Výsledky vyhledávání - Christian Sutter

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  1. 1
    Systematic identification of genes with coding microsatellites mutated in DNA mismatch repair-deficient cancer cells

    Systematic identification of genes with coding microsatellites mutated in DNA mismatch repair-deficient cancer cells Autor Stefan M. Woerner, Johannes Gebert, Yan P. Yuan, Christian Sutter, Ruediger Ridder, Peer Bork, Magnus von Knebel Doeberitz

    Vydáno 2001
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  2. 2
    Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk

    Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk Autor Bernd Frank, Justo Lorenzo Bermejo, Kari Hemminki, Christian Sutter, Barbara Wappenschmidt, Alfons Meindl, M. Kiechle-Bahat, Peter Bugert, Rita K. Schmutzler, Claus R. Bartram, Barbara Burwinkel

    Vydáno 2007
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  3. 3
    Next Generation Sequencing and Pediatric Brain Tumors: Detection of Cancer Predisposition Syndromes in Patients and Their Families

    Next Generation Sequencing and Pediatric Brain Tumors: Detection of Cancer Predisposition Syndromes in Patients and Their Families Autor Kerstin Grund, Dominik Sturm, Christian Sutter, Felix Sahm, Katrin Hinderhofer, Christian P. Kratz, Daniel Schrimpf, Andreas von Deimling, Kristian W. Pajtler, David Jones, Stefan M. Pfister, Nicola Dikow

    Vydáno 2017
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  4. 4
    T25 Repeat in the 3′ Untranslated Region of the <i>CASP2</i> Gene: A Sensitive and Specific Marker for Microsatellite Instability in Colorectal Cancer

    T25 Repeat in the 3′ Untranslated Region of the <i>CASP2</i> Gene: A Sensitive and Specific Marker for Microsatellite Instability in Colorectal Cancer Autor Peter Findeisen, Matthias Kloor, Sabine Merx, Christian Sutter, Stefan M. Woerner, Nicole Dostmann, Axel Benner, Bolormaa Dondog, Michael Pawlita, Wolfgang Dippold, Rudolf Wagner, Johannes Gebert, Magnus von Knebel Doeberitz

    Vydáno 2005
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  5. 5
    Successful immune checkpoint blockade in a patient with advanced stage microsatellite-unstable biliary tract cancer

    Successful immune checkpoint blockade in a patient with advanced stage microsatellite-unstable biliary tract cancer Autor Elena Czink, Matthias Kloor, Benjamin Goeppert, Stefan Fröhling, Sebastian Uhrig, Tim Frederik Weber, Jörn Meinel, Christian Sutter, Karl Heinz Weiss, Peter Schirmacher, Magnus von Knebel Doeberitz, Dirk Jäger, Christoph Springfeld

    Vydáno 2017
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  6. 6
    Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer

    Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer Autor Heide Hellebrand, Christian Sutter, Ellen Honisch, Eva Groß, Barbara Wappenschmidt, Christian Schem, Helmut Deißler, Nina Ditsch, Verena Gress, Marion Kiechle, Claus R. Bartram, Rita K. Schmutzler, Dieter Niederacher, Norbert Arnold, Alfons Meindl

    Vydáno 2011
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  7. 7
    A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women

    A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women Autor Sandrine Tchatchou, Anke Jung, Kari Hemminki, Christian Sutter, Barbara Wappenschmidt, Peter Bugert, Bernhard H. F. Weber, Dieter Niederacher, Norbert Arnold, Raymonda Varon-Mateeva, Nina Ditsch, Alfons Meindl, Rita K. Schmutzler, Claus R. Bartram, Barbara Burwinkel

    Vydáno 2008
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  8. 8
    The association between breast cancer and S100P methylation in peripheral blood by multicenter case–control studies

    The association between breast cancer and S100P methylation in peripheral blood by multicenter case–control studies Autor Rongxi Yang, Sarah Stöcker, Sarah Schott, Jörg Heil, Frederik Marmé, Katarina Ćuk, Bowang Chen, Michael Golatta, Yan Zhou, Christian Sutter, Barbara Wappenschmidt, Rita K. Schmutzler, Peter Bugert, Bin Qu, Claus R. Bartram, Christof Sohn, Andreas Schneeweiß, Barbara Burwinkel

    Vydáno 2017
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  9. 9
    Pan-cancer analysis of genomic scar patterns caused by homologous repair deficiency (HRD)

