Cecilia Surace

1.2k total citations
33 papers, 595 citations indexed

About

Cecilia Surace is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Cecilia Surace has authored 33 papers receiving a total of 595 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 12 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in Cecilia Surace's work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (5 papers) and Acute Myeloid Leukemia Research (4 papers). Cecilia Surace is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (5 papers) and Acute Myeloid Leukemia Research (4 papers). Cecilia Surace collaborates with scholars based in Italy, United States and France. Cecilia Surace's co-authors include Mariano Rocchi, Clelia Tiziana Storlazzi, Adriano Angioni, Pietro Sirleto, Angelo Lonoce, Pietro D’Addabbo, Stefania Purgato, Peter F. Ambros, Massimo Carella and Alberto L’Abbate and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and PLoS ONE.

In The Last Decade

Cecilia Surace

32 papers receiving 564 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Cecilia Surace Italy	12	328	201	128	75	68	33	595
Umut Aypar United States	12	273 0.8×	127 0.6×	118 0.9×	54 0.7×	88 1.3×	33	557
Johanna Sandgren Sweden	12	425 1.3×	335 1.7×	241 1.9×	71 0.9×	83 1.2×	21	818
Daniël Olde Weghuis Netherlands	15	412 1.3×	238 1.2×	174 1.4×	44 0.6×	91 1.3×	20	744
Peter C. Verlander United States	14	695 2.1×	255 1.3×	206 1.6×	82 1.1×	132 1.9×	18	921
Karl Vandepoele Belgium	12	256 0.8×	122 0.6×	79 0.6×	55 0.7×	55 0.8×	23	428
Anita S. Kulharya United States	14	509 1.6×	452 2.2×	60 0.5×	106 1.4×	26 0.4×	31	843
Marie Trková Czechia	13	272 0.8×	145 0.7×	60 0.5×	23 0.3×	146 2.1×	33	589
Rodney Staggs United States	7	385 1.2×	74 0.4×	90 0.7×	33 0.4×	121 1.8×	8	556
Jonathan P. Park United States	19	462 1.4×	267 1.3×	83 0.6×	63 0.8×	177 2.6×	36	898
Anne Marie Ottesen Denmark	11	371 1.1×	390 1.9×	109 0.9×	70 0.9×	54 0.8×	15	733

Countries citing papers authored by Cecilia Surace

Since Specialization

Citations

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

Fields of papers citing papers by Cecilia Surace

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cecilia Surace

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

All Works

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20 of 20 papers shown

Ciciriello, Fabiana, Nicolò de Pretis, Laura Bernardoni, et al.. (2024). CFTR function is impaired in a subset of patients with pancreatitis carrying rare CFTR variants. Pancreatology. 24(3). 394–403.

Zangari, Paola, Cristina Cifaldi, Silvia Di Cesare, et al.. (2019). Novel Compound Heterozygous Mutations in IL-7 Receptor α Gene in a 15-Month-Old Girl Presenting With Thrombocytopenia, Normal T Cell Count and Maternal Engraftment. Frontiers in Immunology. 10. 2471–2471. 3 indexed citations

Alesi, Viola, Silvia Genovese, Sara Loddo, et al.. (2017). Interstitial 10q21.1q23.31 Duplication due to Meiotic Recombination of a Paternal Balanced Complex Rearrangement: Cytogenetic and Molecular Characterization. Cytogenetic and Genome Research. 151(4). 179–185. 2 indexed citations

Sofia, Valentina, Letizia Da Sacco, Cecilia Surace, et al.. (2016). Extensive Molecular Analysis Suggested the Strong Genetic Heterogeneity of Idiopathic Chronic Pancreatitis. Molecular Medicine. 22(1). 300–309. 18 indexed citations

Garibaldi, Matteo, Johann Böhm, Fabiana Fattori, et al.. (2016). Novel Dominant Mutation in BIN1 Gene Causing Mild Centronuclear Myopathy Revealed by Myalgias and CK Elevation. Journal of Neuromuscular Diseases. 3(1). 111–114. 5 indexed citations

