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
21 - 30 of 93
- Kufor-Rakeb Syndrome/PARK9(2018)
Authors: Rivka Inzelberg, Alejandro Estrada, Yael Laitman, Els De Vriendt, Eitan Friedman, Albena Jordanova
Pages: 399 - 403 - Three novel SLC2A1 mutations in Bulgarian patients with different forms of genetic generalized epilepsy reflecting the clinical and genetic diversity of GLUT1-deficiency syndrome(2018)
Authors: Nevyana Ivanova, Valentina Peycheva, Kunka Kamenarova, Dalia Kancheva, Irina Tsekova, Iliana Aleksandrova, Dimitrina Hristova, Ivan Litvinenko, Diana Todorova, Gergana Sarailieva, et al.
Pages: 41 - 44 - Identification of novel causal genes for autosomal recessive Charcot-Marie-Tooth neuropathies(2018)
Authors: Derek Atkinson, Albena Jordanova
Number of pages: 163 - Chromosomal microarray analysis of Bulgarian patients with epilepsy and intellectual disability(2018)
Authors: Valentina Peycheva, Kunka Kamenarova, Neviana Ivanova, Albena Jordanova, Dimitar Stamatov, Daniela Avdjieva-Tzavella, Iliana Alexandrova, Sashka Zhelyazkova, Iliana Pacheva, Petya Dimova, et al.
Pages: 45 - 55 - Pontocerebellar hypoplasia type 1 for the neuropediatrician(2018)
Authors: I. Ivanov, D. Atkinson, I. Litvinenko, L. Angelova, S. Andonova, H. Mumdjiev, I. Pacheva, M. Panova, R. Yordanova, V. Belovejdov, et al.
Pages: 674 - 681 - MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability(2017)
Authors: Emil Ylikallio, Rosa Woldegebriel, Manuela Tumiati, Pirjo Isohanni, Monique M. Ryan, Zornitza Stark, Maie Walsh, Sarah L. Sawyer, Katrina M. Bell, Alicia Oshlack, et al.
Pages: 2093 - 2103 - Alternative stable conformation capable of protein misinteraction links tRNA synthetase to peripheral neuropathy(2017)
Authors: David Blocquel, Sheng Li, Na Wei, Herwin Daub, Mathew Sajish, Maria-Luise Petrovic-Erfurth, Grace Kooi, Jiadong Zhou, Ge Bai, Paul Schimmel, et al.
Pages: 8091 - 8104 - Intermediate Charcot-Marie-Tooth disease(2017)
Authors: José Berciano, Antonio García, Elena Gallardo, Kristien Peeters, Ana L. Pelayo-Negro, Silvia Alvarez-Paradelo, José Gazulla, Miriam Martínez-Tames, Jon Infante, Albena Jordanova
Pages: 1655 - 1677 - A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy(2017)
Authors: Daniela Rossi, Johanna Palmio, Anni Evila, Lucia Galli, Virginia Barone, Tracy A. Caldwell, Rachel A. Policke, Esraa Aldkheil, Christopher E. Berndsen, Nathan T. Wright, et al.
- Impact of KCNQ2 mutations in Bulgarian patients with electroclinical syndromes with onset in the first year of life(2017)
Authors: Valentina Peycheva, Neviana Ivanova, Kunka Kamenarova, Irina Tsekova, Iliyana Aleksandrova, Veneta Bozhinova, Maria Bozhidarova, Ivan Litvinenko, Dimitrina Hristova, Vanyo Mitev, et al.
Pages: 138 - 142
Patents
1 - 1 of 1