Researcher
Albena Jordanova
- Keywords (University of Antwerp):Chemistry (incl. biochemistry)
- Disciplines (Flanders Institute for Biotechnology):Analysis of next-generation sequence data, Behavioural neuroscience
- Disciplines (University of Antwerp):Analytical chemistry, Inorganic chemistry, Macromolecular and materials chemistry, Medicinal and biomolecular chemistry, Organic chemistry, Physical chemistry, Sustainable chemistry, Theoretical and computational chemistry, Other chemical sciences, Biochemistry and metabolism, Other biological sciences, Other natural sciences
- See also: Albena Jordanova (Flanders Institute for Biotechnology)
Affiliations
- Jordanova Lab (Research group)
Responsible
From1 Jan 2017 → Today - VIB CMN - Molecular Neurogenomics (Research group)
Responsible
From1 Jan 2011 → Today - Neurogenetics Group (Research group)
Member
From1 Oct 2006 → 31 Dec 2010
Projects
21 - 30 of 39
- Unraveling the nuclear function of tyrosyl-tRNA synthetase and its connection to Dominant Intermediate Charcot-Marie -Tooth type C disease.From1 Jan 2014 → 31 Dec 2017Funding: FWO research project (including WEAVE projects)
- Identification of recessive genes and networks for Charcot-Marie-Tooth neuropathies.From1 Jan 2014 → 30 Sep 2014Funding: Fund Recuperation Fiscal Exemption
- Unraveling the molecular architecture of peripheral nerves- a system genetics approach.From1 Jan 2014 → 31 Dec 2017Funding: BOF - Other initiatives
- Unraveling the nuclear function of mutant tyrosyl-tRNA synthetase and the link with dominant intermediate Charcot-Marie-Tooth disease type C.From1 Jan 2014 → 31 Dec 2017Funding: IWT personal funding - strategic basic research grants
- Unraveling the molecular basis and genetic epidemiology of Charcot-Marie-Tooth neurpathies: contribution from Northeast Brazil.From1 Sep 2013 → 31 Aug 2016Funding: International Cooperation and Mobility
- Unravelling the molecular architecture of autosomal recessive Charcot-Marie-Tooth neuropathiess.From1 Jan 2013 → 31 Dec 2016Funding: FWO research project (including WEAVE projects)
- Identification and characterization of novel causal genes for autosomal recessive Charcot-Marie-Tooth neuropathies.From1 Jan 2013 → 31 Dec 2013Funding: BOF - Other initiatives
- Identification of molecular players and drug targets for DICMTC neuropathy.From1 Oct 2012 → 30 Sep 2014Funding: 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
- Large scale genetic approach for the molecular characterization of autosomalrecessive Charcot-Marie-Tooth disease.From1 Oct 2011 → 30 Sep 2013Funding: FWO fellowships
Publications
1 - 10 of 93
- An adapted GeneSwitch toolkit for comparable cellular and animal models(2023)
Authors: Laura Morant, Maria-Luise Petrovic-Erfurth, Albena Jordanova
Pages: 1 - 18 - Tyrosyl-tRNA synthetase has a noncanonical function in actin bundling(2023)
Authors: Biljana Ermanoska, Bob Asselbergh, Laura Morant, Maria-Luise Petrovic-Erfurth, Seyyedmohsen Hosseinibarkooie, Ricardo Leitao-Goncalves, Leonardo de Almeida Souza, Sven Bervoets, Litao Sun, LaTasha Lee, et al.
Pages: 1 - 19 - Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity(2022)
Authors: Alina Kurolap, Florian Kreuder, Claudia Gonzaga-Jauregui, Morasha Plesser Duvdevani, Tamar Harel, Luna Tammer, Baozhong Xin, Somayeh Bakhtiari, James Rice, Clare L. van Eyk, et al.
Pages: 518 - 532 - Phenotypic and genetic heterogeneity of adult patients with hereditary spastic paraplegia from Serbia(2022)
Authors: Stojan Peric, Vladana Markovic, Ayşe Candayan Niron, Els De Vriendt, Nikola Momcilovic, Andrija Savic, Natasa Dragasevic-Miskovic, Marina Svetel, Zorica Stevic, Ivo Bozovic, et al.
Pages: 1 - 14 - HINT1 neuropathy in Lithuania(2022)
Authors: Matilde Malcorps, Silvia Amor Barris, Birute Burnyte, Ramune Vilimiene, Kristina Grigalioniene, Alexandra Ekshteyn, Ausra Morkuniene, Arunas Vaitkevicius, Els De Vriendt, Jonathan Baets, et al.
Pages: 1 - 11 - LRSAM1 and the RING domain(2021)
Authors: Paulius Palaima, José Berciano, Kristien Peeters, Albena Jordanova
- Genetic survey of autosomal recessive peripheral neuropathy cases unravels high genetic heterogeneity in a Turkish cohort(2021)
Authors: Ayşe Candayan Niron, Arman Cakar, Gulshan Yunisova, Ayse Nur Ozdag Acarli, Derek Atkinson, Pinar Topaloglu, Hacer Durmus, Zuhal Yapici, Albena Jordanova, Yesim Parman, et al.
- HINT1 neuropathy in Norway(2021)
Authors: Silvia Amor Barris, Helle Hoyer, Lin V. Brauteset, Els De Vriendt, Linda Strand, Albena Jordanova, Geir J. Braathen, Kristien Peeters
- Drosophila Models for Charcot-Marie-Tooth Neuropathy Related to Aminoacyl-tRNA Synthetases(2021)
Authors: Laura Morant, Maria-Luise Petrovic-Erfurth, Albena Jordanova
- HINT1 founder mutation causing axonal neuropathy with neuromyotonia in South America(2021)
Authors: Bianca de Aguiar Coelho Silva Madeiro, Kristien Peeters, Elker Lene Santos de Lima, Silvia Amor Barris, Els De Vriendt, Albena Jordanova, Maria Tereza Cartaxo Muniz, Carolina da Cunha Correia
Patents
1 - 1 of 1