Angelo Notarangelo
Impact in
- Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
- Cell Biology top 10%
- Cellular transport and secretion
- Endoplasmic Reticulum Stress and Disease
Papers in
-
- Epigenetics and DNA Methylation 3
- DNA Repair Mechanisms 2
- Genetics 6
- Glioma Diagnosis and Treatment 5
- Genomic variations and chromosomal abnormalities 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Co-authors
- Leopoldo Zelante (7 shared papers)Paolo Gasparini (4 shared papers)Luigi Bisceglia (3 shared papers)Massimo Carella (5 shared papers)Bruno Dallapiccola (3 shared papers)María L. Arbonés (1 shared paper)Tama Sobe (1 shared paper)Salvatore Melchionda (1 shared paper)
- Journals
- International Journal of Molecular Sciences (2 papers)Human Genetics (2 papers)Thrombosis and Haemostasis (1 paper)Human Molecular Genetics (1 paper)European Journal of Medicinal Chemistry (1 paper)
- Partner nations
- ItalyUnited StatesSpain
In The Last Decade
Angelo Notarangelo
29 papers receiving 806 citations
Peers
Comparison fields: 5 of 84
- Sensory Systems 123
- Cell Biology 153
- Nephrology 60
- Biochemistry 55
- Molecular Biology 437
Countries citing papers authored by Angelo Notarangelo
This map shows the geographic impact of Angelo Notarangelo'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 Angelo Notarangelo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Angelo Notarangelo more than expected).
Fields of papers citing papers by Angelo Notarangelo
This network shows the impact of papers produced by Angelo Notarangelo. 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 Angelo Notarangelo. The network helps show where Angelo Notarangelo may publish in the future.
Co-authors
The 25 scholars most cited alongside Angelo Notarangelo, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 195 | |
| 2 | 2012 | 135 | |
| 3 | 2011 | 88 | |
| 4 | Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity. | 1995 | 78 |
| 5 | 1986 | 66 | |
| 6 | 2010 | 64 | |
| 7 | 2015 | 44 | |
| 8 | 1998 | 38 | |
| 9 | 2009 | 25 | |
| 10 | 1993 | 18 | |
| 11 | 2019 | 13 | |
| 12 | 2014 | 12 | |
| 13 | 2020 | 12 | |
| 14 | 2006 | 10 | |
| 15 | 1993 | 10 | |
| 16 | Homocysteine levels in amniotic fluid. Relationship with birth-weight. | 2006 | 10 |
| 17 | 2013 | 7 | |
| 18 | 2003 | 6 | |
| 19 | 2019 | 4 | |
| 20 | 2021 | 4 |
About Angelo Notarangelo
Angelo Notarangelo is a scholar working on Molecular Biology, Genetics, Genetics, Cancer Research and Pediatrics, Perinatology and Child Health, having authored 29 papers that have together received 860 indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (5 papers), Folate and B Vitamins Research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Epigenetics and DNA Methylation (3 papers), MicroRNA in disease regulation (3 papers), Prenatal Screening and Diagnostics (3 papers) and DNA Repair Mechanisms (2 papers). The work is most often cited by research in Sensory Systems (123 citations), Cell Biology (153 citations), Nephrology (60 citations), Biochemistry (55 citations) and Molecular Biology (437 citations). Angelo Notarangelo has collaborated with scholars based in Italy, United States and Spain. Frequent co-authors include Leopoldo Zelante, Paolo Gasparini, Luigi Bisceglia, Massimo Carella, Bruno Dallapiccola, María L. Arbonés, Tama Sobe, Salvatore Melchionda, Fabian Glaser and Enzo Di Iorio. Their work appears in journals such as International Journal of Molecular Sciences, Human Genetics, Thrombosis and Haemostasis, Human Molecular Genetics and European Journal of Medicinal Chemistry.
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.