Maaike P G Vreeswijk (Mpg Vreeswijk, Maaike Pg Vreeswijk)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 18

Top Venues

Cancers

Journal of medical genetics

Cancer research

Human mutation

Leiden University Medical Center

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Leiden University Medical Center

Netherlands

Assistant Professor :: Human Genetics

Publications

Lise Marit van Wijk, Sylvia Vermeulen, Natalja T Ter Haar, Claire J H Kramer, Diantha Terlouw, Harry Vrieling, Danielle Cohen, Maaike P G Vreeswijk
Performance of a RAD51-based functional HRD test on paraffin-embedded breast cancer tissue. Breast cancer research and treatment (2023)
Claire J H Kramer, Alba Llop-Guevara, Elisa Yaniz-Galende, Benedetta Pellegrino, Natalja T Ter Haar, Andrea Herencia-Ropero, Nicoletta Campanini, Antonino Musolino, Tjalling Bosse, Alexandra Leary, Violeta Serra, Maaike P G Vreeswijk
RAD51 as a biomarker for homologous recombination deficiency in high-grade serous ovarian carcinoma: robustness and interobserver variability of the RAD51 test. The journal of pathology. Clinical research (2023)
Mads Thomassen, Romy L S Mesman, Thomas V O Hansen, Mireia Menendez, Maria Rossing, Ada Esteban-Sánchez, Emma Tudini, Therese Törngren, Michael T Parsons, Inge S Pedersen, Soo H Teo, Torben A Kruse, Pål Møller, Åke Borg, Uffe B Jensen, Lise L Christensen, Christian F Singer, Daniela Muhr, Marta Santamarina, Rita Brandao, Brage Storstein Andresen, Bing-Jian Feng, Daffodil Canson, Marcy E Richardson, Rachid Karam, Tina Pesaran, Holly LaDuca, Blair R Conner, Nelly Abualkheir, Lily Hoang, Fabienne M G R Calléja, Lesley Andrews, Paul A James, Dave Bunyan, Amanda Hamblett, Paolo Radice, David E Goldgar, Logan C Walker, Christoph Engel, Kathleen B M Claes, Eva Macháčková, Htoo Aung Wai, Alessandra Viel, Barbara Wappenschmidt, Conxi Lazaro, Ana Vega, null null, Maaike P G Vreeswijk, Miguel de la Hoya, Amanda B Spurdle
Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants: Application of a points-based ACMG/AMP approach. Human mutation (2022)
Rick A C M Boonen, Wouter W Wiegant, Nandi Celosse, Bas Vroling, Stephan Heijl, Zsofia Kote-Jarai, Martina Mijuskovic, Simona Cristea, Nienke Solleveld-Westerink, J Tom van Wezel, Niko Beerenwinkel, Rosalind A Eeles, Peter Devilee, Maaike P G Vreeswijk, Giancarlo Marra, Haico van Attikum
Functional Analysis Identifies Damaging CHEK2 Missense Variants Associated with Increased Cancer Risk. Cancer research 82 (4) (2022)
Claire J H Kramer, Maaike P G Vreeswijk, Bram Thijssen, Tjalling Bosse, Jelle Wesseling
Beyond the snapshot: optimizing prognostication and prediction by moving from fixed to functional multidimensional cancer pathology. The Journal of pathology 257 (4) (2022)
Lise Marit van Wijk, Andreea B Nilas, Harry Vrieling, Maaike P G Vreeswijk
RAD51 as a functional biomarker for homologous recombination deficiency in cancer: a promising addition to the HRD toolbox? Expert review of molecular diagnostics 22 (2) (2022)
