Ivan Macciocca
Impact in
- Genetics top 2%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
-
- Cardiomyopathy and Myosin Studies
- Cardiac electrophysiology and arrhythmias
- Cardiovascular Effects of Exercise
Papers in
- Genetics 13
- Genomics and Rare Diseases 13
-
- Cardiomyopathy and Myosin Studies 11
- Cardiac pacing and defibrillation studies 1
- Co-authors
- Clara Gaff (7 shared papers)Jodie Ingles (6 shared papers)Zornitza Stark (6 shared papers)Susan M. White (3 shared papers)Christopher Semsarian (5 shared papers)Khurshid Alam (1 shared paper)DEBORAH J. SCHOFIELD (1 shared paper)Rupendra N. Shrestha (1 shared paper)
- Journals
- Genetics in Medicine (9 papers)European Journal of Human Genetics (4 papers)Clinical Genetics (2 papers)European Heart Journal (2 papers)Journal of Developmental Origins of Health and Disease (2 papers)
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
Ivan Macciocca
45 papers receiving 2.1k citations
Ivan Macciocca's Hit Papers
Peers
Comparison fields: 5 of 56
- Genetics 729
- Cardiology and Cardiovascular Medicine 417
- Clinical Biochemistry 25
- Hematology 89
- Pediatrics, Perinatology and Child Health 46
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 48 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 317 | |
| 2 | The Global State of the Genetic Counseling Profession Hit paper breakdown → | 2018 | 281 |
| 3 | 2017 | 247 | |
| 4 | 2017 | 196 | |
| 5 | 2013 | 106 | |
| 6 | 2015 | 86 | |
| 7 | 2005 | 78 | |
| 8 | 2014 | 75 | |
| 9 | 2016 | 56 | |
| 10 | 2021 | 55 | |
| 11 | 2011 | 52 | |
| 12 | 2016 | 52 | |
| 13 | 2011 | 51 | |
| 14 | 2019 | 42 | |
| 15 | 2024 | 39 | |
| 16 | 2019 | 38 | |
| 17 | 2020 | 37 | |
| 18 | 2022 | 35 | |
| 19 | 2017 | 34 | |
| 20 | 2004 | 30 |
About Ivan Macciocca
Ivan Macciocca is a scholar working on Genetics, Cardiology and Cardiovascular Medicine, Hematology, Health and Pediatrics, Perinatology and Child Health, having authored 48 papers that have together received 2.2k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (13 papers), Cardiomyopathy and Myosin Studies (11 papers), Iron Metabolism and Disorders (4 papers), Lysosomal Storage Disorders Research (1 paper), Occupational and Professional Licensing Regulation (1 paper), Hereditary Neurological Disorders (1 paper), Cardiac pacing and defibrillation studies (1 paper) and Indigenous Health, Education, and Rights (1 paper). The work is most often cited by research in Genetics (729 citations), Cardiology and Cardiovascular Medicine (417 citations), Clinical Biochemistry (25 citations), Hematology (89 citations) and Pediatrics, Perinatology and Child Health (46 citations). Ivan Macciocca has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Clara Gaff, Jodie Ingles, Zornitza Stark, Susan M. White, Christopher Semsarian, Khurshid Alam, DEBORAH J. SCHOFIELD, Rupendra N. Shrestha, Paul Andrew James and Laura Yeates. Their work appears in journals such as Genetics in Medicine, European Journal of Human Genetics, Clinical Genetics, European Heart Journal and Journal of Developmental Origins of Health and Disease.
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.