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Published in European journal of human genetics : EJHG (01.05.2021)
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Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants
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Published in Proceedings of the National Academy of Sciences - PNAS (12.04.2016)
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Published in European journal of human genetics : EJHG (01.06.2005)
Published in European journal of human genetics : EJHG (01.06.2005)
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‘We don’t know for sure’: discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations
Medendorp, Niki M., Hillen, Marij A., van Maarschalkerweerd, Pomme E. A., Aalfs, Cora M., Ausems, Margreet G. E. M., Verhoef, Senno, van der Kolk, Lizet E., Berger, Lieke P. V., Wevers, Marijke R., Wagner, Anja, Caanen, Barbara A. H., Stiggelbout, Anne M., Smets, Ellen M. A.
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Genetic Testing in Li-Fraumeni Syndrome: Uptake and Psychosocial Consequences
LAMMENS, Chantal R. M, AARONSON, Neil K, KLUIJT, Irma, NAGTEGAAL, Tanja, VERHOEF, Senno, BLEIKER, Eveline M. A, WAGNER, Anja, SIJMONS, Rolf H, AUSEMS, Margreet G. E. M, VRIENDS, Annette H. J. T, RUIJS, Mariëlle W. G, VAN OS, Theo A. M, SPRUIJT, Liesbeth, GOMEZ GARCIA, Encarna B
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Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome
Wijnen, Juul T, Brohet, Richard M, van Eijk, Ronald, Jagmohan-Changur, Shanty, Middeldorp, Anneke, Tops, Carli M, van Puijenbroek, Mario, Ausems, Margreet G E M, Gómez García, Encarna, Hes, Frederik J, Hoogerbrugge, Nicoline, Menko, Fred H, van Os, Theo A M, Sijmons, Rolf H, Verhoef, Senno, Wagner, Anja, Nagengast, Fokko M, Kleibeuker, Jan H, Devilee, Peter, Morreau, Hans, Goldgar, David, Tomlinson, Ian P, Houlston, Richard S, van Wezel, Tom, Vasen, Hans F A
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Published in Gastroenterology (New York, N.Y. 1943) (01.01.2009)
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The single-nucleotide polymorphism 309 in the MDM2 gene contributes to the Li -Fraumeni syndrome and related phenotypes
RUIJS, Mariëlle W. G, SCHMIDT, Marjanka K, NEVANLINNA, Heli, TOMMISKA, Johanna, AITTOMÄKI, Kristiina, PRUNTEL, Roelof, VERHOEF, Senno, VAN'T VEER, Laura J
Published in European journal of human genetics : EJHG (01.01.2007)
Published in European journal of human genetics : EJHG (01.01.2007)
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Behavioral and psychosocial effects of rapid genetic counseling and testing in newly diagnosed breast cancer patients: design of a multicenter randomized clinical trial
Wevers, Marijke R, Ausems, Margreet G E M, Verhoef, Senno, Bleiker, Eveline M A, Hahn, Daniela E E, Hogervorst, Frans B L, van der Luijt, Rob B, Valdimarsdottir, Heiddis B, van Hillegersberg, Richard, Rutgers, Emiel J T H, Aaronson, Neil K
Published in BMC cancer (10.01.2011)
Published in BMC cancer (10.01.2011)
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High Rate of Mosaicism in Tuberous Sclerosis Complex
Verhoef, Senno, Bakker, Lida, Tempelaars, Anita M.P., Hesseling-Janssen, Arjenne L.W., Mazurczak, Tadeusz, Jozwiak, Sergiusz, Fois, Alberto, Bartalini, Gabriella, Zonnenberg, Bernard A., van Essen, Anthonie J., Lindhout, Dick, Halley, Dicky J.J., van den Ouweland, Ans M.W.
