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14 results for van+Hest,+Liselotte+P

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Germ-line and somatic DICER1 mutations in pineoblastoma
Author / Creator:de Kock, Leanne ; Sabbaghian, Nelly ; Druker, Harriet ; Weber, Evan ; Hamel, Nancy ; Miller, Suzanne ; Choong, Catherine S. ; Gottardo, Nicholas G. ; Kees, Ursula R. ; Rednam, Surya P. ; van Hest, Liselotte P. ; Jongmans, Marjolijn C. ; Jhangiani, Shalini ; Lupski, James R. ; Zacharin, Margaret ; Bouron-Dal Soglio, Dorothée ; Huang, Annie ; Priest, John R. ; Perry, Arie ; Mueller, Sabine ; Albrecht, Steffen ; Malkin, David ; Grundy, Richard G. ; Foulkes, William D.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Acta neuropathologica, 2014-10, Vol.128 (4), p.583-595
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First estimates of diffuse gastric cancer risks for carriers of CTNNA1 germline pathogenic variants
Author / Creator:Coudert, Marie ; Drouet, Youenn ; Delhomelle, Hélène ; Svrcek, Magali ; Benusiglio, Patrick R ; Coulet, Florence ; Clark, Dana Farengo ; Katona, Bryson W ; van Hest, Liselotte P ; van der Kolk, Lizet E ; Cats, Annemieke ; van Dieren, Jolanda M ; Nehoray, Bita ; Slavin, Thomas ; Spier, Isabel ; Hüneburg, Robert ; Lobo, Silvana ; Oliveira, Carla ; Boussemart, Lise ; Masson, Laure ; Chiesa, Jean ; Schwartz, Mathias ; Buecher, Bruno ; Golmard, Lisa ; Bouvier, Anne-Marie ; Bonadona, Valérie ; Stoppa-lyonnet, Dominique ; Lasset, Christine ; Colas, Chrystelle
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2022-12, Vol.59 (12), p.1189-1195
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Increased colorectal cancer risk during follow-up in patients with hyperplastic polyposis syndrome: a multicentre cohort study
Author / Creator:Boparai, Karam S ; Mathus-Vliegen, Elisabeth M H ; Koornstra, Jan J ; Nagengast, Fokko M ; van Leerdam, Monique ; van Noesel, Carel J M ; Houben, Martin ; Cats, Annemieke ; van Hest, Liselotte P ; Fockens, Paul ; Dekker, Evelien
Publisher:London: BMJ Publishing Group Ltd and British Society of Gastroenterology
Journal title:Gut, 2010-08, Vol.59 (8), p.1094-1100
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Families with BAP1-Tumor Predisposition Syndrome in The Netherlands: Path to Identification and a Proposal for Genetic Screening Guidelines
Author / Creator:Chau, Cindy ; van Doorn, Remco ; van Poppelen, Natasha M ; van der Stoep, Nienke ; Mensenkamp, Arjen R ; Sijmons, Rolf H ; van Paassen, Barbara W ; van den Ouweland, Ans M W ; Naus, Nicole C ; van der Hout, Annemieke H ; Potjer, Thomas P ; Bleeker, Fonnet E ; Wevers, Marijke R ; van Hest, Liselotte P ; Jongmans, Marjolijn C J ; Marinkovic, Marina ; Bleeker, Jaco C ; Jager, Martine J ; Luyten, Gregorius P M ; Nielsen, Maartje
Publisher:Switzerland: MDPI AG
Journal title:Cancers, 2019-08, Vol.11 (8), p.1114
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Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing
