Lavinia Caba

489 total citations
37 papers, 283 citations indexed

About

Lavinia Caba is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lavinia Caba has authored 37 papers receiving a total of 283 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 16 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lavinia Caba's work include Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Lavinia Caba is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Lavinia Caba collaborates with scholars based in Romania, United States and Pakistan. Lavinia Caba's co-authors include Eusebiu Vlad Gorduza, Laura Florea, Cristina Gug, Alina Delia Popa, Roxana Popescu, Lidia Iuliana Arhire, Laura Mihalache, Otilia Niță, Lăcrămioara Ionela Butnariu and Cristina Rusu and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Gene.

In The Last Decade

Lavinia Caba

32 papers receiving 279 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Lavinia Caba Romania 11 140 119 48 40 40 37 283
Eusebiu Vlad Gorduza Romania 12 161 1.1× 149 1.3× 72 1.5× 65 1.6× 45 1.1× 49 385
Angeline Lai Singapore 10 152 1.1× 133 1.1× 23 0.5× 67 1.7× 28 0.7× 31 349
Banu Nur Türkiye 12 150 1.1× 125 1.1× 35 0.7× 51 1.3× 10 0.3× 36 358
Azmy M. Al-Hadidy Jordan 9 94 0.7× 89 0.7× 18 0.4× 49 1.2× 22 0.6× 21 274
Karen E. Hemmings United Kingdom 11 186 1.3× 49 0.4× 57 1.2× 49 1.2× 35 0.9× 18 402
Moira Blyth United Kingdom 12 139 1.0× 162 1.4× 51 1.1× 57 1.4× 16 0.4× 22 379
Alvaro Mesoraca Italy 11 140 1.0× 69 0.6× 95 2.0× 35 0.9× 38 0.9× 38 349
Hala Mégarbané Lebanon 12 325 2.3× 161 1.4× 20 0.4× 39 1.0× 15 0.4× 24 495
J. Garcı́a Rodrı́guez Spain 9 161 1.1× 163 1.4× 60 1.3× 120 3.0× 18 0.5× 54 431
Tzu-Ping Lin Taiwan 9 174 1.2× 114 1.0× 14 0.3× 43 1.1× 15 0.4× 23 333

Countries citing papers authored by Lavinia Caba

Since Specialization
Citations

This map shows the geographic impact of Lavinia Caba'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 Lavinia Caba with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lavinia Caba more than expected).

Fields of papers citing papers by Lavinia Caba

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lavinia Caba. 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 Lavinia Caba. The network helps show where Lavinia Caba may publish in the future.

Co-authorship network of co-authors of Lavinia Caba

This figure shows the co-authorship network connecting the top 25 collaborators of Lavinia Caba. A scholar is included among the top collaborators of Lavinia Caba 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 Lavinia Caba. Lavinia Caba 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.
Caba, Lavinia, Petru Cianga, Vasile Drug, et al.. (2025). Genetic and Epigenetic Factors in Ulcerative Colitis: A Narrative Literature Review. Genes. 16(9). 1085–1085.
2.
Andreescu, Nicoleta, et al.. (2025). The Landscape of Genetic Variation and Disease Risk in Romania: A Single-Center Study of Autosomal Recessive Carrier Frequencies and Molecular Variants. International Journal of Molecular Sciences. 26(22). 10912–10912.
3.
Caba, Lavinia, Roxana Popescu, Laura Florea, et al.. (2024). Unlocking the Genetic Secrets of Acromegaly: Exploring the Role of Genetics in a Rare Disorder. Current Issues in Molecular Biology. 46(8). 9093–9121.
4.
Popa, Alina Delia, Lavinia Caba, Otilia Niță, et al.. (2024). Cathelicidin: Insights into Its Impact on Metabolic Syndrome and Chronic Inflammation. Metabolites. 14(12). 672–672. 5 indexed citations
5.
Popa, Alina Delia, Otilia Niță, Lavinia Caba, et al.. (2023). From the Sun to the Cell: Examining Obesity through the Lens of Vitamin D and Inflammation. Metabolites. 14(1). 4–4. 4 indexed citations
6.
7.
Budișteanu, Magdalena, Lavinia Caba, Lăcrămioara Ionela Butnariu, et al.. (2023). Exome sequencing in a Romanian Bardet‐Biedl syndrome cohort revealed an overabundance of causal BBS12 variants. American Journal of Medical Genetics Part A. 191(9). 2376–2391. 4 indexed citations
8.
Caba, Lavinia, et al.. (2023). Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counseling. World Journal of Clinical Cases. 11(12). 2604–2620. 10 indexed citations
9.
Popescu, Roxana, et al.. (2023). Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome. International Journal of Molecular Sciences. 24(11). 9206–9206. 8 indexed citations
10.
Caba, Lavinia, et al.. (2022). Clinical Aspects of a Rare Disease: Bardet Biedl Syndrome. Medicina Moderna - Modern Medicine. 29(1). 37–42. 2 indexed citations
11.
Caba, Lavinia, et al.. (2022). Monitoring and Management of Bardet-Biedl Syndrome: What the Multi-Disciplinary Team Can Do. Journal of Multidisciplinary Healthcare. Volume 15. 2153–2167. 11 indexed citations
12.
Caba, Lavinia, et al.. (2022). Genomics and Epigenomics in the Molecular Biology of Melanoma—A Prerequisite for Biomarkers Studies. International Journal of Molecular Sciences. 24(1). 716–716. 9 indexed citations
13.
Florea, Laura, Lavinia Caba, & Eusebiu Vlad Gorduza. (2022). Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance. Frontiers in Pediatrics. 10. 908655–908655. 9 indexed citations
14.
Haba, Danisia, Lavinia Caba, Vasile Drug, et al.. (2021). Novel Mutation in APC Gene Associated with Multiple Osteomas in a Family and Review of Genotype-Phenotype Correlations of Extracolonic Manifestations in Gardner Syndrome. Diagnostics. 11(9). 1560–1560. 8 indexed citations
15.
Popescu, Roxana, Lavinia Caba, Lăcrămioara Ionela Butnariu, et al.. (2021). A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature. Genes. 12(12). 1957–1957. 2 indexed citations
16.
Popa, Alina Delia, et al.. (2021). Observational study on dietary patterns in pregnancy. SHILAP Revista de lepidopterología. 16(2). 259–264. 2 indexed citations
17.
18.
Cozma, Sebastian, Roxana Popescu, Luminiţa Rădulescu, et al.. (2020). Genetics of Hearing Impairment in North-Eastern Romania—A Cost-Effective Improved Diagnosis and Literature Review. Genes. 11(12). 1506–1506. 5 indexed citations
19.
Petriş, Antoniu Octavian, et al.. (2018). Holt-Oram Syndrome With Multiple Cardiac Abnormalities. Cardiology Research. 9(5). 324–329. 9 indexed citations
20.
Caba, Lavinia, et al.. (2013). Drug adiction – it is just a medical problem?. 6(4).

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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