Florindo Mollica

648 total citations
25 papers, 471 citations indexed

About

Florindo Mollica is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Florindo Mollica has authored 25 papers receiving a total of 471 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Genetics and 6 papers in Genetics. Recurrent topics in Florindo Mollica's work include Hemoglobinopathies and Related Disorders (5 papers), Metabolism and Genetic Disorders (4 papers) and Metabolomics and Mass Spectrometry Studies (3 papers). Florindo Mollica is often cited by papers focused on Hemoglobinopathies and Related Disorders (5 papers), Metabolism and Genetic Disorders (4 papers) and Metabolomics and Mass Spectrometry Studies (3 papers). Florindo Mollica collaborates with scholars based in Italy, United States and Switzerland. Florindo Mollica's co-authors include S. Li Volti, Andrew Cassidy, Robert Hume, Anne McGeehan, Brian Burchell, A. Thomas McLellan, Gemma Monaghan, John M. Opitz, Mario La Rosa and Piero Pavone and has published in prestigious journals such as The Lancet, Blood and Neurology.

In The Last Decade

Florindo Mollica

22 papers receiving 452 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Florindo Mollica Italy 10 228 178 141 126 87 25 471
Eilish Twomey Ireland 9 193 0.8× 167 0.9× 176 1.2× 42 0.3× 56 0.6× 20 521
G. Fekete Hungary 12 281 1.2× 75 0.4× 32 0.2× 173 1.4× 48 0.6× 32 490
Peter Durie Canada 12 161 0.7× 78 0.4× 63 0.4× 224 1.8× 459 5.3× 16 860
Sunita Arya United States 9 185 0.8× 36 0.2× 125 0.9× 94 0.7× 35 0.4× 18 431
Jürgen R. Bierich Germany 9 289 1.3× 137 0.8× 51 0.4× 163 1.3× 25 0.3× 13 715
D G Barr United Kingdom 14 186 0.8× 93 0.5× 37 0.3× 269 2.1× 32 0.4× 28 530
Marion Gérard‐Blanluet France 13 200 0.9× 72 0.4× 22 0.2× 158 1.3× 23 0.3× 24 399
S Vestermark Denmark 12 102 0.4× 113 0.6× 19 0.1× 102 0.8× 30 0.3× 38 447
Ryszard Ślężak Poland 13 155 0.7× 57 0.3× 18 0.1× 129 1.0× 35 0.4× 50 472
SONGJA PANG United States 13 689 3.0× 93 0.5× 284 2.0× 123 1.0× 30 0.3× 21 884

Countries citing papers authored by Florindo Mollica

Since Specialization
Citations

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

Fields of papers citing papers by Florindo Mollica

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florindo Mollica

This figure shows the co-authorship network connecting the top 25 collaborators of Florindo Mollica. A scholar is included among the top collaborators of Florindo 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 Florindo Mollica. Florindo Mollica 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.
Pavone, Piero, et al.. (2009). Familial centronuclear myopathy. Acta Neurologica Scandinavica. 62(1). 33–40.
2.
Bianca, Sebastiano, et al.. (2002). Hyperphenylalaninemia and birth weight. Annales de Génétique. 45(3). 105–107.
3.
Monaghan, Gemma, A. Thomas McLellan, Anne McGeehan, et al.. (1999). Gilbert’s syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn. The Journal of Pediatrics. 134(4). 441–446. 110 indexed citations
4.
Cataldo, Andrea Di, Marcella Renis, Gino Schilirò, et al.. (1999). Deletions in the mitochondrial DNA and decrease in the oxidative phosphorylation activity of children with fanconi syndrome secondary to antiblastic therapy. American Journal of Kidney Diseases. 34(1). 98–106. 11 indexed citations
5.
Bosco, Paolo, Francesco Calı̀, Concetta Meli, et al.. (1998). Eight new mutations of the phenylalanine hydroxylase gene in Italian patients with hyperphenylalaninemia. Human Mutation. 11(3). 240–243. 7 indexed citations
6.
Mollica, Florindo, et al.. (1995). Severe case of al Awadi/Raas‐Rothschild syndrome or new, possibly autosomal recessive facio‐skeleto‐genital syndrome. American Journal of Medical Genetics. 56(2). 168–172. 13 indexed citations
7.
Opitz, John M., et al.. (1993). Acrofacial dysostoses: Review and report of a previously undescribed condition: The autosomal or X‐linked dominant catania form of acrofacial dysostosis. American Journal of Medical Genetics. 47(5). 660–678. 43 indexed citations
8.
Volti, S. Li, et al.. (1993). Acute post-streptococcal glomerulonephritis in an 8-month-old girl. Pediatric Nephrology. 7(6). 737–738. 5 indexed citations
9.
Guldberg, Per, Valentino Romano, N. Ceratto, et al.. (1993). Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenyl-alaninemia in Southern Europe. Human Molecular Genetics. 2(10). 1703–1707. 104 indexed citations
10.
Schilirò, Gino, Maria Antonietta Romeo, & Florindo Mollica. (1988). Prenatal diagnosis of thalassemia: The viewpoint of patients. Prenatal Diagnosis. 8(3). 231–233. 4 indexed citations
11.
Distefano, Giuseppe, Mario Romeo, Sebastiano Grasso, et al.. (1987). Dextrocardia with and without situs viscerum inversus in two sibs. American Journal of Medical Genetics. 27(4). 929–934. 19 indexed citations
12.
Volti, S. Li, et al.. (1986). Familial Optic Atrophy with Sex-Influenced Severity. Ophthalmologica. 192(1). 28–33. 7 indexed citations
13.
Pavone, Lorenzo, Gemma Incorpora, Mario La Rosa, S. Li Volti, & Florindo Mollica. (1981). Treatment of Infantile Spasms with Sodium Dipropylacetic Acid. Developmental Medicine & Child Neurology. 23(5). 454–461. 39 indexed citations
14.
Pavone, Piero, et al.. (1981). Ocular manifestations in a family with probably X‐linked cataracts. Clinical Genetics. 20(4). 243–246. 10 indexed citations
15.
Pavone, Piero, et al.. (1979). Muscle involvement in thalassemia major. Neurology. 29(5). 754–754. 1 indexed citations
16.
Mollica, Florindo, et al.. (1977). Neonatal hepatitis in five children of a hepatitis B surface antigen carrier woman. The Journal of Pediatrics. 90(6). 949–951. 9 indexed citations
17.
Russo, Giuseppe, Florindo Mollica, Piero Pavone, S Musumeci, & Corrado Baglioni. (1973). Genetic Implications of the Interaction of Two Types of Beta-Thalassemia Genes in a Patient With Thalassemia Major. Blood. 42(5). 763–769. 1 indexed citations
18.
Russo, Giuseppe, Florindo Mollica, Piero Pavone, & Salvatore Musumeci. (1972). Robin's Syndrome in Three Children of Consanguineous Parents —A Pedigree Suggesting Autosomal Recessive Inheritance. Acta geneticae medicae et gemellologiae. 21(4). 349–353.
19.
Russo, Giuseppe, Florindo Mollica, Piero Pavone, & Gino Schilirò. (1972). HEMOLYTIC CRISES OF FAVISM IN SICILIAN FEMALES HETEROZYGOUS FOR G-6-PD DEFICIENCY. PEDIATRICS. 49(6). 854–859. 9 indexed citations
20.
Mollica, Florindo, et al.. (1971). INTRATHECAL METHOTREXATE. The Lancet. 298(7727). 771–771. 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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