    Pan-cancer analysis of genomic scar patterns caused by homologous repair deficiency (HRD) Autor Eugen Rempel, Klaus Kluck, Susanne Beck, Iordanis Ourailidis, Daniel Kazdal, Olaf Neumann, Anna‐Lena Volckmar, Martina Kirchner, H. Goldschmid, Nicole Pfarr, Wilko Weichert, Daniel Hübschmann, Stefan Fröhling, Christian Sutter, Christian P. Schaaf, Peter Schirmacher, Volker Endris, Albrecht Stenzinger, Jan Budczies

    Vydáno 2022
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  10. 10
    Evaluation of SNPs in<i>miR-146a</i>,<i>miR196a2</i>and<i>miR-499</i>as low-penetrance alleles in German and Italian familial breast cancer cases

    Evaluation of SNPs in<i>miR-146a</i>,<i>miR196a2</i>and<i>miR-499</i>as low-penetrance alleles in German and Italian familial breast cancer cases Autor Irene Catucci, Rongxi Yang, Paolo Verderio, Sara Pizzamiglio, Ludwig Heesen, Kari Hemminki, Christian Sutter, Barbara Wappenschmidt, Michèlle Dick, Norbert Arnold, Peter Bugert, Dieter Niederacher, Alfons Meindl, Rita K. Schmutzler, Claus C. Bartram, Filomena Ficarazzi, Laura Tizzoni, Daniela Zaffaroni, Siranoush Manoukian, Monica Barile, Marco A. Pierotti, Paolo Radice, Barbara Burwinkel, Paolo Peterlongo

    Vydáno 2009
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  11. 11
    Gene panel testing of 5589 <i><scp>BRCA</scp>1/2</i>‐negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer

    Gene panel testing of 5589 <i><scp>BRCA</scp>1/2</i>‐negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Bre... Autor Jan Hauke, Judit Horváth, Eva Groß, Andrea Gehrig, Ellen Honisch, Karl Hackmann, Gunnar Schmidt, Norbert Arnold, Ulrike Faust, Christian Sutter, Julia Hentschel, Shan Wang‐Gohrke, Mateja Smogavec, Bernhard H. F. Weber, Nana Weber‐Lassalle, Konstantin Weber‐Lassalle, Julika Borde, Corinna Ernst, Janine Altmüller, Alexander E. Volk, Hölger Thiele, Verena Hübbel, Peter Nürnberg, Katharina Keupp, Beatrix Versmold, Esther Pohl, Christian Kubisch, Sabine Grill, Victoria Paul, N Herold, Nadine Lichey, Kerstin Rhiem, Nina Ditsch, Christian Rückert, Barbara Wappenschmidt, Bernd Auber, Andreas Rump, Dieter Niederacher, Thomas Haaf, Juliane Ramser, Bernd Dworniczak, Christoph Engel, Alfons Meindl, Rita K. Schmutzler, Eric Hahnen

    Vydáno 2018
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  12. 12
    Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology

    Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology Autor Dominik Sturm, David Capper, Felipe Andreiuolo, Marco Gessi, Christian Kölsche, Annekathrin Reinhardt, Philipp Sievers, Annika K. Wefers, Azadeh Ebrahimi, Abigail K. Suwala, Gerrit H. Gielen, Martin Sill, Daniel Schrimpf, Damian Stichel, Volker Hovestadt, Bjarne Daenekas, Agata Rode, Stefan Hamelmann, Christopher Previti, Natalie Jäger, Ivo Buchhalter, Mirjam Blattner-Johnson, Barbara C. Jones, Monika Warmuth‐Metz, Brigitte Bison, Kerstin Grund, Christian Sutter, Steffen Hirsch, Nicola Dikow, Martin Hasselblatt, Ulrich Schüller, Arend Koch, Nicolas U. Gerber, Christine L. White, Molly K. Buntine, Kathryn M. Kinross, Elizabeth M. Algar, Jordan R. Hansford, Nicholas G. Gottardo, Martin U. Schuhmann, Ulrich W. Thomale, Pablo Hernáiz Driever, Astrid Gnekow, Olaf Witt, Hermann L. Müller, Gabriele Calaminus, Gudrun Fleischhack, Uwe Kordes, Martin Mynarek, Stefan Rutkowski, Michael C. Frühwald, Christof M. Kramm, Andreas von Deimling, Torsten Pietsch, Felix Sahm, Stefan M. Pfister, David Jones

