Debra Saxe
Impact in
- Hematology top 2%
- Multiple Myeloma Research and Treatments
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Hematology 14
- Acute Myeloid Leukemia Research 5
- Chronic Myeloid Leukemia Treatments 4
- Genetics 8
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- Fuping Zhang (1 shared paper)Maura Pieretti (1 shared paper)David L. Nelson (1 shared paper)Stephen T. Warren (1 shared paper)James S. Sutcliffe (1 shared paper)J A Kant (1 shared paper)Albert J. Fornace (1 shared paper)Robert H. Crabtree (1 shared paper)
- Journals
- Prenatal Diagnosis (4 papers)Genetics in Medicine (4 papers)Archives of Pathology & Laboratory Medicine (3 papers)Journal of Molecular Diagnostics (2 papers)British Journal of Haematology (2 papers)
- Partner nations
- United StatesCanadaJapan
In The Last Decade
Debra Saxe
48 papers receiving 2.1k citations
Debra Saxe's Hit Papers
Peers
Comparison fields: 5 of 92
- Hematology 477
- Genetics 732
- Genetics 252
- Molecular Biology 978
- Cognitive Neuroscience 234
Countries citing papers authored by Debra Saxe
This map shows the geographic impact of Debra Saxe'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 Debra Saxe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Debra Saxe more than expected).
Fields of papers citing papers by Debra Saxe
This network shows the impact of papers produced by Debra Saxe. 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 Debra Saxe. The network helps show where Debra Saxe may publish in the future.
Co-authors
The 25 scholars most cited alongside Debra Saxe, 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 | DNA methylation represses FMR-1 transcription in fragile X syndrome Hit paper breakdown → | 1992 | 599 |
| 2 | 1985 | 229 | |
| 3 | 1984 | 186 | |
| 4 | 2013 | 166 | |
| 5 | 1982 | 122 | |
| 6 | 1996 | 88 | |
| 7 | 2009 | 80 | |
| 8 | 1998 | 67 | |
| 9 | 2018 | 53 | |
| 10 | 2016 | 51 | |
| 11 | 2022 | 47 | |
| 12 | 2018 | 45 | |
| 13 | 2014 | 42 | |
| 14 | 1987 | 35 | |
| 15 | 2012 | 30 | |
| 16 | 2010 | 26 | |
| 17 | 2017 | 26 | |
| 18 | 1984 | 25 | |
| 19 | 2010 | 23 | |
| 20 | 1988 | 22 |
About Debra Saxe
Debra Saxe is a scholar working on Hematology, Genetics, Pathology and Forensic Medicine, Genetics and Cancer Research, having authored 48 papers that have together received 2.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Lymphoma Diagnosis and Treatment (6 papers), Acute Myeloid Leukemia Research (5 papers), Cancer Genomics and Diagnostics (4 papers), Prenatal Screening and Diagnostics (4 papers), Acute Lymphoblastic Leukemia research (4 papers), Chronic Myeloid Leukemia Treatments (4 papers) and Protein Degradation and Inhibitors (3 papers). The work is most often cited by research in Hematology (477 citations), Genetics (732 citations), Genetics (252 citations), Molecular Biology (978 citations) and Cognitive Neuroscience (234 citations). Debra Saxe has collaborated with scholars based in United States, Canada and Japan. Frequent co-authors include Fuping Zhang, Maura Pieretti, David L. Nelson, Stephen T. Warren, James S. Sutcliffe, J A Kant, Albert J. Fornace, Robert H. Crabtree, Mathieu Simon and O. Wesley McBride. Their work appears in journals such as Prenatal Diagnosis, Genetics in Medicine, Archives of Pathology & Laboratory Medicine, Journal of Molecular Diagnostics and British Journal of Haematology.
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.