Sandra Passe

2.7k citations
21 papers · 2.1k · 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 · 533 citations
5330+6+13Years since publication100200300400500

Peers

Sandra Passe
Comparison fields: 5 of 83
  • Genetics 1.4k
  • Cancer Research 687
  • Neurology 259
  • Radiology, Nuclear Medicine and Imaging 369
  • Molecular Biology 983
Replace Jörg Balß with:
Jörg Balß Germany
Shuichi Izumoto Japan
Hendrik Witt Germany
Marianne Labussière France
Kazuhiko Kurozumi Japan
Joy Gumin United States
Louisa von Baumgarten Germany
Andrey Golanov Russia
Sabina Eigenbrod Germany
Mariarita Santi United States
Sandra Passe relative to Jörg Balß Germany Jörg Balß's profile →
Citations per field
00.5×1.5×
Jörg Balß · 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 →
2006533
2 2001493
3 2005170
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 200895
8 200189
9 200586
10 200475
11 201459
12 201350
13 201336
14 201431
15 201518
16 201510
17 20028
18 20118
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 2.1k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (12 papers), Orthopedic Surgery and Rehabilitation (5 papers), Cancer Genomics and Diagnostics (4 papers), Tendon Structure and Treatment (4 papers), Peripheral Nerve Disorders (4 papers), Shoulder Injury and Treatment (2 papers), Brain Metastases and Treatment (2 papers) and Chromatin Remodeling and Cancer (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, Heather C. Flynn and Robert M. Arusell. 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.

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