsetti Grazziotin, Nelleke A. Gruis, Johan Hansson, Marko Hočevar, Veronica Höiom, Elizabeth A. Holland, Christian Ingvar, Gilles Landman, Alejandra Larre-Borges, Graham J. Mann, Montserrat Molgó, Luciana Facure Moredo, Håkan Olsson, Jacoba J. Out‐Luiting, Barbara Perić, Dace Pjanova, Susana Puig, Julio C. Salas‐Alanís, Helen Schmid, Karin Wadt, Julia Newton‐Bishop, Peter A. Kanetsky

    Argitaratua 2021
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  8. 8
    Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study

    Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study nork Florence Démenais, Hamida Mohamdi, Valérie Chaudru, Alisa M. Goldstein, Julia Newton‐Bishop, D. Timothy Bishop, Peter A. Kanetsky, Nicholas K. Hayward, Elizabeth M. Gillanders, David E. Elder, Marie‐Françoise Avril, Esther Azizi, Patricia Van Belle, W. Bergman, Giovanna Bianchi‐Scarrà, Brigitte Bressac–de Paillerets, Donato Calista, Cristina Carrera, Johan Hansson, Mark Harland, David Hogg, Veronica Höiom, Elizabeth A. Holland, Christian Ingvar, M. T. Landi, Julie Lang, R.M. MACKIE, Graham J. Mann, M.E. Ming, Ching-Ni-Jenny Njauw, Håkan Olsson, Jane M. Palmer, Lorenza Pastorino, Susana Puig, Juliette A. Randerson‐Moor, Mitchell Stark, Hensin Tsao, Margaret A. Tucker, Pieter van der Velden, X. R. Yang, Nelleke A. Gruis

    Argitaratua 2010
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  9. 9
    Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT

    Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT nork Nicholas J. Taylor, Nandita Mitra, Qian Lü, Marie‐Françoise Avril, D. Timothy Bishop, Brigitte Bressac–de Paillerets, William Bruno, Donato Calista, Francisco Cuéllar, Anne Ε. Cust, Florence Démenais, David E. Elder, Anne‐Marie Gerdes, Paola Ghiorzo, Alisa M. Goldstein, Thaís Corsetti Grazziotin, Nelleke A. Gruis, Johan Hansson, Mark Harland, Nicholas K. Hayward, Marko Hočevar, Veronica Höiom, Elizabeth A. Holland, Christian Ingvar, Maria Teresa Landi, Gilles Landman, Alejandra Larre-Borges, Graham J. Mann, Eduardo Nagore, Håkan Olsson, Jane M. Palmer, Barbara Perić, Dace Pjanova, Antonia L. Pritchard, Susana Puig, Helen Schmid, Nienke van der Stoep, Margaret A. Tucker, Karin Wadt, Xiaohong R. Yang, Julia Newton‐Bishop, Peter A. Kanetsky

    Argitaratua 2019
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  10. 10
    Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families

    Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families nork Nicholas J. Taylor, Elizabeth A. Handorf, Nandita Mitra, Marie-Françoise Avril, Esther Azizi, Wilma Bergman, Giovanna Bianchi‐Scarrà, D. Timothy Bishop, Brigitte Bressac–de Paillerets, Donato Calista, Lisa Cannon‐Albright, Francisco Cuéllar, Anne Ε. Cust, Florence Démenais, David E. Elder, Eitan Friedman, Anne‐Marie Gerdes, Paola Ghiorzo, Alisa M. Goldstein, Thaís Corsetti Grazziotin, Johan Hansson, Nicholas K. Hayward, Marko Hočevar, Veronica Höiom, Elizabeth A. Holland, Christian Ingvar, Maria Teresa Landi, Gilles Landman, Alejandra Larre-Borges, Sancy A. Leachman, Graham J. Mann, Eduardo Nagore, Håkan Olsson, Jane M. Palmer, Barbara Perić, Dace Pjanova, Susana Puig, Helen Schmid, Nienke van der Stoep, Margaret A. Tucker, Karin Wadt, Linda Whitaker, Xiaohong R. Yang, Julia Newton‐Bishop, Nelleke A. Gruis, Peter A. Kanetsky

    Argitaratua 2016
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  11. 11
    Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families

    Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families nork Nicholas J. Taylor, Nandita Mitra, Alisa M. Goldstein, Margaret A. Tucker, Marie-Françoise Avril, Esther Azizi, Wilma Bergman, D. Timothy Bishop, Brigitte Bressac–de Paillerets, William Bruno, Donato Calista, Lisa Cannon‐Albright, Francisco Cuéllar, Anne Ε. Cust, Florence Démenais, David E. Elder, Anne‐Marie Gerdes, Paola Ghiorzo, Thaís Corsetti Grazziotin, Johan Hansson, Mark Harland, Nicholas K. Hayward, Marko Hočevar, Veronica Höiom, Christian Ingvar, Maria Teresa Landi, Gilles Landman, Alejandra Larre-Borges, Sancy A. Leachman, Graham J. Mann, Eduardo Nagore, Håkan Olsson, Jane M. Palmer, Barbara Perić, Dace Pjanova, Antonia L. Pritchard, Susana Puig, Nienke van der Stoep, Karin Wadt, Linda Whitaker, Xiaohong R. Yang, Julia Newton‐Bishop, Nelleke A. Gruis, Peter A. Kanetsky

    Argitaratua 2017
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  12. 12
    Genome-wide association study identifies three loci associated with melanoma risk

    Genome-wide association study identifies three loci associated with melanoma risk nork D. Timothy Bishop, Florence Démenais, Mark M. Iles, Mark Harland, John Taylor, Eve Corda, Juliette A. Randerson‐Moor, Joanne F. Aitken, Marie‐Françoise Avril, Esther Azizi, Egbert Bakker, Giovanna Bianchi‐Scarrà, Brigitte Bressac–de Paillerets, Donato Calista, Lisa Cannon‐Albright, Thomas F. C. Chin‐A‐Woeng, Tadeusz Dębniak, Gilli Galore-Haskel, Paola Ghiorzo, Marta Gut, Johan Hansson, Marko Hočevar, Veronica Höiom, John L. Hopper, Christian Ingvar, Peter A. Kanetsky, Richard Kefford, Maria Teresa Landi, Julie Lang, Jan Lubiński, Rona M. MacKie, Josep Malvehy, Graham J. Mann, Nicholas G. Martin, Grant W. Montgomery, Frans A. van Nieuwpoort, Srdjan Novaković, Håkan Olsson, Susana Puig, Marjan M. Weiss, Wilbert van Workum, Diana Zélénika, Kevin M. Brown, Alisa M. Goldstein, Elizabeth M. Gillanders, Anne Boland, Pilar Galán, David E. Elder, Nelleke A. Gruis, Nicholas K. Hayward, G.M. Lathrop, Jennifer H. Barrett, Julia Newton‐Bishop

    Argitaratua 2009
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  13. 13
    New common variants affecting susceptibility to basal cell carcinoma

    New common variants affecting susceptibility to basal cell carcinoma nork Simon Stacey, Patrick Sulem, Gísli Másson, Sigurjón A. Guðjónsson, Guðmar Þorleifsson, Margret Jakobsdottir, Ásgeir Sigurðsson, Daníel F. Guðbjartsson, Bárður Sigurgeirsson, Kristrún R. Benediktsdóttir, Kristin Thorisdottir, Rafn Ragnarsson, Dominique Scherer, Kari Hemminki, Péter Rudnai, Eugen Gurzău, Kvetoslava Koppová, Rafael Botella‐Estrada, Vincent Soriano, Pablo Juberías, Berta Sáez, Yolanda Gilaberte, Victoria Fuentelsaz, Cristina Corredera, Matilde Grasa, Veronica Höiom, Annika Lindblom, Johannes J. Bonenkamp, Michelle M. van Rossum, Katja K.H. Aben, Esther de Vries, Mario Santinami, Maria Gaetana Di Mauro, Andrea Maurichi, Judith Wendt, Pia Hochleitner, Hubert Pehamberger, Jūlı́us Guðmundsson, Droplaug N. Magnúsdóttir, Sólveig Grétarsdóttir, Hilma Hólm, Valgerður Steinthórsdóttir, Michael L. Frigge, Thórarinn Blöndal, Jona Saemundsdottir, Hjördis Bjarnason, Kristleifur Kristjánsson, Gyða Björnsdóttir, Ichiro Okamoto, Licia Rivoltini, Monica Rodolfo, Lambertus A. Kiemeney, Johan Hansson, Eduardo Nagore, José Mayordomo, Rajiv Kumar, Margaret R. Karagas, Heather H. Nelson, Jeffrey R. Gulcher, Þórunn Rafnar, Unnur Þorsteinsdóttir, Jón Ólafsson, Augustine Kong, Kāri Stefánsson

    Argitaratua 2009
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  14. 14
    The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length

