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
41 - 50 of 93
- 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 - Metabolite profile of a mouse model of Charcot-Marie-Tooth type 2D neuropathy(2016)
Authors: Preeti Bais, Kirk Beebe, Kathryn H. Morelli, Meagan E. Currie, Sara N. Norberg, Alexei V. Evsikov, Kathy E. Miers, Kevin L. Seburn, Velina Guergueltcheva, Ivo Kremensky, et al.
Pages: 908 - 920 - 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 - Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach(2015)
Authors: Magdalena Zimon, Esra Battaloglu, Yesim Parman, Sevim Erdem, Jonathan Baets, Els De Vriendt, Derek Atkinson, Leonardo de Almeida Souza, Tine Deconinck, Burcak Ozes, et al.
Pages: 33 - 42 - CMT2D neuropathy is linked to the neomorphic binding activity of glycyl-tRNA synthetase(2015)
Authors: Weiwei He, Ge Bai, Huihao Zhou, Na Wei, Nicholas M. White, Janelle Lauer, Huaqing Liu, Yi Shi, Calin Dan Dumitru, Karen Lettieri, et al.
Pages: 710 - 714 - Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2(2015)
Authors: Alexander M. Rossor, Emily C. Oates, Hannah K. Salter, Albena Jordanova, et al.
Pages: 293 - 310 - 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 - 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 - Reply(2015)
Authors: Alexander M. Rossor, Emily C. Oates, Hannah K. Salter, Yang Liu, Sinead M. Murphy, Rebecca Schule, Michael A. Gonzales, Mariacristina Scoto, Rahul Phadke, Caroline A. Sewry, et al.
- Mutations in the GABA transporter SLC6A1 cause epilepsy with myoclonic-atonic seizures(2015)
Authors: Gemma L. Carvill, Jacinta M. McMahon, Amy Schneider, Matthew Zemel, Candace T. Myers, Julia Saykally, John Nguyen, Angela Robbiano, Federico Zara, Nicola Specchio, et al.
Pages: 808 - 815
Patents
1 - 1 of 1