F. Mollica

995 total citations
70 papers, 677 citations indexed

About

F. Mollica is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, F. Mollica has authored 70 papers receiving a total of 677 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 15 papers in Genetics and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in F. Mollica's work include Neonatal Respiratory Health Research (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Metabolism and Genetic Disorders (6 papers). F. Mollica is often cited by papers focused on Neonatal Respiratory Health Research (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Metabolism and Genetic Disorders (6 papers). F. Mollica collaborates with scholars based in Italy, United Kingdom and United States. F. Mollica's co-authors include Piero Pavone, S. Li Volti, Giovanna Russo, Giovanni Sorge, Teresa Mattina, Allan J. Richards, G. Pampiglione, F M Pope, M. G. S. Dunnill and Robin A.J. Eady and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Human Molecular Genetics.

In The Last Decade

F. Mollica

66 papers receiving 643 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F. Mollica Italy	15	231	187	139	90	86	70	677
A D'agostino United States	17	233 1.0×	55 0.3×	88 0.6×	73 0.8×	57 0.7×	30	667
Angela Robbiano Italy	9	265 1.1×	82 0.4×	160 1.2×	34 0.4×	39 0.5×	10	629
Fumiya Uchino Japan	18	545 2.4×	108 0.6×	61 0.4×	53 0.6×	50 0.6×	74	953
Gal Finer United States	11	346 1.5×	71 0.4×	103 0.7×	19 0.2×	71 0.8×	19	610
S Tamura Japan	17	142 0.6×	68 0.4×	181 1.3×	33 0.4×	51 0.6×	64	667
Maruša Debeljak Slovenia	15	396 1.7×	173 0.9×	48 0.3×	37 0.4×	155 1.8×	84	870
Burcu Öztürk Hişmi Türkiye	13	233 1.0×	55 0.3×	38 0.3×	41 0.5×	104 1.2×	50	611
Marie Gonzalès France	14	348 1.5×	207 1.1×	156 1.1×	51 0.6×	353 4.1×	33	883
Албена Тодорова Bulgaria	14	363 1.6×	132 0.7×	39 0.3×	41 0.5×	47 0.5×	71	661
B. G. Ockenden United Kingdom	8	204 0.9×	248 1.3×	64 0.5×	10 0.1×	131 1.5×	10	556

Countries citing papers authored by F. Mollica

Since Specialization

Citations

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

Fields of papers citing papers by F. Mollica

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F. Mollica

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

All Works

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20 of 20 papers shown

Mollica, F., et al.. (2023). New trends in pediatric pulmonology: our experience. 1(1). 4–4.

Papale, Maria, et al.. (2023). Sleep Respiratory Disorders in Children and Adolescents with Cystic Fibrosis and Primary Ciliary Dyskinesia. Children. 10(10). 1707–1707. 1 indexed citations

Rosenfeld, Margaret, Erin Sullivan, Frankline Onchiri, et al.. (2022). Airway Disease in Children with Primary Ciliary Dyskinesia: Impact of Ciliary Ultrastructure Defect and Genotype. Annals of the American Thoracic Society. 20(4). 539–547. 14 indexed citations

Volti, S. Li, et al.. (1998). Hyporesponsiveness to intradermal administration of hepatitis B vaccine in insulin dependent diabetes mellitus. Archives of Disease in Childhood. 78(1). 54–57. 37 indexed citations

Condorelli, D. F., et al.. (1996). Routine clinical application of the FRAXA Pfu PCR assay: limits and utility. Clinical Genetics. 50(5). 366–371. 8 indexed citations

Garuti, Rita, Roberta Tiozzo, M. Ghisellini, et al.. (1996). Two novel partial deletions of LDL-receptor gene in Italian patients with familial hypercholesterolemia (FHSiracusa and FHReggio Emilia). Atherosclerosis. 121(1). 105–117. 8 indexed citations

Volti, S. Li, et al.. (1995). Duration of hepatitis B antibody response in children immunised with hepatitis B and compulsory vaccines. European Journal of Epidemiology. 11(2). 217–219. 5 indexed citations

Dunnill, M. G. S., et al.. (1994). A novel homozygous point mutation in the collagen VII gene (COL7A1) in two cousins with recessive dystrophic epidermolysis bullosa. Human Molecular Genetics. 3(9). 1693–1694. 28 indexed citations

Renieri, Alessandra, Lucia Galli, F. Mollica, et al.. (1994). Single base pair deletions in exons 39 and 42 of the COL4A5 gene in Alport syndrome. Human Molecular Genetics. 3(1). 201–202. 9 indexed citations

10.

Volti, S. Li, et al.. (1993). Impaired Antioxidant Defense Mechanisms in Two Children with Hemolytic—Uremic Syndrome. Renal Failure. 15(4). 523–528. 8 indexed citations

11.

Mollica, F., et al.. (1992). Effectiveness of early prednisone treatment in preventing the development of nephropathy in anaphylactoid purpura. European Journal of Pediatrics. 151(2). 140–144. 87 indexed citations

12.

Romeo, Mario, et al.. (1991). Familial Jarcho‐Levin syndrome. Clinical Genetics. 39(4). 253–259. 9 indexed citations

13.

Mollica, F.. (1991). Genetic aspects of immune response.. PubMed. 66(6). 490–2. 1 indexed citations

14.

Mollica, F., et al.. (1991). Familial congenital brachial palsy. American Journal of Medical Genetics. 41(3). 322–324. 2 indexed citations

15.

Neri, Giovanni, Piero Pavone, F. Mollica, et al.. (1988). The fragile X in sicily: An epidemiological survey. American Journal of Medical Genetics. 30(1-2). 665–672. 12 indexed citations

16.

Mattina, Teresa, et al.. (1988). Wolfram's syndrome and HLA. Ophthalmic Paediatrics and Genetics. 9(1). 25–28. 1 indexed citations

17.

Pavone, Piero, F. Mollica, Gemma Incorpora, & G. Pampiglione. (1985). Infantile spasms syndrome in monozygotic twins. A 7-year follow-up. Neurological Sciences. 6(4). 503–506. 3 indexed citations

18.

Feingold, Murray, et al.. (1980). Picture of the month. Metaphyseal chondrodysplasia, Schmid type.. PubMed. 134(7). 699–700. 2 indexed citations

19.

Pavone, L, et al.. (1977). Haematological studies in a case of oculocerebrorenal syndrome.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 31(6). 509–14. 1 indexed citations

20.

Mollica, F., et al.. (1967). Hemolysis in typhoid fever.. BMJ. 2(5545). 175.1–175. 3 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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