Marcello Niceta

2.4k total citations
53 papers, 810 citations indexed

About

Marcello Niceta is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Marcello Niceta has authored 53 papers receiving a total of 810 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 25 papers in Genetics and 6 papers in Cell Biology. Recurrent topics in Marcello Niceta's work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Rare Diseases (5 papers). Marcello Niceta is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Rare Diseases (5 papers). Marcello Niceta collaborates with scholars based in Italy, United States and Germany. Marcello Niceta's co-authors include Marco Tartaglia, L. Alio, Clelia Cicerone, Antonio Maiorana, Bruno Dallapiccola, Enrico Bertini, Andrea Ciolfi, Maria Lisa Dentici, Richard P. Harbottle and Suet Ping Wong and has published in prestigious journals such as Brain, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Marcello Niceta

47 papers receiving 799 citations

Peers

Countries citing papers authored by Marcello Niceta

Since Specialization

Citations

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

Fields of papers citing papers by Marcello Niceta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marcello Niceta

This figure shows the co-authorship network connecting the top 25 collaborators of Marcello Niceta. A scholar is included among the top collaborators of Marcello Niceta 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 Marcello Niceta. Marcello Niceta 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

#	Work	Indexed citations
1	Oxytocin Deficiency in Childhood and Adolescence: Clinical Features, Diagnostic Challenges and Therapeutic Perspectives 2025 ·Current Issues in Molecular Biology ·(unknown), Amy K. Bei, (unknown), C. Fiorentini, (unknown), (unknown), (unknown), F. Pastore, (unknown), Marcello Niceta, Marco Fiore, Brunella Caronti, Mario Vitali, Ida Pucarelli, Luigi Tarani	0
2	Water-Soluble Vitamins: Hypo- and Hypervitaminosis in Pediatric Population 2025 ·Pharmaceutics ·(unknown), (unknown), Lucia Leonardi, Ida Pucarelli, (unknown), (unknown), (unknown), Marcello Niceta, Debora Rasio, Rouzha Pancheva, Marco Fiore, Luigi Tarani	7
3	The p.Ile202Thr Substitution in TUBB2B Can Be Associated with Syndromic Presentation of Congenital Fibrosis of the Extraocular Muscles 2025 ·Genes ·(unknown), (unknown), Alessandro Bruselles, Paola D′Ambrosio, Andrea Ciolfi, (unknown), (unknown), (unknown), Francesca Clementina Radio, Viviana Cordeddu, Marcello Niceta, (unknown), Rossella Capolino, (unknown), (unknown), Mario Muto, Manuela Priolo, Marco Tartaglia	1
4	Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome 2024 ·Movement Disorders ·Serena Galosi, Cecilia Mancini, (unknown), Paolo Calligari, Viviana Caputo, Francesca Nardecchia, Claudia Carducci, Lambertus P. van den Heuvel, Simone Pizzi, Alessandro Bruselles, Marcello Niceta, Simone Martinelli, Richard J. Rodenburg, Marco Tartaglia, Vincenzo Leuzzi	2
5	Whole Genome Sequencing Solves an Atypical Form of Bardet–Biedl Syndrome: Identification of Novel Pathogenic Variants of BBS9 2024 ·International Journal of Molecular Sciences ·Emilia Stellacci, Marcello Niceta, Alessandro Bruselles, (unknown), Massimo Tatti, (unknown), Cecilia Mancini, Serena Cecchetti, Mariacristina Parravano, (unknown), Monica Varano, Marco Tartaglia, Lucia Ziccardi, Viviana Cordeddu	0
6	Case report: Novel compound heterozygosity for pathogenic variants in MED23 in a syndromic patient with postnatal microcephaly 2023 ·Frontiers in Neurology ·(unknown), Marcello Niceta, Simone Pizzi, Francesca Clementina Radio, (unknown), (unknown), Sabina Barresi, (unknown), Cecilia Mancini, Marco Tartaglia, Maria Piccione	1
7	Case report: Expanding the phenotype of FOXP1-related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures 2023 ·Frontiers in Neurology ·(unknown), Marzia Pollazzon, Cecilia Mancini, (unknown), (unknown), Simone Pizzi, Daniele Frattini, Carlotta Spagnoli, Stefano Giuseppe Caraffi, Roberta Zuntini, (unknown), Marcello Niceta, Francesca Clementina Radio, Marco Tartaglia, Livia Garavelli, Carlo Fusco	3
8	Clinical profiling of MRD48 and functional characterization of two novel pathogenic RAC1 variants 2023 ·European Journal of Human Genetics ·Manuela Priolo, (unknown), Francesca Clementina Radio, Andrea Ciolfi, Francesca Spadaro, Emanuele Bellacchio, Cecilia Mancini, Francesca Pantaleoni, Viviana Cordeddu, (unknown), Marcello Niceta, (unknown), Corrado Mammì, Daniela Melis, Simona Coppola, Marco Tartaglia	4
