M. Cioni

629 citations
22 papers · 428 · h-index 13

Impact in

    • Sperm and Testicular Function
  • Genetics top 10%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Genetics and Neurodevelopmental Disorders 6
    • Genomic variations and chromosomal abnormalities 3
    • Genomics and Rare Diseases 3
    • RNA regulation and disease 4
    • RNA Research and Splicing 2

M. Cioni

22 papers receiving 409 citations

Peers

M. Cioni
Comparison fields: 5 of 70
  • Reproductive Medicine 50
  • Genetics 170
  • Clinical Biochemistry 31
  • Pediatrics, Perinatology and Child Health 76
  • Psychiatry and Mental health 47
Replace Irene Mademont‐Soler with:
Irene Mademont‐Soler Spain
Kentaro Katayama Japan
Shangang Li China
Rik Hendrickx Belgium
Haijun Gao United States
Masaru Fukuda Japan
Anton Mlikotic United States
J.G. Bearn United States
Ziva Ben Neriah Israel
Ana Monteagudo United States
M. Cioni relative to Irene Mademont‐Soler Spain Irene Mademont‐Soler's profile →
Citations per field
00.5×5.6×
Irene Mademont‐Soler · 1×
Citations per year

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-authors

The 25 scholars most cited alongside M. Cioni, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with M. Cioni Line = papers co-authored together M. Cioni links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 22 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2009108
2 200544
3 200540
4 199938
5 200131
6 198620
7 200520
8 199817
9 200216
10 199815
11 201014
12 200314
13 198614
14 199211
15 20029
16 19884
17 19943
18 19903
19 20002
20 19992

About M. Cioni

M. Cioni is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Biomedical Engineering and Rheumatology, having authored 22 papers that have together received 428 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Thermochemical Biomass Conversion Processes (4 papers), RNA regulation and disease (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (3 papers), Folate and B Vitamins Research (2 papers), Metabolism and Genetic Disorders (2 papers) and RNA Research and Splicing (2 papers). The work is most often cited by research in Reproductive Medicine (50 citations), Genetics (170 citations), Clinical Biochemistry (31 citations), Pediatrics, Perinatology and Child Health (76 citations) and Psychiatry and Mental health (47 citations). M. Cioni has collaborated with scholars based in Italy, United States and France. Frequent co-authors include Paolo Balestri, Salvatore Grosso, G Morgese, Maria Margollicci, Leonardo Tognotti, Enrico Biagini, Vincenzo De Leo, Laura Gambera, Paola Piomboni and Alice Luddi. Their work appears in journals such as Journal of Inherited Metabolic Disease, Brain and Development, Annals of Neurology, European Journal of Medical Genetics and Neonatology.

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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