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L. Lovrečić · SciRah

Researcher profile · Semantic Scholar

L. Lovrečić

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L. Lovrečić — researcher profile on SciRah

h-index: 20
Works: 87
Citations: 1,984

Most-cited papers

Genome-wide expression profiling of human blood reveals biomarkers for Huntington's disease.
F. Borovecki, L. Lovrečić, J. Zhou, H. Jeong +7 more
2005Proceedings of the National Academy of Sciences of the United States of America419 citations Open access
Semantic Scholar
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
C. Brownstein, A. Beggs, N. Homer, Barry Merriman +194 more
2014Genome Biology308 citations Open access
Semantic Scholar
Therapeutic perspectives of epigenetically active nutrients
M. Remely, L. Lovrečić, A. L. de la Garza, L. Migliore +4 more
2015British Journal of Pharmacology115 citations Open access
Semantic Scholar
Sodium phenylbutyrate in Huntington's disease: A dose‐finding study
P. Hogarth, L. Lovrečić, D. Krainc
2007Movement Disorders93 citations
Semantic Scholar
Legislation of direct-to-consumer genetic testing in Europe: a fragmented regulatory landscape
L. Kalokairinou, H. Howard, S. Slokenberga, E. Fisher +21 more
2017Journal of Community Genetics89 citations Open access
Semantic Scholar
Comprehensive use of extended exome analysis improves diagnostic yield in rare disease: a retrospective survey in 1,059 cases
G. Bergant, A. Maver, L. Lovrečić, G. Čuturilo +2 more
2017Genetics in Medicine81 citations Open access
Semantic Scholar
Points to consider for laboratories reporting results from diagnostic genomic sequencing
D. Vears, K. Sénécal, A. J. Clarke, L. Jackson +7 more
2017European Journal of Human Genetics65 citations Open access
Semantic Scholar
Nutriepigenomics: the role of nutrition in epigenetic control of human diseases
M. Remely, B. Stefańska, L. Lovrečić, U. Magnet +1 more
2015Current opinion in clinical nutrition and metabolic care62 citations
Semantic Scholar
Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis
Polona Lavtar, G. Rudolf, A. Maver, A. Hodzic +12 more
2018PLoS ONE50 citations Open access
Semantic Scholar
Recommendations for reporting results of diagnostic genomic testing
Z. Deans, J. Ahn, I. Carreira, E. Dequeker +6 more
2022European Journal of Human Genetics46 citations Open access
Semantic Scholar
Transcriptomic Analysis and Meta-Analysis of Human Granulosa and Cumulus Cells
T. BurnikPapler, Eda Vrtacnik Bokal, A. Maver, A. Kopitar +1 more
2015PLoS ONE36 citations Open access
Semantic Scholar
Mutations in the hemochromatosis gene (HFE) and multiple sclerosis.
S. Ristić, L. Lovrečić, B. Brajenović-Milić, Nada Starčević-Čižmarević +4 more
2005Neuroscience Letters35 citations
Semantic Scholar
No Specific Gene Expression Signature in Human Granulosa and Cumulus Cells for Prediction of Oocyte Fertilisation and Embryo Implantation
T. BurnikPapler, Eda Vrtacnik Bokal, L. Lovrečić, A. Kopitar +1 more
2015PLoS ONE33 citations Open access
Semantic Scholar
High frequency of pathogenic ACAN variants including an intragenic deletion in selected individuals with short stature
Lana Stavber, T. Hovnik, P. Kotnik, L. Lovrečić +7 more
2019European Journal of Endocrinology32 citations Open access
Semantic Scholar
Specific gene expression differences in cumulus cells as potential biomarkers of pregnancy.
T. BurnikPapler, Eda Vrtacnik Bokal, A. Maver, L. Lovrečić
2015Reproductive Biomedicine Online28 citations Open access
Semantic Scholar
Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome.
J. van der Spek, J. den Hoed, Lot Snijders Blok, A. Dingemans +42 more
2022Genetics in Medicine27 citations Open access
Semantic Scholar
Clinical utility of array comparative genomic hybridisation in prenatal setting
L. Lovrečić, Ž. I. Remec, M. Volk, G. Rudolf +2 more