Author / Creator:Vogelaar, Ingrid P ; van der Post, Rachel S ; van Krieken, J Han Jm ; Spruijt, Liesbeth ; van Zelst-Stams, Wendy Ag ; Kets, C Marleen ; Lubinski, Jan ; Jakubowska, Anna ; Teodorczyk, Urszula ; Aalfs, Cora M ; van Hest, Liselotte P ; Pinheiro, Hugo ; Oliveira, Carla ; Jhangiani, Shalini N ; Muzny, Donna M ; Gibbs, Richard A ; Lupski, James R ; de Ligt, Joep ; Vissers, Lisenka E L M ; Hoischen, Alexander ; Gilissen, Christian ; van de Vorst, Maartje ; Goeman, Jelle J ; Schackert, Hans K ; Ranzani, Guglielmina N ; Molinaro, Valeria ; Gómez García, Encarna B ; Hes, Frederik J ; Holinski-Feder, Elke ; Genuardi, Maurizio ; Ausems, Margreet G E M ; Sijmons, Rolf H ; Wagner, Anja ; van der Kolk, Lizet E ; Bjørnevoll, Inga ; Høberg-Vetti, Hildegunn ; van Kessel, Ad Geurts ; Kuiper, Roland P ; Ligtenberg, Marjolijn J L ; Hoogerbrugge, Nicoline
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2017-11, Vol.25 (11), p.1246-1252
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Functional analysis of MSH2 unclassified variants found in suspected Lynch syndrome patients reveals pathogenicity due to attenuated mismatch repair
Author / Creator:Wielders, Eva AL ; Hettinger, Jan ; Dekker, Rob ; Kets, C Marleen ; Ligtenberg, Marjolijn J ; Mensenkamp, Arjen R ; van den Ouweland, Ans MW ; Prins, Judith ; Wagner, Anja ; Dinjens, Winand NM ; Dubbink, Hendrikus Jan ; van Hest, Liselotte P ; Menko, Fred ; Hogervorst, Frans ; Verhoef, Senno ; te Riele, Hein
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2014-04, Vol.51 (4), p.245-253
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Two TP53 germline mutations in a classical Li-Fraumeni syndrome family
Author / Creator:van Hest, Liselotte P ; Ruijs, Mariëlle W G ; Wagner, Anja ; van der Meer, Conny A ; Verhoef, Senno ; van't Veer, Laura J ; Meijers-Heijboer, Hanne
Publisher:Netherlands: Springer Nature B.V
Journal title:Familial cancer, 2007-01, Vol.6 (3), p.311-316
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The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
Author / Creator:Lakeman, Inge M. M. ; Vos, Juliën A. M. ; Barnes, Daniel R. ; Adlard, Julian ; Andrulis, Irene L. ; Arason, Adalgeir ; Arnold, Norbert ; Arun, Banu K. ; Balmaña, Judith ; Barrowdale, Daniel ; Benitez, Javier ; Borg, Ake ; Caldés, Trinidad ; Caligo, Maria A. ; Chung, Wendy K. ; Claes, Kathleen B. M. ; Collée, J. Margriet ; Couch, Fergus J. ; Daly, Mary B. ; Dennis, Joe ; Dhawan, Mallika ; Domchek, Susan M. ; Eeles, Ros ; Engel, Christoph ; Evans, D. Gareth ; Feliubadaló, Lidia ; Foretova, Lenka ; Friedman, Eitan ; Frost, Debra ; Ganz, Patricia A. ; Gayther, Simon A. ; Gerdes, Anne-Marie ; Godwin, Andrew K. ; Goldgar, David E. ; Hahnen, Eric ; Hake, Christopher R. ; Hamann, Ute ; Hogervorst, Frans B. L. ; Hooning, Maartje J. ; Hopper, John L. ; Hulick, Peter J. ; Imyanitov, Evgeny N. ; Isaacs, Claudine ; Izatt, Louise ; Jakubowska, Anna ; James, Paul A. ; Janavicius, Ramunas ; Jensen, Uffe Birk ; Jiao, Yue ; John, Esther M. ; Karlan, Beth Y. ; Kets, Carolien M. ; Kwong, Ava ; Legrand, Clémentine ; Leslie, Goska ; Lesueur, Fabienne ; Loud, Jennifer T. ; Manoukian, Siranoush ; McGuffog, Lesley ; Miller, Austin ; Gomes, Denise Molina ; Montagna, Marco ; Mouret-Fourme, Emmanuelle ; Neuhausen, Susan L. ; Nevanlinna, Heli ; Yie, Joanne Ngeow Yuen ; Olah, Edith ; Olopade, Olufunmilayo I. ; Park, Sue K. ; Parsons, Michael T. ; Peterlongo, Paolo ; Radice, Paolo ; Rantala, Johanna ; Rennert, Gad ; Schmutzler, Rita K. ; Sharma, Priyanka ; Simard, Jacques ; Singer, Christian F. ; Stadler, Zsofia ; Stoppa-Lyonnet, Dominique ; Sutter, Christian ; Tan, Yen Yen ; Teixeira, Manuel R. ; Teo, Soo Hwang ; Teulé, Alex ; Thomassen, Mads ; Thull, Darcy L. ; Tischkowitz, Marc ; Toland, Amanda E. ; Tung, Nadine ; Vega, Ana ; Wappenschmidt, Barbara ; Devilee, Peter ; van Asperen, Christi J. ; Bernstein, Jonine L. ; Offit, Kenneth ; Easton, Douglas F. ; Rookus, Matti A. ; Chenevix-Trench, Georgia ; Schmidt, Marjanka K.