    Vydáno 2023
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  13. 13
    The Pediatric Precision Oncology INFORM Registry: Clinical Outcome and Benefit for Patients with Very High-Evidence Targets

    The Pediatric Precision Oncology INFORM Registry: Clinical Outcome and Benefit for Patients with Very High-Evidence Targets Autor Cornelis M. van Tilburg, Elke Pfaff, Kristian W. Pajtler, Karin P.S. Langenberg, Petra Fiesel, Barbara C. Jones, Gnana Prakash Balasubramanian, Sebastian Stark, Pascal D. Johann, Mirjam Blattner-Johnson, Kathrin Schramm, Nicola Dikow, Steffen Hirsch, Christian Sutter, Kerstin Grund, Arend von Stackelberg, Andreas E. Kulozik, Andrej Lissat, Arndt Borkhardt, Roland Meisel, Dirk Reinhardt, Jan‐Henning Klusmann, Gudrun Fleischhack, Stephan Tippelt, Dietrich von Schweinitz, Irene Schmid, Christof M. Kramm, André O. von Bueren, Gabriele Calaminus, Peter Vorwerk, Norbert Graf, Frank Westermann, Matthias Fischer, Angelika Eggert, Birgit Burkhardt, Wilhelm Wößmann, Michaela Nathrath, Stefanie Hecker‐Nolting, Michael C. Frühwald, Dominik T. Schneider, Ines B. Brecht, Petra Ketteler, Simone Fulda, Ewa Kościelniak, Michael T. Meister, Monika Scheer, Simone Hettmer, Matthias Schwab, Roman Tremmel, Ingrid Øra, Caroline Hutter, Nicolas U. Gerber, Olli Lohi, Bernarda Kazanowska, Antonis Kattamis, Maria Filippidou, Bianca F. Goemans, C. Michel Zwaan, Till Milde, Natalie Jäger, Stephan Wolf, David Reuß, Felix Sahm, Andreas von Deimling, Uta Dirksen, Angelika Freitag, Ruth Witt, Peter Lichter, Annette Kopp‐Schneider, David Jones, Jan J. Molenaar, David Capper, Stefan M. Pfister, Olaf Witt

    Vydáno 2021
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  14. 14
    <i>FANCM</i>c.5791C&gt;T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor

    <i>FANCM</i>c.5791C&gt;T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor Autor Paolo Peterlongo, Irene Catucci, Mara Colombo, Laura Caleca, Eliseos J. Mucaki, Massimo Bogliolo, Maria Marín, Francesca Damiola, Loris Bernard, Valeria Pensotti, Sara Volorio, Valentina Dall’Olio, Alfons Meindl, Claus R. Bartram, Christian Sutter, Harald Surowy, Valérie Sornin, Marie‐Gabrielle Dondon, Séverine Eon‐Marchais, Dominique Stoppa‐Lyonnet, Nadine Andrieu, Olga M. Sinilnikova, Gillian Mitchell, Paul A. James, Ella R. Thompson, Marina Marchetti, Cristina Verzeroli, Carmen Julia Tartari, Gabriele Lorenzo Capone, Anna Laura Putignano, Maurizio Genuardi, Veronica Medici, Isabella Marchi, Massimo Federico, Silvia Tognazzo, Laura Matricardi, Simona Agata, Riccardo Dolcetti, Lara Della Puppa, Giulia Cini, Viviana Gismondi, Valeria Viassolo, Chiara Perfumo, Maria Antonietta Mencarelli, Margherita Baldassarri, Bernard Peissel, Gaia Roversi, Valentina Silvestri, Piera Rizzolo, Francesca Spina, Caterina Vivanet, Maria Grazia Tibiletti, Maria A. Caligo, Gaetana Gambino, Stefania Tommasi, Brunella Pilato, Carlo Tondini, Chiara Corna, Bernardo Bonanni, Monica Barile, Ana Osório, Javier Benı́tez, Luisa Balestrino, Laura Ottini, Siranoush Manoukian, Marco A. Pierotti, Alessandra Renieri, Liliana Varesco, Fergus J. Couch, Xianshu Wang, Peter Devilee, Florentine Hilbers, Christi J. van Asperen, Alessandra Viel, Marco Montagna, Laura Cortesi, Orland Dı́ez, Judith Balmañà, Jan Hauke, Rita K. Schmutzler, Laura Papi, Miguel Ángel Pujana, Conxi Lázaro, Anna Falanga, Kenneth Offit, Joseph Vijai, Ian Campbell, Barbara Burwinkel, Anders Kvist, Hans Ehrencrona, Sylvie Mazoyer, Sara Pizzamiglio, Paolo Verderio, Jordi Surrallés, Peter K. Rogan, Paolo Radice

