Daniel B. Bellissimo
Impact in
- Hematology top 1%
- Platelet Disorders and Treatments
- Blood groups and transfusion
- Genetics top 5%
- Genomics and Rare Diseases
- Blood disorders and treatments
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Papers in
- Hematology 33
- Platelet Disorders and Treatments 23
- Blood groups and transfusion 18
- Genetics 14
- Blood disorders and treatments 7
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 4
- Myeloproliferative Neoplasms: Diagnosis and Treatment 3
- Hemoglobinopathies and Related Disorders 3
- Co-authors
- Wayne W. Grody (2 shared papers)C. Sue Richards (2 shared papers)Soma Das (1 shared paper)Madhuri Hegde (2 shared papers)Brian E. Ward (1 shared paper)Sherri J. Bale (1 shared paper)Elaine Lyon (1 shared paper)Nigel M. Crawford (1 shared paper)
- Journals
- Blood (17 papers)Transfusion (4 papers)Archives of Biochemistry and Biophysics (2 papers)Journal of Thrombosis and Haemostasis (2 papers)Research and Practice in Thrombosis and Haemostasis (2 papers)
- Partner nations
- United StatesUnited KingdomItaly
In The Last Decade
Daniel B. Bellissimo
45 papers receiving 1.7k citations
Daniel B. Bellissimo's Hit Papers
Peers
Comparison fields: 5 of 106
- Hematology 706
- Genetics 423
- Genetics 111
- Cardiology and Cardiovascular Medicine 140
- Cancer Research 87
Countries citing papers authored by Daniel B. Bellissimo
This map shows the geographic impact of Daniel B. Bellissimo'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 Daniel B. Bellissimo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel B. Bellissimo more than expected).
Fields of papers citing papers by Daniel B. Bellissimo
This network shows the impact of papers produced by Daniel B. Bellissimo. 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 Daniel B. Bellissimo. The network helps show where Daniel B. Bellissimo may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniel B. Bellissimo, 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 47 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007 Hit paper breakdown → | 2008 | 574 |
| 2 | 1988 | 162 | |
| 3 | 2006 | 136 | |
| 4 | 1994 | 122 | |
| 5 | 2011 | 73 | |
| 6 | 2015 | 69 | |
| 7 | 2019 | 61 | |
| 8 | 2008 | 56 | |
| 9 | 2018 | 56 | |
| 10 | 2009 | 53 | |
| 11 | 2012 | 49 | |
| 12 | 1995 | 41 | |
| 13 | 2005 | 33 | |
| 14 | 1984 | 32 | |
| 15 | 2010 | 24 | |
| 16 | 2005 | 20 | |
| 17 | 2011 | 18 | |
| 18 | 1997 | 12 | |
| 19 | 2000 | 12 | |
| 20 | 2018 | 12 |
About Daniel B. Bellissimo
Daniel B. Bellissimo is a scholar working on Hematology, Genetics, Genetics, Molecular Biology and Surgery, having authored 47 papers that have together received 1.7k indexed citations. Recurring topics across this work include Platelet Disorders and Treatments (23 papers), Blood groups and transfusion (18 papers), Blood disorders and treatments (7 papers), Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers), Immunodeficiency and Autoimmune Disorders (4 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (3 papers) and Hemoglobinopathies and Related Disorders (3 papers). The work is most often cited by research in Hematology (706 citations), Genetics (423 citations), Genetics (111 citations), Cardiology and Cardiovascular Medicine (140 citations) and Cancer Research (87 citations). Daniel B. Bellissimo has collaborated with scholars based in United States, United Kingdom and Italy. Frequent co-authors include Wayne W. Grody, C. Sue Richards, Soma Das, Madhuri Hegde, Brian E. Ward, Sherri J. Bale, Elaine Lyon, Nigel M. Crawford, Ronald W. Davis and Martin A. Smith. Their work appears in journals such as Blood, Transfusion, Archives of Biochemistry and Biophysics, Journal of Thrombosis and Haemostasis and Research and Practice in Thrombosis and Haemostasis.
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.