Angelita Calı̀

1.5k citations
9 papers · 1.1k indexed · 1 hit paper · h-index 7

Angelita Calı̀

9 papers receiving 1.1k citations

Hit Papers

The gene TFR2 is mutated in a new type of haemochromatosi...6222000202620082017200400600

Peers

Angelita Calı̀
Comparison fields: 5 of 59
  • Hematology 868
  • Genetics 780
  • Nutrition and Dietetics 725
  • Genetics 132
  • Rheumatology 47
Replace Steven M. Starnes with:
Steven M. Starnes United States
Flavia Guillem France
Shall Jue United States
Zi Xu China
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Frédéric Bilan France
Michael L. Bloom United States
Xiangpeng Guo China
Rashim Pal Singh Germany
Angelita Calı̀ relative to Steven M. Starnes United States Steven M. Starnes's profile →
Citations per field
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Citations per year

Countries citing papers authored by Angelita Calı̀

Since Specialization
Citations

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

Fields of papers citing papers by Angelita Calı̀

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Angelita Calı̀. 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 Angelita Calı̀. The network helps show where Angelita Calı̀ may publish in the future.

Co-authorship network

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

All Works

9 of 9 papers shown
#Work
1 200239
2 200266
3 2001129
4 2001189
5
The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22breakdown →
2000622
6
Non-HFE hemochromatosis: insights into regulation on iron metabolisms from novel iron loading disorders.
20002
7 200018
8
Mutations in transferrin receptor-2 in hemochromatosis type 3.
20001
9
FISH characterization of two supernumerary r(1) associated with distinct clinical phenotypes.
199911

About Angelita Calı̀

Angelita Calı̀ is a scholar working on Hematology, Genetics and Nutrition and Dietetics, having authored 9 papers that have together received 1.1k indexed citations. Recurring topics across this work include Iron Metabolism and Disorders (7 papers), Hemoglobinopathies and Related Disorders (5 papers), Trace Elements in Health (4 papers), Genomic variations and chromosomal abnormalities (2 papers), Chromosomal and Genetic Variations (2 papers), Prenatal Screening and Diagnostics (2 papers) and Child Nutrition and Water Access (1 paper). The work is most often cited by research in Hematology (868 citations), Genetics (780 citations) and Nutrition and Dietetics (725 citations). Angelita Calı̀ has collaborated with scholars based in Italy, Belarus and United States. Frequent co-authors include Clara Camaschella, Antonella Roetto, Marco De Gobbi, Antonio Totaro, Paolo Gasparini, Giovanni Garozzo, Massimo Carella, Antonio Piga, Filomena Longo and Alberto Piperno.

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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