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Д. Тончева, Р. Въжарова, С. Хаджидекова, И. Димова, М. Малинов, Диагноза на редки генетични болести. В „Редки генетични болести“, П/Р Д. Тончева, ISBN:978-619-183-012-1, Симелпрес
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2014
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| Дисертация д-р |
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Радослава Василева Въжарова, АНАЛИТИЧЕН ПОДХОД ЗА РАЗКРИВАНЕ НА ГЕНЕТИЧНИ НАРУШЕНИЯ ПРИ РЕДКИ БОЛЕСТИ ЧРЕЗ ДНК СЕКВЕНИРАНЕ ОТ НОВО ПОКОЛЕНИЕ, Медицински университет София, Ръководител:чл. кор. проф. д-р Драга Тончева
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2016
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| Статия в научно списание |
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1
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Emma Keuleyan, Theodor Todorov, Deyan Donchev, Ani Kevorkyan, Radoslava Vazharova, Alexander Kukov, Georgi Todorov, Boriana Georgieva, Iskra Altankova, Yordanka Uzunova, Characterization of Streptococcus pyogenes Strains from Tonsillopharyngitis and Scarlet Fever Resurgence, 2023—FIRST Detection of M1UK in Bulgaria, Microorganisms, 2025, doi:10.3390/microorganisms13010179, Ref, Web of Science
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2025
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2
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Maya Atanasoska, Radoslava Vazharova, Galina Stevanović, Irena Bradinova, Slavyana Yaneva Staykova, Lubomir Balabanski, Daniela Mircheva, Daniela Avdjieva-Tzavella, Draga Toncheva, Dopa-responsive dystonia in Bulgarian patients: report of three cases, European Journal of Human Genetics, vol:31, issue:5, 2023, pages:1-5, ISSN (print):1018-4813, ISSN (online):1476-5438, doi:https://doi.org/10.1038/s41431-023-01370-4, Ref, Web of Science, IF (5.351 - 2021), Web of Science Quartile: Q1 (2023), SCOPUS, SJR (1.764 - 2021), International, PhD
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2023
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3
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Славяна Янева Стайкова, Мая Атанасоска, Спасимир Шишиньов, Любомир Балабански, Даниела Мирчева, Ирена Брадинова, Радослава Въжарова, NESCAV синдром: клиничен случай, Редки болести и лекарства сираци, 2023, PhD
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2023
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4
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Е. Кьолеян, Й. Узунова, Г. Тодоров, Б. Георгиева, А. Куков, Р. Въжарова, Т. Тодоров, И. Алтънкова, ЕПИДЕМИЧЕН ВЗРИВ ОТ STREPTOCOCCUS PYOGENES – ФАРИНГИТИ И СКАРЛАТИНА – 2023. АНАЛИЗ НА СЛУЧАИТЕ ОТ УНИВЕРСИТЕТСКА БОЛНИЦА "ЛОЗЕНЕЦ" В СОФИЯ И КРАТКА ЕПИДЕМИОЛОГИЯ НА ИНФЕКЦИИТЕ, Детски и инфекциозни болести, vol:XV, issue:2, 2023
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2023
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5
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Alexander Kukov, Milena Peruhova, Atanas Syarov, Iskra Altankova, Nonka Yurukova, Andrei Goncharov, Radoslava Vazharova, Anoaneta Mihova, Tsvetelina Velikova, Yordanka Uzunova, Alterations of gut bacteria Akkermansia muciniphila and Faecalibacterium prausnitzii in late post-transplant period after liver transplantation., Iberoamerican Journal of Medicine, vol:4, issue:1, 2022, pages:45-51, ISSN (online):2695-5075, doi:https://doi.org/10.53986/ibjm.2022.0010, Ref
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2022
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6
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Irena Bradinova, Silvia Andonova, Radoslava Vazharova, Stiliyana Tomova, Lubomir Balabanski, Alexey Savov, Spinal muscular atrophy with congenital bone fractures 2 caused by a rare loss-of-function ASCC1 gene mutation in two Bulgarian Roma patients, Clinical Genetics, vol:102, issue:1, 2022, pages:78-79, ISSN (online):1399-0004, doi:https://doi.org/10.1111/cge.14130, Ref, IF, IF (4.296 - 2021), Web of Science Quartile: Q1 (2022)
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2022
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7
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Мая Атанасоска, Радослава Въжарова, Славяна Янева Стайкова, Любомир Балабански, Драга Тончева, Наследствена сфероцитоза тип 4, установена чрез цялостно екзомно секвениране, Редки болести и лекарства сираци, том:13, брой:1, 2022, стр.:14-21, ISSN (online):1314-3581, doi:https://doi.org/10.36865/2022.v13i1.158, Ref
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2022
