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
31 - 40 of 93
- TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis(2017)
Authors: Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, Federica Perrone, Lubina Dillen, Bavo Heeman, Veerle Bäumer, Sebastiaan Engelborghs, Jan De Bleecker, Ellen Gelpi, et al.
Pages: 297 - 309 - Axonal neuropathy with neuromyotonia(2017)
Authors: Kristien Peeters, Teodora Chamova, Ivailo Tournev, Albena Jordanova
Pages: 868 - 877 - ATP13A2/PARK9 regulates endo-/lysosomal cargo sorting and proteostasis through a novel PI(3,5)P2-mediated scaffolding function(2017)
Authors: S. Demirsoy, S. Martin, S. Motamedi, S. van Veen, T. Holemans, C. Van den Haute, Albena Jordanova, V. Baekelandt, P. Vangheluwe, P. Agostinis
Pages: 1656 - 1669 - Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78)(2017)
Authors: Alejandro Estrada-Cuzcano, Shaun Martin, Teodora Chamova, Matthis Synofzik, Dagmar Timmann, Tine Holemans, Albena Andreeva, Jennifer Reichbauer, Riet De Rycke, Dae-In Chang, et al.
Pages: 287 - 305 - Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy(2017)
Authors: Derek Atkinson, J. Nikodinovic Glumac, Bob Asselbergh, D. Blocquel, D. Steiner, A. Estrada-Cuzcano, Kristien Peeters, Tinne Ooms, Els De Vriendt, X.L. Yang, et al.
Pages: 533 - 542 - Charcot-Marie-Tooth disease type 2G redefined by a novel mutation in LRSAM1(2016)
Authors: Kristien Peeters, Paulius Palaima, Ana L. Pelayo-Negro, Antonio García, Elena Gallardo, Rosario García-Barredo, Ligia Monica Mateiu, Jonathan Baets, Björn Menten, Els De Vriendt, et al.
Pages: 823 - 833 - Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing(2016)
Authors: Derek Atkinson, Magdalena Zimon, Teodora Chamova, Vanyo Mitev, Ahmet Yaramis, Gian Maria Fabrizi, Haluk Topaloglu, Ivailo Tournev, Yesim Parma, Esra Battaloglu, et al.
Pages: 600 - 607 - De novo PMP2 mutations in families with type 1 CharcotMarieTooth disease(2016)
Authors: William W. Motley, Paulius Palaima, Sabrina W. Yum, Els De Vriendt, Albena Jordanova, et al.
Pages: 1649 - 1656 - Unravelling 5-oxoprolinuria (pyroglutamic aciduria) due to bi-allelic OPLAH mutations(2016)
Authors: Joern Oliver Sass, Corinne Gemperle-Britschgi, Maja Tarailo-Graovac, Nisha Patel, Melanie Walter, Albena Jordanova, Majid Alfadhel, Ivo Baric, Mahmut Coker, Aynur Damli-Huber, et al.
Pages: 44 - 49 - Clinical, neurophysiological and morphological study of dominant intermediate Charcot-Marie-Tooth type C neuropathy(2016)
Authors: Florian P. Thomas, Velina Guergueltcheva, Francisco A. A. Gondim, Ivailo Tournev, Chitharanjan V. Rao, Boryana Ishpekova, Laurence J. Kinsella, Yi Pan, Thomas J. Geller, Ivan Litvinenko, et al.
Pages: 467 - 476
Patents
1 - 1 of 1