Nancy E. Hasselt

2.1k citations
7 papers · 1.1k · 1 hit paper · h-index 7

Impact in

  • Genetics top 2%
    • Glioma Diagnosis and Treatment
  • Neurology top 5%
    • Neuroblastoma Research and Treatments

Papers in

    • Glioma Diagnosis and Treatment 3
    • Neuroblastoma Research and Treatments 2

Nancy E. Hasselt

7 papers receiving 1.1k citations

Nancy E. Hasselt's Hit Papers

Integrated Genomics Identifies Five Medulloblastoma Subtypes with Distinct Genetic Profiles, Pathway Signatures and Clinicopathological Features 2008 · 536 citations
5360+6+12Years since publication100200300400500

Peers

Nancy E. Hasselt
Comparison fields: 5 of 53
  • Genetics 362
  • Neurology 301
  • Cancer Research 265
  • Molecular Biology 722
  • Oncology 145
Replace Jesse Chung‐Sean Pang with:
Jesse Chung‐Sean Pang Hong Kong
Matthew Grimmer United States
Pilar González‐Gómez Spain
Dorota Denkhaus Germany
Francisco J. Cordero United States
Caterina Marchetti Italy
Danielle Schüler France
Emmanuelle Crinière France
Arjan Lakeman Netherlands
Jan Gronych Germany
Nancy E. Hasselt relative to Jesse Chung‐Sean Pang Hong Kong Jesse Chung‐Sean Pang's profile →
Citations per field
00.5×1.5×2.0×
Jesse Chung‐Sean Pang · 1×
Citations per year

Countries citing papers authored by Nancy E. Hasselt

Since Specialization
Citations

This map shows the geographic impact of Nancy E. Hasselt'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 Nancy E. Hasselt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nancy E. Hasselt more than expected).

Fields of papers citing papers by Nancy E. Hasselt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nancy E. Hasselt. 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 Nancy E. Hasselt. The network helps show where Nancy E. Hasselt may publish in the future.

Co-authors

The 25 scholars most cited alongside Nancy E. Hasselt, 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 Nancy E. Hasselt Line = papers co-authored together Nancy E. Hasselt links everyone, so they are left out of the graph.

All Works

7 of 7 papers shown
#Work
1
Integrated Genomics Identifies Five Medulloblastoma Subtypes with Distinct Genetic Profiles, Pathway Signatures and Clinicopathological Features
Hit paper breakdown →
2008536
2 2015270
3 2019101
4 201165
5 200846
6 201038
7 201123

About Nancy E. Hasselt

Nancy E. Hasselt is a scholar working on Genetics, Neurology, Molecular Biology, Cancer Research and Radiology, Nuclear Medicine and Imaging, having authored 7 papers that have together received 1.1k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (3 papers), Genomics and Chromatin Dynamics (3 papers), Neuroblastoma Research and Treatments (2 papers), Protein Degradation and Inhibitors (1 paper), RNA Research and Splicing (1 paper), Telomeres, Telomerase, and Senescence (1 paper), Cancer-related Molecular Pathways (1 paper) and Cell death mechanisms and regulation (1 paper). The work is most often cited by research in Genetics (362 citations), Neurology (301 citations), Cancer Research (265 citations), Molecular Biology (722 citations) and Oncology (145 citations). Nancy E. Hasselt has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Rogier Versteeg, Jan Köster, Peter van Sluis, Marcel Kool, Danny A. Zwijnenburg, Jens Bunt, Arjan Lakeman, Dirk Troost, Huib N. Caron and Wiesława Grajkowska. Their work appears in journals such as PLoS ONE, International Journal of Cancer, Molecular Cancer Research, Nature Communications and Nature Genetics.

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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