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2021-09, Vol.23 (9), p.1726-1737
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ArticlesPeer ReviewedFull Text
Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility
Author / Creator:Weren, Robbert D A ; van der Post, Rachel S ; Vogelaar, Ingrid P ; van Krieken, J Han ; Spruijt, Liesbeth ; Lubinski, Jan ; Jakubowska, Anna ; Teodorczyk, Urszula ; Aalfs, Cora M ; van Hest, Liselotte P ; Oliveira, Carla ; Kamping, Eveline J ; Schackert, Hans K ; Ranzani, Guglielmina N ; Gómez García, Encarna B ; Hes, Frederik J ; Holinski-Feder, Elke ; Genuardi, Maurizio ; Ausems, Margreet G E M ; Sijmons, Rolf H ; Wagner, Anja ; van der Kolk, Lizet E ; Cats, Annemieke ; Bjørnevoll, Inga ; Hoogerbrugge, Nicoline ; Ligtenberg, Marjolijn J L
Publisher:England: BMJ Publishing Group LTD
Journal title:Journal of medical genetics, 2018-10, Vol.55 (10), p.669-674
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PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients
Author / Creator:Giardiello, Daniele ; Hooning, Maartje J ; Hauptmann, Michael ; Keeman, Renske ; Heemskerk-Gerritsen, B A M ; Becher, Heiko ; Blomqvist, Carl ; Bojesen, Stig E ; Bolla, Manjeet K ; Camp, Nicola J ; Czene, Kamila ; Devilee, Peter ; Eccles, Diana M ; Fasching, Peter A ; Figueroa, Jonine D ; Flyger, Henrik ; García-Closas, Montserrat ; Haiman, Christopher A ; Hamann, Ute ; Hopper, John L ; Jakubowska, Anna ; Leeuwen, Floor E ; Lindblom, Annika ; Lubiński, Jan ; Margolin, Sara ; Martinez, Maria Elena ; Nevanlinna, Heli ; Nevelsteen, Ines ; Pelders, Saskia ; Pharoah, Paul D P ; Siesling, Sabine ; Southey, Melissa C ; van der Hout, Annemieke H ; van Hest, Liselotte P ; Chang-Claude, Jenny ; Hall, Per ; Easton, Douglas F ; Steyerberg, Ewout W ; Schmidt, Marjanka K
Publisher:England: BioMed Central Ltd
Journal title:Breast cancer research : BCR, 2022-10, Vol.24 (1), p.69-69, Article 69
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PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ∼ 200,000 patients (vol 24, 69, 2022)
Author / Creator:Giardiello, D ; Hooning, MJ ; Hauptmann, M ; Keeman, R ; Heemskerk-Gerritsen, BAM ; Becher, H ; Blomqvist, C ; Bojesen, SE ; Bolla, MK ; Camp, NJ
Journal title:BREAST CANCER RESEARCH, 2022-11, Vol.24 (1)
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Correction: PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients
Author / Creator:Giardiello, Daniele ; Hooning, Maartje J ; Hauptmann, Michael ; Keeman, Renske ; Heemskerk-Gerritsen, B A M ; Becher, Heiko ; Blomqvist, Carl ; Bojesen, Stig E ; Bolla, Manjeet K ; Camp, Nicola J ; Czene, Kamila ; Devilee, Peter ; Eccles, Diana M ; Fasching, Peter A ; Figueroa, Jonine D ; Flyger, Henrik ; García-Closas, Montserrat ; Haiman, Christopher A ; Hamann, Ute ; Hopper, John L ; Jakubowska, Anna ; Leeuwen, Floor E ; Lindblom, Annika ; Lubiński, Jan ; Margolin, Sara ; Martinez, Maria Elena ; Nevanlinna, Heli ; Nevelsteen, Ines ; Pelders, Saskia ; Pharoah, Paul D P ; Siesling, Sabine ; Southey, Melissa C ; van der Hout, Annemieke H ; van Hest, Liselotte P ; Chang-Claude, Jenny ; Hall, Per ; Easton, Douglas F ; Steyerberg, Ewout W ; Schmidt, Marjanka K
