Sara Bargiacchi

700 total citations
18 papers, 102 citations indexed

About

Sara Bargiacchi is a scholar working on Molecular Biology, Ophthalmology and Nutrition and Dietetics. According to data from OpenAlex, Sara Bargiacchi has authored 18 papers receiving a total of 102 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Ophthalmology and 5 papers in Nutrition and Dietetics. Recurrent topics in Sara Bargiacchi's work include Retinal Development and Disorders (7 papers), Biochemical Analysis and Sensing Techniques (4 papers) and melanin and skin pigmentation (3 papers). Sara Bargiacchi is often cited by papers focused on Retinal Development and Disorders (7 papers), Biochemical Analysis and Sensing Techniques (4 papers) and melanin and skin pigmentation (3 papers). Sara Bargiacchi collaborates with scholars based in Italy, Belgium and United States. Sara Bargiacchi's co-authors include Sabrina Giglio, Roberto Caputo, Giacomo Maria Bacci, Stefano Stagi, Maurizio de Martino, Elisabetta Lapi, Salvatore Seminara, Silvia Romano, Andrea Sodi and Dario Pasquale Mucciolo and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Orphanet Journal of Rare Diseases.

In The Last Decade

Sara Bargiacchi

14 papers receiving 102 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sara Bargiacchi Italy 6 54 31 27 21 17 18 102
Zhenggen Wu China 6 37 0.7× 74 2.4× 40 1.5× 8 0.4× 12 0.7× 16 118
Valeria Lo Faro Netherlands 7 36 0.7× 27 0.9× 12 0.4× 33 1.6× 5 0.3× 10 91
Noa Kapelushnik Israel 7 17 0.3× 39 1.3× 29 1.1× 5 0.2× 16 0.9× 24 97
Vasumathy Vedantham India 9 34 0.6× 140 4.5× 56 2.1× 6 0.3× 4 0.2× 17 178
Leonardo Mastropasqua Italy 7 30 0.6× 113 3.6× 90 3.3× 18 0.9× 77 4.5× 13 177
Claudia Priglinger Germany 4 78 1.4× 27 0.9× 7 0.3× 10 0.5× 4 0.2× 5 97
Maurizio Digiuni Italy 9 40 0.7× 188 6.1× 109 4.0× 8 0.4× 44 2.6× 14 229
George J. Manayath India 9 72 1.3× 256 8.3× 147 5.4× 12 0.6× 17 1.0× 38 303
Marc Rosenblatt United States 5 17 0.3× 95 3.1× 50 1.9× 16 0.8× 8 0.5× 5 140
Laura Frost United States 5 109 2.0× 94 3.0× 17 0.6× 5 0.2× 6 0.4× 7 185

Countries citing papers authored by Sara Bargiacchi

Since Specialization
Citations

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

Fields of papers citing papers by Sara Bargiacchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sara Bargiacchi

