Resultats de la cerca - Senno Verhoef
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The single-nucleotide polymorphism 309 in the MDM2 gene contributes to the Li–Fraumeni syndrome and related phenotypes per Mariëlle Ruijs, Marjanka K. Schmidt, Heli Nevanlinna, Johanna Tommiska, Kristiina Aittomäki, Roelof Pruntel, Senno Verhoef, Laura J. vanʼt Veer
Publicat 2006Artigo -
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Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype – phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex... per Őzgür Sancak, Mark Nellist, Miriam Goedbloed, Peter Elfferich, Carine Wouters, Anneke Maat‐Kievit, Bernard A. Zonnenberg, Senno Verhoef, Dicky Halley, Ans van den Ouweland
Publicat 2005Artigo -
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Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation per Marjon van Slegtenhorst, Senno Verhoef, A.M.P. Tempelaars, Lida Bakker, Qi Wang, Marja W. Wessels, Remco Bakker, Mark Nellist, Dick Lindhout, Dicky Halley, Ans van den Ouweland
Publicat 1999Artigo -
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Psychological distress and use of psychosocial support in familial adenomatous polyposis per Kirsten F. L. Douma, Neil K. Aaronson, Hans F. A. Vasen, Miranda A. Gerritsma, Chad M. Gundy, Esther P. A. Janssen, A. H. J. T. Vriends, Annemieke Cats, Senno Verhoef, Eveline M. A. Bleiker
Publicat 2009Artigo -
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Comparative Genomic Hybridization Profiles in Human BRCA1 and BRCA2 Breast Tumors Highlight Differential Sets of Genomic Aberrations per Erik H. van Beers, Tibor van Welsem, Lodewyk F.A. Wessels, Yunlei Li, Rogier A. Oldenburg, Peter Devilee, Cees J. Cornelisse, Senno Verhoef, Frans B.L. Hogervorst, Laura J. vanʼt Veer, Petra M. Nederlof
Publicat 2005Artigo -
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Prediction of BRCA1-association in hereditary non-BRCA1/2 breast carcinomas with array-CGH per Simon A. Joosse, Erik H. van Beers, Ivon H. G. Tielen, Hugo M. Horlings, Johannes L. Peterse, Nicoline Hoogerbrugge, Marjolijn J. L. Ligtenberg, Lodewyk F.A. Wessels, Priscilla Axwijk, Senno Verhoef, Frans B.L. Hogervorst, Petra M. Nederlof
Publicat 2008Artigo -
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Malignant pancreatic tumour within the spectrum of tuberous sclerosis complex in childhood per Senno Verhoef, R. van Diemen-Steenvoorde, W.L. Akkersdijk, N. M. A. Bax, Yavuz Ariyürek, Caroline Hermans, Onno van Nieuwenhuizen, P. G. J. Nikkels, Dick Lindhout, D. J. J. Halley, Kees J.M. Lips, A. M. W. van den Ouweland
Publicat 1999Artigo -
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High Rate of Mosaicism in Tuberous Sclerosis Complex per Senno Verhoef, Lida Bakker, Anita M.P. Tempelaars, Arjenne L.W. Hesseling-Janssen, Tadeusz Mazurczak, Sergiusz Jóźwiak, A. Fois, G. Bartalini, Bernard A. Zonnenberg, Anthonie J. van Essen, Dick Lindhout, D. J. J. Halley, Ans M.W. van den Ouweland
Publicat 1999Artigo -
