| Genome-wide expression profiling of human blood reveals biomarkers for Huntington's disease F Borovecki, L Lovrecic, J Zhou, H Jeong, F Then, HD Rosas, SM Hersch, ... Proceedings of the National Academy of Sciences 102 (31), 11023-11028, 2005 | 497 | 2005 |
| Therapeutic perspectives of epigenetically active nutrients M Remely, L Lovrecic, AL De La Garza, L Migliore, B Peterlin, FI Milagro, ... British journal of pharmacology 172 (11), 2756-2768, 2015 | 135 | 2015 |
| Sodium phenylbutyrate in Huntington's disease: A dose‐finding study P Hogarth, L Lovrecic, D Krainc Movement Disorders 22 (13), 1962-1964, 2007 | 124 | 2007 |
| An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge CA Brownstein, AH Beggs, N Homer, B Merriman, TW Yu, KC Flannery, ... Genome biology 15, 1-18, 2014 | 119 | 2014 |
| Legislation of direct-to-consumer genetic testing in Europe: a fragmented regulatory landscape L Kalokairinou, HC Howard, S Slokenberga, E Fisher, M Flatscher-Thöni, ... Journal of Community Genetics 9, 117-132, 2018 | 112 | 2018 |
| Nutriepigenomics: the role of nutrition in epigenetic control of human diseases M Remely, B Stefanska, L Lovrecic, U Magnet, AG Haslberger Current Opinion in Clinical Nutrition & Metabolic Care 18 (4), 328-333, 2015 | 89 | 2015 |
| 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 | 68 | 2018 |
| Points to consider for laboratories reporting results from diagnostic genomic sequencing DF Vears, K Sénécal, AJ Clarke, L Jackson, AM Laberge, L Lovrecic, ... European journal of human genetics 26 (1), 36-43, 2018 | 63 | 2018 |
| Transcriptomic analysis and meta-analysis of human granulosa and cumulus cells T Burnik Papler, E Vrtacnik Bokal, A Maver, AN Kopitar, L Lovrečić PloS one 10 (8), e0136473, 2015 | 52 | 2015 |
| 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 |
| 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 |
| No specific gene expression signature in human granulosa and cumulus cells for prediction of oocyte fertilisation and embryo implantation T Burnik Papler, E Vrtacnik Bokal, L Lovrecic, AN Kopitar, A Maver PloS one 10 (3), e0115865, 2015 | 42 | 2015 |
| Tumor necrosis factor-α-308 gene polymorphism in Croatian and Slovenian multiple sclerosis patients S Ristić, L Lovrečić, N Starčević-Čizmarević, B Brajenović-Milić, ... European neurology 57 (4), 203-207, 2007 | 40 | 2007 |
| Gene expression changes in blood as a putative biomarker for Huntington's disease L Lovrecic, A Kastrin, J Kobal, Z Pirtosek, D Krainc, B Peterlin Movement disorders: official journal of the Movement Disorder Society 24 (15 …, 2009 | 37 | 2009 |
| Specific gene expression differences in cumulus cells as potential biomarkers of pregnancy TB Papler, EV Bokal, A Maver, L Lovrečić Reproductive Biomedicine Online 30 (4), 426-433, 2015 | 34 | 2015 |
| Mutations in the hemochromatosis gene (HFE) and multiple sclerosis S Ristić, L Lovrečić, B Brajenović-Milić, N Starčević-Čizmarević, ... Neuroscience letters 383 (3), 301-304, 2005 | 31 | 2005 |
| High frequency of pathogenic ACAN variants including an intragenic deletion in selected individuals with short stature L Stavber, T Hovnik, P Kotnik, L Lovrečić, J Kovač, T Tesovnik, S Bertok, ... European journal of endocrinology 182 (3), 243-253, 2020 | 29 | 2020 |
| The role of epigenetics in neurodegenerative diseases L Lovrečić, A Maver, M Zadel, B Peterlin Neurodegenerative diseases 10, 54744, 2013 | 29 | 2013 |
| Angiotensin‐converting enzyme I/D gene polymorphism and risk of multiple sclerosis L Lovrečić, S Ristić, N Starčević‐Čizmarević, SŠ Jazbec, J Sepčić, ... Acta neurologica scandinavica 114 (6), 374-377, 2006 | 27 | 2006 |
| Clinical utility of array comparative genomic hybridisation in prenatal setting L Lovrecic, ZI Remec, M Volk, G Rudolf, K Writzl, B Peterlin BMC Medical Genetics 17, 1-8, 2016 | 25 | 2016 |
