| Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1 V Guergueltcheva, DN Azmanov, D Angelicheva, KR Smith, T Chamova, ... The American Journal of Human Genetics 91 (3), 553-564, 2012 | 106 | 2012 |
| LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population DN Azmanov, S Dimitrova, L Florez, S Cherninkova, D Draganov, B Morar, ... European journal of human genetics 19 (3), 326-333, 2011 | 79 | 2011 |
| GNE myopathy in Roma patients homozygous for the p. I618T founder mutation T Chamova, V Guergueltcheva, M Gospodinova, S Krause, S Cirak, ... Neuromuscular Disorders 25 (9), 713-718, 2015 | 46 | 2015 |
| Neurological symptoms, genotype-phenotype correlations and ethnic-specific differences in Bulgarian patients with Wilson disease V Mihaylova, T Todorov, H Jelev, I Kotsev, L Angelova, O Kosseva, ... The neurologist 18 (4), 184-189, 2012 | 39 | 2012 |
| X-linked inheritance and its implication in the diagnosis and management of female patients in Fabry disease DP Germain, K Benistan, L Angelova La Revue de medecine interne 31, S209-S213, 2010 | 39 | 2010 |
| Pontocerebellar hypoplasia type 1 for the neuropediatrician: Genotype–phenotype correlations and diagnostic guidelines based on new cases and overview of the literature I Ivanov, D Atkinson, I Litvinenko, L Angelova, S Andonova, H Mumdjiev, ... European Journal of Paediatric Neurology 22 (4), 674-681, 2018 | 27 | 2018 |
| Chlamydia psittaci genotype B in a pigeon (Columba livia) inhabiting a public place in San José, Costa Rica G Dolz, A Solórzano-Morales, L Angelova, C Tien, L Fonseca, MC Bonilla Open veterinary journal 3 (2), 135-139, 2013 | 22 | 2013 |
| Ethnicity-related DMD genotype landscapes in European and non-European countries R Selvatici, R Rossi, F Fortunato, C Trabanelli, Y Sifi, A Margutti, M Neri, ... Neurology: Genetics 7 (1), e536, 2020 | 16 | 2020 |
| Application of chemical and biological tests for estimation of current state of a tailing dump and surrounding soil from the region of Tarniţa, Suceava, Romania DM Ilieva, M Argirova, LY Angelova, RV Gradinaru, G Drochioiu, ... Environmental Science and Pollution Research 27 (2), 1386-1396, 2020 | 11 | 2020 |
| Characterization of production of an extracellular proteinase inhibitor from Streptomyces chromofuscus 34–1 with alkaline phosphatase activity and antiviral effect L Angelova, S Danova, I Iliev, I Ivanova, J Serkedjieva Biotechnology & Biotechnological Equipment 19 (2), 126-131, 2005 | 10 | 2005 |
| Potential role of dynein‐related genes in the etiology of male infertility: A systematic review and a meta‐analysis M Levkova, M Radanova, L Angelova Andrology 10 (8), 1484-1499, 2022 | 6 | 2022 |
| Association between polymorphic markers human leucocyte antigen-G and tumour necrosis factor alpha and susceptibility to recurrent miscarriages among Bulgarian women M Levkova, T Chervenkov, M Hachmeriyan, L Angelova Turkish Journal of Obstetrics and Gynecology 17 (1), 34, 2020 | 6 | 2020 |
| Comparison between thrombophilic gene polymorphisms among high risk patients M Levkova, M Hachmeriyan, M Stoyanova, V Miteva, L Angelova Romanian Journal of Internal Medicine 58 (1), 20-26, 2020 | 6 | 2020 |
| Maternal biochemical screening -- an approach for genetic prevention. part 2. sequential approach with integrated risk assessment L Angelova, V Gadancheva, D Konstantinova, M Stoianova, ... Akusherstvo i ginekologiia 52 (5), 14-18, 2013 | 6 | 2013 |
| Clinical and molecular data on mental retardation in Bulgaria T Todorov, A Todorova, D Avdjieva, P Dimova, L Angelova, R Tincheva, ... Balkan Journal of Medical Genetics 13 (2), 11-25, 2010 | 5 | 2010 |
| Роля на семейния лекар за ранна диагноза, лечение и профилактика на вродените аномалии Л Ангелова Практическа педиатрия 6, 24-25, 2004 | 5 | 2004 |
| CFTR gene variants as a reason for impaired spermatogenesis: a pilot study and a Meta-analysis of published data M Levkova, T Chervenkov, M Hachmeriyan, L Angelova Human Fertility 25 (4), 728-737, 2022 | 4 | 2022 |
| Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders C Lowther, MM Mehrjouy, RL Collins, MC Bak, O Dudchenko, H Brand, ... medRxiv, 2022.02. 15.22270795, 2022 | 4 | 2022 |
| Double aneuploidy 48, ХХХ,+ 21 of a Bulgarian newborn with Down phenotype: a case report M Tsvetkova, M Levkova, S Tsvetkova, M Hachmeriyan, E Kovachev, ... Egyptian Journal of Medical Human Genetics 21, 1-5, 2020 | 4 | 2020 |
| Standard karyotyping-a look through the European guidelines M Hachmeriyan, M Levkova, M Stoyanova, V Miteva, L Angelova Varna Medical Forum 8 (1), 90-96, 2019 | 4 | 2019 |