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8
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Victoria Spasova Boris Mladenov, Simeon Rangelov Zora Hammoudeh, Desislava Nesheva Dimitar Serbezov, Rada Staneva Savina Hadjidekova, Mihail Ganev, Lubomir Balabanski, Radoslava Vazharova, Chavdar Slavov, Draga Toncheva, Olga Sergeevna Antonova, Clinical impact of copy number variation changes in bladder cancer samples, Experimental and Therapeutic Medicine, vol:22, issue:2, 2021, pages:1-15, ISSN (print):1792-0981, ISSN (online):1792-1015, doi:10.3892/etm.2021.10333, Ref, Web of Science, др., PhD
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2021
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9
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Lubomir Balabanski, Dimitar Serbezov, Maya Atanasoska, Sena Karachanak-Yankova, Savina Hadjidekova, Dragomira Nikolova, Olga Sergeevna Antonova, Rada Staneva, Radoslava Vazharova, Marta Mihailova, Rare genetic variants prioritize molecular pathways for semaphorin interactions in Alzheimer’s disease patients, Biotechnology & Biotechnological Equipment, vol:35, issue:1, 2021, pages:1256-1262, ISSN (print):1310-2818, ISSN (online):1314-3530, doi:10.1080/13102818.2021.1964382, Ref, IR , SCOPUS, SJR (38 - 2021), SCOPUS Quartile: Q3 (2021), PhD
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2021
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10
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Даниела Денева, В. Божинова, И. Александрова, Р. Въжарова, Полимикрогирия при патогенни варианти в COL18A1 гена, асоциирани с Knobloch синдром тип 1, Българска Неврология, том:22, брой:1, 2021, стр.:32-35, ISSN (print):1311-8641, ISSN (online):2815-2522
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2021
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11
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Balabanski L, Serbezov D, Nikolova D, Atonova O, Nesheva D, Hammoudeh Z, Vazharova R, Karachanak-Yankova S, Staneva R, Mihaylova M, Damyanova V, Hadjidekova S, Toncheva D., Centenarian Exomes as a Tool for Evaluating the Clinical Relevance of Germline Tumor Suppressor Mutations. , Technology in Cancer Research & Treatment, vol:19, 2020, pages:1-6, ISSN (print):1533-0346, ISSN (online):1533-0338, doi:10.1177/1533033820911082., Ref, Web of Science, IF (2.068 - 2019), SCOPUS, SJR (0.526 - 2019), SCOPUS Quartile: Q2 (2020)
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2020
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12
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Serbezov D, Balabanski L, Karachanak-Yankova S, Vazharova R, Nesheva D, Hammoudeh Z, Staneva R, Mihaylova M, Damyanova V, Antonova O, Nikolova D, Hadjidekova S, Toncheva D., Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study. , J Transl Genet Genom , vol:4, 2020, pages:446-454, ISSN (online):2578-5281, doi:10.20517/jtgg.2020.41, Ref, SCOPUS, SJR ( - 2022)
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2020
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13
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Sabina Zacharieva, Ralitsa Robeva, Silvia Andonova, Radoslava Vazharova, Lubomir Balabanski, Maya Atanasoska, Draga Toncheva, Atanaska Elenkova, Alexey Savov, Long-term follow-up of a female patient with non-classical 11β-hydroxylase deficiency and two novel mutations in CYP11B1, Gynecological Endocrinology, vol:35, issue:1, 2019, pages:23-27, ISSN (print):0951-3590, ISSN (online):1473-0766, doi:https://doi.org/10.1080/09513590.2018.1482870, Ref, IR , SCOPUS, SJR (1.406 - 2018)
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2019
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14
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Dimitar Serbezov, Balabanski L, Karachanak-Yankova S, Vazharova R, Nesheva D, Hammoudeh Z, Staneva R, Mihaylova M, Damyanova V, Antonova O, Nikolova D, Hadjidekova S, Toncheva D., POOL-SEQ Study of Bulgarian Centenarians Highlights the Relevance for Human Longevity of Gene Expression Pathways. , Journal of Aging Science, vol:7, issue:3, 2019, pages:1-14, ISSN (print):2329-8847, doi:10.35248/2329-8847.19.07.208
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2019
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15
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Ganev M, Balabanski L, Serbezov D, Karachanak-Yankova S, Vazharova R, Nesheva D, Hammoudeh Z, Nikolova D Antonova O,, Staneva R, Mihaylova M, Damyanova V, Hadjidekova S, Toncheva D, Prioritization of genetic variants predisposing to coronary heart disease in the Bulgarian population using centenarian exomes. , Biotechnology & Biotechnological Equipment, vol:33, issue:1, 2019, pages:1757-1765, ISSN (print):1310-2818, ISSN (online):1314-3530, doi:10.1080/13102818.2019.1700164 , Ref, Web of Science, IF (1.18 - 2019), Web of Science Quartile: Q3 (2019), SCOPUS, SJR (0.376 - 2019), SCOPUS Quartile: Q3 (2019)