This figure shows the co-authorship network connecting the top 25 collaborators of Sara Bargiacchi. A scholar is included among the top collaborators of Sara Bargiacchi 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 Sara Bargiacchi. Sara Bargiacchi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Uner, Ogul E., Margaret Reynolds, Giacomo Maria Bacci, et al.. (2025). Phosphoribosyl pyrophosphate synthetase 1 ( PRPS1 ) associated retinal degeneration: an international study. Ophthalmic Genetics. 46(2). 133–143.
2.
Bacci, Giacomo Maria, Sara Bargiacchi, Michel Pâques, et al.. (2024). Multimodal phenotyping of foveal hypoplasia in albinism and albino-like conditions: a pediatric case series with adaptive optics insights. Scientific Reports. 14(1). 15454–15454. 1 indexed citations
3.
Barbato, Alessandro, Michele Sacchini, Sara Bargiacchi, et al.. (2024). Endocrinological features and epileptic encephalopathy in COX deficiency due to SCO1 mutations: case series and review of literature. Endocrine Connections. 13(10). 2 indexed citations
4.
Landini, Samuela, Rosangela Artuso, Pina Fortunato, et al.. (2024). Broadening the ocular phenotypic spectrum of ultra-rare BRPF1 variants: report of two cases. Ophthalmic Genetics. 45(4). 390–394.
5.
Murro, Vittoria, Sandro Banfi, Francesco Testa, et al.. (2023). A multidisciplinary approach to inherited retinal dystrophies from diagnosis to initial care: a narrative review with inputs from clinical practice. Orphanet Journal of Rare Diseases. 18(1). 223–223. 20 indexed citations
6.
Bargiacchi, Sara, Pina Fortunato, Roberto Caputo, et al.. (2022). Optic nerve involvement in CACNA1F-related disease: observations from a multicentric case series. Ophthalmic Genetics. 44(2). 152–162.
7.
Bargiacchi, Sara, Viviana Palazzo, Samuela Landini, et al.. (2022). Expanding the Spectrum of Oculocutaneous Albinism: Does Isolated Foveal Hypoplasia Really Exist?. International Journal of Molecular Sciences. 23(14). 7825–7825. 6 indexed citations
8.
Fortunato, Pina, Angelica Pagliazzi, Sara Bargiacchi, et al.. (2022). X-linked retinoschisis: mutation spectrum and genotype-phenotype relationship in an Italian pediatric cohort. Ophthalmic Genetics. 44(1). 35–42. 3 indexed citations
9.
Brizola, Evelise, Maria Gnoli, Morena Tremosini, et al.. (2020). Variable clinical expression of Stickler Syndrome: A case report of a novel COL11A1 mutation. Molecular Genetics & Genomic Medicine. 8(9). e1353–e1353. 5 indexed citations
10.
Bacci, Giacomo Maria, Sara Bargiacchi, Pina Fortunato, et al.. (2020). Novel mutations in MFRP and PRSS56 are associated with posterior microphthalmos. Ophthalmic Genetics. 41(1). 49–56. 9 indexed citations
11.
Lembo, Andrea, Giacomo Maria Bacci, Massimiliano Serafino, et al.. (2020). Unusual presentation of early-onset X-linked retinoschisis: Report after 1 year of multimodal follow-up. European Journal of Ophthalmology. 31(3). NP60–NP64. 3 indexed citations
12.
Murro, Vittoria, Dario Pasquale Mucciolo, Dario Giorgio, et al.. (2019). Optical coherence tomography (OCT) features of cystoid spaces in choroideremia (CHM). Graefe s Archive for Clinical and Experimental Ophthalmology. 257(12). 2655–2663. 5 indexed citations
13.
Callea, Michele, Francisco Cammarata‐Scalisi, Colin E. Willoughby, et al.. (2017). Estudio clínico y molecular en una familia con displasia ectodérmica hipohidrótica autosómica dominante. Archivos Argentinos de Pediatria. 115(1). e34–e38.
14.
Murro, Vittoria, Roberto Caputo, Giacomo Maria Bacci, et al.. (2017). Case report of an atypical early onset X-linked retinoschisis in monozygotic twins. BMC Ophthalmology. 17(1). 19–19. 10 indexed citations
15.
Bargiacchi, Sara, Matteo Della Monica, Roberto Biagiotti, et al.. (2017). Metatropic dysplasia in third trimester of pregnancy and a novel causative variant in the TRPV4 gene. European Journal of Medical Genetics. 60(7). 365–368. 2 indexed citations
16.
Delvecchio, Maurizio, Paola Primignani, Roberto Caputo, et al.. (2016). A novel OTX2 gene frameshift mutation in a child with microphthalmia, ectopic pituitary and growth hormone deficiency. Journal of Pediatric Endocrinology and Metabolism. 29(5). 603–5. 3 indexed citations
17.
Straniero, Letizia, Valeria Rimoldi, Giulia Soldà, et al.. (2015). Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites. Journal of Human Genetics. 60(9). 467–471. 5 indexed citations
18.
Stagi, Stefano, Elisabetta Lapi, Silvia Romano, et al.. (2015). Determinants of Vitamin D Levels in Children and Adolescents with Down Syndrome. International Journal of Endocrinology. 2015. 1–11. 28 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Zhenggen Wu Breakdown of academic impact, for papers by Valeria Lo Faro Breakdown of academic impact, for papers by Noa Kapelushnik Breakdown of academic impact, for papers by Vasumathy Vedantham Breakdown of academic impact, for papers by Leonardo Mastropasqua Breakdown of academic impact, for papers by Claudia Priglinger Breakdown of academic impact, for papers by Maurizio Digiuni Breakdown of academic impact, for papers by George J. Manayath Breakdown of academic impact, for papers by Marc Rosenblatt Breakdown of academic impact, for papers by Laura Frost
Rankless by CCL
2026