Candidate Gene Discovery in Hereditary Colorectal Cancer and Polyposis Syndromes–Considerations for Future Studies

por te Paske, Iris B. A. W., Ligtenberg, Marjolijn J. L., Hoogerbrugge, Nicoline, de Voer, Richarda M.
Publicado 2020

Lagging Immune Response to Haemophilus influenzae Serotype b (Hib) Conjugate Vaccine after the Primary Vaccination with Hib of Infants in The Netherlands

por Schouls, Leo, Schot, Corrie, de Voer, Richarda M., van der Klis, Fiona, Knol, Mirjam, Tcherniaeva, Irina, Berbers, Guy
Publicado 2020

Monoallelic NTHL1 Loss-of-Function Variants and Risk of Polyposis and Colorectal Cancer

por Elsayed, Fadwa A., Grolleman, Judith E., Ragunathan, Abiramy, Buchanan, Daniel D., van Wezel, Tom, de Voer, Richarda M.
Publicado 2020

Evaluating the role of NTHL1 p.Q90* allele in inherited breast cancer predisposition

por Kumpula, Timo, Tervasmäki, Anna, Mantere, Tuomo, Koivuluoma, Susanna, Huilaja, Laura, Tasanen, Kaisa, Winqvist, Robert, de Voer, Richarda M., Pylkäs, Katri
Publicado 2020

Age-Related Immunity to Meningococcal Serogroup C Vaccination: An Increase in the Persistence of IgG2 Correlates with a Decrease in the Avidity of IgG

por de Voer, Richarda M., van der Klis, Fiona R. M., Schepp, Rutger M., Rijkers, Ger T., Sanders, Elisabeth A. M., Berbers, Guy A. M.
Publicado 2011

The Role of Haematological Parameters in Predicting the Response To Radical Chemoradiotherapy in Patients with Anal Squamous Cell Cancer

por Stojanovic-Rundic, Suzana, Marinkovic, Mladen, Cavic, Milena, Karapandzic, Vesna Plesinac, Gavrilovic, Dusica, Jankovic, Radmila, de Voer, Richarda M., Castellvi-Bel, Sergi, Krivokapic, Zoran
Publicado 2021

Microsatellite instability in noncolorectal and nonendometrial malignancies in patients with Lynch syndrome

por Elze, 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
Publicado 2023

Challenges of Neoantigen Targeting in Lynch Syndrome and Constitutional Mismatch Repair Deficiency Syndrome

por Abidi, Asima, Gorris, Mark A. J., Brennan, Evan, Jongmans, Marjolijn C. J., Weijers, Dilys D., Kuiper, Roland P., de Voer, Richarda M., Hoogerbrugge, Nicoline, Schreibelt, Gerty, de Vries, I. Jolanda M.
Publicado 2021

Mutational signature analysis in non-small cell lung cancer patients with a high tumor mutational burden

por van den Heuvel, Guus R. M., Kroeze, Leonie I., Ligtenberg, Marjolijn J. L., Grünberg, Katrien, Jansen, Erik A. M., von Rhein, Daniel, de Voer, Richarda M., van den Heuvel, Michel M.
Publicado 2021

A mosaic PIK3CA variant in a young adult with diffuse gastric cancer: case report

por te Paske, Iris B. A. W., Garcia-Pelaez, José, Sommer, Anna K., Matalonga, Leslie, Starzynska, Teresa, Jakubowska, Anna, van der Post, Rachel S., Lubinski, Jan, Oliveira, Carla, Hoogerbrugge, Nicoline, de Voer, Richarda M.
Publicado 2021

TINF2 is a haploinsufficient tumor suppressor that limits telomere length

por Schmutz, Isabelle, Mensenkamp, Arjen R, Takai, Kaori K, Haadsma, Maaike, Spruijt, Liesbeth, de Voer, Richarda M, Choo, Seunga Sara, Lorbeer, Franziska K, van Grinsven, Emma J, Hockemeyer, Dirk, Jongmans, Marjolijn CJ, de Lange, Titia
Publicado 2020

Immunity against Neisseria meningitidis Serogroup C in the Dutch Population before and after Introduction of the Meningococcal C Conjugate Vaccine

por de Voer, Richarda M., Mollema, Liesbeth, Schepp, Rutger M., de Greeff, Sabine C., van Gageldonk, Pieter G. M., de Melker, Hester E., Sanders, Elisabeth A. M., Berbers, Guy A. M., van der Klis, Fiona R. M.
Publicado 2010