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2019
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16
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Slavica Josifovska, Radoslava Vazharova, Lubomir Balabanski, Maxim Malinov, Anna Kaneva, Sasho Panov, Savina Hadjidekova, Draga Toncheva, Double heterozygosity of novel variants found in patients with severe clinical phenotype of cardiovascular disorders, Biotechnology & Biotechnological Equipment, vol:32, issue:3, 2018, pages:679-685, ISSN (print):1310-2818, ISSN (online):1314-3530, doi:10.1080/13102818.2018.1433064, Ref, IR , SCOPUS, SJR (0.394 - 2018), International, PhD
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2018
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17
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Slavica Josifovska, Radoslava Vazharova, Lubomir Balabanski, Maxim Malinov, Draga Toncheva, Sasho Panov, Genetic profiling of a patient with a complex phenotype revealed variants in the CPT2 gene , Medicus , vol:23, issue:1, 2018, pages:44-48, ISSN (print):1409-6366, Ref, Web of Science, International
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2018
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18
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Josifovska S, Vazharova R, Balabanski L, Malinov M, Kaneva A, Panov S, Toncheva D., Mutations in ACTA2 gene detected by Next Generation Sequencing in patients with pathology of great vessels. , Genetics and Plant Physiology, vol:8, issue:1-2, 2018, pages:62-67, ISSN (print):1314-6394, ISSN (online):1314-5770, International
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2018
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19
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Veneta Stoykova, Radoslava Vazharova, Evgeni Grigorov, Ivo Kremensky, Dimiter Markov, Stoimen Ivanov, PAPP-A LEVELS AND THE RISK OF PREECLAMPSIA, Comptes rendus de l’Acade'mie bulgare des Sciences, vol:71, issue:11, 2018, pages:1557-1565, doi:10.7546/CRABS.2018.11.16, Ref, SCOPUS, SJR (0.205 - 2018)
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2018
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20
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Ivanov, H. Y., Stoyanova, V, Ivanov, I., Linev, A., Vazharova, R., Ivanov, S., Balabanski, L., R. V. Vazharova, RARE CASE OF A HETEROZYGOUS MICRODELETION 9q21.11-q21.2: CLINICAL AND GENETIC CHARACTERISTICS, BALKAN JOURNAL OF MEDICAL GENETICS, vol:21, issue:2, 2018, pages:59-62, ISSN (print):1311-0160, doi:10.2478/bjmg-2018-0021
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2018
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21
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Maya Atanasoska, Radoslava Vazharova, Ivan Ivanov, Lubomir Balabanski, Silvia Andonova, Samuil Ivanov, Iliana Pacheva, Maxim Malinov, Draga Toncheva, SCN8A p.Arg1872Gln mutation in early infantile epileptic encephalopathy type 13: Review and case report, Biotechnology and Biotechnological Equipment, vol:32, issue:6, 2018, pages:1345-1351, ISSN (print):1310-2818, ISSN (online):1314-3530, doi:10.1080/13102818.2018.1532815, Ref, Web of Science, IF (1.174 - 2018), SCOPUS, SJR (0.394 - 2018)
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2018
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22
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Сербезов Д, Балабански Л, Николова Д, Хаджидекова С, Станева, Р, Карачанак-Янкова С, Михайлова М, Дамянова В, Антов Г, Въжарова Р, Тончева Д., Варианти в гени, свързани с онкогенеза и сърдечно-съдови заболявания, при суперстолетници, Съвременна медицина, том:LXII, брой:1, 2018, стр.:3-9, ISSN (print):0562-7192
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2018
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23
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Andonova S., Robeva R., Vazharova R., Ledig S., Grozdanova L., Stefanova E., Bradinova I., Todorov T., Hadjidekov G., Sirakov M., New Territory for an Old Disease: 5-Alpha-Reductase Type 2 Deficiency in Bulgaria, Sexual Development, vol:11, issue:1, 2017, pages:21-28, ISSN (print):1661-5425, ISSN (online):1661-5433, doi:10.1159/000454974, Ref, Web of Science, IF (2.25 - 2017), SCOPUS, SJR (0.903 - 2017)
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2017
