Mita Mancini

1.2k citations
11 papers · 986 · 1 hit paper · h-index 9

Impact in

    • Nuclear Structure and Function
    • RNA Research and Splicing
    • Genomics and Chromatin Dynamics
    • Muscle Physiology and Disorders
    • RNA regulation and disease
  • Cell Biology top 10%

Papers in

    • RNA Research and Splicing 3
    • Epigenetics and DNA Methylation 2
    • Genomics and Chromatin Dynamics 2
    • Nuclear Structure and Function 2
    • Caveolin-1 and cellular processes 2

Mita Mancini

11 papers receiving 941 citations

Mita Mancini's Hit Papers

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy 1994 · 723 citations
7230+10+21Years since publication200400600

Peers

Mita Mancini
Comparison fields: 5 of 56
  • Molecular Biology 852
  • Cell Biology 137
  • Cardiology and Cardiovascular Medicine 142
  • Genetics 54
  • Genetics 124
Replace Francesco Muntoni with:
Francesco Muntoni United Kingdom
Luiza Bengtsson Germany
Y Nabeshima Japan
Matthew Wheeler United Kingdom
S. Manilal United Kingdom
Sylvia Vlcek Austria
Yanfeng Kong United States
Guillaume Précigout France
Rüdiger J. Blaschke Germany
Norma Towers United Kingdom
Mita Mancini relative to Francesco Muntoni United Kingdom Francesco Muntoni's profile →
Citations per field
00.5×1.6×
Francesco Muntoni · 1×
Citations per year

Countries citing papers authored by Mita Mancini

Since Specialization
Citations

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

Fields of papers citing papers by Mita Mancini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Mita Mancini, 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 Mita Mancini Line = papers co-authored together Mita Mancini links everyone, so they are left out of the graph.

All Works

11 of 11 papers shown
#Work
1
Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy
Hit paper breakdown →
1994723
2 199368
3 199440
4 199239
5 200029
6 199427
7 200026
8 199922
9 19958
10 19962
11 19992

About Mita Mancini

Mita Mancini is a scholar working on Molecular Biology, Cell Biology, Genetics, Cardiology and Cardiovascular Medicine and Atomic and Molecular Physics, and Optics, having authored 11 papers that have together received 986 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), RNA Research and Splicing (3 papers), Epigenetics and DNA Methylation (2 papers), Caveolin-1 and cellular processes (2 papers), Genomics and Chromatin Dynamics (2 papers), Nuclear Structure and Function (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Molecular Biology (852 citations), Cell Biology (137 citations), Cardiology and Cardiovascular Medicine (142 citations), Genetics (54 citations) and Genetics (124 citations). Mita Mancini has collaborated with scholars based in Italy and United States. Frequent co-authors include Stefano Rivella, Daniela Toniolo, Elena Maestrini, Silvia Bione, Giovanni Romeo, Stefano Regis, Anna Villa, Paolo Vezzoni, Annamaria Fra and Elena Pasqualetto. Their work appears in journals such as Genomics, Human Molecular Genetics, Gene, Nucleic Acids Research and Nature Genetics.

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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