Novel desmoplakin mutations in familial Carvajal syndrome

por YERMAKOVICH, DANAT, SIVITSKAYA, LARYSA, VAIKHANSKAYA, TATIYANA, DANILENKO, NINA, MOTUK, IRYNA
Publicado 2018

LMNA-related dilated cardiomyopathy

por Vaikhanskaya, Tatiyana, Sivitskaya, Larysa, Danilenko, Nina, Davydenko, Oleg, Kurushka, Tatsiyana, Sidorenko, Irina
Publicado 2014

Association of MIR137 With Symptom Severity and Cognitive Functioning in Belarusian Schizophrenia Patients

por Kandratsenka, Hanna, Nestsiarovich, Anastasiya, Goloenko, Inna, Danilenko, Nina, Makarevich, Anna, Obyedkov, Victor, Davydenko, Oleg, Waszkiewicz, Napoleon
Publicado 2018

Spectrum of Genetic Changes in Patients with Non-Syndromic Hearing Impairment and Extremely High Carrier Frequency of 35delG GJB2 Mutation in Belarus

por Danilenko, Nina, Merkulava, Elena, Siniauskaya, Marina, Olejnik, Olga, Levaya-Smaliak, Anastasia, Kushniarevich, Alena, Shymkevich, Andrey, Davydenko, Oleg
Publicado 2012

Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia

por Zytsar, Marina V., Barashkov, Nikolay A., Bady-Khoo, Marita S., Shubina-Olejnik, Olga A., Danilenko, Nina G., Bondar, Alexander A., Morozov, Igor V., Solovyev, Aisen V., Danilchenko, Valeriia Yu., Maximov, Vladimir N., Posukh, Olga L.
Publicado 2018

Uniparental Genetic Heritage of Belarusians: Encounter of Rare Middle Eastern Matrilineages with a Central European Mitochondrial DNA Pool

por Kushniarevich, Alena, Sivitskaya, Larysa, Danilenko, Nina, Novogrodskii, Tadeush, Tsybovsky, Iosif, Kiseleva, Anna, Kotova, Svetlana, Chaubey, Gyaneshwer, Metspalu, Ene, Sahakyan, Hovhannes, Bahmanimehr, Ardeshir, Reidla, Maere, Rootsi, Siiri, Parik, Jüri, Reisberg, Tuuli, Achilli, Alessandro, Hooshiar Kashani, Baharak, Gandini, Francesca, Olivieri, Anna, Behar, Doron M., Torroni, Antonio, Davydenko, Oleg, Villems, Richard
Publicado 2013