APC promoter 1B deletion in familial polyposis-implications for mutation-negative families
Kadiyska, T.K., Todorov, T.P., Bichev, S.N., Vazharova, R.V., Nossikoff, A.V., Savov, A.S., Mitev, V.I.
Published in Clinical genetics (01.05.2014)
Published in Clinical genetics (01.05.2014)
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Rare case of a heterozygous microdeletion 9q21.11-q21.2: Clinical and genetic characteristics
Ivanov, HY, Stoyanova, V, Ivanov, I, Linev, A, Vazharova, R, Ivanov, S, Balabanski, L, Toncheva, D
Published in Balkan journal of medical genetics (31.12.2018)
Published in Balkan journal of medical genetics (31.12.2018)
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Genome‐wide association study on bipolar disorder in the Bulgarian population
Yosifova, A., Mushiroda, T., Kubo, M., Takahashi, A., Kamatani, Y., Kamatani, N., Stoianov, D., Vazharova, R., Karachanak, S., Zaharieva, I., Dimova, I., Hadjidekova, S., Milanova, V., Madjirova, N., Gerdjikov, I., Tolev, T., Poryazova, N., O'Donovan, M. C., Owen, M. J., Kirov, G., Toncheva, D., Nakamura, Y.
Published in Genes, brain and behavior (01.10.2011)
Published in Genes, brain and behavior (01.10.2011)
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NGS Nominated CELA1, HSPG2, and KCNK5 as Candidate Genes for Predisposition to Balkan Endemic Nephropathy
Dimitrov, P., Karachanak, S., Staneva, R., Vazharova, R., Mihailova-Hristova, M., Toncheva, D., Simeonov, V., Ivanov, S., Balabanski, L., Serbezov, D., Malinov, M., Stefanovic, Vladisav, Čukuranović, Rade, Polenakovic, M., Jankovic-Velickovic, Ljubinka, Djordjević, Vidosava B., Jevtovic-Stoimenov, T., Plaseska-Karanfilska, D., Galabov, A., Djonov, V., Dimova, I.
Published in BioMed research international (01.01.2014)
Published in BioMed research international (01.01.2014)
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TruSight Cancer Sequencing Panel reveals pharmacogenetic variants associated with sensitivity to chemotherapy in lung cancer
Chilingirova, N., Hammoudeh, Z., Balabanski, L., Ivanov, S., Vazharova, R., Nikolova, D., Kurteva, G., Toncheva, D., Chilingirov, P.
Published in Memo - Magazine of European medical oncology (01.02.2016)
Published in Memo - Magazine of European medical oncology (01.02.2016)
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Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene
Betcheva, Elitza T, Yosifova, Adelina G, Mushiroda, Taisei, Kubo, Michiaki, Takahashi, Atsushi, Karachanak, Sena K, Zaharieva, Irina T, Hadjidekova, Savina P, Dimova, Ivanka I, Vazharova, Radoslava V, Stoyanov, Drozdstoy S, Milanova, Vihra K, Tolev, Todor, Kirov, George, Kamatani, Naoyuki, Toncheva, Draga I, Nakamura, Yusuke
Published in Psychiatric genetics (01.02.2013)
Published in Psychiatric genetics (01.02.2013)
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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
Andonova, Silvia, Vazharova, Radoslava, Dimitrova, Violeta, Mazneikova, Valentina, Toncheva, Draga, Kremensky, Ivo
Published in Prenatal diagnosis (01.03.2004)
Published in Prenatal diagnosis (01.03.2004)
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Полимикрогирия при патогенни варианти в COL18A1 гена, асоциирани с Knobloch синдром тип 1
Daniela Deneva, V. Bojinova, I. Аleksandrova, R. Vazharova
Published in Bŭlgarska nevrologii︠a︡ : izdanie na Bŭlgarskoto druzhestvo po nevrologii︠a︡ = Bulgarian neurology : official journal of the Bulgarian Society of Neurology (01.04.2021)
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Published in Bŭlgarska nevrologii︠a︡ : izdanie na Bŭlgarskoto druzhestvo po nevrologii︠a︡ = Bulgarian neurology : official journal of the Bulgarian Society of Neurology (01.04.2021)
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