Sandra Passe
Impact in
- Genetics top 0.5%
- Glioma Diagnosis and Treatment
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
- MicroRNA in disease regulation
- Cancer, Hypoxia, and Metabolism
Papers in
- Genetics 12
- Glioma Diagnosis and Treatment 12
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- Tendon Structure and Treatment 4
- Co-authors
- Robert B. JenkinsJan C. BucknerMark E. LawHilary BlairCaterina GianniniKarla V. BallmanC. David JamesKen Aldape
- Journals
- Journal of Orthopaedic Research® (5 papers)Genes Chromosomes and Cancer (2 papers)Cancer (1 paper)JNCI Journal of the National Cancer Institute (1 paper)Clinical Cancer Research (1 paper)
- Partner nations
- United StatesNetherlandsCanada
In The Last Decade
Sandra Passe
21 papers receiving 2.1k citations
Hit Papers
Peers
Comparison fields: 5 of 83
- Genetics 1.4k
- Cancer Research 687
- Neurology 259
- Radiology, Nuclear Medicine and Imaging 369
- Molecular Biology 983
Countries citing papers authored by Sandra Passe
This map shows the geographic impact of Sandra Passe'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 Sandra Passe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandra Passe more than expected).
Fields of papers citing papers by Sandra Passe
This network shows the impact of papers produced by Sandra Passe. 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 Sandra Passe. The network helps show where Sandra Passe may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Sandra Passe, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 10 | |
| 2 | 2015 | 18 | |
| 3 | 2014 | 59 | |
| 4 | 2013 | 36 | |
| 5 | 2013 | 50 | |
| 6 | 2011 | 8 | |
| 7 | 2009 | 7 | |
| 8 | 2008 | 95 | |
| 9 | A t(1;19)(q10;p10) Mediates the Combined Deletions of 1p and 19q and Predicts a Better Prognosis of Patients with Oligodendroglioma Hit paper breakdown → | 2006 | 533 |
| 10 | Histone deacetylase inhibitors (HDACIs) induce HIF-1 transcriptional activity. | 2006 | 1 |
| 11 | 2005 | 86 | |
| 12 | 2005 | 6 | |
| 13 | 2005 | 170 | |
| 14 | 2004 | 75 | |
| 15 | 2002 | 8 | |
| 16 | Genetic aberrations defined by comparative genomic hybridization distinguish long-term from typical survivors of glioblastoma. | 2002 | 117 |
| 17 | Aberrant p53, mdm2, and proliferation differ in glioblastomas from long-term compared with typical survivors. | 2002 | 107 |
| 18 | 2001 | 89 | |
| 19 | 2001 | 151 | |
| 20 | 2001 | 493 |
About Sandra Passe
Sandra Passe is a scholar working on Genetics, Orthopedics and Sports Medicine, Cancer Research, Radiology, Nuclear Medicine and Imaging and Surgery, having authored 21 papers that have together received 2.1k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (12 papers), Orthopedic Surgery and Rehabilitation (5 papers), Peripheral Nerve Disorders (4 papers), Tendon Structure and Treatment (4 papers), Cancer Genomics and Diagnostics (4 papers), Brain Metastases and Treatment (2 papers), Chromatin Remodeling and Cancer (2 papers) and Myofascial pain diagnosis and treatment (2 papers). The work is most often cited by research in Genetics (1.4k citations), Cancer Research (687 citations), Neurology (259 citations), Radiology, Nuclear Medicine and Imaging (369 citations) and Molecular Biology (983 citations). Sandra Passe has collaborated with scholars based in United States, Netherlands and Canada. Frequent co-authors include Robert B. Jenkins, Jan C. Buckner, Mark E. Law, Hilary Blair, Caterina Giannini, Karla V. Ballman, C. David James, Ken Aldape, Paul D. Brown and Heather C. Flynn. Their work appears in journals such as Journal of Orthopaedic Research®, Genes Chromosomes and Cancer, Cancer, JNCI Journal of the National Cancer Institute and Clinical Cancer 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.