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Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits per Chantal R.M. Lammens, Eveline M. A. Bleiker, Neil K. Aaronson, Anja Wagner, Rolf H. Sijmons, Margreet G.E.M. Ausems, A. H. J. T. Vriends, Mariëlle Ruijs, Theo A.M. van Os, Liesbeth Spruijt, E. Gómez, Annemieke Cats, Tanja Nagtegaal, Senno Verhoef
Publicat 2010Artigo -
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Genetic Testing in Li-Fraumeni Syndrome: Uptake and Psychosocial Consequences per Chantal R.M. Lammens, Neil K. Aaronson, Anja Wagner, Rolf H. Sijmons, Margreet G.E.M. Ausems, A. H. J. T. Vriends, Mariëlle Ruijs, Theo A.M. van Os, Liesbeth Spruijt, E. Gómez, Irma Kluijt, Tanja Nagtegaal, Senno Verhoef, Eveline M. A. Bleiker
Publicat 2010Artigo -
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Physical activity and the risk of breast cancer in BRCA1/2 mutation carriers per Anouk Pijpe, Peggy Manders, Richard M. Brohet, J. Margriet Collée, Senno Verhoef, Hans F. A. Vasen, Nicoline Hoogerbrugge, Christi J. van Asperen, Charlotte J. Dommering, Margreet G.E.M. Ausems, Cora M. Aalfs, E. Gómez, Laura J. vanʼt Veer, Flora E. van Leeuwen, Matti A. Rookus
Publicat 2009Artigo -
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Chromosome 8q23.3 and 11q23.1 Variants Modify Colorectal Cancer Risk in Lynch Syndrome per Juul Wijnen, Richard M. Brohet, Ronald van Eijk, S. Jagmohan-Changur, Anneke Middeldorp, Carli M.J. Tops, Mario van Puijenbroek, Margreet G.E.M. Ausems, E. Gómez, Frederik J. Hes, Nicoline Hoogerbrugge, Fred H. Menko, Theo A.M. van Os, Rolf H. Sijmons, Senno Verhoef, Anja Wagner, Fokko M. Nagengast, Jan H. Kleibeuker, Peter Devilee, Hans Morreau, David E. Goldgar, Ian Tomlinson, Richard S. Houlston, Tom van Wezel, Hans F. A. Vasen
Publicat 2008Artigo -
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A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example per Leila Mohammadi, Maaike P.G. Vreeswijk, Rogier A. Oldenburg, Ans van den Ouweland, Jan C. Oosterwijk, Annemarie H. van der Hout, Nicoline Hoogerbrugge, Marjolijn J. L. Ligtenberg, Margreet G.E.M. Ausems, Rob B. van der Luijt, Charlotte J. Dommering, Gilles Thomas, Senno Verhoef, Frans B.L. Hogervorst, Theo A. van Os, E. Gómez, Marinus J. Blok, Juul Wijnen, Quinta Helmer, Peter Devilee, Christi J. van Asperen, Hans C. van Houwelingen
Publicat 2009Artigo -
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Comprehensive Mutation Analysis of<i>PMS2</i>in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome per Heleen M. van der Klift, Arjen R. Mensenkamp, Mark Drost, Elsa C. Bik, Yvonne J. Vos, Gilles Thomas, B. Redeker, Yvonne Tiersma, José B.M. Zonneveld, E. Gómez, Tom G.W. Letteboer, Maran J.W. Olderode-Berends, Liselotte P. van Hest, Theo A. van Os, Senno Verhoef, Anja Wagner, Christi J. van Asperen, Sanne W. ten Broeke, Frederik J. Hes, Niels de Wind, Maartje Nielsen, Peter Devilee, Marjolijn J. L. Ligtenberg, Juul Wijnen, Carli M.J. Tops
Publicat 2016Artigo -
