Debra Saxe
Impact in
- Hematology top 2%
- Multiple Myeloma Research and Treatments
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Hematology 13
- Acute Myeloid Leukemia Research 5
- Chronic Myeloid Leukemia Treatments 3
- Multiple Myeloma Research and Treatments 3
- Co-authors
- Fuping Zhang (1 shared paper)David L. Nelson (1 shared paper)Maura Pieretti (1 shared paper)Stephen T. Warren (1 shared paper)James S. Sutcliffe (1 shared paper)Mathieu Simon (1 shared paper)O. Wesley McBride (1 shared paper)J A Kant (1 shared paper)
- Journals
- Genetics in Medicine (4 papers)Prenatal Diagnosis (3 papers)Archives of Pathology & Laboratory Medicine (3 papers)Human Pathology (2 papers)American Journal of Clinical Pathology (2 papers)
- Partner nations
- United StatesCanadaIsrael
In The Last Decade
Debra Saxe
44 papers receiving 2.0k citations
Debra Saxe's Hit Papers
Peers
Comparison fields: 5 of 90
- Hematology 448
- Genetics 700
- Genetics 244
- Molecular Biology 925
- Cognitive Neuroscience 227
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 47 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 | 587 |
| 2 | 1985 | 227 | |
| 3 | 1984 | 185 | |
| 4 | 2013 | 146 | |
| 5 | 1982 | 124 | |
| 6 | 1996 | 81 | |
| 7 | 2009 | 77 | |
| 8 | 1998 | 66 | |
| 9 | 2018 | 49 | |
| 10 | 2022 | 44 | |
| 11 | 2014 | 41 | |
| 12 | 2018 | 36 | |
| 13 | 1987 | 35 | |
| 14 | 2012 | 30 | |
| 15 | 1984 | 25 | |
| 16 | 2010 | 23 | |
| 17 | 2010 | 23 | |
| 18 | 1988 | 22 | |
| 19 | 2010 | 22 | |
| 20 | 2017 | 22 |
About Debra Saxe
Debra Saxe is a scholar working on Molecular Biology, Hematology, Genetics, Genetics and Pathology and Forensic Medicine, having authored 47 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Lymphoma Diagnosis and Treatment (6 papers), Prenatal Screening and Diagnostics (5 papers), Acute Myeloid Leukemia Research (5 papers), Chronic Myeloid Leukemia Treatments (3 papers), Acute Lymphoblastic Leukemia research (3 papers), Multiple Myeloma Research and Treatments (3 papers) and Congenital Anomalies and Fetal Surgery (3 papers). The work is most often cited by research in Hematology (448 citations), Genetics (700 citations), Genetics (244 citations), Molecular Biology (925 citations) and Cognitive Neuroscience (227 citations). Debra Saxe has collaborated with scholars based in United States, Canada and Israel. Frequent co-authors include Fuping Zhang, David L. Nelson, Maura Pieretti, Stephen T. Warren, James S. Sutcliffe, Mathieu Simon, O. Wesley McBride, J A Kant, Albert J. Fornace and Robert H. Crabtree. Their work appears in journals such as Genetics in Medicine, Prenatal Diagnosis, Archives of Pathology & Laboratory Medicine, Human Pathology and American Journal of Clinical Pathology.
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.