Publisher:England: BioMed Central Ltd
Journal title:Breast cancer research : BCR, 2022-11, Vol.24 (1), p.82-82, Article 82
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Germ-line and somatic D1CER1 mutations in pineoblastoma
Author / Creator:de Kock, Leanne ; Sabbaghian, Nelly ; Druker, Harriet ; Weber, Evan ; Hamel, Nancy ; Miller, Suzanne ; Choong, Catherine S ; Gottardo, Nicholas G ; Kees, Ursula R ; Rednam, Surya P ; van Hest, Liselotte P ; Jongmans, Marjolijn C ; Jhangiani, Shalini ; Lupski, James R ; Zacharin, Margaret ; Soglio, Dorothee Bouron-Dal ; Huang, Annie ; Priest, John R ; Perry, Arie ; Mueller, Sabine ; Albrecht, Steffen ; Malkin, David ; Grundy, Richard G ; Foulkes, William D
Publisher:Springer
Journal title:Acta neuropathologica, 2014-10, Vol.128 (4), p.583
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Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect
Author / Creator:Vogelaar, Ingrid P. ; Ligtenberg, Marjolijn J. L. ; van der Post, Rachel S. ; de Voer, Richarda M. ; Kets, C. Marleen ; Jansen, Trees J. G. ; Jacobs, Liesbeth ; Schreibelt, Gerty ; de Vries, I. Jolanda M. ; Netea, Mihai G. ; Hoogerbrugge, Nicoline
Publisher:Dordrecht: Springer Netherlands
Journal title:Familial cancer, 2016-04, Vol.15 (2), p.289-296
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Germ-line and somatic DICER1 mutations in pineoblastoma

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First estimates of diffuse gastric cancer risks for carriers of CTNNA1 germline pathogenic variants

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Increased colorectal cancer risk during follow-up in patients with hyperplastic polyposis syndrome: a multicentre cohort study

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Families with BAP1-Tumor Predisposition Syndrome in The Netherlands: Path to Identification and a Proposal for Genetic Screening Guidelines

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Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing

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Functional analysis of MSH2 unclassified variants found in suspected Lynch syndrome patients reveals pathogenicity due to attenuated mismatch repair

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Two TP53 germline mutations in a classical Li-Fraumeni syndrome family

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The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

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Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility

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PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients

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PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ∼ 200,000 patients (vol 24, 69, 2022)

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Correction: PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients

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Germ-line and somatic D1CER1 mutations in pineoblastoma

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Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect

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