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24
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Zora Hammoudeh, Dragomira Nikolova, Lubomir Balabanski, Samuil Ivanov, Radoslava Vazharova, Sabine Weidner, Maxim Malinov, Draga Toncheva, Screening of pharmacogenetic variants associated with drug sensitivity in patients with papillary thyroid carcinoma using next generation sequencing , Biotechnology & Biotechnological Equipment, vol:31, issue:4, 2017, pages:761-765, ISSN (print):1310-2818, ISSN (online):1314-3530, doi:10.1080/13102818.2017.1335614, Ref, IR , SCOPUS, SJR (0.394 - 2018)
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2017
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25
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В Атанасов, С Николова, Р. Въжарова, А Тодорова, А Савов, И Кременски, Скрининг за инверсия 22 (Inv22) в гена за коагулационен фактор VIII при български пациенти с тежка форма на хемофилия А , Science & Technologies , том:7, брой:3, 2017, стр.:153-161, ISSN (print):1314-4111
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2017
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26
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Vazharova R., Kremensky I., Individual capacity for DNA repair and maintenance of genomic integrity: a fertile ground for studies in the field of assisted reproduction, Biotechnology and Biotechnological Equipment, vol:Volume 30, 2016, issue:Issue 3, 2016, pages:419-433, ISSN (print):1310-2818, ISSN (online):1314-3530, doi:10.1080/13102818.2016.1159923, Ref, IR , SCOPUS, SJR (0.394 - 2018)
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2016
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27
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Radoslava Vazharova, Svetlana Vragaleva, Violeta Dimitrova, Samuil Ivanov, Lubomir Balabanski, Maxim Malinov, Draga Toncheva, Novel Hypomorphic Mutation in FANCD2 Gene Observed in a Fetus with Multiple Congenital Anomalies, Case Reports in Obstetrics and Gynecology, vol:Volume 2016, issue:Article ID 1462818, 4 pages, 2016, ISSN (print):2090-6684, ISSN (online):2090-6692, doi:10.1155/2016/1462818, Ref, др.(Academic Search Alumni Edition Academic Search Com)
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2016
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28
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N. Chilingirova, Z. Hammoudeh, L. Balabanski, S. Ivanov, R. Vazharova, D. Nikolova, G. Kurteva, D. Toncheva, P. Chilingirov, TruSight Cancer Sequencing Panel reveals pharmacogenetic variants associated with sensitivity to chemotherapy in lung cancer, memo - Magazine of European Medical Oncology, vol:9, issue:1, 2016, pages:30-38, ISSN (print):1865-5041, ISSN (online):1865-5076, doi:10.1007/s12254-015-0244-2, Ref, IR , SCOPUS, SJR (0.48 - 2018)
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2016
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29
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Симеонов, Е., Р. Въжарова, Д. Митева, Ал. Савов, И. Кременски, П. Переновска, Гeномна медицина в педиатричната клинична практика, Педиатрия, том:LVI, брой:1, 2016, ISSN (print):0479-7876, Ref, др.(Excerpta Medica Database EMBASE)
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2016
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30
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Ivanov HY, Stoyanova VK, Vazharova R., Linev A, Ivanov I, Ivanov S, Balabanski L, Toncheva D, A de novo microdeletion 2p24.3-25.1 identified in a girl with global development delay. , Biodiscovery, том:18, брой:1, 2015, doi:10.7750/BioDiscovery.2015.18.1, Ref
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2015
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31
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Kadiyska T.K., Todorov T.P., Bichev S.N., Vazharova, R.V., Nossikoff A.V., Savov A.S., Mitev V.I., APC promoter 1B deletion in familial polyposis-implications for mutation-negative families, Clinical Genetics, vol:85, issue:5, 2014, pages:452-457, ISSN (print):0009-9163, ISSN (online):1399-0004, doi:10.1111/cge.12210, Ref, Web of Science, IF (3.931 - 2014), SCOPUS, SJR (1.729 - 2014), SCOPUS Quartile: Q1 (2014)
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2014
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32
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E. Keuleyan, R. Vazharova, D. Hamidov, T. Todorov, A. Syarov, Lyudmila Belenska-Todorova, CARBAPENEMASES IN CLINICALLY SIGNIFICANT MICROORGANISMS
FROM THE ORDER ENTEROBACTERALES – CHARACTERIZATION.
