Ivan Macciocca
Impact in
-
- Cardiomyopathy and Myosin Studies
- Cardiovascular Effects of Exercise
- Cardiac electrophysiology and arrhythmias
- Cardiovascular Function and Risk Factors
- Genetics top 10%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Papers in
-
- Cardiomyopathy and Myosin Studies 12
- Cardiac electrophysiology and arrhythmias 2
- Genetics 12
- Genomics and Rare Diseases 8
- BRCA gene mutations in cancer 6
- Hemoglobinopathies and Related Disorders 4
- Co-authors
- Jodie Ingles (6 shared papers)Clara Gaff (7 shared papers)Zornitza Stark (6 shared papers)Susan M. White (3 shared papers)Christopher Semsarian (5 shared papers)Rupendra Shrestha (1 shared paper)William Wilson (1 shared paper)Khurshid Alam (1 shared paper)
- Journals
- Genetics in Medicine (6 papers)European Journal of Human Genetics (3 papers)Journal of Developmental Origins of Health and Disease (2 papers)Clinical Genetics (2 papers)Genome Medicine (1 paper)
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
Ivan Macciocca
34 papers receiving 972 citations
Peers
Comparison fields: 5 of 67
- Cardiology and Cardiovascular Medicine 391
- Genetics 303
- Hematology 96
- Genetics 63
- Developmental Neuroscience 18
Countries citing papers authored by Ivan Macciocca
This map shows the geographic impact of Ivan Macciocca'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 Ivan Macciocca with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ivan Macciocca more than expected).
Fields of papers citing papers by Ivan Macciocca
This network shows the impact of papers produced by Ivan Macciocca. 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 Ivan Macciocca. The network helps show where Ivan Macciocca may publish in the future.
Co-authors
The 25 scholars most cited alongside Ivan Macciocca, 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 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 159 | |
| 2 | 2013 | 93 | |
| 3 | 2005 | 77 | |
| 4 | 2014 | 74 | |
| 5 | 2016 | 58 | |
| 6 | 2015 | 56 | |
| 7 | 2011 | 51 | |
| 8 | 2019 | 41 | |
| 9 | 2011 | 39 | |
| 10 | 2016 | 39 | |
| 11 | 2019 | 37 | |
| 12 | 2004 | 29 | |
| 13 | 2020 | 26 | |
| 14 | 2024 | 23 | |
| 15 | 2022 | 22 | |
| 16 | 2015 | 17 | |
| 17 | 2014 | 15 | |
| 18 | 2018 | 14 | |
| 19 | 2017 | 13 | |
| 20 | 2021 | 13 |
About Ivan Macciocca
Ivan Macciocca is a scholar working on Cardiology and Cardiovascular Medicine, Genetics, Genetics, Molecular Biology and Hematology, having authored 36 papers that have together received 986 indexed citations. Recurring topics across this work include Cardiomyopathy and Myosin Studies (12 papers), Genomics and Rare Diseases (8 papers), BRCA gene mutations in cancer (6 papers), Hemoglobinopathies and Related Disorders (4 papers), Iron Metabolism and Disorders (4 papers), Cardiac electrophysiology and arrhythmias (2 papers), Cancer Genomics and Diagnostics (2 papers) and Trace Elements in Health (2 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (391 citations), Genetics (303 citations), Hematology (96 citations), Genetics (63 citations) and Developmental Neuroscience (18 citations). Ivan Macciocca has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Jodie Ingles, Clara Gaff, Zornitza Stark, Susan M. White, Christopher Semsarian, Rupendra Shrestha, William Wilson, Khurshid Alam, Deborah Schofield and Laura Yeates. Their work appears in journals such as Genetics in Medicine, European Journal of Human Genetics, Journal of Developmental Origins of Health and Disease, Clinical Genetics and Genome 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.