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Nicoline Hoogerbrugge

netherlands cancer institute

72H指数
435论文数
1.8W被引数
收录论文 158
发表时间
ERN GENTURIS cancer surveillance guideline for individuals with PTEN hamartoma tumour syndrome (PHTS)ERNGENTURIS癌症监测指南:针对PTEN错构瘤肿瘤综合征(PHTS)个体的监测指南
err2026-07-16
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PREAI
errNicoline Hoogerbrugge; Ana Blatnik; Charlotte Kvist Lautrup; Robert Hüneburg; Daniela Turchetti; Anne van Altena; Frédéric Caux; Sophie Da Mota Gomes; Kelly Kearley; Chella RS van der Post; Alex Teulé; Jolanda Schieving; Inga-Lena Nilsson; Ritse Mann; Per-Olof Lundgren; Thera Links; Emma Tham; Sjaak Pouwels; Marc Tischkowitz
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Hereditary cancer: Germline testing practices across ERN GENTURIS member countries遗传性癌症:ERN GENTURIS成员国中的生殖细胞系检测实践
err2026-06-09
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errOAAI
errMilena Kiljańczyk; Zanda Daneberga; Mikk Tooming; Katarzyna Urbańczyk; Minna Pöyhönen; Tiina Kahre; Lenka Foretova; Emma Tham; Tamara Milagre; Béla Melegh; Maria K. Haanpää; Ana Blatnik; Katharina Wimmer; Robin de Putter; Karin Wadt; Claude Houdayer; Elke Holinski-Feder; Antonis Kattamis; Barbara Klink; Hildegunn Høberg-Vetti; Ignacio Blanco Guillermo; Nicoline Hoogerbrugge; Jan Lubiński
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Personalized risk estimates of advanced neoplasia development in individuals with a family history of colorectal cancer具有结直肠癌家族史个体的进展性新生物发展个性化风险估计
err2026-05-14
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errOAAI
errGreuter, Marjolein J. E.; Akwiwu, Eddymurphy U.; Hennink, Simone D.; Bisseling, Tanya M.; Spanier, Marcel B. W.; Nagtegaal, Iris D.; Canfell, Karen; Dekker, Evelien; Klausch, Thomas; Lansdorp-Vogelaar, Iris; van Leerdam, Monique E.; Hoogerbrugge, Nicoline; Coupe, Veerle M. H.
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Breast cancer germline multigene panel testing in mainstream oncology based on clinical–public health utility: ESMO Precision Oncology Working Group recommendations基于临床-公共卫生效用的主流肿瘤学中乳腺癌胚系多基因-panel检测:ESMO精准肿瘤学工作组建议
err2025-06-15
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PREAI
errC. Turnbull; M.I. Achatz; J. Balmaña; E. Castro; G. Curigliano; C. Cybulski; S.M. Domchek; D.G. Evans; H. Hanson; N. Hoogerbrugge; P.A. James; A. Krause; K.L. Nathanson; J. Ngeow Yuen Yie; M. Robson; M. Tischkowitz; B. Westphalen; W.D. Foulkes
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The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS)PTEN错构瘤综合征(PHTS)中第二原发癌的风险
err2025-05-24
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errOAAI
errLinda A.J. Hendricks; Katja C.J. Verbeek; Janneke H.M. Schuurs-Hoeijmakers; Mirjam M. de Jong; Thera P. Links; Hilde Brems; Mio Aerden; Joan Brunet; Roser Lleuger-Pujol; Robert Hüneburg; Stefan Aretz; Chrystelle Colas; Marie-Charlotte Villy; Emma R. Woodward; D. Gareth Evans; Daniëlle G.M. Bosch; Stephany H. Donze; Lenka Foretová; Ana Blatnik; Edward M. Leter; Marc Tischkowitz; Arne Jahn; Robin de Putter; Juliette Dupont; Siri Briskemyr; Verena Steinke-Lange; Margherita Baldassarri; Violetta C. Anastasiadou; Arvīds Irmejs; Carla Oliveira; Rachel S. van der Post; Arjen R. Mensenkamp; Bianca Tesi; Ninni Mu; Patrick R. Benusiglio; Anna Gerasimenko; Giovanni Innella; Daniela Turchetti; Claude Houdayer; Maud Branchaud; Hildegunn Høberg Vetti; Marianne Tveit Haavind; Judith Balmaña; Maite Torres; Maurizio Genuardi; Arianna Panfili; Kjersti Jørgensen; Lovise Mæhle; Nicoline Hoogerbrugge; Janet R. Vos
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Unraveling mutagenic processes influencing the tumor mutational patterns of individuals with constitutional mismatch repair deficiency解析影响常染色体错配修复缺陷个体肿瘤突变模式的致突变过程
err2025-05-14
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errOAAI
errWeijers, Dilys D.; Hinic, Snezana; Kroeze, Emma; Gorris, Mark A. J.; Schreibelt, Gerty; Middelkamp, Sjors; Mensenkamp, Arjen R.; Bladergroen, Reno; Verrijp, Kiek; Hoogerbrugge, Nicoline; Wesseling, Pieter; van der Post, Rachel S.; Loeffen, Jan L. C.; Gidding, Corrie E. M.; van Kouwen, Mariette C. A.; de Vries, I. Jolanda M.; van Boxtel, Ruben; de Voer, Richarda M.; Jongmans, Marjolijn C. J.; Kuiper, Roland P.
