Olivier M. Vanakker

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Gonadal Mosaicism As a Rare Inheritance Pattern in Recessive Genodermatoses: Report of Two Cases with Pseudoxanthoma Elasticum and Literature Review

Lisa Dangreau,Mohammad J Hosen,Julie De Zaeytijd,Bart P Leroy,Paul J Coucke,Olivier M Vanakker

Current issues in molecular biologyno. 9 (2024): 9998-10007

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Clinical Impact of RNA-sequencing in Diagnostics

Laurenz De Cock, Erika D'haenens,Sarah Vergult, Lies Vantomme,Annelies Dheedene, Robin de Putter,Tim Van Damme, Jo Sourbron,Bert Callewaert,Olivier Vanakker,Bjorn Menten

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 648-648

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Rapidly Progressive Peripheral Artery Disease: Importance of Oligogenic Inheritance and Functional Validation

Lisa Dangreau,Yvonne Nitschke,Frank Rutsch,Olivier M Vanakker

Circulation Genomic and precision medicine (2024)

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Full Characterization of Unresolved Structural Variation Through Long-Read Sequencing and Optical Genome Mapping

Griet De Clercq,Lies Vantomme,Barbara Dewaele,Bert Callewaert,Olivier Vanakker,Sandra Janssens, Bart Loeys,Mojca Strazisar,Wouter De Coster,Joris R Vermeesch,Annelies Dheedene,Björn Menten

medrxiv（2024）

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Significance of Premature Vertebral Mineralization in Zebrafish Models in Mechanistic and Pharmaceutical Research on Hereditary Multisystem Diseases

Judith Van Wynsberghe,Olivier M. Vanakker

Biomoleculesno. 11 (2023): 1621

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Valuable insights after one year whole exome sequencing in a fetal/prenatal setting

Sarah Delbaere,Machteld Baetens,Candy Kumps,Ellen Roets,Noortje Van Oostrum,Bert Callewaert,Sandra Janssens,Olivier Vanakker,Bjorn Menten

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 356-356

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The Activation of JAK/STAT3 Signaling and the Complement System Modulate Inflammation in the Primary Human Dermal Fibroblasts of PXE Patients

Christopher Lindenkamp,Ricarda Pluemers, Michel R. Osterhage,Olivier M. Vanakker,Judith Van Wynsberghe,Cornelius Knabbe,Doris Hendig

Biomedicinesno. 10 (2023)

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Inherited pathogenic variants in neurodevelopmental disorders: a potential pitfall in trio-based analysis of clinical exomes

Annelies Dheedene,Erika D'haenens, Evelien Pouillie,Sarah Delbaere,Olivier Vanakker,Bert Callewaert,Bjorn Menten

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 460-460

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C-terminal Frameshift Variant of TDP-43 with Pronounced Aggregation-Propensity Causes Rimmed Vacuole Myopathy but Not ALS/FTD

Acta Neuropathologicano. 6 (2023): 793-814

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Multicentric longitudinal performance monitoring of different non-invasive prenatal screening technologies used in Belgium

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 46-47

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论文共 166 篇作者统计合作学者相似作者