Enrico Alfei

887 total citations
25 papers, 333 citations indexed

About

Enrico Alfei is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Enrico Alfei has authored 25 papers receiving a total of 333 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Enrico Alfei's work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Congenital heart defects research (5 papers). Enrico Alfei is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Congenital heart defects research (5 papers). Enrico Alfei collaborates with scholars based in Italy, United Kingdom and United States. Enrico Alfei's co-authors include Chiara Pantaleoni, Stefano D’Arrigo, Orsetta Zuffardi, Donatella Milani, Pierangelo Veggiotti, Umberto Balottin, Francesca L. Sciacca, Sara Bulgheroni, Veronica Saletti and Daria Riva and has published in prestigious journals such as Journal of Autism and Developmental Disorders, Pharmacological Research and Human Mutation.

In The Last Decade

Enrico Alfei

24 papers receiving 304 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Enrico Alfei Italy 11 160 140 64 58 39 25 333
Luigina Spaccini Italy 13 159 1.0× 208 1.5× 43 0.7× 104 1.8× 39 1.0× 47 455
Francisca Millan United States 11 250 1.6× 261 1.9× 14 0.2× 49 0.8× 34 0.9× 19 479
Bret L. Bostwick United States 9 215 1.3× 225 1.6× 43 0.7× 29 0.5× 35 0.9× 17 414
Devon Lamb Thrush United States 10 141 0.9× 218 1.6× 26 0.4× 26 0.4× 29 0.7× 19 334
Bouchra Ouled Amar Bencheikh Canada 9 79 0.5× 105 0.8× 62 1.0× 52 0.9× 15 0.4× 13 307
Ayelet Zerem Israel 11 127 0.8× 180 1.3× 19 0.3× 24 0.4× 40 1.0× 22 321
Alya Qari Saudi Arabia 8 76 0.5× 106 0.8× 19 0.3× 30 0.5× 56 1.4× 17 244
Giuseppina Vitiello Italy 8 49 0.3× 131 0.9× 64 1.0× 49 0.8× 10 0.3× 16 260
Vamsee Pillalamarri United States 9 222 1.4× 204 1.5× 21 0.3× 98 1.7× 18 0.5× 10 388
Qi Zeng China 11 228 1.4× 266 1.9× 17 0.3× 52 0.9× 23 0.6× 21 524

