M. Cioni

627 total citations
22 papers, 426 citations indexed

About

M. Cioni is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, M. Cioni has authored 22 papers receiving a total of 426 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in M. Cioni's work include Genetics and Neurodevelopmental Disorders (6 papers), RNA regulation and disease (4 papers) and Thermochemical Biomass Conversion Processes (4 papers). M. Cioni is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), RNA regulation and disease (4 papers) and Thermochemical Biomass Conversion Processes (4 papers). M. Cioni collaborates with scholars based in Italy, United States and Spain. M. Cioni's co-authors include Paolo Balestri, Salvatore Grosso, G Morgese, Enrico Biagini, Maria Margollicci, Leonardo Tognotti, Alice Luddi, Paola Piomboni, Laura Gambera and Vincenzo De Leo and has published in prestigious journals such as New England Journal of Medicine, Annals of Neurology and Chemosphere.

In The Last Decade

M. Cioni

22 papers receiving 407 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Cioni Italy	13	186	163	98	58	50	22	426
W. Scholz Germany	14	201 1.1×	217 1.3×	78 0.8×	23 0.4×	65 1.3×	43	600
Lap-Chee Tsui Canada	9	118 0.6×	389 2.4×	39 0.4×	6 0.1×	29 0.6×	9	1.3k
Kentaro Katayama Japan	13	151 0.8×	188 1.2×	14 0.1×	10 0.2×	11 0.2×	39	396
Jostein Westvik Norway	9	172 0.9×	246 1.5×	35 0.4×	41 0.7×	4 0.1×	14	364
Yufen Xie United States	15	40 0.2×	316 1.9×	80 0.8×	32 0.6×	28 0.6×	21	621
J. M. Cant� Mexico	11	220 1.2×	189 1.2×	81 0.8×	31 0.5×	5 0.1×	17	378
Maria Papadopoulos United Kingdom	15	34 0.2×	147 0.9×	15 0.2×	14 0.2×	16 0.3×	32	867
Douglas R. Lazzaro United States	17	61 0.3×	213 1.3×	96 1.0×	3 0.1×	5 0.1×	51	865
Nidhi Shah United States	12	136 0.7×	96 0.6×	59 0.6×	4 0.1×	23 0.5×	40	339
J.G. Bearn United States	10	39 0.2×	80 0.5×	56 0.6×	32 0.6×	3 0.1×	38	355

Countries citing papers authored by M. Cioni

Since Specialization

Citations

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

Fields of papers citing papers by M. Cioni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Cioni

This figure shows the co-authorship network connecting the top 25 collaborators of M. Cioni. A scholar is included among the top collaborators of M. Cioni 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 M. Cioni. M. Cioni 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:

20 of 20 papers shown

Uliana, Vera, Salvatore Grosso, M. Cioni, et al.. (2010). 3.2 Mb microdeletion in chromosome 7 bands q22.2–q22.3 associated with overgrowth and delayed bone age. European Journal of Medical Genetics. 53(3). 168–170. 14 indexed citations

Luddi, Alice, Maria Margollicci, Laura Gambera, et al.. (2009). Spermatogenesis in a Man with Complete Deletion of USP9Y. New England Journal of Medicine. 360(9). 881–885. 107 indexed citations

Luddi, Alice, Maria Margollicci, Laura Gambera, et al.. (2009). Brief Report: Spermatogenesis in a Man with Complete Deletion of USP9Y.. 1 indexed citations

Grosso, Salvatore, Daniela Galimberti, M. A. Farnetani, et al.. (2005). Efficacy and safety of topiramate in infants according to epilepsy syndromes. Seizure. 14(3). 183–189. 40 indexed citations

Grosso, Salvatore, Lucia Pucci, Rosanna Maria Di Bartolo, et al.. (2005). Chromosome 18 aberrations and epilepsy: A review. American Journal of Medical Genetics Part A. 134A(1). 88–94. 20 indexed citations

Grosso, Salvatore, et al.. (2003). Schinzel–Giedion syndrome: a further cause of West syndrome. Brain and Development. 25(4). 294–298. 14 indexed citations

Grosso, Salvatore, et al.. (2002). Pontocerebellar hypoplasia type 2. Journal of Neurology. 249(5). 596–600. 9 indexed citations

Grosso, Salvatore, M. Cioni, Lucia Pucci, et al.. (2002). De novo complete trisomy 5p: Clinical and neuroradiological findings. American Journal of Medical Genetics. 112(1). 56–60. 16 indexed citations

Vivarelli, Rossella, Salvatore Grosso, M. Cioni, et al.. (2001). Pseudo-TORCH syndrome or Baraitser–Reardon syndrome: diagnostic criteria. Brain and Development. 23(1). 18–23. 31 indexed citations

10.

Ferrari, Fabrizio, Claudio De Felice, Franco Bagnoli, et al.. (2000). EEG in Assessing Hydroxycobalamin Therapy in Neonatal Methylmalonic Aciduria with Homocystinuria. Neonatology. 78(4). 327–330. 1 indexed citations

11.

Guerrini, Renzo, Francesca Moro, Emilio Fernández‐Álvarez, et al.. (1999). Intracellular levels of the LIS1 protein correlate with clinical and neuroradiological findings in patients with classical lissencephaly. Annals of Neurology. 45(2). 154–161. 2 indexed citations

12.

Grosso, Salvatore, Rosario Berardi, M. Cioni, & G Morgese. (1998). Transient neonatal hypothyroidism after gestational exposure to amiodarone: A follow-up of two cases. Journal of Endocrinological Investigation. 21(10). 699–702. 17 indexed citations

13.

Grosso, Salvatore, M. Cioni, Sabrina Buoni, et al.. (1998). Growth hormone secretion in Prader-Willi syndrome. Journal of Endocrinological Investigation. 21(7). 418–422. 15 indexed citations

14.

Cioni, M., et al.. (1994). PCDD/PCDF formation and destruction during co-firing of coal and RDF in a slag forming combustor. Analytical and Bioanalytical Chemistry. 348(1-2). 136–140. 3 indexed citations

15.

Bartalini, G., Maria Margollicci, Paolo Balestri, et al.. (1992). Biochemical diagnosis of Canavan disease. Child s Nervous System. 8(8). 468–470. 11 indexed citations

16.

Cioni, M., et al.. (1990). Evaluation of PCDD/PCDF emission from the combined combustion of RDF with coal. Chemosphere. 20(10-12). 1891–1897. 3 indexed citations

17.

Cioni, M., et al.. (1988). Determination of trace organic compounds in effluents from a coal-fired power plant. Journal of Mass Spectrometry. 16(1-12). 175–178. 4 indexed citations

18.

Cioni, M., et al.. (1986). Characterization of solid emissions from a coal-fired power plant. Journal of Aerosol Science. 17(3). 627–628. 2 indexed citations

19.

Fois, A., M. Cioni, R. Frezzotti, et al.. (1986). Presentation of the data of the Italian registry for oculocutaneous tyrosinaemia. Journal of Inherited Metabolic Disease. 9(S2). 262–264. 20 indexed citations

20.

Fois, A., M. Cioni, Paolo Balestri, et al.. (1986). Biotinidase deficiency: metabolites in CSF. Journal of Inherited Metabolic Disease. 9(3). 284–285. 14 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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