Licia Turolla

946 total citations
23 papers, 345 citations indexed

About

Licia Turolla is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Licia Turolla has authored 23 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 7 papers in Surgery and 5 papers in Molecular Biology. Recurrent topics in Licia Turolla's work include Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Congenital Ear and Nasal Anomalies (3 papers). Licia Turolla is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Congenital Ear and Nasal Anomalies (3 papers). Licia Turolla collaborates with scholars based in Italy, Switzerland and Cuba. Licia Turolla's co-authors include Romano Tenconi, Maurizio Clementi, Guido Barbujani, Isabella Mammi, Maria Elisabetta Clementi, Lidia Larizza, Elisa Calzolari, Francesca Romana Grati, Giuseppe Simoni and Federico Maggi and has published in prestigious journals such as Journal of Medical Genetics, Human Mutation and Human Genetics.

In The Last Decade

Licia Turolla

21 papers receiving 322 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Licia Turolla Italy 11 175 95 90 83 67 23 345
Yoshitsugu Sugio Japan 10 120 0.7× 107 1.1× 32 0.4× 58 0.7× 45 0.7× 20 257
Anne De Paepe Belgium 12 298 1.7× 85 0.9× 21 0.2× 77 0.9× 73 1.1× 21 434
H. Cortina Spain 12 124 0.7× 64 0.7× 36 0.4× 122 1.5× 17 0.3× 20 385
P. Berlier France 10 51 0.3× 84 0.9× 114 1.3× 66 0.8× 61 0.9× 23 387
Daniele De Brasi Italy 14 256 1.5× 224 2.4× 36 0.4× 73 0.9× 86 1.3× 44 478
Patrick Lo Australia 11 277 1.6× 85 0.9× 87 1.0× 210 2.5× 38 0.6× 24 521
Eusebiu Vlad Gorduza Romania 12 149 0.9× 161 1.7× 18 0.2× 65 0.8× 72 1.1× 49 385
Cheryl S. Reid United States 11 321 1.8× 89 0.9× 15 0.2× 152 1.8× 47 0.7× 18 483
Danny Halim Indonesia 13 65 0.4× 66 0.7× 34 0.4× 99 1.2× 89 1.3× 27 350
Diana Carli Italy 14 272 1.6× 279 2.9× 31 0.3× 124 1.5× 152 2.3× 51 599