Published in American journal of human genetics (01.06.1999)
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Molecular characterization of novel germline deletions affecting SDHD and SDHC in pheochromocytoma and paraganglioma patients
Bayley, Jean-Pierre, Weiss, Marjan M, Grimbergen, Anneliese, van Brussel, Bernadette T J, Hes, Frederik J, Jansen, Jeroen C, Verhoef, Senno, Devilee, Peter, Corssmit, Eleonora P, Vriends, Annette H J T
Published in Endocrine-related cancer (01.09.2009)
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The contribution of CHEK2 to the TP53-negative Li-Fraumeni phenotype
Ruijs, Marielle W G, Broeks, Annegien, Menko, Fred H, Ausems, Margreet G E M, Wagner, Anja, Oldenburg, Rogier, Meijers-Heijboer, Hanne, van't Veer, Laura J, Verhoef, Senno
Published in Hereditary cancer in clinical practice (17.02.2009)
Published in Hereditary cancer in clinical practice (17.02.2009)
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Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer
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Published in JAMA : the journal of the American Medical Association (07.04.2015)
Published in JAMA : the journal of the American Medical Association (07.04.2015)
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Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Beesley, Jonathan, Canisius, Sander, Shah, Mitul, Czene, Kamila, Nordestgaard, Børge G, Flyger, Henrik, Nielsen, Sune F, Rahman, Nazneen, Fletcher, Olivia, Rudolph, Anja, Behrens, Sabine, Aaltonen, Kirsimari, Ahsan, Habibul, Kibriya, Muhammad G, John, Esther M, Santella, Regina M, Makalic, Enes, Casey, Graham, Haiman, Christopher A, Schumacher, Fredrick, Le Marchand, Loic, Berg, Christine D, Chanock, Stephen J, Hoover, Robert N, Cornelissen, Sten, Olson, Janet E, Hallberg, Emily, Waisfisz, Quinten, van der Luijt, Rob B, Liu, Jianjun, Kang, Daehee, Choi, Ji-Yeob, Matsuo, Keitaro, Iwata, Hiroji, Guénel, Pascal, Truong, Thérèse, Mulot, Claire, Surowy, Harald, Sohn, Christof, Wu, Anna H, Van Den Berg, David, Stram, Daniel O, González-Neira, Anna, Zamora, M Pilar, Perez, Jose Ignacio Arias, Gao, Yu-Tang, Cox, Angela, Cross, Simon S, Andrulis, Irene L, Knight, Julia A, Kerin, Michael J, Miller, Nicola, Margolin, Sara, Taib, Nur Aishah Mohd, Tan, Gie-Hooi, Hollestelle, Antoinette, Martens, John W M, Collée, J Margriet, Signorello, Lisa B, Cai, Qiuyin, Tsimiklis, Helen, Apicella, Carmel, Shen, Chen-Yang, Hsiung, Chia-Ni, Wu, Pei-Ei, Hou, Ming-Feng, Kristensen, Vessela N, Nord, Silje, Giles, Graham G, McLean, Catriona, Peeters, Petra, Yang, Rongxi, Muir, Kenneth, Stewart-Brown, Sarah, Hartman, Mikael, Hein, Alexander, Beckmann, Matthias W, Brenner, Hermann, Dieffenbach, Aida Karina, Arndt, Volker, Stegmaier, Christa, Garcia-Closas, Montserrat, Zheng, Wei, Goldberg, Mark S, Grip, Mervi, Bernard, Loris, Bogdanova, Natalia V, Dörk, Thilo, Kosma, Veli-Matti, Hartikainen, Jaana M, Tollenaar, Robert A E M, Seynaeve, Caroline, Ambrosone, Christine B, Kabisch, Maria, Neuhausen, Susan L, Anton-Culver, Hoda, Baynes, Caroline, Ahmed, Shahana, Tessier, Daniel C, Herrero, Daniel
Published in Nature genetics (01.04.2015)
Published in Nature genetics (01.04.2015)
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Prediction of breast cancer risk based on profiling with common genetic variants