9	Biallelic Inactivating TUB Variants Cause Retinal Ciliopathy Impairing Biogenesis and the Structure of the Primary Cilium 2022 ·International Journal of Molecular Sciences ·Lucia Ziccardi, Marcello Niceta, Emilia Stellacci, Andrea Ciolfi, Massimo Tatti, Alessandro Bruselles, Cecilia Mancini, (unknown), Serena Cecchetti, Eliana Costanzo, Marco Cappa, Mariacristina Parravano, Monica Varano, Marco Tartaglia, Viviana Cordeddu	2
10	SHP2 's gain‐of‐function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction 2022 ·Clinical Genetics ·Manuela Priolo, (unknown), (unknown), Andrea Ciolfi, Luca Pannone, Valentina Muto, Marialetizia Motta, Cecilia Mancini, Francesca Clementina Radio, Marcello Niceta, Chiara Leoni, (unknown), Rosalba Carrozzo, (unknown), Corrado Mammì, Giuseppe Zampino, Simone Martinelli, Bruno Dallapiccola, Pietro Pichierri, Marco Tartaglia	2
11	CDKL5 deficiency disorder in males: Five new variants and review of the literature 2021 ·European Journal of Paediatric Neurology ·(unknown), Costanza Varesio, Elena Freri, Francesca Darra, Simone Gana, Davide Mei, Francesco Porta, Elena Fontana, Giulia Galati, Roberta Solazzi, Marcello Niceta, Pierangelo Veggiotti, Enrico Alfei	19
12	Co-occurrence of mutations in KIF7 and KIAA0556 in Joubert syndrome with ocular coloboma, pituitary malformation and growth hormone deficiency: a case report and literature review 2020 ·BMC Pediatrics ·Marcello Niceta, Maria Lisa Dentici, Andrea Ciolfi, (unknown), Sabina Barresi, Francesca Romana Lepri, Antonio Novelli, Enrico Bertini, Marco Cappa, M. Cristina Digilio, Bruno Dallapiccola, Marco Tartaglia	13
13	Expanding the clinical spectrum associated with PACS2 mutations 2019 ·Clinical Genetics ·Maria Lisa Dentici, Sabina Barresi, Marcello Niceta, Andrea Ciolfi, Marina Trivisano, Andrea Bartuli, M. Cristina Digilio, Nicola Specchio, Bruno Dallapiccola, Marco Tartaglia	17
14	Skeletal abnormalities are common features in Aymé‐Gripp syndrome 2019 ·Clinical Genetics ·Marcello Niceta, Domenico Barbuti, Neerja Gupta, Carlos Ruggiero, Eduardo F. Tizzano, Luitgard Graul‐Neumann, Sabina Barresi, Gen Nishimura, Irene Valenzuela, (unknown), Paula Fernández‐Álvarez, Chiara Leoni, Christiane Zweier, Andreas Tzschach, Emilia Stellacci, Andrea Del Fattore, Bruno Dallapiccola, Giuseppe Zampino, Marco Tartaglia	10
15	Clinical and hormonal characteristics in heterozygote carriers of congenital adrenal hyperplasia 2019 ·The Journal of Steroid Biochemistry and Molecular Biology ·Valentina Guarnotta, Marcello Niceta, (unknown), (unknown), Carmelo Fabiano, Serena Indelicato, Francesca Di Gaudio, Piernicola Garofalo, Carla Giordano	16
16	TARP syndrome: Long-term survival, anatomic patterns of congenital heart defects, differential diagnosis and pathogenetic considerations 2018 ·European Journal of Medical Genetics ·Marcello Niceta, Sabina Barresi, Francesca Pantaleoni, Rossella Capolino, Maria Lisa Dentici, Andrea Ciolfi, Simone Pizzi, Andrea Bartuli, Bruno Dallapiccola, Marco Tartaglia, M. Cristina Digilio	16
17	A mild form of adenylosuccinate lyase deficiency in absence of typical brain MRI features diagnosed by whole exome sequencing 2017 ·The Italian Journal of Pediatrics/Italian journal of pediatrics ·Marina Macchiaiolo, Sabina Barresi, Francesco Cecconi, Ginevra Zanni, Marcello Niceta, Emanuele Bellacchio, Giacomo Lazzarino, Angela Maria Amorini, Enrico Bertini, Salvatore Rizza, (unknown), Marco Tartaglia, Andrea Bartuli	10
18	A large view of CYP21 locus among Sicilians and other populations: identification of a novel CYP21A2 variant in Sicily. 2011 ·PubMed ·Marcello Niceta, (unknown), Carmelo Fabiano, Fanny Pojero, (unknown), (unknown), Giovanni Corsello, Piernicola Garofalo	3
19	Persistent episomal transgene expression in liver following delivery of a scaffold/matrix attachment region containing non-viral vector 2008 ·Gene Therapy ·Orestis Argyros, Suet Ping Wong, Marcello Niceta, Simon N. Waddington, Steven J. Howe, Charles Coutelle, Andrew D. Miller, Richard P. Harbottle	73
20	Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndrome 2008 ·European Journal of Pediatrics ·Maria Piccione, Vincenzo Antona, Marcello Niceta, Carmelo Fabiano, (unknown), Alberto Bianchi, Giovanni Corsello	11

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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