D’Elia, Gemma, Silvia Genovese, Cecilia Surace, et al.. (2015). Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma. BMC Cancer. 15(1). 841–841. 21 indexed citations

Sofia, Valentina, Cecilia Surace, Fabio Majo, et al.. (2015). Relationship between CFTR and CTRC Variants and the Clinical Phenotype in Late-Onset Cystic Fibrosis Disease with Chronic Pancreatitis. Journal of Molecular Diagnostics. 17(2). 171–178. 6 indexed citations

Ciocca, Leonardo, Cecilia Surace, M. Cristina Digilio, et al.. (2013). Array-CGH characterization and genotype-phenotype analysis in a patient with a ring chromosome 6. BMC Medical Genomics. 6(1). 3–3. 9 indexed citations

D’Elia, Gemma, Francesca Del Bufalo, Maria Antonietta De Ioris, et al.. (2013). Two novel cases of trilateral retinoblastoma: genetics and review of the literature. Cancer Genetics. 206(11). 398–401. 9 indexed citations

10.

Digilio, M. Cristina, Laura Bernardini, Federica Consoli, et al.. (2012). Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: Rare association with pulmonary valve stenosis. European Journal of Medical Genetics. 56(3). 144–149. 47 indexed citations

11.

Storlazzi, Clelia Tiziana, Angelo Lonoce, Maria Corsignano Guastadisegni, et al.. (2010). Gene amplification as double minutes or homogeneously staining regions in solid tumors: Origin and structure. Genome Research. 20(9). 1198–1206. 168 indexed citations

12.

Starza, Roberta La, Cecilia Surace, Pietro Sirleto, et al.. (2009). RABGAP1L gene rearrangement resulting from a der(Y)t(Y;1)(q12;q25) in acute myeloid leukemia arising in a child with Klinefelter syndrome. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 454(3). 311–316. 11 indexed citations

13.

Sirleto, Pietro, Cecilia Surace, Helena G. Dos Santos, et al.. (2009). Lyonization Effects of the t(X;16) Translocation on the Phenotypic Expression in a Rare Female With Menkes Disease. Pediatric Research. 65(3). 347–351. 18 indexed citations

14.

Surace, Cecilia, et al.. (2008). Masked complex chromosome rearrangement in a child thought to have del(8qter) as the sole cytogenetic abnormality. Cytogenetic and Genome Research. 121(3-4). 215–221. 2 indexed citations

15.

Surace, Cecilia, Florence Pédeutour, Domenico Trombetta, et al.. (2008). Episomal amplification of MYCN in a case of medulloblastoma. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 452(5). 491–497. 4 indexed citations

16.

Marisavljević, Dragomir, Cecilia Surace, Olivera Marković, et al.. (2006). A Ph-negative chronic myeloid leukemia with a complex BCR/ABL rearrangement and a t(6;9)(p21;q34.1). Cancer Genetics and Cytogenetics. 166(2). 180–185. 11 indexed citations

17.

Surace, Cecilia, Ioannis Panagopoulos, Eva Pålsson, et al.. (2004). A novel FISH assay for SS18–SSX fusion type in synovial sarcoma. Laboratory Investigation. 84(9). 1185–1192. 20 indexed citations

18.

Surace, Cecilia, Anna Leszl, Giorgio Perilongo, et al.. (2002). Fluorescent in situ hybridization (FISH) reveals frequent and recurrent numerical and structural abnormalities in hepatoblastoma with no informative karyotype. Medical and Pediatric Oncology. 39(5). 536–539. 11 indexed citations

19.

Sainati, Laura, Anna Leszl, Cecilia Surace, et al.. (2002). Fluorescence in situ hybridization improves cytogenetic results in the analysis of hepatoblastoma. Cancer Genetics and Cytogenetics. 134(1). 18–20. 9 indexed citations

20.

Storlazzi, Clelia Tiziana, Luisa Anelli, Cecilia Surace, et al.. (2002). Molecular cytogenetic characterization of a novel additional chromosomal aberration in blast crisis of a Ph-positive chronic myeloid leukemia. Cancer Genetics and Cytogenetics. 134(2). 109–113. 1 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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