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Exome-based cancer predisposition gene testing can provide a genetic diagnosis for individuals with heterogeneous tumor phenotypes
err2025-02-20
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errOAAI
errHinic, Snezana; Mensenkamp, Arjen R.; Schuurs-Hoeijmakers, Janneke H. M.; Brugnoletti, Fulvia; Vreede, Lilian; van Veen, Elke M.; Mijzen, Barend; van der Post, Rachel S.; Genuardi, Maurizio; Ligtenberg, Marjolijn J. L.; Hoogerbrugge, Nicoline; de Voer, Richarda M.
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Salpingectomy With Delayed Oophorectomy Versus Salpingo-Oophorectomy in BRCA1/2 Carriers: Three-Year Outcomes of a Prospective Preference Trial输卵管切除联合延迟卵巢切除术与输卵管卵巢联合切除术在BRCA1/2携带者中的比较:一项前瞻性偏好试验的三年结果
err2025-01-17
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errOAAI
errVan Bommel, Majke H. D.; Steenbeek, Miranda P.; Inthout, Joanna; Van Garderen, Tessa; Harmsen, Marline G.; Arts-De Jong, Marieke; Maas, Angela H. E. M.; Prins, Judith B.; Bulten, Johan; Van Doorn, Helena C.; Mourits, Marian J. E.; Tros, Rachel; Zweemer, Ronald P.; Gaarenstroom, Katja N.; Slangen, Brigitte F. M.; Brood-Van Zanten, Monique M. A.; Vos, M. Caroline; Piek, Jurgen M. J.; van Lonkhuijzen, Luc R. C. W.; Apperloo, Mirjam J. A.; Coppus, Sjors F. P. J.; Hoogerbrugge, Nicoline; Hermens, Rosella P. M. G.; De Hullu, Joanne A.
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Exploring the Prevalence of Oral Features for Early Detection of PTEN Hamartoma Tumour Syndrome
err2024-12-01
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errOAAI
errSchei-Andersen, Ane J.; van Oirschot, Bart; Drissen, Meggie M. C. M.; Schieving, Jolanda; Schuurs-Hoeijmakers, Janneke H. M.; Vos, Janet R.; Barton, Claire M.; Hoogerbrugge, Nicoline
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Population-based germline breast cancer gene association studies and meta-analysis to inform wider mainstream testing基于人群的生殖系乳腺癌基因关联研究和荟萃分析,为更广泛的主流检测提供信息
err2024-10-01
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errOAAI
errRowlands, C. F.; Allen, S.; Balmana, J.; Domchek, S. M.; Evans, D. G.; Hanson, H.; Hoogerbrugge, N.; James, P. A.; Nathanson, K. L.; Robson, M.; Tischkowitz, M.; Foulkes, W. D.; Turnbull, C.
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Genomic instability in non-breast or ovarian malignancies of individuals with germline pathogenic variants in BRCA1/2在BRCA1/2中具有种系致病性变异的个体的非乳腺或卵巢恶性肿瘤中的基因组不稳定性
err2024-07-03
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errOAAI
errElze, Lisa; van der Post, Rachel S.; Vos, Janet R.; Mensenkamp, Arjen R.; Naga, Samhita Pamidimarri; Hampstead, Juliet E.; Vermeulen, Emma; Oorsprong, Michiel; Hofste, Tom; Simons, Michiel; Nagtegaal, Iris D.; Hoogerbrugge, Nicoline; de Voer, Richarda M.; Ligtenberg, Marjolijn J. L.
