| Vaginal microbiome signature is associated with spontaneous preterm delivery K Hočevar, A Maver, M Vidmar Šimic, A Hodžić, A Haslberger, ... Frontiers in medicine 6, 201, 2019 | 91 | 2019 |
| Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases G Bergant, A Maver, L Lovrecic, G Čuturilo, A Hodzic, B Peterlin Genetics in Medicine 20 (3), 303-312, 2018 | 70 | 2018 |
| Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis A Maver, P Lavtar, S Ristić, S Stopinšek, S Simčič, K Hočevar, J Sepčić, ... Scientific reports 7 (1), 3715, 2017 | 66 | 2017 |
| Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis P Lavtar, G Rudolf, A Maver, A Hodžić, N Starčević Čizmarević, M Živković, ... PloS one 13 (1), e0190601, 2018 | 50 | 2018 |
| Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice B Tumienė, A Maver, K Writzl, A Hodžić, G Čuturilo, R Kuzmanić‐Šamija, ... Clinical genetics 93 (5), 1057-1062, 2018 | 48 | 2018 |
| Phenotype-driven gene target definition in clinical genome-wide sequencing data interpretation M Ales, L Luca, V Marija, R Gorazd, W Karin, B Ana, H Alenka, B Peterlin Genetics in Medicine 18 (11), 1102-1110, 2016 | 45 | 2016 |
| Genetic variation in circadian rhythm genes CLOCK and ARNTL as risk factor for male infertility A Hodžić, M Ristanović, B Zorn, C Tulić, A Maver, I Novaković, B Peterlin PloS one 8 (3), e59220, 2013 | 42 | 2013 |
| Loss‐of‐Function Mutations in NR4A2 Cause Dopa‐Responsive Dystonia Parkinsonism T Wirth, LL Mariani, G Bergant, M Baulac, MO Habert, N Drouot, E Ollivier, ... Movement Disorders 35 (5), 880-885, 2020 | 28 | 2020 |
| De novo mutations in idiopathic male infertility—A pilot study A Hodžić, A Maver, D Plaseska‐Karanfilska, M Ristanović, P Noveski, ... Andrology 9 (1), 212-220, 2021 | 23 | 2021 |
| Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion A Hodžić, P Lavtar, M Ristanović, I Novaković, J Dotlić, B Peterlin PLoS One 13 (5), e0196345, 2018 | 20 | 2018 |
| A single nucleotide polymorphism of DNA methyltransferase 3B gene is a risk factor for recurrent spontaneous abortion A Barišić, N Pereza, A Hodžić, S Ostojić, B Peterlin American journal of reproductive immunology 78 (6), e12765, 2017 | 17 | 2017 |
| The −2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortion N Pereza, S Ostojić, A Smirčić, A Hodžić, M Kapović, B Peterlin Journal of assisted reproduction and genetics 32, 1789-1794, 2015 | 17 | 2015 |
| Genetic variation in the maternal vitamin D receptor FokI gene as a risk factor for recurrent pregnancy loss A Barišić, N Pereza, A Hodžić, MG Krpina, S Ostojić, B Peterlin The Journal of Maternal-Fetal & Neonatal Medicine 34 (14), 2221-2226, 2021 | 16 | 2021 |
| Genetic variation in leptin and leptin receptor genes as a risk factor for idiopathic male infertility A Hodžić, M Ristanović, B Zorn, C Tulić, A Maver, I Novaković, ... Andrology 5 (1), 70-74, 2017 | 13 | 2017 |
| Transcriptome profiling uncovers potential common mechanisms in fetal trisomies 18 and 21 M Volk, A Maver, A Hodžić, L Lovrečić, B Peterlin OMICS: A Journal of Integrative Biology 21 (10), 565-570, 2017 | 12 | 2017 |
| Genetic variation in leptin and leptin receptor genes is a risk factor for idiopathic recurrent spontaneous abortion A Müller, J Wagner, A Hodžić, A Maver, I Škrlec, M Heffer, L Zibar, ... Croatian medical journal 57 (6), 566-571, 2016 | 10 | 2016 |
| The role of next generation sequencing in the differential diagnosis of caroli’s syndrome B Smolović, D Muhović, A Hodžić, G Bergant, B Peterlin Balkan Journal of Medical Genetics 21 (2), 49-53, 2018 | 7 | 2018 |
| Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion A Barišić, N Pereza, A Hodžić, M Kapović, B Peterlin, S Ostojić Journal of assisted reproduction and genetics 34, 365-371, 2017 | 4 | 2017 |
| Case Report: Non-ossifying fibromas with pathologic fractures in a patient with NONO-associated X-linked syndromic intellectual developmental disorder K Writzl, B Mavčič, A Maver, A Hodžić, B Peterlin Frontiers in Genetics 14, 1167054, 2023 | 3 | 2023 |
| Transcriptomic signatures for human male infertility A Hodžić, A Maver, B Zorn, D Petrovič, T Kunej, B Peterlin Frontiers in molecular biosciences 10, 2023 | 2 | 2023 |