    The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length nork Mark M. Iles, D. Timothy Bishop, John Taylor, Nicholas K. Hayward, Myriam Brossard, Anne Ε. Cust, Alison M. Dunning, Jeffrey E. Lee, Eric K. Moses, Lars A. Akslen, Per Arne Andresen, Marie‐Françoise Avril, Esther Azizi, Giovanna Bianchi‐Scarrà, Kevin M. Brown, Tadeusz Dębniak, David E. Elder, Eitan Friedman, Paola Ghiorzo, Elizabeth M. Gillanders, Alisa M. Goldstein, Nelleke A. Gruis, Johan Hansson, Mark Harland, Per Helsing, Marko Hočevar, Veronica Höiom, Christian Ingvar, Peter A. Kanetsky, Maria Teresa Landi, Julie Lang, G.M. Lathrop, Jan Lubiński, Rona M. MacKie, Nicholas G. Martin, Anders Molven, Grant W. Montgomery, Srdjan Novaković, Håkan Olsson, Susana Puig, Joan Anton Puig‐Butille, Graham Radford‐Smith, Juliette A. Randerson‐Moor, Nienke van der Stoep, Remco van Doorn, David C. Whiteman, Stuart MacGregor, Karen A. Pooley, Sarah V. Ward, Graham J. Mann, Christopher I. Amos, Paul D.P. Pharoah, Florence Démenais, Matthew H. Law, Julia Newton‐Bishop, Jennifer H. Barrett

    Argitaratua 2014
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  15. 15
    Genome-wide association study identifies three new melanoma susceptibility loci

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

    Argitaratua 2011
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  16. 16
    Comprehensive Study of the Clinical Phenotype of Germline<i>BAP1</i>Variant-Carrying Families Worldwide

    Comprehensive Study of the Clinical Phenotype of Germline<i>BAP1</i>Variant-Carrying Families Worldwide nork Sebastian Walpole, Antonia L. Pritchard, Colleen M. Cebulla, Robert Pilarski, Meredith Stautberg, Frederick H. Davidorf, Arnaud de la Fouchardière, Odile Cabaret, Lisa Golmard, Dominique Stoppa‐Lyonnet, Erin M. Garfield, Ching-Ni Jenny Njauw, Mitchell Cheung, Joni A. Turunen, Pauliina Repo, Reetta-Stiina Järvinen, Remco van Doorn, Martine J. Jager, Gregorius P. M. Luyten, Marina Marinkovic, Cindy Chau, Míriam Potrony, Veronica Höiom, Hildur Helgadóttir, Lorenza Pastorino, William Bruno, Virginia Andreotti, Bruna Dalmasso, Giulia Ciccarese, Paola Queirolo, Luca Mastracci, Karin Wadt, Jens Folke Kiilgaard, Michael R. Speicher, Natasha van Poppelen, Emine Kılıç, Rana’a T. Al‐Jamal, Irma Dianzani, Marta Betti, Carsten Bergmann, Sandro Santagata, Sonika Dahiya, Saleem Taibjee, Jo Burke, Nicola Poplawski, Sally J. O’Shea, Julia Newton‐Bishop, Julian Adlard, David J. Adams, Anne-Marie Lane, Ivana K. Kim, Sonja Klebe, Hilary Racher, J. William Harbour, Michael L. Nickerson, Rajmohan Murali, Jane M. Palmer, Madeleine Howlie, Judith Symmons, Hayley R. Hamilton, Sunil Warrier, William Glasson, Peter A. Johansson, Carla Daniela Robles‐Espinoza, Raúl Ossio, Annelies de Klein, Susana Puig, Paola Ghiorzo, Maartje Nielsen, Tero Kivelä, Hensin Tsao, Joseph R. Testa, Pedram Gerami, Marc‐Henri Stern, Brigitte Bressac–de Paillerets, Mohamed H. Abdel‐Rahman, Nicholas K. Hayward

    Argitaratua 2018
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  17. 17
    Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma

    Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma nork Matthew H. Law, D. Timothy Bishop, Jeffrey E. Lee, Myriam Brossard, Nicholas G. Martin, Eric K. Moses, Fengju Song, Jennifer H. Barrett, Rajiv Kumar, Douglas F. Easton, Paul D.P. Pharoah, Anthony J. Swerdlow, K. Kypreou, John Taylor, Mark Harland, Juliette A. Randerson‐Moor, Lars A. Akslen, Per Arne Andresen, Marie-Françoise Avril, Esther Azizi, Giovanna Bianchi‐Scarrà, Kevin M. Brown, Tadeusz Dębniak, David L. Duffy, David E. Elder, Shenying Fang, Eitan Friedman, Pilar Galán, Paola Ghiorzo, Elizabeth M. Gillanders, Alisa M. Goldstein, Nelleke A. Gruis, Johan Hansson, Per Helsing, Marko Hočevar, Veronica Höiom, Christian Ingvar, Peter A. Kanetsky, Wei V. Chen, Maria Teresa Landi, Julie Lang, G.M. Lathrop, Jan Lubiński, Rona M. MacKie, Graham J. Mann, Anders Molven, Grant W. Montgomery, Srdjan Novaković, Håkan Olsson, Susana Puig, Joan Anton Puig‐Butille, Abrar A. Qureshi, Graham Radford‐Smith, Nienke van der Stoep, Remco van Doorn, David C. Whiteman, Jamie E. Craig, Dirk Schadendorf, Lisa A. Simms, Kathryn P. Burdon, Dale R. Nyholt, Karen A. Pooley, Nick Orr, Alexander J. Stratigos, Anne Ε. Cust, Sarah V. Ward, Nicholas K. Hayward, Jiali Han, H. J. Schulze, Alison M. Dunning, Julia Newton‐Bishop, Florence Démenais, Christopher I. Amos, Stuart MacGregor, Mark M. Iles

    Argitaratua 2015
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  18. 18
    Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

    Sequence variants at the TERT-CLPTM1L locus associate with many cancer types nork Þórunn Rafnar, Patrick Sulem, Simon Stacey, Frank Geller, Jūlı́us Guðmundsson, Ásgeir Sigurðsson, Margret Jakobsdottir, Hafdís T. Helgadóttir, Steinunn Thorlacius, Katja K.H. Aben, Thórarinn Blöndal, Thorgeir E. Thorgeirsson, Guðmar Þorleifsson, Kristleifur Kristjánsson, Kristin Thorisdottir, Rafn Ragnarsson, Bárður Sigurgeirsson, Halla Skúladóttir, Tómas Guðbjartsson, Helgi J. Ísaksson, Guðmundur Einarsson, Kristrún R. Benediktsdóttir, Bjarni A. Agnarsson, Karl Olafsson, Anna Salvarsdottir, Hjördis Bjarnason, Margret Asgeirsdottir, Kári Kristinsson, Sigurborg Matthiasdottir, Steinunn G Sveinsdottir, Silvia Polidoro, Veronica Höiom, Rafael Botella‐Estrada, Kari Hemminki, Péter Rudnai, D. Timothy Bishop, Marcello Campagna, Eliane Kellen, Maurice P. Zeegers, Petra de Verdier, A. Pérez, Dolores Isla, María Vidal, R. Andrés, Berta Sáez, Pablo Juberías, Javier Banzo, Sebastián Navarrete, A. Trés, Donghui Kan, Annika Lindblom, Eugen Gurzău, Kvetoslava Koppová, Femmie de Vegt, Jack A. Schalken, Erik H.F.M. van der Heijden, Hans J.M. Smit, René A. R. Termeer, Egbert Oosterwijk, Onno van Hooij, Eduardo Nagore, Stefano Porru, Gunnar Steineck, Johan Hansson, Frank Buntinx, William J. Catàlona, Giuseppe Matullo, Paolo Vineis, Anne E. Kiltie, José Mayordomo, Rajiv Kumar, Lambertus A. Kiemeney, Michael L. Frigge, Þorvaldur Jónsson, Hafsteinn Saemundsson, Rósa B. Barkardóttir, Eiríkur Jónsson, Steinn Jónsson, Jón Ólafsson, Jeffrey R. Gulcher, Gísli Másson, Daníel F. Guðbjartsson, Augustine Kong, Unnur Þorsteinsdóttir, Kāri Stefánsson

    Argitaratua 2009
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  19. 19
    A variant in FTO shows association with melanoma risk not due to BMI