Brook, Mark N, Bolla, Manjeet K, Dennis, Joe, Dunning, Alison M, Bojesen, Stig E, Nordestgaard, Børge G, Nielsen, Sune F, Darabi, Hatef, Johnson, Nichola, Broeks, Annegien, Verhoef, Senno, Rutgers, Emiel J, Schoemaker, Minouk J, Figueroa, Jonine, Brinton, Louise, Olson, Janet E, Lambrechts, Diether, Wildiers, Hans, Van Ongeval, Chantal, van Limbergen, Erik, Grenaker Alnæs, Grethe, Nevanlinna, Heli, Fasching, Peter A, Haeberle, Lothar, Beckmann, Matthias W, Newcomb, Polly, Titus, Linda, Egan, Kathleen M, Tamimi, Rulla M, Kraft, Peter, Renwick, Anthony, Seal, Sheila, Humphreys, Keith, Jakubowska, Anna, Lubinski, Jan, Antonenkova, Natalia N, Anton-Culver, Hoda, Neuhausen, Susan L, Seynaeve, Caroline, Cox, Angela, Reed, Malcolm W R, Khusnutdinova, Elza, Bermisheva, Marina, Prokofyeva, Darya, Takhirova, Zalina, Meindl, Alfons, Sutter, Christian, Schürmann, Peter, Bremer, Michael, Park-Simon, Tjoung-Won, Hillemanns, Peter, Guénel, Pascal, Truong, Thérèse, Menegaux, Florence, Peterlongo, Paolo, Manoukian, Siranoush, Hopper, John L, Apicella, Carmel, Ulmer, Hans-Ulrich, Försti, Asta, Chenevix-Trench, Georgia, Balleine, Rosemary, Milne, Roger L, McLean, Catriona, Margolin, Sara, Henderson, Brian E, Schumacher, Fredrick, Le Marchand, Loic, Wang-Gohrke, Shan, Hooning, Maartje J, Hollestelle, Antoinette, Clarke, Christine, Scott, Rodney, Kataja, Vesa, Kosma, Veli-Matti, Hartikainen, Jaana M, Arndt, Volker, Stegmaier, Christa, Karina Dieffenbach, Aida, Winqvist, Robert, Grip, Mervi, Robson, Mark, Rau-Murthy, Rohini, Dwek, Miriam, Annie Perkins, Katherine, Labrèche, France, Dumont, Martine, John, Esther M, Slager, Susan, Toland, Amanda E, Zheng, Wei, González-Neira, Anna, Pita, Guillermo, Tessier, Daniel C, Vincent, Daniel, Bacot, Francois, Luccarini, Craig, Ahmed, Shahana, Hall, Per, Easton, Douglas F
Published in JNCI : Journal of the National Cancer Institute (01.05.2015)
Published in JNCI : Journal of the National Cancer Institute (01.05.2015)
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PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
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Published in Journal of medical genetics (01.12.2016)
Published in Journal of medical genetics (01.12.2016)
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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Aittomäki, Kristiina, Anton-Culver, Hoda, Arndt, Volker, Aronson, Kristan J, Arun, Banu K, Azzollini, Jacopo, Barnes, Daniel R, Beckmann, Matthias W, Bermisheva, Marina, Białkowska, Katarzyna, Blomqvist, Carl, Bolla, Manjeet K, Borg, Ake, Campbell, Ian, Carter, Jonathan, Chang-Claude, Jenny, Chanock, Stephen J, Christiansen, Hans, Couch, Fergus J, Dennis, Joe, Diez, Orland, Dunning, Alison M, Ejlertsen, Bent, Fasching, Peter A, Fletcher, Olivia, Flyger, Henrik, Friedman, Eitan, Frost, Debra, Gago-Dominguez, Manuela, Glendon, Gord, Goldgar, David E, González-Neira, Anna, Greene, Mark H, Guénel, Pascal, Hollestelle, Antoinette, Hoover, Robert N, Hopper, John L, Imyanitov, Evgeny N, Isaacs, Claudine, Jakimovska, Milena, Janavicius, Ramunas, Joseph, Vijai, Khusnutdinova, Elza, Ko, Yon-Dschun, Konstantopoulou, Irene, Lambrechts, Diether, Lazaro, Conxi, Leslie, Goska, Lesueur, Fabienne, Long, Jirong, Lubiński, Jan, Makalic, Enes, Mannermaa, Arto, Margolin, Sara, Maurer, Tabea, Mavroudis, Dimitrios, Meindl, Alfons, Menon, Usha, Michailidou, Kyriaki, Montagna, Marco, Moserle, Lidia, Mulligan, Anna Marie, Nevanlinna, Heli, Nevelsteen, Ines, Olsson, Håkan, Osorio, Ana, Park-Simon, Tjoung-Won, Parsons, Michael T, Pedersen, Inge Sokilde, Peixoto, Ana, Plaseska-Karanfilska, Dijana, Poppe, Bruce, Radice, Paolo, Rantala, Johanna, Rennert, Gad, Saloustros, Emmanouil, Schmutzler, Rita K, Simard, Jacques, Spurdle, Amanda B, Stone, Jennifer, Swerdlow, Anthony J, Tapper, William J, Teixeira, Manuel R, Teulé, Alex, Thomassen, Mads, Thöne, Kathrin, Tischkowitz, Marc, Toland, Amanda E, Truong, Thérèse, Tung, Nadine, Vachon, Celine M, van Rensburg, Elizabeth J, Viel, Alessandra, Wang, Qin, Wappenschmidt, Barbara, Weitzel, Jeffrey N, Winqvist, Robert, Kraft, Peter, Milne, Roger L, Beesley, Jonathan
