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Researcher
Kristien Peeters
- Keywords:Biology
- Disciplines:Animal biology, Bioinformatics and computational biology, Ecology, Evolutionary biology, General biology, Genetics, Microbiology, Molecular and cell biology, Plant biology, Systems biology, Other biological sciences, Other natural sciences
Affiliations
- VIB CMN - Molecular Neurogenomics (Research group)
Member
From1 Jan 2011 → 31 Aug 2021 - Neurogenetics Group (Research group)
Member
From15 Jul 2010 → 31 Dec 2010
Projects
1 - 4 of 4
- Characterization of HINT1 knockout Drosophila model for peripheral neuropathy.From1 Apr 2019 → 30 Mar 2020Funding: BOF - projects
- Establishment and therapeutic targeting of disease signatures in patient-derived neuronal model of HINT1 neuropathy.From1 Oct 2018 → 30 Sep 2022Funding: FWO fellowships
- Identification of novel genes implicated in Charcot-Marie- Tooth neuropathies using next generation whole genome sequencing.From1 Oct 2012 → 30 Sep 2015Funding: FWO fellowships
- Identification of novel genes implicated in Charcot-Marie-Tooth neuropathies using next generation full genome sequencing.From1 Oct 2010 → 30 Sep 2012Funding: FWO fellowships
Publications
1 - 10 of 19
- HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling(2022)Published in: Orphanet journal of rare diseasesISSN: 1750-1172Volume: 17Pages: 1 - 11
- LRSAM1 and the RING domain: Charcot–Marie–Tooth disease and beyond(2021)Published in: Orphanet journal of rare diseasesISSN: 1750-1172Volume: 16
- HINT1 founder mutation causing axonal neuropathy with neuromyotonia in South America(2021)Published in: Molecular genetics & genomic medicineISSN: 2324-9269Volume: 9
- HINT1 neuropathy in Norway: clinical, genetic and functional profiling(2021)Published in: Orphanet journal of rare diseasesISSN: 1750-1172Volume: 16
- The search of novel genetic causes of dominantly inherited Charcot-Marie-Tooth disease(2019)Number of pages: 174
- Peripheral myelin protein 2-a novel cluster of mutations causing Charcot-Marie-Tooth neuropathy(2019)Published in: Orphanet journal of rare diseasesISSN: 1750-1172Volume: 14
- Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review(2017)Published in: Journal of neurologyISSN: 0340-5354Volume: 264Pages: 1655 - 1677
- Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy(2017)Published in: NeurologyISSN: 0028-3878Volume: 88Pages: 533 - 542
- Axonal neuropathy with neuromyotonia: there is a HINT(2017)Published in: BrainISSN: 0006-8950Volume: 140Pages: 868 - 877
- Charcot-Marie-Tooth disease type 2G redefined by a novel mutation in LRSAM1(2016)Published in: Annals of neurologyISSN: 0364-5134Volume: 80Pages: 823 - 833