2016BMC Medical Genetics25 citations Open access
Semantic Scholar
The Role of Epigenetics in Neurodegenerative Diseases
L. Lovrečić, A. Maver, M. Zadel, B. Peterlin
201323 citations Open access
Semantic Scholar
Epidemiology of Huntington’s disease in Slovenia
B. Peterlin, J. Kobal, N. Teran, D. Flisar +1 more
2009Acta Neurologica Scandinavica23 citations Open access
Semantic Scholar
Tumor Necrosis Factor-α-308 Gene Polymorphism in Croatian and Slovenian Multiple Sclerosis Patients
S. Ristić, L. Lovrečić, Nada Starčević-Čižmarević, B. Brajenović-Milić +4 more
2007European Neurology21 citations
Semantic Scholar
The genetic approach to stillbirth: A »systematic review«
M. Merc, B. Peterlin, L. Lovrečić
2023Prenatal Diagnosis20 citations Open access
Semantic Scholar
Angiotensin‐converting enzyme I/D gene polymorphism and risk of multiple sclerosis
L. Lovrečić, S. Ristić, N. Starčević Čizmarević, S. Jazbec +3 more
2006Acta Neurologica Scandinavica20 citations Open access
Semantic Scholar
Human Y-specific STR haplotypes in the Western Croatian population sample.
L. Lovrečić, S. Ristić, Bojana Brajenović, M. Kapović +1 more
2005Forensic Science International19 citations
Semantic Scholar
No association of CCR5D32 gene mutation with multiple sclerosis in Croatian and Slovenian patients
S. Ristić, L. Lovrečić, Nada Starčević-Čižmarević, B. Brajenović-Milić +6 more
2005Multiple Sclerosis19 citations
Semantic Scholar
Diagnostic efficacy and new variants in isolated and complex autism spectrum disorder using molecular karyotyping
L. Lovrečić, Polona Rajar, M. Volk, S. Bertok +4 more
2018Journal of Applied Genetics18 citations
Semantic Scholar
The Role of TPA I/D and PAI-1 4G/5G Polymorphisms in Multiple Sclerosis
M. Živković, N. Starčević Čizmarević, L. Lovrečić, Inge Klupka-Sarić +13 more
2014Disease Markers18 citations Open access
Semantic Scholar
Interleukin 7 receptor alpha polymorphism rs6897932 and susceptibility to multiple sclerosis in the Western Balkans
A. Stanković, E. Dinčić, S. Ristić, L. Lovrečić +8 more
2010Multiple Sclerosis18 citations Open access
Semantic Scholar
11q terminal deletion and combined immunodeficiency (Jacobsen syndrome): Case report and literature review on immunodeficiency in Jacobsen syndrome
S. Blazina, A. Ihan, L. Lovrečić, T. Hovnik
2016American Journal of Medical Genetics. Part A17 citations
Semantic Scholar
Expression Signature as a Biomarker for Prenatal Diagnosis of Trisomy 21
M. Volk, A. Maver, L. Lovrečić, P. Juvan +1 more
2013PLoS ONE16 citations Open access
Semantic Scholar
PAI and TPA gene polymorphisms in multiple sclerosis
L. Lovrečić, S. Ristić, Nada Starčević-Čižmarević, B. Brajenović-Milić +4 more
2008Multiple Sclerosis15 citations
Semantic Scholar
The Endometrial Transcriptome of Metabolic and Inflammatory Pathways During the Window of Implantation Is Deranged in Infertile Obese Polycystic Ovarian Syndrome Women
V. Šalamun, M. Rizzo, L. Lovrečić, Keli Hočevar +6 more
2022Metabolic Syndrome and Related Disorders13 citations
Semantic Scholar
ADP-Ribosylation Factor Guanine Nucleotide-Exchange Factor 2 (ARFGEF2): A New Potential Biomarker in Huntington's Disease
L. Lovrečić, Ivica Slavkov, S. Džeroski, B. Peterlin
2010Journal of International Medical Research13 citations Open access
Semantic Scholar
Transcriptome Profiling Uncovers Potential Common Mechanisms in Fetal Trisomies 18 and 21
M. Volk, A. Maver, A. Hodzic, L. Lovrečić +1 more
2017Omics12 citations Open access
Semantic Scholar
A Systematic Clinical Review of Prenatally Diagnosed Tetrasomy 9p
M. Vinkšel, M. Volk, B. Peterlin, L. Lovrečić
2019Balkan Journal of Medical Genetics10 citations Open access
Semantic Scholar
Combination of QF‐PCR and aCGH is an efficient diagnostic strategy for the detection of chromosome aberrations in recurrent miscarriage
L. Lovrečić, N. Pereza, H. Jaklic, S. Ostojić +1 more