Countries citing papers authored by Enrico Alfei

Since Specialization
Citations

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

Fields of papers citing papers by Enrico Alfei

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Enrico Alfei

This figure shows the co-authorship network connecting the top 25 collaborators of Enrico Alfei. A scholar is included among the top collaborators of Enrico Alfei 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 Enrico Alfei. Enrico Alfei 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.
Pezzani, Lidia, Enrico Alfei, Laura Pezzoli, et al.. (2023). Rock around DYRK1A: Ethnic diversity, clinical challenges. American Journal of Medical Genetics Part A. 191(5). 1459–1464.
2.
Alfei, Enrico, et al.. (2023). Paradigm shift in the treatment of tuberous sclerosis: Effectiveness of everolimus. Pharmacological Research. 195. 106884–106884. 6 indexed citations
3.
Alfei, Enrico, Maria Iascone, Daniela Marchetti, et al.. (2023). Menkes disease complicated by concurrent ACY1 deficiency: A case report. Frontiers in Genetics. 14. 1077625–1077625. 2 indexed citations
4.
Ionio, Chiara, Gianluca Lista, Pierangelo Veggiotti, et al.. (2022). Cognitive, Behavioral and Socioemotional Development in a Cohort of Preterm Infants at School Age: A Cross-Sectional Study. Pediatric Reports. 14(1). 115–126. 4 indexed citations
5.
Varesio, Costanza, Elena Freri, Francesca Darra, et al.. (2021). CDKL5 deficiency disorder in males: Five new variants and review of the literature. European Journal of Paediatric Neurology. 33. 9–20. 19 indexed citations
6.
Alfei, Enrico, Elisa Cattaneo, Luigina Spaccini, et al.. (2021). Progressive Clinical and Neuroradiological Findings in a Child with BCL11B Missense Mutation: Expanding the Phenotypic Spectrum of Related Disorder. Neuropediatrics. 53(4). 283–286. 5 indexed citations
7.
Scelsa, Barbara, Mariano Lanna, Andrea Righini, et al.. (2021). Prenatal Diagnosis and Neurodevelopmental Outcome in Isolated Cerebellar Hypoplasia of Suspected Hemorrhagic Etiology: a Retrospective Cohort Study. The Cerebellum. 21(6). 944–953. 7 indexed citations
8.
Albani, Elena, Luigina Spaccini, Enrico Alfei, et al.. (2021). Efficacy of Everolimus Low-Dose Treatment for Cardiac Rhabdomyomas in Neonatal Tuberous Sclerosis: Case Report and Literature Review. Pediatric Reports. 13(1). 104–112. 8 indexed citations
9.
Bulgheroni, Sara, Stefano D’Arrigo, Silvia Esposito, et al.. (2021). CGH Findings in Children with Complex and Essential Autistic Spectrum Disorder. Journal of Autism and Developmental Disorders. 53(2). 615–623. 4 indexed citations
10.
Ciaccio, Claudia, Veronica Saletti, Stefano D’Arrigo, et al.. (2018). Clinical spectrum of PTEN mutation in pediatric patients. A bicenter experience. European Journal of Medical Genetics. 62(12). 103596–103596. 43 indexed citations
11.
Magri, Stefania, Massimo Plumari, Enrico Alfei, et al.. (2018). Concurrent AFG3L2 and SPG7 mutations associated with syndromic parkinsonism and optic atrophy with aberrant OPA1 processing and mitochondrial network fragmentation. Human Mutation. 39(12). 2060–2071. 27 indexed citations
12.
Milani, Donatella, et al.. (2017). ZC4H2 deletions can cause severe phenotype in female carriers. American Journal of Medical Genetics Part A. 173(5). 1358–1363. 20 indexed citations
13.
Milani, Donatella, Giulia Cagnoli, Marco Baccarin, et al.. (2016). Insights into 6q21‐q22: Refinement of the critical region for acro‐cardio‐facial syndrome. Congenital Anomalies. 56(4). 187–189. 6 indexed citations
14.
Natacci, Federica, Enrico Alfei, Stefano D’Arrigo, et al.. (2015). Chromosome 17q21.31 duplication syndrome: Description of a new familiar case and further delineation of the clinical spectrum. European Journal of Paediatric Neurology. 20(1). 183–187. 19 indexed citations
15.
Baranello, Giovanni, Enrico Alfei, Diego Martinelli, et al.. (2014). Hyperargininemia: 7-Month Follow-Up Under Sodium Benzoate Therapy in an Italian Child Presenting Progressive Spastic Paraparesis, Cognitive Decline, and Novel Mutation in ARG1 Gene. Pediatric Neurology. 51(3). 430–433. 9 indexed citations
16.
Alfei, Enrico, Federico Raviglione, Silvana Franceschetti, et al.. (2014). Seizures and EEG features in 74 patients with genetic‐dysmorphic syndromes. American Journal of Medical Genetics Part A. 164(12). 3154–3161. 12 indexed citations
17.
Battini, Roberta, Stefano D’Arrigo, Denise Cassandrini, et al.. (2013). Novel Mutations in TSEN54 in Pontocerebellar Hypoplasia Type 2. Journal of Child Neurology. 29(4). 520–525. 8 indexed citations
18.
Novara, Francesca, Enrico Alfei, Stefano D’Arrigo, et al.. (2012). 5p13 microduplication syndrome: A new case and better clinical definition of the syndrome. European Journal of Medical Genetics. 56(1). 54–58. 24 indexed citations
19.
Antonaci, Fabio, et al.. (2009). Therapy-resistant cluster headache in childhood: Case report and literature review. Cephalalgia. 30(2). 233–238. 15 indexed citations
20.
Veggiotti, Pierangelo, Federica Teutonico, Enrico Alfei, et al.. (2009). Glucose transporter type 1 deficiency: Ketogenic diet in three patients with atypical phenotype. Brain and Development. 32(5). 404–408. 30 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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