Diego Lorenzetti
Impact in
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- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
- Neurology top 10%
- Neurological diseases and metabolism
- Parkinson's Disease Mechanisms and Treatments
Papers in
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- Genetic Neurodegenerative Diseases 6
- Hereditary Neurological Disorders 2
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- Mitochondrial Function and Pathology 3
- Pluripotent Stem Cells Research 2
- DNA Repair Mechanisms 2
- Signaling Pathways in Disease 2
- Co-authors
- Huda Yahya Zoghbi (3 shared papers)Colin E. Bishop (3 shared papers)Monica J. Justice (2 shared papers)Saeed Bohlega (1 shared paper)Shannon F. Kramer (1 shared paper)Richard R. Sinden (1 shared paper)David L. Nelson (1 shared paper)Evan E. Eichler (1 shared paper)
- Journals
- Mammalian Genome (2 papers)Neurology (2 papers)genesis (1 paper)Cells Tissues Organs (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- United StatesItalyFrance
In The Last Decade
Diego Lorenzetti
13 papers receiving 904 citations
Peers
Comparison fields: 5 of 67
- Cellular and Molecular Neuroscience 580
- Neurology 199
- Neurology 101
- Geriatrics and Gerontology 34
- Reproductive Medicine 67
Countries citing papers authored by Diego Lorenzetti
This map shows the geographic impact of Diego Lorenzetti'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 Diego Lorenzetti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Diego Lorenzetti more than expected).
Fields of papers citing papers by Diego Lorenzetti
This network shows the impact of papers produced by Diego Lorenzetti. 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 Diego Lorenzetti. The network helps show where Diego Lorenzetti may publish in the future.
Co-authors
The 25 scholars most cited alongside Diego Lorenzetti, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 186 | |
| 2 | 1998 | 137 | |
| 3 | 1996 | 100 | |
| 4 | 2000 | 82 | |
| 5 | 2004 | 81 | |
| 6 | 2013 | 71 | |
| 7 | 1997 | 67 | |
| 8 | 2012 | 63 | |
| 9 | A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies. | 1995 | 42 |
| 10 | 2004 | 41 | |
| 11 | 2006 | 35 | |
| 12 | 2013 | 13 | |
| 13 | 1993 | 13 |
About Diego Lorenzetti
Diego Lorenzetti is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Genetics and Cell Biology, having authored 13 papers that have together received 931 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Pluripotent Stem Cells Research (2 papers), Neurological disorders and treatments (2 papers), DNA Repair Mechanisms (2 papers), Hereditary Neurological Disorders (2 papers) and Signaling Pathways in Disease (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (580 citations), Neurology (199 citations), Neurology (101 citations), Geriatrics and Gerontology (34 citations) and Reproductive Medicine (67 citations). Diego Lorenzetti has collaborated with scholars based in United States, Italy and France. Frequent co-authors include Huda Yahya Zoghbi, Colin E. Bishop, Monica J. Justice, Saeed Bohlega, Shannon F. Kramer, Richard R. Sinden, David L. Nelson, Evan E. Eichler, Christopher E. Pearson and Paul A. Overbeek. Their work appears in journals such as Mammalian Genome, Neurology, genesis, Cells Tissues Organs and European Journal of Human 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.