Sandra Passe

2.8k citations
21 papers · 2.2k · 1 hit paper · h-index 15

Impact in

  • Genetics top 0.5%
    • Glioma Diagnosis and Treatment
    • Cancer Genomics and Diagnostics
    • MicroRNA in disease regulation
    • Cancer, Hypoxia, and Metabolism

Papers in

Sandra Passe

21 papers receiving 2.1k citations

Sandra Passe's Hit Papers

A t(1;19)(q10;p10) Mediates the Combined Deletions of 1p and 19q and Predicts a Better Prognosis of Patients with Oligodendroglioma 2006 · 535 citations
5350+6+13Years since publication100200300400500

Peers

Sandra Passe
Comparison fields: 5 of 75
  • Genetics 1.3k
  • Cancer Research 545
  • Neurology 214
  • Radiology, Nuclear Medicine and Imaging 293
  • Molecular Biology 821
Replace Shuichi Izumoto with:
Shuichi Izumoto Japan
Hendrik Witt Germany
Jörg Balß Germany
Maciej Mrugala United States
Joy Gumin United States
Michel Wager France
Andrey Golanov Russia
Marion Rapp Germany
Griffith Harsh United States
Kazuhiko Kurozumi Japan
Sandra Passe relative to Shuichi Izumoto Japan Shuichi Izumoto's profile →
Citations per field
00.5×4.0×
Shuichi Izumoto · 1×
Citations per year

Countries citing papers authored by Sandra Passe

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authors

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.

Border = papers with Sandra Passe Line = papers co-authored together Sandra Passe links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 21 papers — load more, or switch the sort, to bring in the rest.

#Work
1
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 →
2006535
2 2001493
3 2005171
4 2001151
5
Genetic aberrations defined by comparative genomic hybridization distinguish long-term from typical survivors of glioblastoma.
2002117
6
Aberrant p53, mdm2, and proliferation differ in glioblastomas from long-term compared with typical survivors.
2002107
7 200896
8 200189
9 200586
10 200475
11 201459
12 201351
13 201338
14 201432
15 201520
16 201510
17 20118
18 20028
19 20097
20 20056

About Sandra Passe

Sandra Passe is a scholar working on Genetics, Molecular Biology, Surgery, Cancer Research and Radiology, Nuclear Medicine and Imaging, having authored 21 papers that have together received 2.2k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (11 papers), Orthopedic Surgery and Rehabilitation (4 papers), Cancer Genomics and Diagnostics (4 papers), Peripheral Nerve Disorders (4 papers), Tendon Structure and Treatment (4 papers), Myofascial pain diagnosis and treatment (2 papers), Chromatin Remodeling and Cancer (2 papers) and Shoulder Injury and Treatment (2 papers). The work is most often cited by research in Genetics (1.3k citations), Cancer Research (545 citations), Neurology (214 citations), Radiology, Nuclear Medicine and Imaging (293 citations) and Molecular Biology (821 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, Edward G. Shaw and Sara J. Felten. Their work appears in journals such as Journal of Orthopaedic Research®, Genes Chromosomes and Cancer, Journal of Clinical Oncology, Clinical Cancer Research and American Journal Of 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.

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