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
11 - 19 of 19
- NEFL N98S mutation(2016)
Authors: Jose Berciano, Kristien Peeters, Antonio Garcia, Tomas Lopez-Alburquerque, Elena Gallardo, Arantxa Hernandez-Fabian, Ana L. Pelayo-Negro, Els De Vriendt, Jon Infante, Albena Jordanova
Pages: 361 - 369 - NEFL E396K mutation is associated with a novel dominant intermediate Charcot-Marie-Tooth disease phenotype(2015)
Authors: Jose Berciano, Antonio Garcia, Kristien Peeters, Elena Gallardo, Els De Vriendt, Ana L. Pelayo-Negro, Jon Infante, Albena Jordanova
Pages: 1289 - 1300 - Novel mutations in the DYNC1H1 tail domain refine the genetic and clinical spectrum of dyneinopathies(2015)
Authors: Kristien Peeters, Sven Bervoets, Teodora Chamova, Ivan Litvinenko, Els De Vriendt, Stoyan Bichev, Vanyo Mitev, Marina Kennerson, Vincent Timmerman, Ivailo Tournev, et al.
Pages: 287 - 291 - Discovery of novel genes implicated in hereditary neuromuscular disorders combining classical and next generation genetic approaches(2014)
Authors: Kristien Peeters
Number of pages: 178 - Clinical and genetic diversity of SMN1-negative proximal spinal muscular atrophies(2014)
Authors: Kristien Peeters, Teodora Chamova, Albena Jordanova
Pages: 2879 - 2896 - Molecular defects in the motor adaptor BICD2 cause proximal spinal muscular atrophy with autosomal-dominant inheritance(2013)
Authors: Kristien Peeters, Ivan Litvinenko, Bob Asselbergh, Leonardo de Almeida Souza, Elke Ydens, Magdalena Zimon, Joy Irobi-Devolder, Els De Vriendt, Vicky De Winter, Vincent Timmerman, et al.
Pages: 955 - 964 - Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia(2012)
Authors: Magdalena Zimon, Leonardo de Almeida Souza, Els De Vriendt, Erik Fransen, Kristien Peeters, Tinne Ooms, Vincent Timmerman, Albena Jordanova, et al.
Pages: 1080 - 1083 - Genetic spectrum of hereditary neuropathies with onset in the first year of life(2011)
Authors: Jonathan Baets, Tine Deconinck, Els De Vriendt, Magdalena Zimon, Laetitia Yperzeele, Kim Van Hoorenbeeck, Kristien Peeters, R. Spiegel, Y. Parman, Berten Ceulemans, et al.
Pages: 2664 - 2676 - Distal myopathy with upper limb predominance caused by **filamin C** haploinsufficiency(2011)
Authors: V. Guergueltcheva, Kristien Peeters, Chantal De Groote, Jean-Jacques Martin, Vincent Timmerman, Albena Jordanova, et al.
Pages: 2105 - 2114