| Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: A cystic fibrosis mutation of Slavic origin common in Central and East Europe Human Genetics 106 (3), 259-268, 2000 | 173 | 2000 |
| Genetic diversity within the R408W phenylketonuria mutation lineages in Europe O Tighe, D Dunican, C O'Neill, G Bertorelle, D Beattie, C Graham, ... Human mutation 21 (4), 387-393, 2003 | 54 | 2003 |
| Development of micro-entrepreneurs in agriculture in wartime conditions M Malik, S Kravchenko, A Diuk, L Malik, M Nechyporenko Міжнародний науково-виробничий Журнал Економіка АПК. 2023. Т. 30.№ 2. С …, 2023 | 11 | 2023 |
| Analysis of EX5del4232ins268 and EX5del955 PAH gene mutations in Ukrainian patients with phenylketonuria V Pampukha, M Nechyporenko, L Livshyts Genes & diseases 4 (2), 108-110, 2017 | 9 | 2017 |
| Origin of dystrophin gene deletions in Duchenne and Becker muscular dystrophy patients from Ukraine SA Kravchenko, MV Nechyporenko, LA Livshits Cytology and Genetics 51, 185-191, 2017 | 7 | 2017 |
| Analysis of mutations in the phenylalanine hydroxylase gene in Ukrainian families at high risk for phenylketonuria MV Nechiporenko, LA Lalivshits Tsitologiia i Genetika 34 (6), 59-63, 2000 | 7 | 2000 |
| Analysis of mutations and VNTR-polymorphism in the phenylalanine hydroxylase gene LA Hechyporenko, M.V., Kravchenko, S.A., Livshyts Ukrainskii biokhimicheskii zhurnal 73 (2), 63, 2001 | 4* | 2001 |
| Mutation and VNTR-polymorphism analysis of phenylalanine hydroxylase gene Nechyporenko, M.V., Kravchenko, S.A., Livshits, L.A. Ukrain'skyi Biokhimichnyi Zhurnal 73 (2), 66-67, 2001 | 4* | 2001 |
| Allele Polymorphism of Micro- and Mini-Satellite Loci in Population of Different Regions of Ukraine LA Kravchenko, S.A., Pampukha, V.N., Ekshiyan, A.Yu., Nechiporenko, M.V ... Tsitologiia i Genetika 35 (5), 30-37, 2001 | 3 | 2001 |
| Analysis of Relative Average Length of Telomeres in Leukocytes of Women with COVID-19 DS Krasnienkov, OV Gorodna, TM Kaminska, VV Podolskiy, VV Podolskiy, ... Cytology and Genetics 56 (6), 526-529, 2022 | 2 | 2022 |
| Association between genotype and clinical manifestation of the most spread monogenic hereditary disorders LA Livshits, AM Bychkova, MV Nechyporenko, OY Ekshyyan, ... Biopolymers and Cell 20 (1-2), 107-114, 2004 | 2 | 2004 |
| Molecular and genetical study of phenylketonuria in Ukraine MV Nechyporenko, LA Livshits Eur J Hum Genet 10 (Suppl 1), 236, 2002 | 2 | 2002 |
| Molecular genetics analysis of mutations and minihaplotypes of the phenylalanine hydroxylase gene in Ukraine MV Nechyporenko, SA Kravchenko, LA Livshits Biopolymers and Cell 17 (6), 556-559, 2001 | 2 | 2001 |
| Human genome mutation and rearrangement studies–the way to investigate monogenic and complex disease pathogenesis LA Livshits, SA Kravchenko, MV Nechyporenko, VM Pampukha, ... Biopolymers and cell, 330-338, 2013 | 1 | 2013 |
| Розвиток суб’єктів мікропідприємництва у сільському господарстві в умовах воєнного часу M Malik, S Kravchenko, A Diuk, L Malik, M Nechyporenko Ekonomika APK 30 (2), 10-23, 2023 | | 2023 |
| Original Studies-Analysis of mutations of the phenylalanine hydroxylase gene in families of a high risk of phenylketonuria in Ukraine. MV Nechiporenko, LA Livshits Cytology and Genetics 34 (6), 47-51, 2000 | | 2000 |
| Analysis of phenylalanine hydroxilase gene mutations in families with high risk of phenylketonuria in Ukraine LA Nechiporenko, M.V., Livshitz Tsitologiia i Genetika 34 (6), 59-63, 2000 | | 2000 |
| «Наука та інновації» перехід на новий сайт LA Livshits, VM Pampukha, OA Yasinska, GB Livshits, NV Hryshchenko, ... | | |
Ludmila Livshits - Людмила ЛівшицьInstitute of Molecular Biology and Genetics, NAS of Ukraine在 imbg.org.ua 的电子邮件经过验证
