| Bardet–Biedl syndrome—Multiple kaleidoscope images: insight into mechanisms of genotype–phenotype correlations L Florea, L Caba, EV Gorduza Genes 12 (9), 1353, 2021 | 42 | 2021 |
| Circular RNA—Is the Circle Perfect? L Caba, L Florea, C Gug, DC Dimitriu, EV Gorduza Biomolecules 11 (12), 1755, 2021 | 30 | 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 | 28 | 2018 |
| 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 |
| 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 | 18 | 2020 |
| 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 |
| 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 | 14 | 2021 |
| Prenatal diagnosis of 21 trisomy by quantification of methylated fetal DNA in maternal blood: study on 10 pregnancies EV Gorduza, R Popescu, L Caba, I Ivanov, V Martiniuc, F Nedelea, ... Revista Romana de Medicina de Laborator 21 (3), 275-284, 2013 | 14* | 2013 |
| Genetic heterogeneity in Bartter syndrome: clinical and practical importance L Florea, L Caba, EV Gorduza Frontiers in Pediatrics 10, 908655, 2022 | 13 | 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 | 13 | 2022 |
| Comparison between paramagnetic and CD71 magnetic activated cell sorting of fetal nucleated red blood cells from the maternal blood D Nemescu, D Constantinescu, V Gorduza, A Carauleanu, L Caba, ... Journal of Clinical Laboratory Analysis 34 (9), e23420, 2020 | 13 | 2020 |
| Phenotypic variability in Patau syndrome L Caba¹, C Rusu¹, L Butnariu¹, M Panzaru¹, E Braha¹, M Volosciuc, ... | 13 | 2013 |
| Drogodependenţa-numai problemă medicală MC Vicol, OC Stîngă, L Caba, B Ioan, V Astărăstoae Revista Română de Bioetică 6 (4), 2008 | 13* | 2008 |
| Epidermolysis Bullosa—A Different Genetic Approach in Correlation with Genetic Heterogeneity MC Pânzaru, L Caba, L Florea, EE Braha, EV Gorduza Diagnostics 12 (6), 1325, 2022 | 12 | 2022 |
| Genotype-phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literature L BUTNARIU, R Cristina, C Lavinia, M Pânzaru, E Braha, M GRAMESCU, ... The Medical-Surgical Journal 117 (3), 714-721, 2013 | 11 | 2013 |
| Novel Mutation in APC Gene Associated with Multiple Osteomas in a Family and Review of Genotype-Phenotype Correlations of Extracolonic Manifestations in … C Antohi, D Haba, L Caba, ML Ciofu, VL Drug, OB Bărboi, BI Dobrovăț, ... Diagnostics 11 (9), 1560, 2021 | 10 | 2021 |
| Chromosomal evaluation in couples with reproductive disorders--retrospective study of a selected group of 266 couples L Butnariu, M Covic, M Onofriescu, M Grămescu, C Bujoran, L Caba, ... Revista Medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi …, 2010 | 10 | 2010 |
| Detection of chromosomal imbalances using combined MLPA kits in patients with syndromic intellectual disability A Sireteanu, R Popescu, EE Braha, C Bujoran, L Butnariu, L Caba, ... Revista Romana de Medicina de Laborator 22 (2), 157-164, 2014 | 9 | 2014 |
| Benefits of cytogenetic testing in diagnosis of plurimalformative syndromes with congenital heart defects M Pânzaru¹, C Rusu¹, M Voloşciuc, E Braha¹, L Butnariu¹, M Gramescu¹, ... Revista Română de Medicină de Laborator Vol 20 (3/4), 2012 | 8 | 2012 |
| Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counseling MC Panzaru, A Florea, L Caba, EV Gorduza World Journal of Clinical Cases 11 (12), 2604, 2023 | 7 | 2023 |