PROBLEMS IN THE TREATMENT AND CONTROL OF INFECTIONS, BULGARIAN MEDICAL JOURNAL, том:18, брой:1, 2014, стр.:13-22, ISSN (print):1313-1516, ISSN (online):1313-1516, Ref, PhD
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2014
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33
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Георгиева Р, Тинчева Р, Влахова Д, Дянкова Д, Авджиева Д, Кадъм А, Бонева И, Въжарова Р, Jacobsеn Syndrome, Педиатрия, том:LIV, брой:4, 2014
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2014
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34
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Toncheva D, Mihailova-Hristova M, Vazharova R, Staneva R, Karachanak S, Dimitrov P, Simeonov V, Ivanov S, Balabanski L, Serbezov D, Malinov, M, Stefanovic V, Polenakovic M, Jankovic-Velickovic L, Djordjevic V, Jevtovic-Stoimenov T, Plaseska-Karanfilska D, Galabov A, Djonov V, Dimova I, NGS nominated CELA1, HSPG2, and KCNK5 as candidate genes for predisposition to Balkan endemic nephropathy , BioMed Research International, том:2014, 2014, ISSN (print):2314-6133, ISSN (online):2314-6141, doi:10.1155/2014/920723, Ref, Web of Science, IF (2.583 - 2014), SCOPUS, SJR (0.797 - 2014), SCOPUS Quartile: Q2 (2014), в сътрудничество с чуждестранни учени
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2014
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35
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Попова А, Тончева Д, Тинчева Р, Въжарова Р, Иванов С, Балабански Л., Случай на дете с аниридия и мутация в гена VSX1. , Български форум Глаукома, том:4, брой:2, 2014, стр.:88-92, ISSN (print):1314-5800
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2014
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36
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Elitza T. Betcheva, Adelina G. Yosifova,, Taisei Mushiroda, Michiaki Kubo, Atsushi Takahashi, Sena K. Karachanak, Irina T. Zaharieva, Savina P. Hadjidekova, Ivanka I. Dimova, Radoslava V. Vazharova, Drozdstoy S. Stoyanov, Vihra K. Milanova, George Kirov, Naoyuki Kamatani, Draga I. Toncheva, Yusuke Nakamura, Whole-genome-wide association study in the Bulgarian population reveals
HHAT as schizophrenia susceptibility gene
, Psychiatric Genetics, vol:23, issue:1, 2013, pages:11-19, ISSN (print):0955-8829, ISSN (online):1473-5873, doi:10.1097/YPG.0b013e3283586343, Ref, Web of Science, IF (2.242 - 2013), SCOPUS, SJR (1.145 - 2013), SCOPUS Quartile: Q2 (2013), International
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2013
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37
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Ангелова Л., В. Гаданчева, A. Тодорова, M. Стоянова, Д. Константинова, Б. Яков, Р. Въжарова, С. Иванов, Опитът на генетична лаборатория Варна с амниоцентеза с генетичен анализ за периода 2006-2010 година , Акушерство и гинекология, том:51, брой:1, 2012, стр.:8-12, ISSN (print):0324-0959
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2012
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38
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Ангелова Л., В. Гаданчева, Р. Въжарова, Д. Константинова, С. Иванов, И. Кременски, Опитът на генетичната лаборатория Варна с майчин серумен скрининг за шест годишен период , Акушерство и гинекология, том:51, брой:1, 2012, стр.:13-18, ISSN (print):0324-0959
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2012
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39
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Кедикова С., Х. Шивачев, О. Бранков, Е. Филипов, Р. Въжарова, Трансверзален вагинален септум при двумесечна пациентка - клиничен случай , Акушерство и гинекология, том:51, брой:1, 2012, стр.:41-45, ISSN (print):0324-0959
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2012
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40
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Stancheva-Ivanova MK, Wuyts W, van Hul E, Radeva BI, Vazharova RV, Sokolov TP, Vladimirov BY, Apostolova MD, Kremensky IM, Clinical and molecular studies of EXT1/EXT2 in Bulgaria. , J Inherit Metab Dis., vol:34, issue:4, 2011, pages:917-921, ISSN (print):0141-8955, ISSN (online):1573-2665, doi:10.1007/s10545-011-9314-8, Ref, Web of Science, IF (3.577 - 2011), SCOPUS, SJR (1.56 - 2018), International
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2011
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41
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Yosifova A, Mushiroda T, Kubo M, Takahashi A, Kamatani Y, Kamatani N, Stoianov D, Vazharova R, Karachanak S, Zaharieva I, Genome-wide association study on bipolar disorder in the Bulgarian population, Genes Brain Behav., vol:10, issue:7, 2011, pages:789-797, ISSN (print):1601-1848, ISSN (online):1601-183X, doi:10.1111/j.1601-183X.2011.00721.x., Ref, Web of Science, IF (3.476 - 2011), SCOPUS, SJR (1.543 - 2011), International
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2011
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42