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Genetic modifiers of CHEK2*1100delC-associated breast cancer risk per Taru Muranen, Dario Greco, Carl Blomqvist, Kristiina Aittomäki, Sofia Khan, Frans B.L. Hogervorst, Senno Verhoef, Paul D.P. Pharoah, Alison M. Dunning, Mitul Shah, Robert Luben, Stig E. Bojesen, Børge G. Nordestgaard, Minouk J. Schoemaker, Anthony J. Swerdlow, Montserrat García‐Closas, Jonine D. Figueroa, Thilo Dörk, Natalia Bogdanova, Per Hall, Jingmei Li, Э. К. Хуснутдинова, Marina Bermisheva, Vessela Kristensen, Anne‐Lise Børresen‐Dale, Julian Peto, Isabel dos–Santos–Silva, Fergus J. Couch, Janet E. Olson, Peter Hillemans, Tjoung‐Won Park‐Simon, Hiltrud Brauch, Ute Hamann, Barbara Burwinkel, Frederik Marmé, Alfons Meindl, Rita K. Schmutzler, Angela Cox, Simon S. Cross, Elinor J. Sawyer, Ian Tomlinson, Diether Lambrechts, Matthieu Moisse, Annika Lindblom, Sara Margolin, Antoinette Hollestelle, John W.M. Martens, Peter A. Fasching, Matthias W. Beckmann, Irene L. Andrulis, Julia A. Knight, Hoda Anton‐Culver, Argyrios Ziogas, Graham G. Giles, Roger L. Milne, Hermann Brenner, Volker Arndt, Arto Mannermaa, Veli‐Matti Kosma, Jenny Chang‐Claude, Anja Rudolph, Peter Devilee, Caroline Seynaeve, John L. Hopper, Melissa C. Southey, Esther M. John, Alice S. Whittemore, Manjeet K. Bolla, Qin Wang, Kyriaki Michailidou, Joe Dennis, Douglas F. Easton, Marjanka K. Schmidt, Heli Nevanlinna
Publicat 2016Artigo -
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Common Breast Cancer Susceptibility Loci Are Associated with Triple-Negative Breast Cancer per Kristen N. Stevens, Celine M. Vachon, Adam M. Lee, Susan Slager, Timothy G. Lesnick, Curtis Olswold, Peter A. Fasching, Penelope Miron, Diana Eccles, Jane Carpenter, Andrew K. Godwin, Christine B. Ambrosone, Robert Winqvist, Hiltrud Brauch, Marjanka K. Schmidt, Angela Cox, Simon S. Cross, Elinor J. Sawyer, Arndt Hartmann, Matthias W. Beckmann, Rüdiger Schulz-Wendtland, Arif B. Ekici, William Tapper, Susan M. Gerty, Lorraine Durcan, Nikki Graham, Rebecca Hein, Stephan Nickels, Dieter Flesch‐Janys, Judith Heinz, Hans‐Peter Sinn, Irene Konstantopoulou, Florentia Fostira, Dimitrios Pectasides, Meletios Α. Dimopoulos, George Fountzilas, Christine L. Clarke, Rosemary L. Balleine, Janet E. Olson, Zachary Fredericksen, Robert B. Diasio, Harsh B. Pathak, Eric A. Ross, JoEllen Weaver, Thomas Rüdiger, Asta Försti, Thomas Dünnebier, Foluso O. Ademuyiwa, Swati Kulkarni, Katri Pylkäs, Arja Jukkola‐Vuorinen, Yon‐Dschun Ko, Erik Van Limbergen, Hilde Janssen, Julian Peto, Olivia Fletcher, Graham G. Giles, Laura Baglietto, Senno Verhoef, Ian Tomlinson, Veli‐Matti Kosma, Jonathan Beesley, Dario Greco, Carl Blomqvist, Astrid Irwanto, Jianjun Liu, Fiona M. Blows, Sarah‐Jane Dawson, Sara Margolin, Graham J. Mann, Nicholas G. Martin, Grant W. Montgomery, Diether Lambrechts, Isabel dos–Santos–Silva, Gianluca Severi, Ute Hamann, Paul D.P. Pharoah, Douglas F. Easton, Jenny Chang‐Claude, Drakoulis Yannoukakos, Heli Nevanlinna, Xianshu Wang, Fergus J. Couch
