基本信息
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个人简介
His scientific interests lie mostly in Genetics, Glycosylation, Mutation, Molecular biology and Missense mutation. His Mutation, Haplotype, Genotype, Gene and Phosphomannomutase study are his primary interests in Genetics. The Glycosylation study combines topics in areas such as Golgi apparatus, Congenital disorder of glycosylation and Glycoprotein, Glycan.
His study in Mutation is interdisciplinary in nature, drawing from both Hypotonia, Exon and Amyotrophic lateral sclerosis, SOD1. His research integrates issues of Long QT syndrome, KvLQT1, Potassium channel, GATA1 and Zinc finger in his study of Molecular biology. Gert Matthijs interconnects Germline mutation, Compound heterozygosity and Null allele in the investigation of issues within Missense mutation.
研究兴趣
论文共 568 篇作者统计合作学者相似作者
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Dulce Quelhas,Sandra D. K. Kingma,An I. Jonckheere, Claudia S. Smeets-Peels,Daniel Costa Gomes, Jose Duro,Anabela Oliveira,Gert Matthijs, Laura K. M. Steinbusch,Jaak Jaeken,Isabel Rivera,Estela Rubio-Gozalbo
MOLECULAR GENETICS AND METABOLISM REPORTS (2024): 101057-101057
bioRxiv (Cold Spring Harbor Laboratory)no. 5 (2024): eadk8173-eadk8173
Eva Van Steijvoort, Mathilde Cassou, Camille De Schutter,Eftychia Dimitriadou,Hilde Peeters,Karen Peeraer,Gert Matthijs,Pascal Borry
Journal of Assisted Reproduction and Geneticsno. 2 (2024): 451-464
EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 686-686
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HEMATOLOGYno. 1 (2023): 2193770-2193770
Mathilde Geysens,Wouter Bossuyt,Elfride De Baere,Kim De Leeneer,Koenraad Devriendt,Annelies Dheedene,Aime Lumaka,Jeroen Luyten,Gert Matthijs,Bjorn Menten,Marije Meuwissen, Olivier Monestier,
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