Ilaria Stanghellini

776 total citations
15 papers, 400 citations indexed

About

Ilaria Stanghellini is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ilaria Stanghellini has authored 15 papers receiving a total of 400 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ilaria Stanghellini's work include Reproductive Biology and Fertility (4 papers), Congenital heart defects research (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Ilaria Stanghellini is often cited by papers focused on Reproductive Biology and Fertility (4 papers), Congenital heart defects research (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Ilaria Stanghellini collaborates with scholars based in Italy, United States and India. Ilaria Stanghellini's co-authors include Geppino Falco, Minoru S.H. Ko, Uwem C. Bassey, Toshio Hamatani, Antonio Percesepe, Luca Gianaroli, Anna Pia Ferraretti, Maria Cristina Magli, Andor Crippa and V. Mazza and has published in prestigious journals such as Developmental Biology, Fertility and Sterility and Biology of Reproduction.

In The Last Decade

Ilaria Stanghellini

15 papers receiving 393 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ilaria Stanghellini Italy	9	269	94	71	60	53	15	400
Pingyuan Xie China	13	182 0.7×	93 1.0×	196 2.8×	34 0.6×	151 2.8×	36	388
Liangwen Zhong China	9	210 0.8×	57 0.6×	30 0.4×	62 1.0×	77 1.5×	14	321
Jasin Taelman Belgium	10	244 0.9×	117 1.2×	162 2.3×	48 0.8×	85 1.6×	17	419
Bhavini Rana United States	4	191 0.7×	40 0.4×	128 1.8×	31 0.5×	122 2.3×	8	330
Minyue Ma China	9	153 0.6×	126 1.3×	188 2.6×	48 0.8×	128 2.4×	18	347
Giovanni Sestini Austria	6	304 1.1×	81 0.9×	51 0.7×	34 0.6×	26 0.5×	8	402
Sophie Loubersac France	5	376 1.4×	150 1.6×	78 1.1×	51 0.8×	52 1.0×	12	506
Chan Luo China	12	210 0.8×	114 1.2×	55 0.8×	46 0.8×	136 2.6×	35	361
Alexandre Bruneau France	3	372 1.4×	127 1.4×	66 0.9×	35 0.6×	48 0.9×	3	480
Maaike Welling Netherlands	11	551 2.0×	129 1.4×	20 0.3×	23 0.4×	121 2.3×	14	651

Countries citing papers authored by Ilaria Stanghellini

Since Specialization

Citations

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

Fields of papers citing papers by Ilaria Stanghellini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ilaria Stanghellini

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

All Works

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15 of 15 papers shown

Madeo, Simona Filomena, Ilaria Stanghellini, Barbara Predieri, et al.. (2021). Copy Number Variation Analysis Increases the Number of Candidate Loci Associated with Pediatric Obesity. Hormone Research in Paediatrics. 94(7-8). 251–262. 1 indexed citations

Stanghellini, Ilaria, Elisabetta Genovese, Silvia Palma, et al.. (2017). A mild phenotype of sensorineural hearing loss and palmoplantar keratoderma caused by a novel GJB2 dominant mutation. Acta Otorhinolaryngologica Italica. 37(4). 308–311. 2 indexed citations

Stanghellini, Ilaria, et al.. (2015). Role of Genetic Factors in the Pathogenesis of Radial Deficiencies in Humans. Current Genomics. 16(4). 264–278. 14 indexed citations

Stanghellini, Ilaria, Erik Dassi, Roberto Bertorelli, et al.. (2015). Exome sequencing in a patient with Catel–Manzke-like syndrome excludes the involvement of the known genes and reveals a possible candidate. European Journal of Medical Genetics. 58(11). 597–602. 2 indexed citations

Bertucci, Emma, et al.. (2015). Prenatal diagnosis and follow‐up of a case of branchio‐oto‐renal syndrome displays renal growth impairment after the second trimester. Journal of obstetrics and gynaecology research. 41(11). 1831–1834. 3 indexed citations

Stanghellini, Ilaria, et al.. (2014). Predictive diagnostic value for the clinical features accompanying intellectual disability in children with pathogenic copy number variations: a multivariate analysis. The Italian Journal of Pediatrics/Italian journal of pediatrics. 40(1). 39–39. 12 indexed citations

Stanghellini, Ilaria, et al.. (2014). New and Rare GJB2 Alleles in Patients with Nonsyndromic Sensorineural Hearing Impairment: A Genotype/Auditory Phenotype Correlation. Genetic Testing and Molecular Biomarkers. 18(12). 839–844. 5 indexed citations

Gianaroli, Luca, et al.. (2013). Reiterative changes in the Italian regulation on IVF: the effect on PGD patients’ reproductive decisions. Reproductive BioMedicine Online. 28(1). 125–132. 11 indexed citations

Gianaroli, Luca, et al.. (2012). DNA integrity is maintained after freeze-drying of human spermatozoa. Fertility and Sterility. 97(5). 1067–1073.e1. 50 indexed citations

10.

Magli, M.C., et al.. (2011). Prolonged absence of meiotic spindles by birefringence imaging negatively affects normal fertilization and embryo development. Reproductive BioMedicine Online. 23(6). 747–754. 11 indexed citations

11.

Stanghellini, Ilaria, et al.. (2009). Trim43a, Trim43b, and Trim43c: Novel mouse genes expressed specifically in mouse preimplantation embryos. Gene Expression Patterns. 9(8). 595–602. 9 indexed citations

12.

Falco, Geppino, et al.. (2007). Zscan4: A novel gene expressed exclusively in late 2-cell embryos and embryonic stem cells. Developmental Biology. 307(2). 539–550. 227 indexed citations

13.

Lee, Sung‐Lim, Geppino Falco, Ilaria Stanghellini, et al.. (2007). Zscan4: A NOVEL GENE EXPRESSED EXCLUSIVELY IN LATE 2-CELL EMBRYOS. Biology of Reproduction. 77(Suppl_1). 79–79. 1 indexed citations

14.

Stanghellini, Ilaria, et al.. (2006). Quantitation of fetal DNA in maternal serum during the first trimester of pregnancy by the use of a DAZ repetitive probe. Molecular Human Reproduction. 12(9). 587–591. 32 indexed citations

15.

Falco, Geppino, Ilaria Stanghellini, & Minoru S.H. Ko. (2006). Use of Chuk as an internal standard suitable for quantitative RT-PCR in mouse preimplantation embryos. Reproductive BioMedicine Online. 13(3). 394–403. 20 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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