Mark J. Pettenati
Impact in
- Hematology top 0.2%
- Acute Myeloid Leukemia Research
- Hematopoietic Stem Cell Transplantation
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
Papers in
- Hematology 49
- Acute Myeloid Leukemia Research 39
- Hematopoietic Stem Cell Transplantation 7
- Genetics 42
- Genomic variations and chromosomal abnormalities 24
- Genetic Associations and Epidemiology 9
- Co-authors
- Andrew J. Carroll (24 shared papers)Clara Derber Bloomfield (17 shared papers)P. Nagesh Rao (36 shared papers)Robert James Mayer (9 shared papers)Richard A. Larson (14 shared papers)Krzysztof Mrózek (16 shared papers)Charles Alan Schiffer (7 shared papers)Ramana V. Tantravahi (5 shared papers)
- Journals
- Genomics (11 papers)Blood (10 papers)Journal of Clinical Oncology (7 papers)Prenatal Diagnosis (6 papers)Cytogenetic and Genome Research (5 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Mark J. Pettenati
157 papers receiving 6.3k citations
Mark J. Pettenati's Hit Papers
Peers
Comparison fields: 5 of 121
- Hematology 2.8k
- Genetics 1.1k
- Pharmacy 116
- Pediatrics, Perinatology and Child Health 373
- Public Health, Environmental and Occupational Health 751
Countries citing papers authored by Mark J. Pettenati
This map shows the geographic impact of Mark J. Pettenati'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 Mark J. Pettenati with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark J. Pettenati more than expected).
Fields of papers citing papers by Mark J. Pettenati
This network shows the impact of papers produced by Mark J. Pettenati. 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 Mark J. Pettenati. The network helps show where Mark J. Pettenati may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark J. Pettenati, 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 159 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Frequency of prolonged remission duration after high-dose cytarabine intensification in acute myeloid leukemia varies by cytogenetic subtype. Hit paper breakdown → | 1998 | 585 |
| 2 | 2012 | 353 | |
| 3 | 2005 | 326 | |
| 4 | 2009 | 315 | |
| 5 | 2006 | 282 | |
| 6 | 1999 | 267 | |
| 7 | 1986 | 256 | |
| 8 | 2004 | 185 | |
| 9 | 2001 | 142 | |
| 10 | 1987 | 135 | |
| 11 | 2006 | 134 | |
| 12 | 1999 | 123 | |
| 13 | 1995 | 114 | |
| 14 | 2004 | 112 | |
| 15 | 2001 | 106 | |
| 16 | 2001 | 101 | |
| 17 | 1995 | 99 | |
| 18 | 1997 | 99 | |
| 19 | 2004 | 96 | |
| 20 | 2001 | 95 |
About Mark J. Pettenati
Mark J. Pettenati is a scholar working on Hematology, Genetics, Pediatrics, Perinatology and Child Health, Reproductive Medicine and Molecular Biology, having authored 159 papers that have together received 6.8k indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (39 papers), Genomic variations and chromosomal abnormalities (24 papers), Prenatal Screening and Diagnostics (14 papers), Genetic Associations and Epidemiology (9 papers), Acute Lymphoblastic Leukemia research (9 papers), Sarcoma Diagnosis and Treatment (8 papers), Hematopoietic Stem Cell Transplantation (7 papers) and Sperm and Testicular Function (6 papers). The work is most often cited by research in Hematology (2.8k citations), Genetics (1.1k citations), Pharmacy (116 citations), Pediatrics, Perinatology and Child Health (373 citations) and Public Health, Environmental and Occupational Health (751 citations). Mark J. Pettenati has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Andrew J. Carroll, Clara Derber Bloomfield, P. Nagesh Rao, Robert James Mayer, Richard A. Larson, Krzysztof Mrózek, Charles Alan Schiffer, Ramana V. Tantravahi, Bayard L. Powell and Frederick R. Davey. Their work appears in journals such as Genomics, Blood, Journal of Clinical Oncology, Prenatal Diagnosis and Cytogenetic and Genome Research.
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.