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

por 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
Publicado 2015

Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing

por Lorca, Víctor, Rueda, Daniel, Martín-Morales, Lorena, Fernández-Aceñero, María Jesús, Grolleman, Judith, Poves, Carmen, Llovet, Patricia, Tapial, Sandra, García-Barberán, Vanesa, Sanz, Julián, Pérez-Segura, Pedro, de Voer, Richarda M., Díaz-Rubio, Eduardo, de la Hoya, Miguel, Caldés, Trinidad, Garre, Pilar
Publicado 2019

Medullary Pancreatic Carcinoma Due to Somatic POLE Mutation: A Distinctive Pancreatic Carcinoma With Marked Long-Term Survival

por Kryklyva, Valentyna, ter Linden, Esther, Kroeze, Leonie I., de Voer, Richarda M., van der Kolk, B. Marion, Stommel, Martijn W.J., Hermans, John J., Luchini, Claudio, Wood, Laura D., Hruban, Ralph H., Nagtegaal, Iris D., Ligtenberg, Marjolijn J.L., Brosens, Lodewijk A.A.
Publicado 2020

Clonal Hematopoiesis Is Associated With Low CD4 Nadir and Increased Residual HIV Transcriptional Activity in Virally Suppressed Individuals With HIV

por van der Heijden, Wouter A, van Deuren, Rosanne C, van de Wijer, Lisa, van den Munckhof, Inge C L, Steehouwer, Marloes, Riksen, Niels P, Netea, Mihai G, de Mast, Quirijn, Vandekerckhove, Linos, de Voer, Richarda M, van der Ven, Andre J, Hoischen, Alexander
Publicado 2021

Deleterious Germline BLM Mutations and the Risk for Early-onset Colorectal Cancer

por de Voer, Richarda M., Hahn, Marc-Manuel, Mensenkamp, Arjen R., Hoischen, Alexander, Gilissen, Christian, Henkes, Arjen, Spruijt, Liesbeth, van Zelst-Stams, Wendy A., Marleen Kets, C., Verwiel, Eugene T., Nagtegaal, Iris D., Schackert, Hans K., van Kessel, Ad Geurts, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J.L., Kuiper, Roland P.
Publicado 2015

A molecular inversion probe-based next-generation sequencing panel to detect germline mutations in Chinese early-onset colorectal cancer patients

por Zhang, Junxiao, Wang, Xiaoyan, de Voer, Richarda M, Hehir-Kwa, Jayne Y., Kamping, Eveline J, Weren, Robbert D.A., Nelen, Marcel, Hoischen, Alexander, Ligtenberg, Marjolijn J.L., Hoogerbrugge, Nicoline, Yang, Xiangling, Yang, Zihuan, Fan, Xinjuan, Wang, Lei, Liu, Huanliang, Wang, Jianping, Kuiper, Roland P., van Kessel, Ad Geurts
Publicado 2017

Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

por Matalonga, Leslie, Hernández-Ferrer, Carles, Piscia, Davide, Schüle, Rebecca, Synofzik, Matthis, Töpf, Ana, Vissers, Lisenka E. L. M., de Voer, Richarda, Tonda, Raul, Laurie, Steven, Fernandez-Callejo, Marcos, Picó, Daniel, Garcia-Linares, Carles, Papakonstantinou, Anastasios, Corvó, Alberto, Joshi, Ricky, Diez, Hector, Gut, Ivo, Hoischen, Alexander, Graessner, Holm, Beltran, Sergi
Publicado 2021

Immunological and Genomic Analysis Reveals Clinically Relevant Distinctions between Angiosarcoma Subgroups

por van Ravensteijn, Stefan G., Versleijen-Jonkers, Yvonne M. H., Hillebrandt-Roeffen, Melissa H. S., Weidema, Marije E., Nederkoorn, Maikel J. L., Bol, Kalijn F., Gorris, Mark A. J., Verrijp, Kiek, Kroeze, Leonie I., de Bitter, Tessa J. J., de Voer, Richarda M., Flucke, Uta E., Desar, Ingrid M. E.
Publicado 2022