Luigi Memo

3.0k total citations
34 papers, 1.1k citations indexed

About

Luigi Memo is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Luigi Memo has authored 34 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 13 papers in Pediatrics, Perinatology and Child Health and 9 papers in Molecular Biology. Recurrent topics in Luigi Memo's work include Genomic variations and chromosomal abnormalities (9 papers), Neonatal Health and Biochemistry (5 papers) and Genomics and Rare Diseases (4 papers). Luigi Memo is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Neonatal Health and Biochemistry (5 papers) and Genomics and Rare Diseases (4 papers). Luigi Memo collaborates with scholars based in Italy, Spain and United States. Luigi Memo's co-authors include Giovanni Corsello, Alberto Villani, Luigi Tarani, Simona Pichini, Giuseppe Capovilla, Marcella Zollino, Rosetta Lecce, Giovanni Neri, Marina Murdolo and Angelo Selicorni and has published in prestigious journals such as PEDIATRICS, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

Luigi Memo

33 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luigi Memo Italy 16 337 318 285 204 152 34 1.1k
Michael Gottschalk United States 24 652 1.9× 476 1.5× 518 1.8× 211 1.0× 64 0.4× 48 2.3k
Dafne Dain Gandelman Horovitz Brazil 19 197 0.6× 205 0.6× 244 0.9× 861 4.2× 507 3.3× 67 1.9k
Peter Lindgren Sweden 18 171 0.5× 296 0.9× 285 1.0× 283 1.4× 137 0.9× 56 1.2k
Daniel R. Arnold United States 20 230 0.7× 376 1.2× 257 0.9× 418 2.0× 44 0.3× 61 1.4k
Christine Cameron United States 21 72 0.2× 221 0.7× 112 0.4× 375 1.8× 104 0.7× 35 1.8k
Marı́a Belén Herrero Argentina 20 87 0.3× 275 0.9× 123 0.4× 559 2.7× 53 0.3× 50 1.4k
Genevieve L. Wojcik United States 17 846 2.5× 307 1.0× 86 0.3× 75 0.4× 203 1.3× 41 1.4k
Elizabeth Park United States 14 157 0.5× 193 0.6× 48 0.2× 87 0.4× 34 0.2× 41 665
Aparna Duggirala United Kingdom 14 229 0.7× 685 2.2× 209 0.7× 62 0.3× 65 0.4× 18 1.1k
Marion Blumenstein New Zealand 13 47 0.1× 103 0.3× 210 0.7× 287 1.4× 341 2.2× 30 1.1k

Countries citing papers authored by Luigi Memo

Since Specialization
Citations

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

Fields of papers citing papers by Luigi Memo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luigi Memo

This figure shows the co-authorship network connecting the top 25 collaborators of Luigi Memo. A scholar is included among the top collaborators of Luigi Memo 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 Luigi Memo. Luigi Memo 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.
Spedicati, Beatrice, Flavio Faletra, Laura Pignata, et al.. (2023). Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 49(1). 127–127.
2.
Serra, Gregorio, Luigi Memo, Mario Cutrone, et al.. (2022). Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 48(1). 145–145. 10 indexed citations
3.
Bozzola, Elena, Annamaria Staiano, Giulia Spina, et al.. (2021). Social media use to improve communication on children and adolescent’s health: the role of the Italian Paediatric Society influencers. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 47(1). 171–171. 14 indexed citations
4.
Bozzola, Elena, Giulia Spina, Massimiliano Valeriani, et al.. (2021). Management of pediatric post-infectious neurological syndromes. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 47(1). 6 indexed citations
5.
Cianci, Paola, Alex Moretti, Sabrina Paci, et al.. (2020). Children with special health care needs attending emergency department in Italy: analysis of 3479 cases. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 46(1). 173–173. 5 indexed citations
6.
Bozzola, Elena, Giulia Spina, Davide Vecchio, et al.. (2019). Media use during adolescence: the recommendations of the Italian Pediatric Society. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 45(1). 149–149. 40 indexed citations
7.
Jankovic, Momcilo, Lucia De Zen, Pierina Lazzarin, et al.. (2019). A consensus conference report on defining the eligibility criteria for pediatric palliative care in Italy. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 45(1). 89–89. 14 indexed citations
8.
Bozzola, Elena, Giulia Spina, Luigi Memo, et al.. (2018). Media devices in pre-school children: the recommendations of the Italian pediatric society. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 44(1). 69–69. 78 indexed citations
9.
Borghesi, A., Maria Antonietta Mencarelli, Luigi Memo, et al.. (2017). Intersociety policy statement on the use of whole-exome sequencing in the critically ill newborn infant. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 43(1). 100–100. 45 indexed citations
10.
Manzoni, Paolo, Luigi Memo, Michael Mostert, et al.. (2014). Use of erythropoietin is associated with threshold retinopathy of prematurity (ROP) in preterm ELBW neonates: a retrospective, cohort study from two large tertiary NICUs in Italy. Early Human Development. 90. S29–S33. 13 indexed citations
11.
Morini, Luca, Emilia Marchei, Luigi Tarani, et al.. (2013). Testing Ethylglucuronide in Maternal Hair and Nails for the Assessment of Fetal Exposure to Alcohol. Therapeutic Drug Monitoring. 35(3). 402–407. 40 indexed citations
12.
Memo, Luigi, et al.. (2013). Fetal alcohol spectrum disorders and fetal alcohol syndrome: the state of the art and new diagnostic tools. Early Human Development. 89. S40–S43. 46 indexed citations
13.
Salviati, Leonardo, Eva Trevisson, María Hernández, et al.. (2012). Haploinsufficiency of COQ4 causes coenzyme Q10 deficiency. Journal of Medical Genetics. 49(3). 187–191. 85 indexed citations
14.
Resta, Nicoletta & Luigi Memo. (2012). Chromosomal microarray (CMA) analysis in infants with congenital anomalies: when is it really helpful?. The Journal of Maternal-Fetal & Neonatal Medicine. 25(sup4). 116–118. 10 indexed citations
15.
Memo, Luigi, et al.. (2011). Care procedures for healthy term newborn in maternity ward: The “open” nursery. Early Human Development. 87. S87–S88. 1 indexed citations
16.
Gana, Simone, et al.. (2010). Nicolaides–Baraitser syndrome. Clinical Dysmorphology. 20(1). 38–41. 8 indexed citations
17.
Gregori, Manuela De, Tiziano Pramparo, Luigi Memo, et al.. (2005). Direct duplication 12p11.21–p13.31 mediated by segmental duplications: a new recurrent rearrangement?. Human Genetics. 118(2). 207–213. 6 indexed citations
18.
Zollino, Marcella, Rosetta Lecce, Rita Fischetto, et al.. (2003). Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region, WHSCR-2. The American Journal of Human Genetics. 72(3). 590–597. 156 indexed citations
19.
Caufin, Daniele, et al.. (1991). Inv dup (8) (p21.1 → 22.1): further case report and a new hypothesis on the origin of the chromosome abnormality. Clinical Genetics. 39(1). 55–59. 26 indexed citations
20.
Caufin, Daniele, et al.. (1989). Terminal deletion of the long arm of chromosome 10: Case report and review of the literature. American Journal of Medical Genetics. 33(4). 502–504. 31 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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