L. Memo

653 total citations
11 papers, 241 citations indexed

About

L. Memo is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, L. Memo has authored 11 papers receiving a total of 241 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pediatrics, Perinatology and Child Health, 4 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in L. Memo's work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Chromatin Dynamics (3 papers) and Infant Development and Preterm Care (2 papers). L. Memo is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genomics and Chromatin Dynamics (3 papers) and Infant Development and Preterm Care (2 papers). L. Memo collaborates with scholars based in Italy, Spain and Belgium. L. Memo's co-authors include P Maraschio, Claudio Castellan, Cristina Gervasini, Alessandra Baumer, Elena Rossi, Mariluce Riegel, Angela Bentivegna, Orsetta Zuffardi, Teresa Mattina and Paola Castronovo and has published in prestigious journals such as Journal of Medical Genetics, Early Human Development and Clinical Genetics.

In The Last Decade

L. Memo

9 papers receiving 229 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
L. Memo Italy	7	150	131	77	60	15	11	241
Brenda McInnes Canada	7	165 1.1×	47 0.4×	79 1.0×	36 0.6×	7 0.5×	8	242
Anne-Marie Van Der Kevie-Kersemaekers Netherlands	7	124 0.8×	92 0.7×	61 0.8×	35 0.6×	9 0.6×	13	212
Stéphane Serero France	8	188 1.3×	133 1.0×	110 1.4×	46 0.8×	43 2.9×	15	328
Nieves Cremades Portugal	8	116 0.8×	145 1.1×	55 0.7×	32 0.5×	41 2.7×	10	404
Ferdouse Begum United States	7	147 1.0×	103 0.8×	55 0.7×	28 0.5×	7 0.5×	13	231
Vera Ayres Meloni Brazil	9	233 1.6×	122 0.9×	59 0.8×	50 0.8×	17 1.1×	26	272
Rhonda Spiro United States	8	249 1.7×	120 0.9×	120 1.6×	38 0.6×	41 2.7×	8	286
Françoise Girard‐Lemaire France	8	140 0.9×	81 0.6×	98 1.3×	21 0.3×	31 2.1×	12	194
Chen‐Chi Lee Taiwan	11	230 1.5×	69 0.5×	183 2.4×	62 1.0×	40 2.7×	23	270
Shahrin Pereira United States	3	160 1.1×	82 0.6×	71 0.9×	24 0.4×	9 0.6×	3	201

Countries citing papers authored by L. Memo

Since Specialization

Citations

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

Fields of papers citing papers by L. Memo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L. Memo

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

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

Niceta, Marcello, Katia Margiotti, M. Cristina Digilio, et al.. (2017). Biallelic mutations in DYNC2LI1 are a rare cause of Ellis‐van Creveld syndrome. Clinical Genetics. 93(3). 632–639. 19 indexed citations

Rinaldi, Matteo, Paolo Manzoni, Martine De Meyer, et al.. (2012). A3 Bovine lactoferrin supplementation for prevention of necrotising enterocolitis in preterm very-low-birth-weight neonates: a randomised trial. Early Human Development. 88. S102–S102. 5 indexed citations

Vagnarelli, Federica, Ilaria Palmi, Óscar García‐Algar, et al.. (2011). A survey of Italian and Spanish neonatologists and paediatricians regarding awareness of the diagnosis of FAS and FASD and maternal ethanol use during pregnancy. BMC Pediatrics. 11(1). 51–51. 16 indexed citations

Belhaj, Asmae, et al.. (2011). [Gastric adenocarcinoma following "silastic vertical ring gastroplasty": case report].. PubMed. 31(5). 459–62. 6 indexed citations

Memo, L., Luigi Tarani, Roberta Pacifici, et al.. (2011). Survey of Italian neonatologists knowledge regarding awareness of ethanol use during pregnancy and the diagnosis of FAS and FASD. Early Human Development. 87. S93–S94.

Selicorni, Angelo, Silvia Russo, Cristina Gervasini, et al.. (2007). Clinical score of 62 Italian patients with Cornelia de Lange syndrome and correlations with the presence and type of NIPBL mutation. Clinical Genetics. 72(2). 98–108. 72 indexed citations

Rossi, Elena, Mariluce Riegel, Jole Messa, et al.. (2007). Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation. Journal of Medical Genetics. 45(3). 147–154. 83 indexed citations

Memo, L., et al.. (2007). [Follow-up of the neonate with malformation syndrome].. PubMed. 59(5). 503–6.

Lago, Paola, Gina Ancora, Alberto Cavazza, et al.. (2006). [Italian guidelines and recommendations for prevention and treatment of pain in the newborn].. PubMed. 28(1-3). 24–34. 8 indexed citations

10.

Tupler, Rossella, E. Bühler, M. Alkan, et al.. (1992). Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.. Journal of Medical Genetics. 29(1). 53–55. 26 indexed citations

11.

Memo, L., Elisabetta Lenzini, & C Baccichetti. (1988). Trisomy 8p by malsegregation of a t(5;8)(p15;p11)mat in a case of XY pure gonadal dysgenesis.. PubMed. 31(3). 181–5. 6 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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