Lise Marit van Wijk, Claire J H Kramer, Sylvia Vermeulen, Natalja T Ter Haar, Marthe M de Jonge, Judith R Kroep, Cornelis D de Kroon, Katja N Gaarenstroom, Harry Vrieling, Tjalling Bosse, Maaike P G Vreeswijk
The RAD51-FFPE Test; Calibration of a Functional Homologous Recombination Deficiency Test on Diagnostic Endometrial and Ovarian Tumor Blocks. Cancers 13 (12) (2021)
Elena Bueno-Martínez, Lara Sanoguera-Miralles, Alberto Valenzuela-Palomo, Víctor Lorca, Alicia Gómez-Sanz, Sara Carvalho, Jamie Allen, Mar Infante, Pedro Pérez-Segura, Conxi Lázaro, Douglas F Easton, Peter Devilee, Maaike P G Vreeswijk, Miguel de la Hoya, Eladio A Velasco
RAD51D Aberrant Splicing in Breast Cancer: Identification of Splicing Regulatory Elements and Minigene-Based Evaluation of 53 DNA Variants. Cancers 13 (11) (2021)
Michael T Parsons, Emma Tudini, Hongyan Li, Eric Hahnen, Barbara Wappenschmidt, Lidia Feliubadaló, Cora M Aalfs, Simona Agata, Kristiina Aittomäki, Elisa Alducci, María Concepción Alonso-Cerezo, Norbert Arnold, Bernd Auber, Rachel Austin, Jacopo Azzollini, Judith Balmaña, Elena Barbieri, Claus R Bartram, Ana Blanco, Britta Blümcke, Sandra Bonache, Bernardo Bonanni, Åke Borg, Beatrice Bortesi, Joan Brunet, Carla Bruzzone, Karolin Bucksch, Giulia Cagnoli, Trinidad Caldés, Almuth Caliebe, Maria A Caligo, Mariarosaria Calvello, Gabriele L Capone, Sandrine M Caputo, Ileana Carnevali, Estela Carrasco, Virginie Caux-Moncoutier, Pietro Cavalli, Giulia Cini, Edward M Clarke, Paola Concolino, Elisa J Cops, Laura Cortesi, Fergus J Couch, Esther Darder, Miguel de la Hoya, Michael Dean, Irmgard Debatin, Jesús Del Valle, Capucine Delnatte, Nicolas Derive, Orland Diez, Nina Ditsch, Susan M Domchek, Véronique Dutrannoy, Diana M Eccles, Hans Ehrencrona, Ute Enders, D Gareth Evans, Chantal Farra, Ulrike Faust, Ute Felbor, Irene Feroce, Miriam Fine, William D Foulkes, Henrique C R Galvao, Gaetana Gambino, Andrea Gehrig, Francesca Gensini, Anne-Marie Gerdes, Aldo Germani, Jutta Giesecke, Viviana Gismondi, Carolina Gómez, Encarna B Gómez Garcia, Sara González, Elia Grau, Sabine Grill, Eva Gross, Aliana Guerrieri-Gonzaga, Marine Guillaud-Bataille, Sara Gutiérrez-Enríquez, Thomas Haaf, Karl Hackmann, Thomas V O Hansen, Marion Harris, Jan Hauke, Tilman Heinrich, Heide Hellebrand, Karen N Herold, Ellen Honisch, Judit Horvath, Claude Houdayer, Verena Hübbel, Silvia Iglesias, Angel Izquierdo, Paul A James, Linda A M Janssen, Udo Jeschke, Silke Kaulfuß, Katharina Keupp, Marion Kiechle, Alexandra Kölbl, Sophie Krieger, Torben A Kruse, Anders Kvist, Fiona Lalloo, Mirjam Larsen, Vanessa L Lattimore, Charlotte Lautrup, Susanne Ledig, Elena Leinert, Alexandra L Lewis, Joanna Lim, Markus Loeffler, Adrià López-Fernández, Emanuela Lucci-Cordisco, Nicolai Maass, Siranoush Manoukian, Monica Marabelli, Laura Matricardi, Alfons Meindl, Rodrigo D Michelli, Setareh Moghadasi, Alejandro Moles-Fernández, Marco Montagna, Gemma Montalban, Alvaro N Monteiro, Eva Montes, Luigi Mori, Lidia Moserle, Clemens R Müller, Christoph Mundhenke, Nadia Naldi, Katherine L Nathanson, Matilde Navarro, Heli Nevanlinna, Cassandra B