Ghent University Academic Bibliography

Journal Article
A1
open access

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, Robin de Putter (UGent) , Violetta C. Anastasiadou, Marie-Charlotte Villy, Arne Jahn, Verena Steinke-Lange, et al.

(2024) CANCERS. 16(5).

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Cancer prognosis in PTEN Hamartoma Tumor Syndrome : a European cohort study

Linda Hendricks, Katja Verbeek, Hilde Brems, Robin de Putter (UGent) , Lenka Foretova, Chrystelle Colas, Patrick Benusiglio, Claude Houdayer, Arne Jahn, Verena Steinke-Lange, et al.

(2024) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 32(Supplement 1). p.563-564

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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, Sérgio Castedo, Sónia Sousa, Hugo Pinheiro, Liliana Sousa, Rita Monteiro, et al.

(2023) LANCET ONCOLOGY. 24(1). p.91-106

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Journal Article
A1
open access

Identification of codon 146 KRAS variants in isolated epidermal nevus and multiple lesions in oculoectodermal syndrome : confirmation of the phenotypic continuum of mosaic RASopathies

Aude Beyens (UGent) , Laure Dequeker, Hilde Brems, Sandra Janssens (UGent) , Hannes Syryn (UGent) , Anne D’Hooghe, Pascale De Paepe, Lieve Vanwalleghem, Annelies Stockman, Elena Vankwikelberge, et al.

(2022) INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 23(7).

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SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints

Julia Vogt, Kathrin Bengesser, Kathleen Claes (UGent) , Katharina Wimmer, Victor-Felix Mautner, Rick van Minkelen, Eric Legius, Hilde Brems, Meena Upadhyaya, Josef Högel, et al.

(2014) GENOME BIOLOGY. 15(6).

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Jaffe-Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder

Douglas R Stewart, Hilde Brems, Alicia G Gomes, Sarah L Ruppert, Tom Callens, Jennifer Williams, Kathleen Claes (UGent) , Michael B Bober, Rachel Hachen, Leonard B Kaban, et al.

(2014) GENETICS IN MEDICINE. 16(6). p.448-459

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Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of NF1 in neurofibromatosis type I-associated glomus tumors

Douglas R Stewart, Alexander Pemov, Eline Baert, Hilde Brems, Raf Sciot, Kathleen Claes (UGent) , Evgenia Pak, Amalia Dutra, Chyi-Chia Richard Lee and Eric Legius

(2012) GENES CHROMOSOMES & CANCER. 51(5). p.429-437

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Multiple orbital neurofibromas, painful peripheral nerve tumors, distinctive face and marfanoid habitus: a new syndrome

D Babovic-Vuksanovic, Ludwine Messiaen, Christoph Nagel, Hilde Brems, Bernd Scheithauer, Ellen Denayer, Rong Mao, Ralf Sciot, Karen M Janowski, Martin U Schuhmann, et al.

(2012) EUROPEAN JOURNAL OF HUMAN GENETICS. 20(6). p.618-625

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Miscellaneous

Glomus tumors in neurofibromatosis type 1: genetic, functional, and clinical evidence of a novel association (vol 69, pg 7393, 2009)

Hilde Brems, Caroline Park, Ophélia Maertens (UGent) , Alexander Pemov, Ludwine Messiaen, Meena Upadhyaya, Kathleen Claes (UGent) , Eline Beert, Kristel Peeters, Victor Mautner, et al.

(2009) CANCER RESEARCH. 69(20). p.8216-8216

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Glomus tumors in neurofibromatosis type 1: genetic, functional, and clinical evidence of a novel association

Hilde Brems, Caroline Park, Ophélia Maertens (UGent) , Alexander Pemov, Ludwine Messia, Meena Upadhyaya, Kathleen Claes (UGent) , Eline Beert, Kristel Peeters, Victor Mautner, et al.

(2009) CANCER RESEARCH. 69(18). p.7393-7401

Academic Bibliography

Lifestyle factors and breast cancer in females with PTEN Hamartoma Tumor Syndrome (PHTS)

Cancer prognosis in PTEN Hamartoma Tumor Syndrome : a European cohort study

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

Identification of codon 146 KRAS variants in isolated epidermal nevus and multiple lesions in oculoectodermal syndrome : confirmation of the phenotypic continuum of mosaic RASopathies

SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints

Jaffe-Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder

Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of NF1 in neurofibromatosis type I-associated glomus tumors

Multiple orbital neurofibromas, painful peripheral nerve tumors, distinctive face and marfanoid habitus: a new syndrome

Glomus tumors in neurofibromatosis type 1: genetic, functional, and clinical evidence of a novel association (vol 69, pg 7393, 2009)

Glomus tumors in neurofibromatosis type 1: genetic, functional, and clinical evidence of a novel association

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