Eric Rappaport
Impact in
- Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
- Hematology top 1%
- Acute Myeloid Leukemia Research
Papers in
-
- DNA and Nucleic Acid Chemistry 8
- Cancer therapeutics and mechanisms 7
- Congenital heart defects research 5
- Hematology 21
- Acute Myeloid Leukemia Research 11
- Co-authors
- Saul Surrey (35 shared papers)Paolo Fortina (23 shared papers)Carolyn A. Felix (18 shared papers)Elaine Mansfield (8 shared papers)Maureen D. Megonigal (12 shared papers)Elias Schwartz (23 shared papers)Paolo Gasparini (5 shared papers)Leopoldo Zelante (2 shared papers)
- Journals
- Proceedings of the National Academy of Sciences (9 papers)Blood (7 papers)Genome Research (5 papers)Human Mutation (4 papers)Oncogene (3 papers)
- Partner nations
- United StatesItalyAustralia
In The Last Decade
Eric Rappaport
107 papers receiving 4.4k citations
Eric Rappaport's Hit Papers
Peers
Comparison fields: 5 of 126
- Sensory Systems 534
- Hematology 663
- Genetics 430
- Molecular Biology 2.5k
- Neurology 339
Countries citing papers authored by Eric Rappaport
This map shows the geographic impact of Eric Rappaport'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 Eric Rappaport with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eric Rappaport more than expected).
Fields of papers citing papers by Eric Rappaport
This network shows the impact of papers produced by Eric Rappaport. 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 Eric Rappaport. The network helps show where Eric Rappaport may publish in the future.
Co-authors
The 25 scholars most cited alongside Eric Rappaport, 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 108 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Connexin-26 mutations in sporadic and inherited sensorineural deafness Hit paper breakdown → | 1998 | 534 |
| 2 | 2014 | 272 | |
| 3 | 2014 | 240 | |
| 4 | 2009 | 185 | |
| 5 | 1998 | 143 | |
| 6 | 2009 | 122 | |
| 7 | 2005 | 106 | |
| 8 | 1993 | 106 | |
| 9 | 2006 | 102 | |
| 10 | 2000 | 90 | |
| 11 | 2007 | 90 | |
| 12 | 2007 | 83 | |
| 13 | 2008 | 81 | |
| 14 | 2001 | 76 | |
| 15 | 2001 | 74 | |
| 16 | 1999 | 69 | |
| 17 | 2003 | 68 | |
| 18 | 2003 | 63 | |
| 19 | 1998 | 62 | |
| 20 | Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity. | 2005 | 59 |
About Eric Rappaport
Eric Rappaport is a scholar working on Molecular Biology, Hematology, Genetics, Genetics and Neurology, having authored 108 papers that have together received 4.5k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (14 papers), Neuroblastoma Research and Treatments (11 papers), Acute Myeloid Leukemia Research (11 papers), Acute Lymphoblastic Leukemia research (9 papers), Genomic variations and chromosomal abnormalities (8 papers), DNA and Nucleic Acid Chemistry (8 papers), Cancer therapeutics and mechanisms (7 papers) and Congenital heart defects research (5 papers). The work is most often cited by research in Sensory Systems (534 citations), Hematology (663 citations), Genetics (430 citations), Molecular Biology (2.5k citations) and Neurology (339 citations). Eric Rappaport has collaborated with scholars based in United States, Italy and Australia. Frequent co-authors include Saul Surrey, Paolo Fortina, Carolyn A. Felix, Elaine Mansfield, Maureen D. Megonigal, Elias Schwartz, Paolo Gasparini, Leopoldo Zelante, Salvatore Melchionda and Xavier Estivill. Their work appears in journals such as Proceedings of the National Academy of Sciences, Blood, Genome Research, Human Mutation and Oncogene.
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.