Publicat 2011Artigo -
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Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer per Kyriaki Michailidou, Jonathan Beesley, Sara Lindström, Sander Canisius, Joe Dennis, Michael Lush, Mel Maranian, Manjeet K. Bolla, Sophia Wang, Mitul Shah, Barbara Perkins, Kamila Czene, Mikael Eriksson, Hatef Darabi, Judith S. Brand, Stig E. Bojesen, Børge G. Nordestgaard, Henrik Flyger, Sune F. Nielsen, Nazneen Rahman, Clare Turnbull, Olivia Fletcher, Julian Peto, Lorna J. Gibson, Isabel dos–Santos–Silva, Jenny Chang‐Claude, Dieter Flesch‐Janys, Anja Rudolph, Ursula Eilber, Sabine Behrens, Heli Nevanlinna, Taru Muranen, Kristiina Aittomäki, Carl Blomqvist, Sofia Khan, Kirsimari Aaltonen, Habibul Ahsan, Muhammad G. Kibriya, Alice S. Whittemore, Esther M. John, Kathleen E. Malone, Marilie D. Gammon, Regina M. Santella, Giske Ursin, Enes Makalic, Daniel F. Schmidt, Graham Casey, David J. Hunter, Susan M. Gapstur, Mia M. Gaudet, W. Ryan Diver, Christopher A. Haiman, Fredrick R. Schumacher, Brian E. Henderson, Loı̈c Le Marchand, Christine D. Berg, Stephen J. Chanock, Jonine D. Figueroa, Robert N. Hoover, Diether Lambrechts, Patrick Neven, Hans Wildiers, Erik Van Limbergen, Marjanka K. Schmidt, Annegien Broeks, Senno Verhoef, Sten Cornelissen, Fergus J. Couch, Janet E. Olson, Emily Hallberg, Celine M. Vachon, Quinten Waisfisz, Hanne Meijers‐Heijboer, Muriel A. Adank, Rob B. van der Luijt, Jingmei Li, Jianjun Liu, Keith Humphreys, Daehee Kang, Ji‐Yeob Choi, Sue K. Park, Keun-Young Yoo, Keitaro Matsuo, Hidemi Ito, Hiroji Iwata, Kazuo Tajima, Pascal Guénel, Thérèse Truong, Claire Mulot, Marie-Pierre Sanchez, Barbara Burwinkel, Frederik Marmé, Harald Surowy, Christof Sohn, Anna H. Wu, Chiu-Chen Tseng, David Van Den Berg, Daniel O. Stram, Anna González‐Neira, Javier Benı́tez
Publicat 2015Revisão -
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Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers per Antonis C. Antoniou, Karoline Kuchenbaecker, Penny Soucy, Jonathan Beesley, Xiaohong Chen, Lesley McGuffog, Andrew Lee, Daniel Barrowdale, Sue Healey, Olga M. Sinilnikova, Maria A. Caligo, Niklas Loman, Katja Harbst, Annika Lindblom, Brita Arver, Richard Rosenquist, Per Karlsson, Katherine L. Nathanson, Susan M. Domchek, Tim Rebbeck, Anna Jakubowska, Jan Lubiński, Katarzyna Jaworska, Katarzyna Durda, Elżbieta Złowowcka-Perłowska, Ana Osório, M. Durán, Raquel Andrés, Javier Benı́tez, Ute Hamann, Frans B.L. Hogervorst, Theo A. van Os, Senno Verhoef, Hanne Meijers‐Heijboer, Juul Wijnen, E. Gómez, Marjolijn J. L. Ligtenberg, Mieke Kriege, J. Margriet Collée, Margreet G.E.M. Ausems, Jan C. Oosterwijk, Susan Peock, Debra Frost, Steve D. Ellis, Radka Platte, Elena Fineberg, D. Gareth Evans, Fiona Lalloo, Chris Jacobs, Rosalind A. Eeles, Julian Adlard, Rosemarie Davidson, Trevor Cole, Jackie Cook, Joan Paterson, Fiona Douglas, Carole Brewer, Shirley Hodgson, Patrick J. Morrison, Lisa Walker, Mark T. Rogers, Alan Donaldson, Huw Dorkins, Andrew K. Godwin, Betsy