Anna Maria Nardone
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Nuclear Structure and Function
- RNA Research and Splicing
- Genomics and Chromatin Dynamics
- DNA Repair Mechanisms
- CRISPR and Genetic Engineering
Papers in
- Genetics 21
- Genomic variations and chromosomal abnormalities 16
- Genetics and Neurodevelopmental Disorders 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genetic Syndromes and Imprinting 3
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- Genomics and Chromatin Dynamics 4
- Congenital heart defects research 3
- Co-authors
- Giuseppe Novelli (16 shared papers)F Gullotta (7 shared papers)Maria Rosaria D’Apice (8 shared papers)Giovanna Lattanzi (4 shared papers)Marta Columbaro (3 shared papers)Gioacchino Scarano (3 shared papers)Nadir M. Maraldi (2 shared papers)Elisabetta Mattioli (3 shared papers)
- Journals
- European Journal of Medical Genetics (3 papers)Gene (2 papers)The Journal of Maternal-Fetal & Neonatal Medicine (2 papers)Electrophoresis (2 papers)Archives of Pathology & Laboratory Medicine (1 paper)
- Partner nations
- ItalyUnited StatesHong Kong
In The Last Decade
Anna Maria Nardone
36 papers receiving 525 citations
Peers
Comparison fields: 5 of 63
- Genetics 190
- Molecular Biology 359
- Developmental Biology 10
- Cancer Research 29
- Genetics 19
Countries citing papers authored by Anna Maria Nardone
This map shows the geographic impact of Anna Maria Nardone'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 Anna Maria Nardone with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Maria Nardone more than expected).
Fields of papers citing papers by Anna Maria Nardone
This network shows the impact of papers produced by Anna Maria Nardone. 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 Anna Maria Nardone. The network helps show where Anna Maria Nardone may publish in the future.
Co-authors
The 25 scholars most cited alongside Anna Maria Nardone, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 105 | |
| 2 | 2012 | 84 | |
| 3 | 2007 | 47 | |
| 4 | 2002 | 32 | |
| 5 | 2016 | 28 | |
| 6 | 2008 | 22 | |
| 7 | 2004 | 21 | |
| 8 | 2012 | 21 | |
| 9 | 2004 | 20 | |
| 10 | 2006 | 17 | |
| 11 | 2011 | 14 | |
| 12 | 1992 | 13 | |
| 13 | 2015 | 13 | |
| 14 | 2022 | 12 | |
| 15 | 2012 | 11 | |
| 16 | 2006 | 10 | |
| 17 | 2010 | 9 | |
| 18 | 2006 | 9 | |
| 19 | 1998 | 9 | |
| 20 | 2018 | 8 |
About Anna Maria Nardone
Anna Maria Nardone is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Pulmonary and Respiratory Medicine, having authored 38 papers that have together received 556 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Chromosomal and Genetic Variations (4 papers), Genomics and Chromatin Dynamics (4 papers), Congenital heart defects research (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Genetic Syndromes and Imprinting (3 papers). The work is most often cited by research in Genetics (190 citations), Molecular Biology (359 citations), Developmental Biology (10 citations), Cancer Research (29 citations) and Genetics (19 citations). Anna Maria Nardone has collaborated with scholars based in Italy, United States and Hong Kong. Frequent co-authors include Giuseppe Novelli, F Gullotta, Maria Rosaria D’Apice, Giovanna Lattanzi, Marta Columbaro, Gioacchino Scarano, Nadir M. Maraldi, Elisabetta Mattioli, Federica Sangiuolo and Ilaria Filesi. Their work appears in journals such as European Journal of Medical Genetics, Gene, The Journal of Maternal-Fetal & Neonatal Medicine, Electrophoresis and Archives of Pathology & Laboratory Medicine.
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.