    Vydáno 2015
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  15. 15
    Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

    Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers Autor Antonis C. Antoniou, Amanda B. Spurdle, Olga M. Sinilnikova, Sue Healey, Karen A. Pooley, Rita K. Schmutzler, Beatrix Versmold, Christoph Engel, Alfons Meindl, Norbert Arnold, Wera Hofmann, Christian Sutter, Dieter Niederacher, Helmut Deißler, Trinidad Caldés, Kati Kämpjärvi, Heli Nevanlinna, Jacques Simard, Jonathan Beesley, Xiaohong Chen, Susan L. Neuhausen, Timothy R. Rebbeck, Theresa Wagner, Henry T. Lynch, Claudine Isaacs, Jeffrey N. Weitzel, Patricia A. Ganz, Mary B. Daly, Gail E. Tomlinson, Olufunmilayo I. Olopade, Joanne L. Blum, Fergus J. Couch, Paolo Peterlongo, Siranoush Manoukian, Monica Barile, Paolo Radice, Csilla I. Szabo, Lutécia H. Mateus Pereira, Mark H. Greene, Gad Rennert, Flavio Lejbkowicz, Ofra Barnett‐Griness, Irene L. Andrulis, Hilmi Özçelik, Anne‐Marie Gerdes, Maria A. Caligo, Yael Laitman, Bella Kaufman, Roni Milgrom, Eitan Friedman, Susan M. Domchek, Katherine L. Nathanson, Ana Osório, Gemma Llort, Roger L. Milne, Javier Benı́tez, Ute Hamann, Frans B.L. Hogervorst, Peggy Manders, Marjolijn J. L. Ligtenberg, Ans M.W. van den Ouweland, Susan Peock, Margaret Cook, Radka Platte, D. Gareth Evans, Rosalind A. Eeles, Gabriella Pichert, Carol Chu, Diana Eccles, Rosemarie Davidson, Fiona Douglas, Andrew K. Godwin, Laure Barjhoux, Sylvie Mazoyer, Hagay Sobol, Violaine Bourdon, François Eisinger, Agnès Chompret, Corinne Capoulade, Brigitte Bressac–de Paillerets, Gilbert Lenoir, Marion Gauthier‐Villars, Claude Houdayer, Dominique Stoppa‐Lyonnet, Georgia Chenevix‐Trench, Douglas F. Easton

    Vydáno 2008
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  16. 16
    Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort

    Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort Autor Sebastian M. Waszak, Paul A. Northcott, Ivo Buchhalter, Giles Robinson, Christian Sutter, Susanne N. Groebner, Kerstin Grund, Laurence Brugières, David Jones, Kristian W. Pajtler, A. Sorana Morrissy, Marcel Kool, Dominik Sturm, Lukas Chávez, Aurélie Ernst, Sebastian Brabetz, M. Hain, Thomas Zichner, Maia Segura‐Wang, Joachim Weischenfeldt, Tobias Rausch, Balca R. Mardin, Xin Zhou, Cristina Baciu, Christian Lawerenz, Jennifer A. Chan, Pascale Varlet, Léa Guerrini‐Rousseau, Daniel W. Fults, Wiesława Grajkowska, Péter Hauser, Nada Jabado, Young‐Shin Ra, Karel Zitterbart, Suyash Shringarpure, Francisco M. De La Vega, Carlos D. Bustamante, Ho‐Keung Ng, Arie Perry, Tobey J. MacDonald, Pablo Hernáiz Driever, Anne Bendel, Daniel C. Bowers, Geoffrey McCowage, Murali Chintagumpala, Richard J. Cohn, Tim Hassall, Gudrun Fleischhack, Tone Eggen, Finn Wesenberg, Maria Feychting, Birgitta Lannering, Joachim Schüz, Christoffer Johansen, Tina Veje Andersen, Martin Röösli, Claudia E. Kuehni, Michael Grotzer, Kristina Kjærheim, Camelia M. Monoranu, Tenley C. Archer, Elizabeth S. Duke, Scott L. Pomeroy, Shelagh Redmond, Stephan Frank, David Sumerauer, Wolfram Scheurlen, Marina Ryzhova, Till Milde, Christian P. Kratz, David Samuel, Jinghui Zhang, David A. Solomon, Marco A. Marra, Roland Eils, Claus R. Bartram, Katja von Hoff, Stefan Rutkowski, Vijay Ramaswamy, Richard J. Gilbertson, Andrey Korshunov, Michael D. Taylor, Peter Lichter, David Malkin, Amar Gajjar, Jan O. Korbel, Stefan M. Pfister