Bove, Dominique Stoppa‐Lyonnet, Claude Houdayer, Bruno Buecher, Antoine De Pauw, Sylvie Mazoyer, Alain Calender, Mélanie Léoné, Brigitte Bressac–de Paillerets, Olivier Caron, Hagay Sobol, Marc Frénay, Fabienne Prieur, Sandra Fert Ferrer, Isabelle Mortemousque, Saundra S. Buys, Mary B. Daly, Alexander Miron, Mary Beth Terry, John L. Hopper, Esther M. John, Melissa C. Southey, David E. Goldgar, Christian F. Singer, A. Fink-Retter, Muy‐Kheng Tea, Daphne Geschwantler Kaulich, Thomas van Overeem Hansen, Finn C. Nielsen, Rósa B. Barkardóttir, Mia M. Gaudet, Tomas Kirchhoff, Joseph Vijai, Ana Dutra-Clarke, Kenneth Offit, Marion Piedmonte
Publicat 2012Artigo -
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Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia per Amanda B. Spurdle, Fergus J. Couch, Michael T. Parsons, Lesley McGuffog, Daniel Barrowdale, Manjeet K. Bolla, Qin Wang, Sue Healey, Rita K. Schmutzler, Barbara Wappenschmidt, Kerstin Rhiem, Eric Hahnen, Christoph Engel, Alfons Meindl, Nina Ditsch, Norbert Arnold, Hansjoerg Plendl, Dieter Niederacher, Christian Sutter, Shan Wang‐Gohrke, Doris Steinemann, Sabine Preisler-Adams, Karin Kast, Raymonda Varon-Mateeva, Ian O. Ellis, Debra Frost, Radka Platte, Jo Perkins, D. Gareth Evans, Louise Izatt, Rosalind A. Eeles, Julian Adlard, Rosemarie Davidson, Trevor Cole, Giulietta Scuvera, Siranoush Manoukian, Bernardo Bonanni, Frédérique Mariette, Stefano Fortuzzi, Alessandra Viel, Barbara Pasini, Laura Papi, Liliana Varesco, Rosemary L. Balleine, Katherine L. Nathanson, Susan M. Domchek, Kenneth Offitt, Anna Jakubowska, Noralane M. Lindor, Mads Thomassen, Uffe Birk Jensen, Johanna Rantala, Åke Borg, Irene L. Andrulis, Alexander Miron, Thomas van Overeem Hansen, Trinidad Caldés, Susan L. Neuhausen, Amanda E. Toland, Heli Nevanlinna, Marco Montagna, Judy Garber, Andrew K. Godwin, Ana Osório, Rachel E. Factor, Mary Beth Terry, Timothy R. Rebbeck, Beth Y. Karlan, Melissa C. Southey, Muhammad Usman Rashid, Nadine Tung, Paul D.P. Pharoah, Fiona M. Blows, Alison M. Dunning, Elena Provenzano, Per Hall, Kamila Czene, Marjanka K. Schmidt, Annegien Broeks, Sten Cornelissen, Senno Verhoef, Peter A. Fasching, Matthias W. Beckmann, Arif B. Ekici, Dennis J. Slamon, Stig E. Bojesen, Børge G. Nordestgaard, Sune F. Nielsen, Henrik Flyger, Jenny Chang‐Claude, Dieter Flesch‐Janys, Anja Rudolph, Petra Seibold, Kristiina Aittomäki, Taru Muranen, Päivi Heikkilä, Carl Blomqvist, Jonine D. Figueroa, Stephen J. Chanock, Louise A. Brinton
Publicat 2014Artigo
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Matèries relacionades
Biology
Gene
Medicine
Genetics
Cancer
Breast cancer
Internal medicine
Oncology
Mutation
Genotype
Germline mutation
Pathology
Single-nucleotide polymorphism
Cancer research
Environmental health
Phenotype
Population
Tuberous sclerosis
Allele
Apoptosis
Clinical psychology
Computational biology
Computer science
Disease
Estrogen receptor
Genetic association
Genome
Genome-wide association study
Li–Fraumeni syndrome
PI3K/AKT/mTOR pathway