| Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language ZH Rosser, T Zerjal, ME Hurles, M Adojaan, D Alavantic, A Amorim, ... The American Journal of Human Genetics 67 (6), 1526-1543, 2000 | 772 | 2000 |
| Toward male individualization with rapidly mutating y‐chromosomal short tandem repeats KN Ballantyne, A Ralf, R Aboukhalid, NM Achakzai, MJ Anjos, Q Ayub, ... Human mutation 35 (8), 1021-1032, 2014 | 211 | 2014 |
| 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 T Dörk, M Macek Jr, F Mekus, B Tümmler, J Tzountzouris, T Casals, ... Human genetics 106, 259-268, 2000 | 169 | 2000 |
| Children of Chernobyl cleanup workers do not show elevated rates of mutations in minisatellite alleles LA Livshits, SG Malyarchuk, EM Lukyanova, YG Antipkin, LP Arabskaya, ... Radiation research 155 (1), 74-80, 2001 | 116 | 2001 |
| A distribution of two SNPs in exon 10 of the FSHR gene among the women with a diminished ovarian reserve in Ukraine G Livshyts, S Podlesnaja, S Kravchenko, I Sudoma, L Livshits Journal of assisted reproduction and genetics 26, 29-34, 2009 | 76 | 2009 |
| Analysis of CCR5Δ32 geographic distribution and its correlation with some climatic and geographic factors SA Limborska, OP Balanovsky, EV Balanovskaya, PA Slominsky, ... Human heredity 53 (1), 49-54, 2002 | 57 | 2002 |
| 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 | 55 | 2003 |
| Clinical and molecular delineation of PUS3‐associated neurodevelopmental disorders M Nøstvik, SM Kateta, B Schönewolf‐Greulich, A Afenjar, M Barth, ... Clinical Genetics 100 (5), 628-633, 2021 | 31 | 2021 |
| Polymorphism of trinucleotide repeats in loci DM, DRPLA and SCA1 in East European populations SN Popova, PA Slominsky, EA Pocheshnova, EV Balanovskaya, ... European Journal of Human Genetics 9 (11), 829-835, 2001 | 29 | 2001 |
| TGFBI gene mutation analysis in families with hereditary corneal dystrophies from Ukraine VM Pampukha, GI Drozhyna, LA Livshits Ophthalmologica 218 (6), 411-414, 2004 | 25 | 2004 |
| Allelic polymorphism of F2, F5 and MTHFR genes in population of Ukraine P Tatarskyy, A Kucherenko, L Livshits Cytology and genetics 44 (3), 129-133, 2010 | 23 | 2010 |
| A Novel WT1 Mutation Identified in a 46,XX Testicular/Ovotesticular DSD Patient Results in the Retention of Intron 9 D Sirokha, O Gorodna, Y Vitrenko, N Zelinska, R Ploski, S Nef, ... Biology 10 (12), 1248, 2021 | 21 | 2021 |
| IFN-l-3 (IL28B) genotyping by restriction fragment length polymorphism method: detection polymorphism of rs12979860 VM Pampukha, SA Kravchenko, LV Moroz, LA Livshits Вiopolymers and Cell, 2011 | 19 | 2011 |
| Novel L558P mutation of the TGFBI gene found in Ukrainian families with atypical corneal dystrophy VM Pampukha, SA Kravchenko, FA Tereshchenko, LA Livshits, ... Ophthalmologica 223 (3), 207-214, 2009 | 16 | 2009 |
| Allele frequencies for D1S80 (pMCT118) locus in some East European populations DA Verbenko, TV Kekeeva, TV Pogoda, EK Khusnutdinova, AI Mikulich, ... Journal of forensic sciences 48 (1), 207-208, 2003 | 16 | 2003 |
| Association of PvuII polymorphism in ESR1 gene with impaired ovarian reserve in patients from Ukraine G Livshyts, S Podlesnaja, S Kravchenko, L Livshits Reproductive Biology 13 (1), 96-99, 2013 | 14 | 2013 |
| Study on possible role of CYP1A1, GSTT1, GSTM1, GSTP1, NAT2 and ADRB2 genes polymorphisms in bronchial asthma development in children PF Tatarskyy, NG Chumachenko, AM Kucherenko, RV Gulkovskyi, ... Вiopolymers and Cell, 2011 | 14 | 2011 |
| Heritable mutations at some minisatellite loci analysis in children of liquidators of Chernobyl accident consequences LA Livshits Int. J. Radiat. Med. 1, 101-106, 1999 | 14 | 1999 |
| Polymorphism of STR loci of the Y chromosome in three populations of eastern slavs from Belarus, Russia, and Ukraine SA Kravchenko, PA Slominsky, LA Bets, AV Stepanova, AI Mikulich, ... Russian Journal of Genetics 38, 80-86, 2002 | 13 | 2002 |
| The FKBP4 gene, encoding a regulator of the androgen receptor signaling pathway, is a novel candidate gene for androgen insensitivity syndrome E Ilaslan, R Markosyan, P Sproll, BJ Stevenson, M Sajek, MP Sajek, ... International journal of molecular sciences 21 (21), 8403, 2020 | 11 | 2020 |
Sergey KravchenkoInstitute of Molecular biology and Genetics在 imbg.org.ua 的电子邮件经过验证