Nichols, Dieter Niederacher, Henriette R Nielsen, Kai-Ren Ong, Nicholas Pachter, Edenir I Palmero, Laura Papi, Inge Sokilde Pedersen, Bernard Peissel, Pedro Perez-Segura, Katharina Pfeifer, Marta Pineda, Esther Pohl-Rescigno, Nicola K Poplawski, Berardino Porfirio, Anne S Quante, Juliane Ramser, Rui M Reis, Françoise Revillion, Kerstin Rhiem, Barbara Riboli, Julia Ritter, Daniela Rivera, Paula Rofes, Andreas Rump, Monica Salinas, Ana María Sánchez de Abajo, Gunnar Schmidt, Ulrike Schoenwiese, Jochen Seggewiß, Ares Solanes, Doris Steinemann, Mathias Stiller, Dominique Stoppa-Lyonnet, Kelly J Sullivan, Rachel Susman, Christian Sutter, Sean V Tavtigian, Soo H Teo, Alex Teulé, Mads Thomassen, Maria Grazia Tibiletti, Marc Tischkowitz, Silvia Tognazzo, Amanda Ewart Toland, Eva Tornero, Therese Törngren, Sara Torres-Esquius, Angela Toss, Alison H Trainer, Katherine M Tucker, Christi J van Asperen, Marion T van Mackelenbergh, Liliana Varesco, Gardenia Vargas-Parra, Raymonda Varon, Ana Vega, Ángela Velasco, Anne-Sophie Vesper, Alessandra Viel, Maaike P G Vreeswijk, Sebastian A Wagner, Anke Waha, Logan C Walker, Rhiannon J Walters, Shan Wang-Gohrke, Bernhard H F Weber, Wilko Weichert, Kerstin Wieland, Lisa Wiesmüller, Isabell Witzel, Achim Wöckel, Emma Roisin Woodward, Silke Zachariae, Valentina Zampiga, Christine Zeder-Göß, null null, Conxi Lázaro, Arcangela De Nicolo, Paolo Radice, Christoph Engel, Rita K Schmutzler, David E Goldgar, Amanda B Spurdle
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification. Human mutation 40 (9) (2020)
Lara Sanoguera-Miralles, Alberto Valenzuela-Palomo, Elena Bueno-Martínez, Patricia Llovet, Beatriz Díez-Gómez, María José Caloca, Pedro Pérez-Segura, Eugenia Fraile-Bethencourt, Marta Colmena, Sara Carvalho, Jamie Allen, Douglas F Easton, Peter Devilee, Maaike P G Vreeswijk, Miguel de la Hoya, Eladio A Velasco
Comprehensive Functional Characterization and Clinical Interpretation of 20 Splice-Site Variants of the RAD51C Gene. Cancers 12 (12) (2020)
Romy L S Mesman, Fabienne M G R Calléja, Miguel de la Hoya, Peter Devilee, Christi J van Asperen, Harry Vrieling, Maaike P G Vreeswijk
Alternative mRNA splicing can attenuate the pathogenicity of presumed loss-of-function variants in BRCA2. Genetics in medicine : official journal of the American College of Medical Genetics 22 (8) (2020)
Alvaro N A Monteiro, Peter Bouwman, Arne N Kousholt, Diana M Eccles, Gael A Millot, Jean-Yves Masson, Marjanka K Schmidt, Shyam K Sharan, Ralph Scully, Lisa Wiesmuller, Fergus J Couch, Maaike P G Vreeswijk
Variants of uncertain clinical significance in hereditary breast and ovarian cancer genes: best practices in functional analysis for clinical annotation. Journal of medical genetics 57 (8) (2020)
Stefanie de Groot, Rieneke T Lugtenberg, Danielle Cohen, Marij J P Welters, Ilina Ehsan, Maaike P G Vreeswijk, Vincent T H B M Smit, Hiltje de Graaf, Joan B Heijns, Johanneke E A Portielje, Agnes J van de Wouw, Alex L T Imholz, Lonneke W Kessels, Suzan Vrijaldenhoven, Arnold Baars, Elma Meershoek-Klein Kranenbarg, Marjolijn Duijm-de Carpentier, Hein Putter, Jacobus J M van der Hoeven, Johan W R Nortier, Valter Daniel Longo, Hanno Pijl, Judith R Kroep, null null