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Atanassov V, Vazharova R, Ready, Steady, Go—The Current State of Carriership Status Determination and Prenatal Diagnosis of Haemophilia a in Bulgaria, Biotechnology & Biotechnological Equipment, vol:25, issue:4, 2011, pages:2566-2571, ISSN (print): 1310-2818, ISSN (online):1314-3530, doi:10.5504/BBEQ.2011.0104, Ref, Web of Science, SCOPUS Quartile: Q3 (2011)
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2011
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43
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И. Синигерска, Р. Въжарова, И. Брадинова, М. Иванова, И. Хасанова, И. Кременски, Лабораторен подход за диагностика на лизозомни болести на натрупването, Педиатрия, том:LI, брой:1, 2011
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2011
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44
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Иванова, М., И. Брадинова, Р. Въжарова, Д. Димитров, И. Синигерска, И. Кременски, Хиперамониемия - дефекти в урейния цикъл, диагностичен подход, Педиатрия - Suplementum за общопрактикуващия лекар, 2011
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2011
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45
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M. Stancheva, I. Kremenski, M. Apostolova, J. Jaeken, E. van Schaftingen, G. Matthijs, N. Ivanova, V. Bojinova, B. Radeva, P. Perenovska, K. Vladimirova, Vajarova R., D. Todorova, A clinical case with PMM2-CDG and dandy-walker malformation , Acta Medica Bulgarica, vol:37, issue:2, 2010, pages:80-84, ISSN (print):0324-1750, Ref, SCOPUS, SJR (12 - 2010), SCOPUS Quartile: Q4 (2010), International
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2010
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46
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Кременски, И., Р. Въжарова, И. Брадинова, М. Иванова, И. Синигерска, Д. Димитров, А. Савов, С. Бичев, С. Андонова, Нови подходи за скрининг и диагностика при вродени грешки на метаболизма, Педиатрия - Suplementum за общопрактикуващия лекар, 2010
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2010
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47
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Стойкова В, Въжарова Р, Марков Д, Кременски И, Иванов С, Прогностична стойност на ниските нива на PAPP-A между 11 и 13(+6) г. с. за оценка на риска от развитие на прееклампсия., Акушерство и гинекология, том:49, брой:6, 2010, стр.:19-25
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2010
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48
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Иванова М., А. Тодорова, И. Синигерска, Р. Въжарова, И. Брадинова, А. Савов, С. Андонова, Р. Райнова, И. Хасанова, Т. Тодоров, С. Бичев, И. Кременски, Селективен скрининг за диагностика на вродени грешки на обмяната, Практическа педиатрия, том:11, брой:2, 2010, стр.:19-21, ISSN (print):1311-0756
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2010
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49
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Въжарова Р, И. Брадинова, А. Савов, С. Бичев, И. Синигерска, М. Иванова, И. Кременски, Съвременни подходи за генетична диагностика при идиопатично изоставане в умственото развитие, Педиатрия - Suplementum за общопрактикуващия лекар, 2010
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2010
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50
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Elitza T Betcheva, Taisei Mushiroda, Atsushi Takahashi, Michiaki Kubo, Sena K Karachanak, Irina T Zaharieva, Radoslava V Vazharova, Ivanka I Dimova, Vihra K Milanova, Todor Tolev et al., Case–control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population, Journal of Human Genetics, vol:54, issue:2, 2009, pages:98-107, ISSN (print):1434-5161, ISSN (online):1435-232X, doi:https://doi.org/10.1038/jhg.2008.14, Ref, IR , SCOPUS, SJR (1.535 - 2009), International
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2009
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51
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Yosifova A, Mushiroda T, Stoianov D, Vazharova R, Dimova I, Karachanak S, Zaharieva I, Milanova V, Madjirova N, Gerdjikov I, Tolev T, Velkova S, Kirov G, Owen MJ, O'Donovan MC, Toncheva D, Nakamura Y, Case-control association study of 65 candidate genes revealed a possible association of a SNP of HTR5A to be a factor susceptible to bipolar disease in Bulgarian population, Journal of Affective Disorders , vol:117, issue:1-2, 2009, pages:87-97, ISSN (print):0165-0327, ISSN (online):1573-2517, doi:doi:10.1016/j.jad.2008.12.021, Ref, Web of Science, IF (4.491 - 2009), SCOPUS, SJR (2.614 - 2009), International, PhD
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2009
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52
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Yosifova A, Mushiroda T, Stoianov D, Vazharova R,, Dimova I, Karachanak S, Zaharieva I, Milanova V, Madjirova N, Gerdjikov I, Tolev T, Velkova S, Kirov G, Owen MJ, O'Donovan MC, Toncheva D, Nakamura Y, Case-control association study of 65 candidate genes revealed a possible association of a SNP of HTR5A to be a factor susceptible to bipolar disease in Bulgarian population. , Journal of Affective Disorders, том:117, брой:1-2, 2009, стр.:87-97, doi:10.1016/j.jad.2008.12.021, Ref, Web of Science, IF (3.786 - 2009), SCOPUS, SJR (1.876 - 2009), SCOPUS Quartile: Q1 (2009), в сътрудничество с чуждестранни учени, PhD