2019Molecular Genetics & Genomic Medicine10 citations Open access
Semantic Scholar
A New Case of an Extremely Rare 3p21.31 Interstitial Deletion
L. Lovrečić, S. Bertok, Mojca Žerjav Tanšek
2016Molecular Syndromology10 citations Open access
Semantic Scholar
Chronic Lymphocytic Leukemia with Divergent Richter’s Transformation into a Clonally Related Classical Hodgkin’s and Plasmablastic Lymphoma: A Case Report
G. Gašljević, M. Grat, Veronika Kloboves Prevodnik, Biljana Grčar Kuzmanov +3 more
2020Case Reports in Oncology9 citations Open access
Semantic Scholar
Microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disability
L. Lovrečić, C. Gnan, Federica Baldan, A. Franzoni +4 more
2018Molecular Cytogenetics8 citations Open access
Semantic Scholar
Interstitial deletion 2p11.2–p12: Further delineation
K. Writzl, L. Lovrečić, B. Peterlin
2009American Journal of Medical Genetics. Part A8 citations
Semantic Scholar
The interleukin-1 receptor antagonist gene and the inhibitor of kappa B-like protein gene polymorphisms are not associated with myocardial infarction in Slovene population with type 2 diabetes.
S. Kariž, A. Milutinović, D. Bregar, I. Terzić +7 more
2007Collegium Antropologicum8 citations
Semantic Scholar
Further exploration of cardiac channelopathy and cardiomyopathy genes in stillbirth
M. Merc, U. Kotnik, B. Peterlin, L. Lovrečić
2024Prenatal Diagnosis7 citations Open access
Semantic Scholar
Brachytelephalangic chondrodysplasia punctata caused by new small hemizygous deletion in a boy presenting with hearing loss
Irena Vrecar, G. Rudolf, B. Peterlin, L. Lovrečić
2015Molecular Cytogenetics7 citations Open access
Semantic Scholar
MMP-2 -1575G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS?
I. Gašparović, N. S. Čizmarević, L. Lovrečić, O. Perković +6 more
2015Journal of Neuroimmunology7 citations
Semantic Scholar
Direct-to-consumer genetic testing in Slovenia: availability, ethical dilemmas and legislation
Irena Vrecar, B. Peterlin, N. Teran, L. Lovrečić
2015Biochemia Medica6 citations Open access
Semantic Scholar
Heterogeneity of the triple A syndrome and assessment of a case.
L. Lovrečić, A. Pelet, B. Peterlin
2006Genetic Counseling6 citations
Semantic Scholar
A Comprehensive Genetic Analysis of Slovenian Families with Multiple Cases of Orofacial Clefts Reveals Novel Variants in the Genes IRF6, GRHL3, and TBX22
L. Slavec, K. Geršak, A. Eberlinc, T. Hovnik +3 more
2023International Journal of Molecular Sciences5 citations Open access
Semantic Scholar
Optical genome mapping in an atypical Pelizaeus-Merzbacher prenatal challenge
M. Rogač, Anja Kovanda, L. Lovrečić, B. Peterlin
2023Frontiers in Genetics5 citations Open access
Semantic Scholar
Evaluation of Optical Genome Mapping in Clinical Genetic Testing of Facioscapulohumeral Muscular Dystrophy
Anja Kovanda, L. Lovrečić, G. Rudolf, Ivana Babic Bozovic +3 more
2023medRxiv5 citations Open access
Semantic Scholar
Angiotensin-Converting Enzyme Gene Polymorphism in Patients with Multiple Sclerosis from Bosnia and Herzegovina
Inge Klupka-Sarić, B. Peterlin, L. Lovrečić, O. Sinanović +6 more
2011Genetic Testing and Molecular Biomarkers5 citations
Semantic Scholar
Creating the Slovenian genome database and browser as a source of comprehensive variation of the Slovenian population
A. Maver, Peter Juvan, U. Kotnik, L. Lovrečić +2 more
2025Scientific Reports4 citations Open access
Semantic Scholar

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M. Volk — researcher profile on SciRah

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N. Starčević Čizmarević — researcher profile on SciRah

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Eda Vrtacnik Bokal — researcher profile on SciRah

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Nada Starčević-Čižmarević — researcher profile on SciRah