Adele D’Amico

13.4k citations
320 papers · 10.9k · h-index 57

Impact in

  • Genetics top 0.1%
    • Neurogenetic and Muscular Disorders Research
    • Genomics and Rare Diseases
    • Muscle Physiology and Disorders
    • Nuclear Structure and Function

Papers in

    • Neurogenetic and Muscular Disorders Research 128
    • Genomics and Rare Diseases 28
    • Muscle Physiology and Disorders 144
    • Mitochondrial Function and Pathology 10

Adele D’Amico

300 papers receiving 10.6k citations

Peers

Adele D’Amico
Comparison fields: 5 of 141
  • Genetics 3.9k
  • Molecular Biology 5.4k
  • Clinical Biochemistry 334
  • Genetics 911
  • Neurology 361
Replace Anne M. Connolly with:
Anne M. Connolly United States
Claudio Bruno Italy
M. Tulinius Sweden
Basil T. Darras United States
Monique M. Ryan Australia
Adnan Yousaf Manzur United Kingdom
Kathryn J. Swoboda United States
Janbernd Kirschner Germany
Susana Quijano‐Roy France
Lucia Ovidia Morandi Italy
Adele D’Amico relative to Anne M. Connolly United States Anne M. Connolly's profile →
Citations per field
00.5×1.7×
Anne M. Connolly · 1×
Citations per year

Countries citing papers authored by Adele D’Amico

Since Specialization
Citations

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

Fields of papers citing papers by Adele D’Amico

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Adele D’Amico. 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 Adele D’Amico. The network helps show where Adele D’Amico may publish in the future.

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 320 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2011433
2 2011239
3 2008230
4 2007199
5 2009183
6 2010177
7 2014174
8 2016166
9 2021165
10 2015157
11 2009155
12 2011154
13 2006143
14 2012142
15 2007141
16 2008135
17 2014133
18 2016124
19 2003118
20 2011116

About Adele D’Amico

Adele D’Amico is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Clinical Biochemistry and Genetics, having authored 320 papers that have together received 10.9k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (144 papers), Neurogenetic and Muscular Disorders Research (128 papers), Genomics and Rare Diseases (28 papers), Hereditary Neurological Disorders (25 papers), Cardiomyopathy and Myosin Studies (23 papers), Metabolism and Genetic Disorders (16 papers), Genetic Neurodegenerative Diseases (10 papers) and Mitochondrial Function and Pathology (10 papers). The work is most often cited by research in Genetics (3.9k citations), Molecular Biology (5.4k citations), Clinical Biochemistry (334 citations), Genetics (911 citations) and Neurology (361 citations). Adele D’Amico has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Enrico Bertini, Eugenio Maria Mercuri, Francesco Danilo Tiziano, Stefania Petrini, Marika Pane, Claudio Bruno, Sonia Messina, Michela Catteruccia, Filippo Maria Santorelli and Massimiliano Mirabella A. Their work appears in journals such as Neuromuscular Disorders, Neurology, PLoS ONE, European Journal of Paediatric Neurology and Orphanet Journal of Rare Diseases.

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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