Publications by authors named "Hilde Brems"

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The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS).
Linda A J Hendricks, Katja C J Verbeek, Janneke H M Schuurs-Hoeijmakers, Mirjam M de Jong, Thera P Links, Hilde Brems

Genet Med· October 2025

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Reply to Taal et al. Comment on "Iasella et al. Close Follow-Up of Patients with Neurofibromatosis Type 1 Reduces the Incidence of Malignant Peripheral Nerve Sheath Tumour. 2025, , 1306".
Maria Pia Iasella, Dries Ruttens, Daphne Hompes, Vincent Vandecaveye, Raf Sciot, Hilde Brems

Cancers (Basel)· October 2025

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Cancer prognosis and treatment results in patients with PTEN Hamartoma Tumour Syndrome (PHTS)-a European cohort study.
Linda A J Hendricks, Katja C J Verbeek, Janneke H M Schuurs-Hoeijmakers, Robin de Putter, Hilde Brems

BJC Rep· June 2025

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Close Follow-Up of Patients with Neurofibromatosis Type 1 Reduces the Incidence of Malignant Peripheral Nerve Sheath Tumour.
Maria Pia Iasella, Dries Ruttens, Daphne Hompes, Vincent Vandecaveye, Raf Sciot, Hilde Brems

Cancers (Basel)· April 2025

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Legius syndrome mutations in the Ras-regulator SPRED1 abolish its membrane localization and potentially cause neurodegeneration.
Yasuko Hirata, Hilde Brems, Seppe Van der Auweraer, Masaki Ohyagi, Mana Iizuka

J Biol Chem· December 2024

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Pigment epithelium derived factor drives melanocyte proliferation and migration in neurofibromatosis café au lait macules.
Charlotte Lovatt, Megan Williams, Alex Gibbs, Abdullahi Mukhtar, Huw J Morgan, Hilde Brems

Skin Health Dis· October 2024

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Encephalocraniocutaneous lipomatosis phenotype associated with mosaic biallelic pathogenic variants in the gene.
Steven Smeijers, Hilde Brems, Alexander Verhaeghe, Wim van Paesschen, Johannes van Loon

J Med Genet· August 2024

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Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants.
Richard Gallon, Carlijn Brekelmans, Marie Martin, Vincent Bours, Esther Schamschula, Hilde Brems

NPJ Precis Oncol· May 2024

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Mosaic RASopathies concept: different skin lesions, same systemic manifestations?
Marie-Anne Morren, Heidi Fodstad, Hilde Brems, Nicola Bedoni, Emmanuella Guenova

J Med Genet· April 2024

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Capillary malformations in a child caused by a novel HRAS mutation.
Dirk van Gysel, Hannelore de Maeseneer, Eric Legius, Hilde Brems

Pediatr Dermatol· March 2024

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Gonadal and gonadosomatic mosaicism in NF1: report of two families.
Magdalena Seidl-Philipp, Nathalie Veyt, Simon Schnaiter, Anne Krogsdam, Simon Schwendinger, Hilde Brems

J Dtsch Dermatol Ges· March 2024

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Lifestyle Factors and Breast Cancer in Females with PTEN Hamartoma Tumor Syndrome (PHTS).
Linda A J Hendricks, Katja C J Verbeek, Janneke H M Schuurs-Hoeijmakers, Arjen R Mensenkamp, Hilde Brems

Cancers (Basel)· February 2024

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Germline founder variant c.1998delinsTTCT in the RET oncogene: a cohort study in 15 Belgian families.
Axelle Vuylsteke, Laurens Hannes, Hilde Brems, Koen Devis, Marleen Renard

Eur J Endocrinol· September 2023

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PARP inhibitor predictive value of the Leuven HRD test compared with Myriad MyChoice CDx PLUS HRD on 468 ovarian cancer patients from the PAOLA-1/ENGOT-ov25 trial.
Liselore Loverix, Ignace Vergote, Pieter Busschaert, Adriaan Vanderstichele, Tom Venken, Hilde Brems

Eur J Cancer· July 2023

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Preclinical workup using long-read amplicon sequencing provides families with de novo pathogenic variants access to universal preimplantation genetic testing.
Olga Tsuiko, Yasmine El Ayeb, Tatjana Jatsenko, Joke Allemeersch, Cindy Melotte, Hilde Brems

Hum Reprod· March 2023

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Deep genomic analysis of malignant peripheral nerve sheath tumor cell lines challenges current malignant peripheral nerve sheath tumor diagnosis.
Miriam Magallón-Lorenz, Ernest Terribas, Sara Ortega-Bertran, Edgar Creus-Bachiller, Marco Fernández, Hilde Brems

iScience· February 2023

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Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes.
José Garcia-Pelaez, Rita Barbosa-Matos, Silvana Lobo, Alexandre Dias, Luzia Garrido, Hilde Brems

Lancet Oncol· January 2023

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Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohort.
Linda A J Hendricks, Nicoline Hoogerbrugge, Hanka Venselaar, Stefan Aretz, Isabel Spier, Hilde Brems

Eur J Med Genet· December 2022

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Identification of Codon 146 Variants in Isolated Epidermal Nevus and Multiple Lesions in Oculoectodermal Syndrome: Confirmation of the Phenotypic Continuum of Mosaic RASopathies.
Aude Beyens, Laure Dequeker, Hilde Brems, Sandra Janssens, Hannes Syryn

Int J Mol Sci· April 2022

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An update on congenital melanocytic nevus syndrome: A case report and literature review.
Lilaf Abdulmajid, Francesca Maria Bosisio, Hilde Brems, Greet De Vlieger, Marjan Garmyn

J Cutan Pathol· December 2021

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Comprehensive immunomolecular profiling of endometrial carcinoma: A tertiary retrospective study.
Jasper Victoor, Sara Vander Borght, Lien Spans, Stefan Lehnert, Hilde Brems

Gynecol Oncol· September 2021

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Multitumor Case Series of Germline , and -Mutated Patients Responding Favorably on Immune Checkpoint Inhibitors.
Lisa Kinget, Oliver Bechter, Kevin Punie, Philip R Debruyne, Hilde Brems

Curr Oncol· August 2021

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A Patient with neonatal cholestasis.
Kristl G Claeys, Luc Breysem, Eric Legius, Hilde Brems, David Cassiman

J Mother Child· July 2021

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MEK inhibition ameliorates social behavior phenotypes in a Spred1 knockout mouse model for RASopathy disorders.
Sarah C Borrie, Ellen Plasschaert, Zsuzsanna Callaerts-Vegh, Akihiko Yoshimura, Rudi D'Hooge, Hilde Brems

Mol Autism· July 2021

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Impaired instrumental learning in Spred1 mice, a model for a rare RASopathy.
Sarah C Borrie, Alexa E Horner, Akihiko Yoshimura, Eric Legius, Maksym V Kopanitsa, Hilde Brems

Genes Brain Behav· June 2021

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