Bernarda Lozić

464 total citations
33 papers, 178 citations indexed

About

Bernarda Lozić is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Bernarda Lozić has authored 33 papers receiving a total of 178 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Pediatrics, Perinatology and Child Health and 9 papers in Genetics. Recurrent topics in Bernarda Lozić's work include Metabolism and Genetic Disorders (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Bernarda Lozić is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Bernarda Lozić collaborates with scholars based in Croatia, Bosnia and Herzegovina and Canada. Bernarda Lozić's co-authors include Tatijana Zemunik, Vjekoslav Krželj, Dragan Primorac, Joško Markić, Vesna Boraska Perica, Stefan Johansson, Per M. Knappskog, Helge Boman, Dragana Gabrić Pandurić and Angelika F. Hahn and has published in prestigious journals such as Nutrients, Biomolecules and Annals of Medicine.

In The Last Decade

Bernarda Lozić

28 papers receiving 165 citations

Peers

Bernarda Lozić
Mutluay Arslan Türkiye
Muralidharan Sargurupremraj United States
D. Agyapomaa Australia
Ulla Enger Norway
Merry Chen United States
Thipwimol Tim‐Aroon Thailand
Susana Boronat Spain
Ioannis Mavromatis Greece
Qi‐Lun Lai China
Sophia Kitsiou Greece
Mutluay Arslan Türkiye
Bernarda Lozić
Citations per year, relative to Bernarda Lozić Bernarda Lozić (= 1×) peers Mutluay Arslan

Countries citing papers authored by Bernarda Lozić

Since Specialization
Citations

This map shows the geographic impact of Bernarda Lozić's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Bernarda Lozić with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernarda Lozić more than expected).

Fields of papers citing papers by Bernarda Lozić

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bernarda Lozić. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Bernarda Lozić. The network helps show where Bernarda Lozić may publish in the future.

Co-authorship network of co-authors of Bernarda Lozić

This figure shows the co-authorship network connecting the top 25 collaborators of Bernarda Lozić. A scholar is included among the top collaborators of Bernarda Lozić based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Bernarda Lozić. Bernarda Lozić is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Kovačević, Tanja, Branka Polić, Joško Markić, et al.. (2025). Epidemiology and Treatment Outcomes in Neonates with Esophageal Atresia: A 30-Year Population-Based Study. Healthcare. 13(4). 418–418. 3 indexed citations
2.
3.
Odak, Ljubica, et al.. (2024). Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia. Croatian Medical Journal. 65(3). 198–209.
4.
Šoljić, Violeta, et al.. (2023). Spatio-Temporal Expression Pattern of CAKUT Candidate Genes DLG1 and KIF12 during Human Kidney Development. Biomolecules. 13(2). 340–340. 8 indexed citations
5.
Jadrijević, Stipislav, Bernarda Lozić, Marija Petrović, et al.. (2023). SPRTN is involved in hepatocellular carcinoma development through the ER stress response. Cancer Gene Therapy. 31(3). 376–386. 2 indexed citations
6.
7.
Kloth, Katja, Bernarda Lozić, Mariëtte J.V. Hoffer, et al.. (2021). ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants. Neurogenetics. 22(4). 263–269. 14 indexed citations
8.
Lozić, Bernarda, et al.. (2018). Hripavac u dojenačkoj dobi. Paediatria Croatica. 62. 171–175. 1 indexed citations
9.
Torlak, Vesela, Marijana Popović, Bernarda Lozić, et al.. (2017). Dietary Factors Associated with Plasma Thyroid Peroxidase and Thyroglobulin Antibodies. Nutrients. 9(11). 1186–1186. 23 indexed citations
10.
Lozić, Bernarda, Piotr Iwanowski, Tatijana Zemunik, et al.. (2017). Limited survivability of unbalanced progeny of carriers of a unique t(4;19)(p15.32;p13.3): a study in multiple generations. Molecular Cytogenetics. 10(1). 29–29. 12 indexed citations
11.
Lozić, Bernarda, et al.. (2015). Influence of the Inherited Glucose-6-phosphate Dehydrogenase Deficiency on the Appearance of Neonatal Hyperbilirubinemia in Southern Croatia. Acta Informatica Medica. 23(5). 264–264. 1 indexed citations
12.
Lozić, Bernarda, et al.. (2014). Aggressive middle turbinate osteoblastoma with intracranial extension: a case report. Journal of Medical Case Reports. 8(1). 161–161. 7 indexed citations
13.
Krželj, Vjekoslav, et al.. (2012). Introduction of obligatory vaccination against smallpox in Dalmatia and the city of Split during the first half of the 19th century. Paediatria Croatica. 56(1). 83–88. 1 indexed citations
14.
Siebert, Reiner, et al.. (2012). Endobronchial ALK+ Anaplastic Large-cell Lymphoma Resembling Asthma in a 13-Year-Old Girl. Journal of Pediatric Hematology/Oncology. 35(1). e4–e6. 8 indexed citations
15.
Lozić, Bernarda, et al.. (2012). Complete trisomy 10p resulting from an extra stable telocentric chromosome. American Journal of Medical Genetics Part A. 158A(7). 1778–1781. 3 indexed citations
16.
Lozić, Bernarda, et al.. (2011). Analysis of the C609T polymorphism of NQO1 gene in South Croatian patients with hematological malignancies.. PubMed. 35(2). 385–8. 2 indexed citations
17.
Primorac, Dragan, Bernarda Lozić, Vjekoslav Krželj, et al.. (2011). Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy. Croatian Medical Journal. 52(3). 396–402. 14 indexed citations
18.
Lozić, Bernarda, et al.. (2009). Early-onset facioscapulohumeral muscular dystrophy. Paediatria Croatica. 53(3). 153–157. 1 indexed citations
19.
20.
Lozić, Bernarda, et al.. (1998). Control of children with Down syndrome from 0 to 18 years of life. Paediatria Croatica. 42. 33. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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