    A variant in FTO shows association with melanoma risk not due to BMI nork Mark M. Iles, Matthew H. Law, Simon Stacey, Jiali Han, Shenying Fang, Ruth M. Pfeiffer, Mark Harland, Stuart MacGregor, John Taylor, Katja K.H. Aben, Lars A. Akslen, Marie-Françoise Avril, Esther Azizi, Egbert Bakker, Kristrún R. Benediktsdóttir, Wilma Bergman, Giovanna Bianchi‐Scarrà, Kevin M. Brown, Donato Calista, Valérie Chaudru, Maria Concetta Fargnoli, Anne Ε. Cust, Florence Démenais, Anne C. de Waal, Tadeusz Dębniak, David E. Elder, Eitan Friedman, Pilar Galán, Paola Ghiorzo, Elizabeth M. Gillanders, Alisa M. Goldstein, Nelleke A. Gruis, Johan Hansson, Per Helsing, Marko Hočevar, Veronica Höiom, John L. Hopper, Christian Ingvar, Marjolein J. F. W. Janssen, Mark A. Jenkins, Peter A. Kanetsky, Lambertus A. Kiemeney, Julie Lang, G.M. Lathrop, Sancy A. Leachman, Jeffrey E. Lee, Jan Lubiński, Rona M. MacKie, Graham J. Mann, Nicholas G. Martin, José Mayordomo, Anders Molven, Suzanne Mulder, Eduardo Nagore, Srdjan Novaković, Ichiro Okamoto, Jón Ólafsson, Håkan Olsson, Hubert Pehamberger, Ketty Peris, Maria Pilar Grasa, Dolores Planelles, Susana Puig, Susana Puig, Juliette A. Randerson‐Moor, Celia Requena, Licia Rivoltini, Monica Rodolfo, Mario Santinami, Bárður Sigurgeirsson, Helen Snowden, Fengju Song, Patrick Sulem, Kristin Thorisdottir, Rainer Tuominen, Patricia Van Belle, Nienke van der Stoep, Michelle M. van Rossum, Qingyi Wei, Judith Wendt, Diana Zélénika, Mingfeng Zhang, Maria Teresa Landi, Gudrnar Thorleifsson, D. Timothy Bishop, Christopher I. Amos, Nicholas K. Hayward, Hreinn Stefánsson, Julia Newton‐Bishop, Jennifer H. Barrett

    Argitaratua 2013
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  20. 20
    Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

    Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility nork Maria Teresa Landi, D. Timothy Bishop, Stuart MacGregor, Mitchell J. Machiela, Alexander Stratigos, Paola Ghiorzo, Myriam Brossard, Donato Calista, Jiyeon Choi, Maria Concetta Fargnoli, Tongwu Zhang, Monica Rodolfo, Adam J. Trower, Chiara Menin, J. Julian Martinez, Andreas Hadjisavvas, Lei Song, Irene Stefanaki, Richard A. Scolyer, Rose Yang, Alisa M. Goldstein, Míriam Potrony, K. Kypreou, Lorenza Pastorino, Paola Queirolo, Cristina Pellegrini, Laura Cattaneo, Matthew Zawistowski, Pol Giménez‐Xavier, A. L. Rodriguez, Lisa Elefanti, Siranoush Manoukian, Licia Rivoltini, Blair H. Smith, Maria A. Loizidou, Laura Del Regno, Daniela Massi, Mario Mandalà, Kiarash Khosrotehrani, Lars A. Akslen, Christopher I. Amos, Per Arne Andresen, Marie‐Françoise Avril, Esther Azizi, H. Peter Soyer, Véronique Bataille, Bruna Dalmasso, Lisa Bowdler, Kathryn P. Burdon, Wei V. Chen, Veryan Codd, Jamie E. Craig, Tadeusz Dębniak, Mario Falchi, Shenying Fang, Eitan Friedman, Sarah Simi, Pilar Galán, Zaida García‐Casado, Elizabeth M. Gillanders, Scott D. Gordon, Adèle C. Green, Nelleke A. Gruis, Johan Hansson, Mark Harland, Jessica Harris, Per Helsing, Anjali K. Henders, Marko Hočevar, Veronica Höiom, David J. Hunter, Christian Ingvar, Rajiv Kumar, Julie Lang, G.M. Lathrop, Jeffrey E. Lee, Xin Li, Jan Lubiński, Rona M. MacKie, M. Malt, Josep Malvehy, Kerrie McAloney, Hamida Mohamdi, Anders Molven, Eric K. Moses, Rachel Ε. Neale, Srdjan Novaković, Dale R. Nyholt, Håkan Olsson, Nick Orr, Lars G. Fritsche, Joan Anton Puig‐Butille, Abrar A. Qureshi, Graham Radford‐Smith, Juliette A. Randerson‐Moor, Celia Requena, Casey Rowe, Mark M. Iles, Marianna Sanna, Dirk Schadendorf

    Argitaratua 2020
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