Benign, Pathogenic and Copy Number Variations of Unknown Clinical Significance in Patients with Congenital Malformations and Developmental Delay

por Mihaylova, M, Staneva, R, Toncheva, D, Pancheva, M, Hadjidekova, S
Publicado 2017

Genome-Wide Methylation Profiling of Schizophrenia

por Rukova, B, Staneva, R, Hadjidekova, S, Stamenov, G, Milanova, Toncheva, D
Publicado 2015

Detecting EGFR Mutations in Patients with Non-small Cell Lung Cancer

por Hammoudeh, ZA, Antonova, O, Staneva, R, Nikolova, D, Kyuchukov, Y, Penev, A, Mintchev, T, Koleva, V, Hadjidekova, S, Toncheva, D
Publicado 2018

NGS Nominated CELA1, HSPG2, and KCNK5 as Candidate Genes for Predisposition to Balkan Endemic Nephropathy

por 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., Čukuranović, R., Polenakovic, M., Jankovic-Velickovic, L., Djordjevic, V., Jevtovic-Stoimenov, T., Plaseska-Karanfilska, D., Galabov, A., Djonov, V., Dimova, I.
Publicado 2014