E. Di Battista

977 total citations
25 papers, 489 citations indexed

About

E. Di Battista is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, E. Di Battista has authored 25 papers receiving a total of 489 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 10 papers in Pediatrics, Perinatology and Child Health and 8 papers in Molecular Biology. Recurrent topics in E. Di Battista's work include Birth, Development, and Health (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Sexual Differentiation and Disorders (4 papers). E. Di Battista is often cited by papers focused on Birth, Development, and Health (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Sexual Differentiation and Disorders (4 papers). E. Di Battista collaborates with scholars based in Italy, Japan and Netherlands. E. Di Battista's co-authors include Giorgio Aicardi, M. Vignolo, Arturo Naselli, M. Mostert, Silvano Milani, Anna Bossi, Enrico Bertino, C Fabris, L Benso and Giorgio Gimelli and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Lara D. Veeken and Pediatric Research.

In The Last Decade

E. Di Battista

24 papers receiving 462 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. Di Battista Italy 13 141 141 101 101 70 25 489
S Bernasconi Italy 12 87 0.6× 119 0.8× 105 1.0× 89 0.9× 31 0.4× 42 618
Miroslav Živičnjak Germany 17 167 1.2× 96 0.7× 87 0.9× 52 0.5× 56 0.8× 39 661
France Ziereisen Belgium 12 102 0.7× 118 0.8× 146 1.4× 59 0.6× 26 0.4× 29 693
Simon Kipersztok United States 10 120 0.9× 152 1.1× 74 0.7× 96 1.0× 73 1.0× 18 646
B. Leheup France 11 88 0.6× 105 0.7× 126 1.2× 85 0.8× 18 0.3× 29 372
Stéphanie Rouleau France 13 182 1.3× 130 0.9× 179 1.8× 251 2.5× 102 1.5× 25 671
S. Hiéronimus France 16 122 0.9× 87 0.6× 105 1.0× 279 2.8× 118 1.7× 56 667
Lucile Turcot-Lemay Canada 11 65 0.5× 93 0.7× 73 0.7× 75 0.7× 167 2.4× 22 555
Daniëlle C M van der Kaay Netherlands 15 266 1.9× 81 0.6× 111 1.1× 309 3.1× 90 1.3× 38 533
A. Liutkus France 11 231 1.6× 44 0.3× 250 2.5× 42 0.4× 63 0.9× 19 777

Countries citing papers authored by E. Di Battista

Since Specialization
Citations

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

Fields of papers citing papers by E. Di Battista

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E. Di Battista. 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 E. Di Battista. The network helps show where E. Di Battista may publish in the future.

Co-authorship network of co-authors of E. Di Battista

This figure shows the co-authorship network connecting the top 25 collaborators of E. Di Battista. A scholar is included among the top collaborators of E. Di Battista 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 E. Di Battista. E. Di Battista 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.
Capra, Valeria, Mariasavina Severino, Andrea Rossi, et al.. (2013). Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1. American Journal of Medical Genetics Part A. 164(2). 495–499. 9 indexed citations
2.
Traggiai, Cristina, et al.. (2010). Auxological and metabolic study in small for gestational age children during 2 years follow-up. The Journal of Maternal-Fetal & Neonatal Medicine. 24(2). 381–387. 4 indexed citations
3.
Pasquali, Lorenzo, Giuseppe d’Annunzio, Roberto Gastaldi, et al.. (2009). Collectrin gene screening in Turner syndrome patients with kidney malformation. Journal of Genetics. 88(1). 105–108. 8 indexed citations
4.
Capuano, Ermanno, et al.. (2009). Gigantism with Pituitary Macroadenoma: An Unusual Variant of McCune-Albright Syndrome. Journal of Pediatric Endocrinology and Metabolism. 22(2). 177–9. 6 indexed citations
5.
Prodam, Flavia, Simonetta Bellone, Graziano Grugni, et al.. (2009). Influence of age, gender, and glucose tolerance on fasting and fed acylated ghrelin in Prader Willi syndrome. Clinical Nutrition. 28(1). 94–99. 9 indexed citations
6.
Boschetti, Mara, Daniela Larizza, Valeria Calcaterra, et al.. (2008). Effect of environment on growth: Auxological and hormonal parameters in African and Italian children. Growth Hormone & IGF Research. 19(3). 238–241. 2 indexed citations
7.
Vignolo, M., et al.. (2007). Bone quality assessed by phalangeal quantitative ultrasonography in children and adolescents with isolated idiopathic growth hormone deficiency. Journal of Endocrinological Investigation. 30(6). 445–450. 6 indexed citations
8.
Gimelli, Giorgio, Stefania Gimelli, Nazzareno Dimasi, et al.. (2006). Identification and molecular modelling of a novel familial mutation in the SRY gene implicated in the pure gonadal dysgenesis. European Journal of Human Genetics. 15(1). 76–80. 24 indexed citations
9.
Garrè, Maria Luisa, Valeria Capra, E. Di Battista, et al.. (2006). Genetic abnormalities and CNS tumors: report of two cases of ependymoma associated with Klinefelter’s Syndrome (KS). Child s Nervous System. 23(2). 219–223.
10.
Mantovani, Giovanna, Sara Bondioni, Andrea Lania, et al.. (2004). Parental Origin of Gsα Mutations in the McCune-Albright Syndrome and in Isolated Endocrine Tumors. The Journal of Clinical Endocrinology & Metabolism. 89(6). 3007–3009. 49 indexed citations
11.
Milani, Silvano, Anna Bossi, Enrico Bertino, et al.. (2004). Differences in Size at Birth Are Determined by Differences in Growth Velocity during Early Prenatal Life. Pediatric Research. 57(2). 205–210. 30 indexed citations
12.
Bernasconi, Sergio, G Bona, Luciano Cavallo, et al.. (2001). Turner’s Syndrome. Journal of Pediatric Endocrinology and Metabolism. 14(s2). 959–966. 8 indexed citations
13.
Vignolo, M., et al.. (1999). Use of the New US90 Standards for TW-RUS Skeletal Maturity Scores in Youths from the Italian Population. Hormone Research in Paediatrics. 51(4). 168–172. 24 indexed citations
15.
Gimelli, Giorgio, et al.. (1996). The phenotype of a 45, X male with a Y/18 translocation. Clinical Genetics. 49(1). 37–41. 14 indexed citations
16.
Bertino, Enrico, E. Di Battista, Anna Bossi, et al.. (1996). Fetal growth velocity: kinetic, clinical, and biological aspects.. Archives of Disease in Childhood Fetal & Neonatal. 74(1). F10–F15. 48 indexed citations
17.
Aicardi, Giorgio, L Benso, M. Vignolo, et al.. (1993). Dose-Dependent Effects of Deflazacort and Prednisone on Growth and Skeletal Maturation. Lara D. Veeken. 32(suppl 2). 39–43. 15 indexed citations
18.
Vignolo, M., et al.. (1992). FELS, Greulich‐Pyle, and Tanner‐Whitehouse bone age assessments in a group of Italian children and adolescents. American Journal of Human Biology. 4(4). 493–500. 22 indexed citations
19.
Aicardi, Giorgio, Silvano Milani, Bruno P. Imbimbo, et al.. (1991). Comparison of growth retarding effects induced by two different glucocorticoids in prepubertal sick children: An interim long-term analysis. Calcified Tissue International. 48(4). 283–287. 19 indexed citations
20.
Vignolo, M., Arturo Naselli, E. Di Battista, M. Mostert, & Giorgio Aicardi. (1988). Growth and development in simple obesity. European Journal of Pediatrics. 147(3). 242–244. 106 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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