| Single-cell profiling of myeloid cells in glioblastoma across species and disease stage reveals macrophage competition and specialization AR Pombo Antunes, I Scheyltjens, F Lodi, J Messiaen, A Antoranz, ... Nature neuroscience 24 (4), 595-610, 2021 | 439 | 2021 |
| Therapeutic depletion of CCR8+ tumor-infiltrating regulatory T cells elicits antitumor immunity and synergizes with anti-PD-1 therapy H Van Damme, B Dombrecht, M Kiss, H Roose, E Allen, E Van Overmeire, ... Journal for immunotherapy of cancer 9 (2), 2021 | 151 | 2021 |
| Mosaic dominant TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia D Kancheva, T Chamova, V Guergueltcheva, V Mitev, DN Azmanov, ... Movement Disorders 30 (6), 854-858, 2015 | 53 | 2015 |
| Novel mutations in the DYNC 1 H 1 tail domain refine the genetic and clinical spectrum of dyneinopathies K Peeters, S Bervoets, T Chamova, I Litvinenko, E De Vriendt, S Bichev, ... Human mutation 36 (3), 287-291, 2015 | 49 | 2015 |
| Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole … D Kancheva, D Atkinson, P De Rijk, M Zimon, T Chamova, V Mitev, ... Genetics in Medicine 18 (6), 600-607, 2016 | 48 | 2016 |
| Founder p. Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children IS Ivanov, DN Azmanov, MB Ivanova, T Chamova, IH Pacheva, ... Molecular Genetics and Metabolism 113 (1-2), 76-83, 2014 | 31 | 2014 |
| Three novel SLC2A1 mutations in Bulgarian patients with different forms of genetic generalized epilepsy reflecting the clinical and genetic diversity of GLUT1-deficiency syndrome N Ivanova, V Peycheva, K Kamenarova, D Kancheva, I Tsekova, ... Seizure 54, 41-44, 2018 | 16 | 2018 |
| Creatine deficiency syndrome could be missed easily: a case report of guanidinoacetate methyltransferase deficiency presented with neurodevelopmental delay, seizures, and … I Pacheva, I Ivanov, M Penkov, D Kancheva, A Jordanova, M Ivanova Annals of Clinical & Laboratory Science 46 (5), 557-561, 2016 | 11 | 2016 |
| Evidence of an association between bipolar disorder and rs16917237 in the BDNF gene in a Bulgarian sample MA Ivanova, TN Christova, TS Asan, NA Djurova, SS Alexiev, CS Kostov, ... Psychiatric Genetics 23 (3), 141-142, 2013 | 7 | 2013 |
| Unraveling the gene regulatory networks that drive microglia and immune cell activation in Alzheimer's disease at single-cell resolution I Scheyltjens, D Kancheva, H Van Hove, K De Vlaminck, ARP Antunes, ... Glia 67, E600-E600, 2019 | | 2019 |
| Genetic studies in endogamous populations: advantages and challenges: investigation of heterogeneous genetic disorders through exome sequencing and positional cloning in … D Kancheva University of Antwerp, 2016 | | 2016 |
| Reply: Mutations in TUBB4A and spastic paraplegia T Chamova, D Kancheva, V Guergueltcheva, V Mitev, DN Azmanov, ... Movement disorders: official journal of the Movement Disorder Society 30 (13 …, 2015 | | 2015 |
| Hereditary spastic paraplegias, due to mutations in the SPAST gene. Clinical-genetic analysis. TI Andreeva A, Kancheva D, Ivanova N, Jordanova J Bulgarian Neurology 14 (3), 147-151, 2013 | | 2013 |
Albena JordanovaVIB, University of Antwerp, Belgium; Medical University-Sofia, Bulgaria在 molgen.vib-ua.be 的电子邮件经过验证