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2009
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53
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Dimova I, Vazharova R, Nikolova D, Tincheva R, Nesheva D, Uzunova Y, Toncheva D, Whole genome analysis by array-based comparative genomic hybridization in patients with congenital malformations, BJMG , vol:11, issue:1, 2008, pages:33-40, ISSN (print):1311-0160, Ref
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2008
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54
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Р. Въжарова, Микроделеционни синдроми, Практическа педиатрия, том:7, брой:9, 2006, стр.:13-16, ISSN (print):1311-0756
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2006
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55
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Бужов Б Ц, Въжарова Р, Димитрова В, Димова И, Търнев И, ван дер Виелен М, ван дер Маарел С, Бакер Б, Първи случай на пренатална диагностика за фациоскапулохумерална мускулна дистрофия на българска фамилия., Акушерство и гинекология, том:44, брой:2, 2005, стр.:30-32, в сътрудничество с чуждестранни учени
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2005
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56
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Димитрова В, Марков Д, Чернев Т, Карагьозова Ж, Мазнейкова В, Андонова С, Въжарова Р, Ултразвуков скрининг за синдром на Даун и други хромозомни болести чрез измерване на нухалната транслуценция на плода между 11-14 гестационна седмица, Акушерство и гинекология, том:44, брой:1, 2005, стр.:32-37, ISSN (print):0324-0969
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2005
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57
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Богов Б., Р. Въжарова, Б. Киперова, Цитогенетичен анализ при болни със системна амилоидоза, URONET, том:4, брой:2, 2005, стр.:24-27, ISSN (print):1312-1960
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2005
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58
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Andonova S, Vazharova R, Dimitrova V, Mazneikova V, Toncheva D, Kremensky I, Introduction of the QF-PCR analysis for the purposes of prenatal diagnosis in Bulgaria--estimation of applicability of 6 STR markers on chromosomes 21 and 18., Prenat Diagn., vol:24, issue:3, 2004, pages:202-208, ISSN (print):0197-3851, ISSN (online):1097-0223, doi:10.1002/pd.820, Ref, IF, IF (1.76 - 2003)
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2004
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59
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M. Nacheva, Vajarova R., G. Poptodorov, P. Troyanova, Y. Yordanov, B. Peneva., Clinical polymorphism in Neurofibromatosis type 1 , Trakia j. sciences. Series biomed. sci., vol:1, issue:3, 2003, pages:32-35, ISSN (print):1312-1723
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2003
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60
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Vazharova R, Stoyanova V, Ghenev E, Toncheva D, Familial complex translocation involving chromosomes 1,4,9,20, BJMG, vol:5, issue:1-2, 2002, pages:41-44, ISSN (print):1311-0160, Ref
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2002
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61
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Налбански Б., К. Цекова, Р. Въжарова, С. Иванов, А. Димитров, Рядък случай на успешна бременност и родоразрешение при бременна с наследствен ангионевротичен оток , Акушерство и гинекология, том:41, брой:5, 2002, стр.:39-42, ISSN (print):0324-0959
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2002
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62
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Vajarova R., Genetic factors and Schizophrenia, Balkan Journal of Medical Genetics, vol:2, issue:2, 1999, pages:9-19, ISSN (print):1311-0160
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1999
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63
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Начева М., Г. Поптодоров, В. Владимиров, Р. Въжарова, Клинична и генетична хетерогенност на неврофиброматозите , Съвременна медицина, том:50, брой:5-6, 1999, стр.:24-30, ISSN (print):0562-7192
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1999
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| Статия в сборник (на конференция и др.) |
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1
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R. RAYNOVA, I. Bradinova, R. Vazharova, V. Dimitrova, K. Vladimirova, A. Savov, A case of confined placental mosaicism for trisomy 21 and fetus with abnormal ultrasound findings, EJHG, Volume 21 Supplement 2 June 2013, 2013, стр.:591-591
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2013
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2
