| ATP7B Gene Mutations in Croatian Patients with Wilson Disease H Ljubić, M Kalauz, S Telarović, P Ferenci, R Ostojić, MC Noli, MB Lepori, ... Genetic Testing and Molecular Biomarkers 20 (3), 112-117, 2016 | 32 | 2016 |
| Haptoglobin genotype 2-2 associated with atherosclerosis in patients with ischemic stroke A Merkler, J Sertić, AB Martinović, T Križ, I Miličić, M Šimić, D Caban, ... Gene 752, 144786, 2020 | 9 | 2020 |
| Total tau in cerebrospinal fluid detects treatment responders among spinal muscular atrophy types 1–3 patients treated with nusinersen G Šimić, V Vukić, M Babić, M Banović, I Berečić, E Španić, K Zubčić, ... CNS Neuroscience & Therapeutics 30 (3), e14051, 2024 | 5 | 2024 |
| Moderating effect of ppar-γ on the association of c-reactive protein and ischemic stroke in patients younger than 60 AB Martinović, A Merkler, I Ćelić, K Starčević, M Šimić, I Karmelić, ... Gene 809, 146029, 2022 | 4 | 2022 |
| Homocystinuria in adult patients D Muačević Katanec, A Merkler, K Fumić, I Barić, M Merkler, Ž Reiner Paediatria Croatica 58 (3), 208-214, 2014 | 4 | 2014 |
| Can the choice of diet undermine the potential genetic risk of AT1R 1166A> C gene polymorphism? T Božina, J Lovrić, L Šimičević, A Merkler, M Božina, B Jelaković, J Sertić Gene 679, 291-296, 2018 | 3 | 2018 |
| Is there any association of apolipoprotein E gene polymorphisms with metabolic syndrome in a young population of Croatian origin? I Karmelić, J Lovrić, T Božina, A Merkler, N Božina, J Sertić Annals of human biology 44 (3), 287-294, 2017 | 3 | 2017 |
| Nasljedne polineuropatije Charcot-Marie-Tooth Z Mitrović, L Juričić, A Merkler, J Sertić | 2 | 2015 |
| The first report on MODY testing in children in Croatia A Špehar Uroić, A Merkler, N Krnić, I Miličić, N Rojnić Putarek, D Caban, ... 47th Annual Conference of the International Society for Pediatric and …, 2021 | 1 | 2021 |
| Nasljedna hemokromatoza I Šimić, A Merkler, I Jurčević, J Sertić | 1 | 2015 |
| Mutational spectrum of MEN1 and MEN2 syndrome in Croatian patients A Merkler Šorgić, H Ljubić, A Acman Barišić, D Caban, S Kusačić-Kuna, ... European Human Genetics Conference; Hybrid Conference 32, 131-131, 2024 | | 2024 |
| Cistična fibroza–ishodi liječenja u Hrvatskoj uz CFTR modulatore D Tješić-Drinković, I Bambir, D Tješić-Drinković, A Vukić Dugac, I Bambiar, ... Liječnički vjesnik 145 (Supp 5), 121-130, 2023 | | 2023 |
| Cystic Fibrosis–results of CFTR modulators in Croatia D Tješić-Drinković, I Bambir, D Tješić-Drinković, A Vukić Dugac, I Bambiar, ... Liječnički vjesnik 145 (Supp 5), 121-130, 2023 | | 2023 |
| Jesu li bubrežne malformacije jedno od obilježja sindroma MEN2B?–prikaz bolesnika i pregled literature A Špehar Uroić, N Rojnić Putarek, L Kolega Mrkić, S Kusačić-Kuna, ... Liječnički vjesnik 145 (5-6), 212-215, 2023 | | 2023 |
| Gene panel analysis of literature-based infertility genes in Sertoli cell-only syndrome patients ML Klarić, L Žunić, T Marić, L Trgovec-Greif, F Rokić, A Merkler, R Belužić, ... Genetics & applications 7 (1), 20-26, 2023 | | 2023 |
| Angiotensin-converting enzyme 1 gene polymorphisms in patients with systemic sclerosis-associated interstitial lung disease: a single centre retrospective observational study AB Karanović Boris, Barešić Marko, Merkler Šorgić Ana Rheumatology International, 2023 | | 2023 |
| Genetic analysis of azoospermic men by an integrated NGS panel ML Klaric, L Trgovec-Greif, L Zunic, F Rokic, A Vicic, T Maric, A Merkler, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 90-90, 2022 | | 2022 |
| Genetic analysis of azoospermic men by an integrated NGS panel M Logara Klarić, L Trgovec-Greif, L Žunić, F Rokić, A Vičić, T Marić, ... Nepoznat skup, 90-90, 2022 | | 2022 |
| HEMOKROMATOZA-INTERPRETACIJA GENETSKIH PRETRAGA J Sertić, K Kajić, A Acman Barišić, A Merkler Šorgić | | 2022 |
| Molekularna analiza gena BRCA1/2 – sekvenciranje sljedeće generacije, MPLA i sekvenciranje po Sangeru kao komplementarne metode R I, B T, M A, L H, R D, D Plavetić N 10. kongres Hrvatskog društva za medicinsku biokemiju i laboratorijsku …, 2022 | | 2022 |
