Mattias Van Heetvelde

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 8

Top Topics

Dna Methylation

Diabetic Retinopathy

Top Venues

European heart journal

Ophthalmic genetics

Clinical genetics

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

Publications

Richard Mindham, Mattias Van Heetvelde, Susanne S Pedersen
How your patient is really feeling: the emotional hinterland of a cardiac diagnosis. European heart journal 45 (10) (2024)
Marta Del Pozo-Valero, Basamat Almoallem, Alfredo Dueñas Rey, Quinten Mahieu, Mattias Van Heetvelde, Laila Jeddawi, Miriam Bauwens, Elfriede De Baere
Autozygome-guided exome-first study in a consanguineous cohort with early-onset retinal disease uncovers an isolated RIMS2 phenotype and a retina-enriched RIMS2 isoform. Clinical genetics 106 (2) (2024)
Marta Del Pozo-Valero, Basamat Almoallem, Alfredo Dueñas Rey, Quinten Mahieu, Mattias Van Heetvelde, Laila Jeddawi, Miriam Bauwens, Elfriede De Baere
Autozygome-guided exome-first study in a consanguineous cohort with early-onset retinal disease uncovers an isolated RIMS2 phenotype and a retina-enriched RIMS2 isoform. Clinical genetics (2024)
Richard Mindham, Mattias Van Heetvelde, Susanne S Pedersen
How your patient is really feeling: the emotional hinterland of a cardiac diagnosis. European heart journal (2024)
Richard Mindham, Mattias Van Heetvelde, Susanne S Pedersen
How your patient is really feeling: the emotional hinterland of a cardiac diagnosis. European heart journal 45 (10) (2024)
Greet Wieme, Jan Kral, Toon Rosseel, Petra Zemankova, Bram Parton, Michal Vocka, Mattias Van Heetvelde, Petra Kleiblova, Bettina Blaumeiser, Jana Soukupova, Jenneke van den Ende, Petr Nehasil, Sabine Tejpar, Marianna Borecka, Encarna B Gómez García, Marinus J Blok, Marketa Safarikova, Marta Kalousova, Karen Geboes, Robin de Putter, Bruce Poppe, Kim De Leeneer, Zdenek Kleibl, Marketa Janatova, Kathleen B M Claes
Prevalence of Germline Pathogenic Variants in Cancer Predisposing Genes in Czech and Belgian Pancreatic Cancer Patients. Cancers 13 (17) (2021)
Justine Vandeputte, Mattias Van Heetvelde, Caroline Van Cauwenbergh, Sara Seneca, Elfriede De Baere, Bart Peter Leroy, Julie De Zaeytijd
Mild Leber hereditary optic neuropathy (LHON) in a Western European family due to the rare Asian m.14502T>C variant in the MT-ND6 gene. Ophthalmic genetics 42 (4) (2021)
Tom Van Hoorde, Fanny Nerinckx, Elke Kreps, Dimitri Roels, Philippe Huyghe, Mattias Van Heetvelde, Hannah Verdin, Elfriede De Baere, Irina Balikova, Bart Peter Leroy
Expanding the clinical spectrum and management of Traboulsi syndrome: report on two siblings homozygous for a novel pathogenic variant in ASPH. Ophthalmic genetics 42 (4) (2021)