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T. K. Kadiyska, T. Todorov, S. Bichev, R. Vazharova, A. Nossikoff, A. Savov, V. Mitev, A novel full promoter 1B deletion of APC gene in Bulgarian Familial
Adenomatous Polyposis Family, EJHG, Volume 21 Supplement 2 June 2013, 2013, стр.:298-298
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2013
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3
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I. Bradinova, R. Vazharova, V. Bojinova, A. Savov, Mosaic trisomy 9 in a girl with mental retardation and dysmorphic
syndrome, EJHG, Volume 21 Supplement 2 June 2013, 2013, стр.:580-580
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2013
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4
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M. Ivanova, I. Sinigerska, R. Vazharova, I. Bradinova, I. Kremensky, Bulgarian metabolomic approach for diagnosis of Inherited Organic Acidurias, European Journal of Human Genetics, 2009, pages:354-0, Ref
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2009
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5
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M. Ivanova, I. Bradinova, R. Vazharova, I. Kremensky, Gamma-hydroxyburyric aciduria – identification of the first Bulgarian case by metabolomic approach, European Journal of Human Genetics, 2009, pages:351-0, Ref
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2009
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6
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I. Sinigersska, I. Hassanova, M. B. Ivanova, R. Vazharova, I. Bradinova, I. Kremensky, Laboratory approach for biochemical diagnosis of lysosomal Storage Diseases, European Journal of Human Genetics, 2009, pages:354-0, Ref
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2009
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7
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Sinigerska I, M. Ivanova, Vazharova R, Savov A, Kalaydjieva L, Kremensky I, Newborn sceening for phenylketonuria in Bulgaria – past, present and future, Cesko – Slovenska Pediatrie, 2009, pages:202-0
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2009
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8
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R. Vazharova, S. Baklova, A. Savov, R. Rainova, I. Sinigerska, A. Jordanova, A. Todorova, Y. Petrova, M. Ivanova, Prenatal diagnostics in Bulgaria – current experience and future trends, European Journal of Human Genetics, 2009, pages:351-0, Ref
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2009
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9
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M. Ivanova, Sinigerska I., Vazharova R., Bradinova I., Kremensky I., Selective metabolic screening for introduction of expanded newborn sceening for inherited metabolic diseases, Cesko – Slovenska Pediatrie, 2009, pages:207-0
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2009
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10
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Vazharova, R, Nacheva, M, Atanasova, S, Michov, V, Zaharieva, B, Naichova, L, R. V. Vazharova, Frequency and type of structural chromosomal aberrations in patients with schizophrenia., AMERICAN JOURNAL OF MEDICAL GENETICS, vol:96, issue:4, 2000, pages:551-551, ISSN (print):0148-7299
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2000
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11
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Naichova, L, Atanasova, S, Michov, V, Zaharieva, B, Nacheva, M, Vazharova, R, R. V. Vazharova, Frequency of chromosome 22 aberrations in patients with schizophrenia., AMERICAN JOURNAL OF MEDICAL GENETICS, vol:96, issue:4, 2000, pages:550-551, ISSN (print):0148-7299
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2000
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12
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Atanasova, S, Naichova, L, Michov, V, Nacheva, M, Zaharieva, B, Vazharova, R, R. V. Vazharova, Sex chromosomal aberrations in patients with schizophrenia., AMERICAN JOURNAL OF MEDICAL GENETICS, vol:96, issue:4, 2000, pages:553-553, ISSN (print):0148-7299
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2000
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| Участие в конференция |
|
1
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Секционен доклад, Радослава Въжарова, Генетични изследвания при онкологичните заболявания – цел и видове
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2019
|
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2
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Секционен доклад, Радослава Въжарова, WES analysis on rare diseases
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2019
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3
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Пленарен доклад, Радослава Въжарова, Application of targeted NGS in diagnostic work-up of patients with rare diseases
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2017
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