| Bardet–Biedl syndrome—Multiple kaleidoscope images: insight into mechanisms of genotype–phenotype correlations L Florea, L Caba, EV Gorduza Genes 12 (9), 1353, 2021 | 46 | 2021 |
| Circular RNA—Is the Circle Perfect? L Caba, L Florea, C Gug, DC Dimitriu, EV Gorduza Biomolecules 11 (12), 1755, 2021 | 36 | 2021 |
| Increased nuchal translucency in fetuses with a normal karyotype—diagnosis and management An observational study PI Socolov D., Socolov R., Gorduza E.V., Butureanu T., Stanculescu R ... Medicine 96 (29), e7521, 2017 | 34 | 2017 |
| Genetic modifying factors of cystic fibrosis phenotype: a challenge for modern medicine LI Butnariu, E Țarcă, E Cojocaru, C Rusu, ȘM Moisă, ... Journal of Clinical Medicine 10 (24), 5821, 2021 | 32 | 2021 |
| Holt-Oram syndrome with multiple cardiac abnormalities MR Spiridon, AO Petris, EV Gorduza, AS Petras, R Popescu, L Caba Cardiology research 9 (5), 324, 2018 | 30 | 2018 |
| Etiologic puzzle of coronary artery disease: how important is genetic component? LI Butnariu, L Florea, MC Badescu, E Țarcă, II Costache, EV Gorduza Life 12 (6), 865, 2022 | 25 | 2022 |
| Ring autosomes: some unexpected findings L Caba, C Rusu, V Plăiaşu, G Gug, M Grămescu, C Bujoran, D Ochiană, ... Balkan Journal of Medical Genetics 15 (2), 35-46, 2012 | 25 | 2012 |
| Clinical and cytogenetic correlation in primary and secondary amenorrhea: retrospective study on 531 patients L Butnariu, M Covic, I Ivanov, C Bujoran, M Gramescu, EV Gorduza Revista Română de Medicină de Laborator 19 (2/4), 2011 | 24 | 2011 |
| Rare splicing mutation in COL1A1 gene identified by whole exomes sequencing in a patient with osteogenesis imperfecta type I followed by prenatal diagnosis: A case report and … C Gug, L Caba, I Mozos, D Stoian, D Atasie, M Gug, EV Gorduza Gene 741, 144565, 2020 | 19 | 2020 |
| Wolf-Hirschhorn syndrome: clinical and genetic study of 7 new cases, and mini review EC Gavril, AC Luca, AS Curpan, R Popescu, I Resmerita, MC Panzaru, ... Children 8 (9), 751, 2021 | 18 | 2021 |
| Structure-reactivity relationships of antioxidant flavonoides V Gorduza, C Tarabasanu, A Gorduza, C Cernatescu, M Rusu Ovidius University Annals of Chemistry 11 (1), 56-59, 2000 | 17 | 2000 |
| Genetic heterogeneity in corpus callosum agenesis MC Pânzaru, S Popa, A Lupu, C Gavrilovici, VV Lupu, EV Gorduza Frontiers in Genetics 13, 958570, 2022 | 16 | 2022 |
| Genetic heterogeneity in Bartter syndrome: clinical and practical importance L Florea, L Caba, EV Gorduza Frontiers in Pediatrics 10, 908655, 2022 | 15 | 2022 |
| Genetic counseling and management: the first study to report NIPT findings in a Romanian population C Gug, I Mozos, A Ratiu, A Tudor, EV Gorduza, L Caba, M Gug, ... Medicina 58 (1), 79, 2022 | 15 | 2022 |
| Gorham-stout disease with multiple bone involvement—challenging diagnosis of a rare disease and literature review A Momanu, L Caba, NC Gorduza, OE Arhire, AD Popa, V Ianole, ... Medicina 57 (7), 681, 2021 | 15 | 2021 |
| Genetics of Hearing Impairment in North-Eastern Romania—A Cost-Effective Improved Diagnosis and Literature Review I Resmerita, RS Cozma, R Popescu, LM Radulescu, MC Panzaru, ... Genes 11 (12), 1506, 2020 | 15 | 2020 |
| Nutrigenomics in postgenomic era. EV Gorduza, LL Indrei, VM Gorduza Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi …, 2008 | 15 | 2008 |
| Phenotypic variability in Patau syndrome L Caba¹, C Rusu¹, L Butnariu¹, M Panzaru¹, E Braha¹, M Volosciuc, ... | 14 | 2013 |
| Genetic counselling in reproductive disorders GC Cozaru, LI Butnariu, EV Gorduza Procedia-Social and Behavioral Sciences 33, 213-217, 2012 | 14 | 2012 |
| Compendiu de genetică umană şi medicală EV Gorduza, O Stoica, E Braha, L Butnariu Tehnopress, 2008 | 14 | 2008 |