Countries citing papers authored by Licia Turolla

Since Specialization
Citations

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

Fields of papers citing papers by Licia Turolla

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Licia Turolla

This figure shows the co-authorship network connecting the top 25 collaborators of Licia Turolla. A scholar is included among the top collaborators of Licia Turolla 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 Licia Turolla. Licia Turolla 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.
Franz, Leonardo, Chiara Gallo, Licia Turolla, et al.. (2024). Audiological Phenotypes of Connexin Gene Mutation Patterns: A Glance at Different GJB2/GJB6 Gene Mutation Profiles. Children. 11(2). 194–194. 1 indexed citations
2.
Tran, Christel, Licia Turolla, Diana Ballhausen, et al.. (2021). The fate of orally administered sialic acid: First insights from patients with N-acetylneuraminic acid synthase deficiency and control subjects. Molecular Genetics and Metabolism Reports. 28. 100777–100777. 14 indexed citations
3.
Marcon, Maria Lisa, Edward Kiwanuka, Maria Sambataro, et al.. (2019). Can Nurse-Based Management Screening Ensure Adequate Outcomes in Patients With Gestational Diabetes? A Comparison of 2 Organizational Models. Quality Management in Health Care. 28(1). 51–62.
4.
Fernández, Esperanza, Elena Di Gennaro, Filomena Pirozzi, et al.. (2018). FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the FMR1 Gene. Frontiers in Genetics. 9. 442–442. 8 indexed citations
5.
Turolla, Licia, Eva Pompilii, Céline Dupont, et al.. (2014). Prenatal phenotype of Williams–Beuren syndrome and of the reciprocal duplication syndrome. Clinical Case Reports. 2(2). 25–32. 16 indexed citations
6.
Grati, Francesca Romana, Licia Turolla, Anna Ruggeri, et al.. (2007). Chromosome 11 segmental paternal isodisomy in amniocytes from two fetuses with omphalocoele: new highlights on phenotype–genotype correlations in Beckwith–Wiedemann syndrome. Journal of Medical Genetics. 44(4). 257–263. 27 indexed citations
7.
Grati, Francesca Romana, Faustina Lalatta, Licia Turolla, et al.. (2005). Three cases with de novo 6q imbalance and variable prenatal phenotype. American Journal of Medical Genetics Part A. 136A(3). 254–258. 18 indexed citations
8.
Clementi, Maurizio, et al.. (2005). Neonatal growth patterns in a population of consecutively born Down syndrome children. American Journal of Medical Genetics. 37(S7). 71–74. 14 indexed citations
9.
Benedicenti, Francesco, et al.. (2003). Utilization of genetic counseling by parents of a child or fetus with congenital malformation in North‐East Italy. American Journal of Medical Genetics Part A. 121A(3). 214–218. 5 indexed citations
10.
Giardino, Daniela, Palma Finelli, Daniele Caufin, et al.. (2002). Pure 6p22‐pter trisomic patient: Refined FISH characterization and genotype‐phenotype correlation. American Journal of Medical Genetics. 108(1). 36–40. 17 indexed citations
11.
Russo, Silvia, Francesca Cogliati, Maurizio Viri, et al.. (2000). Novel mutations of ubiquitin protein ligase 3A gene in Italian patients with Angelman syndrome. Human Mutation. 15(4). 387–387. 18 indexed citations
12.
Paccagnella, A., et al.. (1994). The Effects of Prolonged Cardiopulmonary Bypass on Cell-Mediated Immunity. The Thoracic and Cardiovascular Surgeon. 42(1). 14–20. 9 indexed citations
13.
Turco, Alberto, Bernard Peissel, Sandro Rossetti, et al.. (1993). Prenatal testing in a fetus at risk for autosomal dominant polycystic kidney disese and autosomal recessive junctional epidermolysis bullosa with pyloric atresia. American Journal of Medical Genetics. 47(8). 1225–1230. 4 indexed citations
14.
Turolla, Licia, et al.. (1992). Clinical anophthalmia: An epidemiological study in Northeast Italy based on 368,256 consecutive births. Teratology. 46(6). 551–553. 34 indexed citations
15.
Clementi, Maurizio, et al.. (1991). Apparent CHARGE association and chromosome anomaly: Chance or contiguous gene syndrome. American Journal of Medical Genetics. 41(2). 246–250. 43 indexed citations
16.
Clementi, Maurizio, Alessandra Murgia, Franca Anglani, et al.. (1991). Linkage analysis of neurofibromatosis type 1. Human Genetics. 87(1). 91–94. 2 indexed citations
17.
Clementi, Maurizio, Guido Barbujani, Licia Turolla, & Romano Tenconi. (1990). Neurofibromatosis-1: a maximum likelihood estimation of mutation rate. Human Genetics. 84(2). 116–8. 60 indexed citations
18.
Turolla, Licia, Maria Elisabetta Clementi, & Rossana Tenconi. (1990). How wide is the clinical spectrum of the acrocallosal syndrome? Report of a mild case.. Journal of Medical Genetics. 27(8). 516–518. 8 indexed citations
19.
Paccagnella, A., Licia Turolla, G. Zanardo, et al.. (1989). Fatal Progression of Behçet's Disease after Cardiac Surgery. The Thoracic and Cardiovascular Surgeon. 37(5). 320–321. 9 indexed citations
20.
Tenconi, Romano, Maria Elisabetta Clementi, & Licia Turolla. (1988). Theoretical recurrence risks for cleft lip derived from a population of consecutive newborns.. Journal of Medical Genetics. 25(4). 243–246. 7 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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