Angelo Notarangelo

1.1k citations
29 papers · 806 · h-index 13

Impact in

    • Hearing, Cochlea, Tinnitus, Genetics
  • Cell Biology top 10%
    • Cellular transport and secretion
    • Endoplasmic Reticulum Stress and Disease

Papers in

    • Epigenetics and DNA Methylation 3
    • RNA regulation and disease 2
    • Glioma Diagnosis and Treatment 6
    • Genomic variations and chromosomal abnormalities 3
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3

Angelo Notarangelo

29 papers receiving 780 citations

Peers

Angelo Notarangelo
Comparison fields: 5 of 85
  • Sensory Systems 113
  • Cell Biology 151
  • Biochemistry 56
  • Nephrology 54
  • Molecular Biology 449
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Michelle Hussain United Kingdom
JT den Dunnen Netherlands
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Sébastien L’Hoste France
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Citations per field
00.5×10×13.3×
Michelle Hussain · 1×
Citations per year

Countries citing papers authored by Angelo Notarangelo

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Angelo Notarangelo Line = papers co-authored together Angelo Notarangelo links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2001180
2 2012133
3 201186
4
Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity.
199572
5 201059
6 198650
7 201541
8 199837
9 200926
10 199314
11 201913
12 202012
13 201412
14 199310
15 200610
16
Homocysteine levels in amniotic fluid. Relationship with birth-weight.
200610
17 20137
18 20035
19 20214
20 20194

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 806 indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (6 papers), Genomic variations and chromosomal abnormalities (3 papers), MicroRNA in disease regulation (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Prenatal Screening and Diagnostics (3 papers), Epigenetics and DNA Methylation (3 papers), Folate and B Vitamins Research (3 papers) and RNA regulation and disease (2 papers). The work is most often cited by research in Sensory Systems (113 citations), Cell Biology (151 citations), Biochemistry (56 citations), Nephrology (54 citations) and Molecular Biology (449 citations). Angelo Notarangelo has collaborated with scholars based in Italy, United States and Spain. Frequent co-authors include Leopoldo Zelante, Paolo Gasparini, Massimo Carella, Luigi Bisceglia, Bruno Dallapiccola, Karen B. Avraham, Salvatore Melchionda, Tama Sobe, Raquel Rabionet and María L. Arbonés. Their work appears in journals such as International Journal of Molecular Sciences, Human Genetics, European Journal of Medicinal Chemistry, Cancer Research and Human Molecular 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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