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Model matchmaking via the Solve-RD Rare Disease Models & Mechanisms Network (RDMM-Europe)
err2024-06-24
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errOAAI
errEllwanger, Kornelia; Brill, Julie A.; de Boer, Elke; Efthymiou, Stephanie; Elgersma, Ype; Icmat, Marynelle; Lecoquierre, Francois; Lobato, Amanda G.; Morleo, Manuela; Ori, Michela; Schaffer, Ashleigh E.; Vitobello, Antonio; Wells, Sara; Yalcin, Binnaz; Zhai, R. Grace; Sturm, Marc; Zurek, Birte; Graessner, Holm; Bermejo-Sanchez, Eva; Evangelista, Teresinha; Hoogerbrugge, Nicoline; Nigro, Vincenzo; Schuele, Rebecca; Verloes, Alain; Brunner, Han; Campeau, Philippe M.; Lasko, Paul; Riess, Olaf
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The genomic landscape of breast and non-breast cancers from individuals with germline CHEK2 deficiency
err2024-06-07
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errOAAI
errHinic, Snezana; van der Post, Rachel S.; Vreede, Lilian; Schuurs-Hoeijmakers, Janneke; Koene, Saskia; Jansen, Erik A. M.; Bervoets-Metge, Franziska; Mensenkamp, Arjen R.; Hoogerbrugge, Nicoline; Ligtenberg, Marjolijn J. L.; de Voer, Richarda M.
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The heterogeneous cancer phenotype of individuals with biallelic germline pathogenic variants in CHEK2CHEK2中双等位基因种系致病变异个体的异质性癌症表型
err2024-05-01
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errOAAI
errHinic, Snezana; Cybulski, Cezary; Van der Post, Rachel S.; Vos, Janet R.; Schuurs-Hoeijmakers, Janneke; Brugnoletti, Fulvia; Koene, Saskia; Vreede, Lilian; van Zelst-Stams, Wendy A. G.; Kets, C. Marleen; Haadsma, Maaike; Spruijt, Liesbeth; Wevers, Marijke R.; Evans, D. Gareth; Wimmer, Katharina; Schnaiter, Simon; Volk, Alexander E.; Mollring, Anna; de Putter, Robin; Soikkonen, Leila; Kahre, Tiina; Tooming, Mikk; de Jong, Mirjam M.; Vaz, Fatima; Mensenkamp, Arjen R.; Genuardi, Maurizio; Lubinski, Jan; Ligtenberg, Marjolijn; Hoogerbrugge, Nicoline; de Voer, Richarda M.
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Detection and yield of thyroid cancer surveillance in adults with PTEN hamartoma tumour syndrome
err2023-07-14
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PREAI
errDrissen, Meggie M. C. M.; Vos, Janet R.; Netea-Maier, Romana T.; Gotthardt, Martin; Hoogerbrugge, Nicoline
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Wnt genes in colonic polyposis predisposition
err2023-05-01
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errOAAI
errQuintana, Isabel; Terradas, Mariona; Mur, Pilar; te Paske, Iris B. A. W.; Peters, Sophia; Spier, Isabel; Steinke-Lange, Verena; Maestro, Claudia; Torrents, David; Puiggros, Montserrat; Royo, Romina; Tonda, Raul; Parra, Genis; Piscia, Davide; Beltran, Sergi; Navarro, Matilde; Pinol, Virginia; Brunet, Joan; Gonzalez-Abuin, Noemi; Aiza, Gemma; Sommer, Anna; van Herwaarden, Yasmijn; Astuti, Galuh; Holinski-Feder, Elke; Hoogerbrugge, Nicoline; de Voer, Richarda M.; Aretz, Stefan; Capella, Gabriel; Valle, Laura
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Microsatellite instability in noncolorectal and nonendometrial malignancies in patients with Lynch syndrome
err2023-04-05
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errOAAI
errElze, Lisa; van der Post, Rachel S.; Vos, Janet R.; Mensenkamp, Arjen R.; de Hullu, Mirjam S. C.; Nagtegaal, Iris D.; Hoogerbrugge, Nicoline; de Voer, Richarda M.; Ligtenberg, Marjolijn J. L.
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Noncoding Aberrations in Mismatch Repair Genes Underlie a Substantial Part of the Missing Heritability in Lynch Syndrome
err2022-12-01
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errOAAI
errTe Paske, Iris B. A. W.; Mensenkamp, Arjen R.; Neveling, Kornelia; Hoogerbrugge, Nicoline; Ligtenberg, Marjolijn J. L.; De Voer, Richarda M.
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