    Vydáno 2018
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  17. 17
    Prediction of Breast and Prostate Cancer Risks in Male <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers Using Polygenic Risk Scores

    Prediction of Breast and Prostate Cancer Risks in Male <i>BRCA1</i> and <i>BRCA2</i> Mutation Carriers Using Polygenic Risk Scores Autor Julie Lecarpentier, Valentina Silvestri, Karoline Kuchenbaecker, Daniel Barrowdale, Joe Dennis, Lesley McGuffog, Penny Soucy, Goska Leslie, Piera Rizzolo, Anna Sara Navazio, Virginia Valentini, Veronica Zelli, Andrew Lee, Ali Amin Al Olama, Jonathan P. Tyrer, Melissa C. Southey, Esther M. John, Thomas Conner, David E. Goldgar, Saundra S. Buys, Ramūnas Janavičius, Linda Steele, Yuan Chun Ding, Susan L. Neuhausen, Thomas van Overeem Hansen, Ana Osório, Jeffrey N. Weitzel, Angela Toss, Veronica Medici, Laura Cortesi, Ines Zanna, Domenico Palli, Paolo Radice, Siranoush Manoukian, Bernard Peissel, Jacopo Azzollini, Alessandra Viel, Giulia Cini, Giuseppe Damante, Stefania Tommasi, Paolo Peterlongo, Florentia Fostira, Ute Hamann, D. Gareth Evans, Alex Henderson, Carole Brewer, Diana Eccles, Jackie Cook, Kai-Ren Ong, Lisa Walker, Lucy Side, Mary Porteous, Rosemarie Davidson, Shirley Hodgson, Debra Frost, Julian Adlard, Louise Izatt, Rosalind A. Eeles, Ian O. Ellis, Marc Tischkowitz, Andrew K. Godwin, Alfons Meindl, Andrea Gehrig, Bernd Dworniczak, Christian Sutter, Christoph Engel, Dieter Niederacher, Doris Steinemann, Eric Hahnen, Jan Hauke, Kerstin Rhiem, Karin Kast, Norbert Arnold, Nina Ditsch, Shan Wang‐Gohrke, Barbara Wappenschmidt, Dorothea Wand, Christine Lasset, Dominique Stoppa‐Lyonnet, Muriel Belotti, Francesca Damiola, Laure Barjhoux, Sylvie Mazoyer, Mattias Van Heetvelde, Bruce Poppe, Kim De Leeneer, Kathleen Claes, Miguel de la Hoya, Vanesa Garcı́a, Miguel de la Hoya, Pedro Pérez Segura, Johanna I. Kiiski, Kristiina Aittomäki, Sofia Khan, Heli Nevanlinna, Christi J. van Asperen, Vaszko Tibor, Miklós Kásler, Edith Oláh, Judith Balmañà

    Vydáno 2017
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  18. 18
    Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

    Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer Autor Manuel A. R. Ferreira, Eric R. Gamazon, Fares Al‐Ejeh, Kristiina Aittomäki, Irene L. Andrulis, Hoda Anton‐Culver, Aðalgeir Arason, Volker Arndt, Kristan J. Aronson, Banu K. Arun, Ella Asseryanis, Jacopo Azzollini, Judith Balmañà, Daniel R. Barnes, Daniel Barrowdale, Matthias W. Beckmann, Sabine Behrens, Javier Benı́tez, Marina Bermisheva, Katarzyna Białkowska, Carl Blomqvist, Natalia Bogdanova, Stig E. Bojesen, Manjeet K. Bolla, Åke Borg, Hiltrud Brauch, Hermann Brenner, Annegien Broeks, Barbara Burwinkel, Trinidad Caldés, Maria A. Caligo, Daniele Campa, Ian Campbell, Federico Canzian, Jonathan Carter, Brian D. Carter, Jose E. Castelao, Jenny Chang‐Claude, Stephen J. Chanock, Hans Christiansen, Wendy K. Chung, Kathleen Claes, Christine L. Clarke, Julian Adlard, Munaza Ahmed, Julian Barwell, Angela Brady, Carole Brewer, Jackie Cook, Rosemarie Davidson, Alan C. Donaldson, Jacqueline Eason, Ros Eeles, D. Gareth Evans, Helen Gregory, Helen Hanson, Alex Henderson, Shirley Hodgson, Louise Izatt, Michael J. Kennedy, Fiona Lalloo, Clare Miller, Patrick J. Morrison, Kai‐Ren Ong, Jo Perkins, Mary Porteous, Mark T. Rogers, Lucy Side, Katie Snape, Lisa Walker, Patricia A. Harrington, Norbert Arnold, Bernd Auber, Nadja Bogdanova-Markov, Julika Borde, Almuth Caliebe, Nina Ditsch, Bernd Dworniczak, Stefanie Engert, Ulrike Faust, Andrea Gehrig, Eric Hahnen, Jan Hauke, Julia Hentschel, Wei He, Ellen Honisch, Walter Just, Karin Kast, Mirjam Larsen, Johannes Lemke, Huu Phuc Nguyen, Dieter Niederacher, Claus‐Eric Ott, Konrad Platzer, Esther Pohl‐Rescigno, Juliane Ramser, Kerstin Rhiem, Doris Steinemann, Christian Sutter, Raymonda Varon-Mateeva

    Vydáno 2019
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  19. 19
    Identification of six new susceptibility loci for invasive epithelial ovarian cancer

    Identification of six new susceptibility loci for invasive epithelial ovarian cancer Autor Karoline Kuchenbaecker, Susan J. Ramus, Jonathan P. Tyrer, Andrew Lee, Howard C. Shen, Jonathan Beesley, Kate Lawrenson, Lesley McGuffog, Sue Healey, Janet M. Lee, Tassja J. Spindler, Yvonne G. Lin, Tanja Pejović, Yukie T. Bean, Qiyuan Li, Simon G. Coetzee, Dennis J. Hazelett, Alexander Miron, Melissa C. Southey, Mary Beth Terry, David E. Goldgar, Saundra S. Buys, Ramūnas Janavičius, Cecilia M. Dorfling, Elizabeth J. van Rensburg, Susan L. Neuhausen, Yuan Chun Ding, Thomas van Overeem Hansen, Lars Jønson, Anne‐Marie Gerdes, Bent Ejlertsen, Daniel Barrowdale, Joe Dennis, Javier Benı́tez, Ana Osório, Maria J. García, Ian K. Komenaka, Jeffrey N. Weitzel, Pamela Ganschow, Paolo Peterlongo, Loris Bernard, Alessandra Viel, Bernardo Bonanni, Bernard Peissel, Siranoush Manoukian, Paolo Radice, Laura Papi, Laura Ottini, Florentia Fostira, Irene Konstantopoulou, Judy E. Garber, Debra Frost, Jo Perkins, Radka Platte, Ian O. Ellis, Andrew K. Godwin, Rita K. Schmutzler, Alfons Meindl, Christoph Engel, Christian Sutter, Olga M. Sinilnikova, Francesca Damiola, Sylvie Mazoyer, Dominique Stoppa‐Lyonnet, Kathleen Claes, Kim De Leeneer, Judy Kirk, Gustavo C. Rodriguez, Marion Piedmonte, David M. O’Malley, Miguel de la Hoya, Trinidad Caldés, Kristiina Aittomäki, Heli Nevanlinna, Margriet Collée, Matti A. Rookus, Jan C. Oosterwijk, Laima Tihomirova, Nadine Tung, Ute Hamann, Claudine Isaccs, Marc Tischkowitz, Evgeny N. Imyanitov, Maria A. Caligo, Ian Campbell, Frans B.L. Hogervorst, Edith Oláh, Orland Dı́ez, Ignacio Blanco, Joan Brunet, Conxi Lázaro, Miquel Angel Pujana, Anna Jakubowska, Jacek Gronwald, Jan Lubiński, Grzegorz Sukiennicki, Rósa B. Barkardóttir, Marie Plante, Jacques Simard, Penny Soucy

    Vydáno 2015
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  20. 20
    Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

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    Vydáno 2014
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