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
1 - 10 of 39
- Investigation of NGS-intractable mutational classes in peripheral neurodegenerationFrom1 Nov 2023 → TodayFunding: FWO junior postdoctoral fellowship
- Establishing neuroimmune brain organoids as a platform for neurodegenerative and neurodevelopmental disease research.From1 Nov 2022 → TodayFunding: BOF - postdoctoral mandates
- Exploring the tissue specific disease mechanisms underlying tRNA-synthetase-associated peripheral neuropathies.From1 Nov 2022 → TodayFunding: FWO fellowships
- Exploring the role of structural variants in peripheral neurodegeneration.From1 Oct 2022 → 30 Sep 2023Funding: BOF - postdoctoral mandates
- Exploring the tissue-specific disease mechanisms underlying tRNA-synthetase-associated peripheral neuropathies.From1 Jan 2022 → TodayFunding: FWO research project (including WEAVE projects)
- Identification and therapeutic targeting of the spatial molecular signatures linked to HINT1 neuropathy.From1 Nov 2021 → TodayFunding: FWO fellowships
- Interactive and intelligent cellomics platform.From1 May 2020 → TodayFunding: FWO Medium Size Research Infrastructure
- Exploring the role of phosphor-signaling in the etiology of tRNA- synthetase-associated peripheral neuropathies.From1 Jan 2020 → 31 Dec 2023Funding: FWO research project (including WEAVE projects)
- Unraveling the genetic architecture of peripheral nerves: A contribution from inherited peripheral neuropathies.From1 Nov 2019 → 31 Oct 2020Funding: BOF - doctoral mandates
- Establishment, characterization and phosphor-profiling of the first iPSC model for aminoacyl-tRNA synthetase induced peripheral neuropathies.From1 Oct 2019 → 30 Sep 2023Funding: FWO senior postdoctoral fellowship
Publications
81 - 90 of 93
- L239F founder mutation in **GDAP1** is associated with a mild CharcotMarieTooth type 4C4 (CMT4C4) phenotype(2010)
Authors: Dagmara Kabzińska, Halina Strugalska-Cynowska, Anna Kostera-Pruszczyk, Barbara Ryniewicz, Renata Posmyk, Alina Midro, Pavel Seeman, Licia Bárankova, Magdalena Zimon, Jonathan Baets, et al.
Pages: 357 - 366 - Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations(2010)
Authors: Liesbet Deprez, Sarah Weckhuysen, Philip Holmgren, Arvid Suls, Tine Van Dyck, Dirk Goossens, Jurgen Del-Favero, Anna Jansen, K. Verhaert, L. Lagae, et al.
Pages: 1159 - 1165 - Mutations in the **SPTLC2** subunit of serine palmitoyltransferase cause hereditary sensory and autonomic neuropathy type I(2010)
Authors: Annelies Rotthier, Michaela Auer-Grumbach, Katrien Janssens, Jonathan Baets, Anke Penno, Leonardo de Almeida Souza, Kim van Hoof, An Jacobs, Els De Vriendt, Beate Schlotter-Weigel, et al.
Pages: 513 - 522 - Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy(2010)
Authors: Yunxiang Liao, Liesbet Deprez, Snezena Maljevic, Julika Pitsch, Godelieve Claes, Dimitrina Hristova, Albena Jordanova, Sirpa Ala-Mello, Astrid Bellan-Koch, Dragica Blazevic, et al.
Pages: 1403 - 1414 - Mutations in SACS cause atypical and late-onset forms of ARSACS(2010)
Authors: Tine Deconinck, Katrien Smets, Dirk Goossens, P. van den Bergh, K. Dahan, E. Schmedding, P. Santens, V. Milic Rasic, Pierre Van Damme, W. Robberecht, et al.
Pages: 1181 - 1188 - Four generations of epilepsy caused by an inherited microdeletion of the **SCN1A** gene(2010)
Authors: Arvid Suls, R. Velizarova, I. Yordanova, Liesbet Deprez, Tine Van Dyck, Jan Wauters, V. Guergueltcheva, Godelieve Claes, I. Kremensky, Albena Jordanova, et al.
Pages: 72 - 76 - Dominant mutations in the cation channel gene **transient receptor potential vanilloid 4** cause an unusual spectrum of neuropathies(2010)
Authors: Magdalena Zimon, Jonathan Baets, Michaela Auer-Grumbach, José Berciano, Antonio Garcia, Eduardo Lopez-Laso, Luciano Merlini, David Hilton-Jones, Meriel McEntagart, Andrew H. Crosby, et al.
Pages: 1798 - 1809 - Genes for hereditary sensory and autonomic neuropathies: a genotypephenotype correlation(2009)
Authors: Annelies Rotthier, Jonathan Baets, Els De Vriendt, An Jacobs, Michaela Auer-Grumbach, Nicolas Lévy, Nathalie Bonello-Palot, Sara Sebnem Kilic, Joachim Weis, Andrés Nacimento, et al.
Pages: 2699 - 2711 - Dominant mutations in the tyrosyl-tRNA synthetase gene recapitulate in **Drosophila** features of human CharcotMarieTooth neuropathy(2009)
Authors: Erik Storkebaum, Ricardo Leitão-Gonçalves, Tanja Godenschwege, Leslie Nangle, Monica Mejia, Inge Bosmans, Tinne Ooms, An Jacobs, Patrick van Dijck, Xiang-Lei Yang, et al.
Pages: 11782 - 11787 - The **SCN1A** variant database: a novel research and diagnostic tool(2009)
Authors: Godelieve Claes, Liesbet Deprez, Arvid Suls, Jonathan Baets, Katrien Smets, Tine Van Dyck, Tine Deconinck, Albena Jordanova, Peter De Jonghe
Pages: E904 - E920
Patents
1 - 1 of 1