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
11 - 20 of 93
- Scn1a mutation spectrum in a cohort of Bulgarian patients with gefs+ phenotype(2020)
Authors: Valentina Peycheva, Nevyana Ivanova, Kunka Kamenarova, Margarita Panova, Iliana Pacheva, Ivan Ivanov, Maria Bojidarova, Genoveva Tacheva, Dimitar Stamatov, Ivan Litvinenko, et al.
Pages: 711 - 725 - Transthyretin familial amyloid polyneuropathy due to lle107Val mutation mimicking atypical chronic inflammatory demyelinating polyneuropathy(2020)
Authors: Francisco Assis Aquino de Gondim, Joana G. Holanda Filha, Albena Jordanova
Pages: 201 - 203 - Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathies(2020)
Authors: C. Paketci, M. Karakaya, P. Edem, E. Bayram, N. Keller, H-S Daimagueler, S. Cirak, Albena Jordanova, S. Hiz, B. Wirth, et al.
Pages: 846 - 855 - The search of novel genetic causes of dominantly inherited Charcot-Marie-Tooth disease(2019)
Authors: Paulius Palaima, Albena Jordanova, Kristien Peeters
Number of pages: 174 - Transcriptional dysregulation by a nucleus-localized aminoacyl-tRNA synthetase associated with Charcot-Marie-Tooth neuropathy(2019)
Authors: Sven Bervoets, Na Wei, Maria-Luise Petrovic-Erfurth, Shazie Yusein-Myashkova, Biljana Ermanoska, Ligia Monica Mateiu, Bob Asselbergh, David Blocquel, Priyanka Kakad, Tyrone Penserga, et al.
- Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family(2019)
Authors: Shelisa Tey, Nortina Shahrizaila, Alexander P. Drew, Sarimah Samulong, Khean-Jin Goh, Esra Battaloglu, Derek Atkinson, Yesim Parman, Albena Jordanova, Ki Wha Chung, et al.
Pages: 117 - 127 - Truncating mutations in UBAP1 cause hereditary spastic paraplegia(2019)
Authors: Mohammad Ali Farazi Fard, Adriana P. Rebelo, Elena Buglo, Hamid Nemati, Hassan Dastsooz, Ina Gehweiler, Selina Reich, Jennifer Reichbauer, Beatriz Quintans, Andres Ordonez-Ugalde, et al.
Pages: 767 - 773 - Peripheral myelin protein 2-a novel cluster of mutations causing Charcot-Marie-Tooth neuropathy(2019)
Authors: Paulius Palaima, Teodora Chamova, Sebastian Jander, Vanyo Mitev, Christine Van Broeckhoven, Ivailo Tournev, Kristien Peeters, Albena Jordanova
- Unraveling the nuclear function of tyrosyl-tRNA synthetase associated with Charcot-Marie-Tooth disease(2019)
Authors: Sven Bervoets, Albena Jordanova, Maria-Luise Petrović-Erfurth
Number of pages: 183 - Expanding the spectrum of genes responsible for hereditary motor neuropathies(2019)
Authors: Stefano C. Previtali, Edward Zhao, Dejan Lazarevic, Giovanni Battista Pipitone, Gian Maria Fabrizi, Fiore Manganelli, Anna Mazzeo, Davide Pareyson, Angelo Schenone, Franco Taroni, et al.
Pages: 1171 - 1179
Patents
1 - 1 of 1