Published in Nature communications (15.04.2019)
Published in Nature communications (15.04.2019)
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Withdrawal from genetic counselling for cancer
Bleiker, Eveline, Wigbout, Gea, van Rens, Anja, Verhoef, Senno, Van't Veer, Laura, Aaronson, Neil
Published in Hereditary cancer in clinical practice (15.02.2005)
Published in Hereditary cancer in clinical practice (15.02.2005)
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A multicentre comparative prospective blinded analysis of EUS and MRI for screening of pancreatic cancer in high-risk individuals
Harinck, F, Konings, I C A W, Kluijt, I, Poley, J W, van Hooft, J E, van Dullemen, H M, Nio, C Y, Krak, N C, Hermans, J J, Aalfs, C M, Wagner, A, Sijmons, R H, Biermann, K, van Eijck, C H, Gouma, D J, Dijkgraaf, M G W, Fockens, P, Bruno, M J
Published in Gut (01.09.2016)
Published in Gut (01.09.2016)
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Somatic mosaicism and clinical variation in tuberous sclerosis complex
Verhoef, Senno, Vrtel, Radek, van Essen, Ton, Bakker, Lida, Sikkens, Ewold, Halley, Dicky, Lindhout, Dick, van den Ouweland, Ans
Published in The Lancet (British edition) (21.01.1995)
Published in The Lancet (British edition) (21.01.1995)
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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk
Couch, Fergus J, Soucy, Penny, Dicks, Ed, Sinilnikova, Olga M, Bacot, François, Vincent, Daniel, Hogervorst, Frans B L, Peock, Susan, Radice, Paolo, Singer, Christian F, Friedman, Eitan, Hansen, Thomas V O, Neuhausen, Susan L, Blanco, Ignacio, Greene, Mark H, Karlan, Beth Y, Montagna, Marco, Godwin, Andrew K, Caldes, Trinidad, van Rensburg, Elizabeth J, Olopade, Olufunmilayo I, Southey, Melissa C, Kwong, Ava, Diez, Orland, Rennert, Gad, Seynaeve, Caroline, Rookus, Matti A, Verhoef, Senno, Wijnen, Juul T, Frost, Debra, Fineberg, Elena, Eccles, Diana M, Douglas, Fiona, Morrison, Patrick J, Rogers, Mark T, Gregory, Helen, McCann, Emma, Murray, Alex, Calender, Alain, Berthet, Pascaline, Lasset, Christine, Rouleau, Etienne, Damiola, Francesca, Sobol, Hagay, Gauthier-Villars, Marion, Lubinski, Jan, Jaworska, Katarzyna, Spurdle, Amanda B, Bonanni, Bernardo, Ottini, Laura, Papi, Laura, Volorio, Sara, Pensotti, Valeria, Arnold, Norbert, Gehrig, Andrea, Kast, Karin, Meindl, Alfons, Ditsch, Nina, Plendl, Hansjoerg, Varon-Mateeva, Raymonda, Weber, Bernhard H F, Arver, Brita, Rosenquist, Richard, Cohn, David E, Small, Laurie, Friedlander, Michael, Fink-Retter, Anneliese, Rappaport, Christine, Gschwantler-Kaulich, Daphne, Pfeiler, Georg, Lindor, Noralane M, Kaufman, Bella, Gerdes, Anne-Marie, Moeller, Sanne Traasdahl, Kruse, Torben A, Robson, Mark, Mulligan, Anna Marie, Andersen, Mette K, Steele, Linda, Foretova, Lenka, Lazaro, Conxi, Brunet, Joan, Pujana, Miquel Angel, Mai, Phuong L, Loud, Jennifer T, Lester, Jenny, Sand, Sharon R, Agata, Simona, Weaver, Joellen, Stavropoulou, Alexandra V, Muranen, Taru A, Duran, Mercedes, Lasa, Adriana, Miron, Alexander, Chan, Salina B, Lejbkowicz, Flavio, Wang, Chen, Pastinen, Tomi, Easton, Douglas F, Antoniou, Antonis C
Published in PLoS genetics (2013)
Published in PLoS genetics (2013)
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