Fasting mimicking diet as an adjunct to neoadjuvant chemotherapy for breast cancer in the multicentre randomized phase 2 DIRECT trial. Nature communications 11 (1) (2020)
Lise Marit van Wijk, Sylvia Vermeulen, Matty Meijers, Manuela F van Diest, Natalja T Ter Haar, Marthe M de Jonge, Nienke Solleveld-Westerink, J Tom van Wezel, Dik C van Gent, Judith R Kroep, Tjalling Bosse, Katja N Gaarenstroom, Harry Vrieling, Maaike P G Vreeswijk
The RECAP Test Rapidly and Reliably Identifies Homologous Recombination-Deficient Ovarian Carcinomas. Cancers 12 (10) (2020)
Laëtitia Meulemans, Romy L S Mesman, Sandrine M Caputo, Sophie Krieger, Marine Guillaud-Bataille, Virginie Caux-Moncoutier, Mélanie Léone, Nadia Boutry-Kryza, Johanna Sokolowska, Françoise Révillion, Capucine Delnatte, Hélène Tubeuf, Omar Soukarieh, Françoise Bonnet-Dorion, Virginie Guibert, Myriam Bronner, Violaine Bourdon, Sarab Lizard, Paul Vilquin, Maud Privat, Aurélie Drouet, Charlotte Grout, Fabienne M G R Calléja, Lisa Golmard, Harry Vrieling, Dominique Stoppat-Lyonnet, Claude Houdayer, Thierry Frebourg, Maaike P G Vreeswijk, Alexandra Martins, Pascaline Gaildrat
Skipping Nonsense to Maintain Function: The Paradigm of BRCA2 Exon 12. Cancer research 80 (7) (2020)
Irene Lopez-Perolio, Raphaël Leman, Raquel Behar, Vanessa Lattimore, John F Pearson, Laurent Castéra, Alexandra Martins, Dominique Vaur, Nicolas Goardon, Grégoire Davy, Pilar Garre, Vanesa García-Barberán, Patricia Llovet, Pedro Pérez-Segura, Eduardo Díaz-Rubio, Trinidad Caldés, Kathleen S Hruska, Vickie Hsuan, Sitao Wu, Tina Pesaran, Rachid Karam, Johan Vallon-Christersson, Ake Borg, null null, Alberto Valenzuela-Palomo, Eladio A Velasco, Melissa Southey, Maaike P G Vreeswijk, Peter Devilee, Anders Kvist, Amanda B Spurdle, Logan C Walker, Sophie Krieger, Miguel de la Hoya
Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants: an ENIGMA report. Journal of medical genetics 56 (7) (2019)
Inge M M Lakeman, Florentine S Hilbers, Mar Rodríguez-Girondo, Andrew Lee, Maaike P G Vreeswijk, Antoinette Hollestelle, Caroline Seynaeve, Hanne Meijers-Heijboer, Jan C Oosterwijk, Nicoline Hoogerbrugge, Edith Olah, Hans F A Vasen, Christi J van Asperen, Peter Devilee
Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families. Journal of medical genetics 56 (9) (2019)
Rick A C M Boonen, Amélie Rodrigue, Chantal Stoepker, Wouter W Wiegant, Bas Vroling, Milan Sharma, Magdalena B Rother, Nandi Celosse, Maaike P G Vreeswijk, Fergus Couch, Jacques Simard, Peter Devilee, Jean-Yves Masson, Haico van Attikum
Functional analysis of genetic variants in the high-risk breast cancer susceptibility gene PALB2. Nature communications 10 (1) (2019)

Maaike P G Vreeswijk.css-eqlu8i{font-size:small;padding-left:4px;} (Mpg Vreeswijk, Maaike Pg Vreeswijk)

Publication Activity (10 Years)

Top Topics

Top Venues

Maaike P G Vreeswijk (Mpg Vreeswijk, Maaike Pg Vreeswijk)