Fanny Cheung

573 citations
6 papers · 430 · h-index 6

Impact in

    • Chromosomal and Genetic Variations
    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

Fanny Cheung

6 papers receiving 416 citations

Peers

Fanny Cheung
Comparison fields: 5 of 49
  • Plant Science 274
  • Genetics 135
  • Molecular Biology 320
  • Cell Biology 51
  • Endocrinology 5
Replace Aiko Iwata‐Otsubo with:
Aiko Iwata‐Otsubo United States
Isabelle Luyten France
Giuliana Giannuzzi Italy
Chantal Goubely France
Cecilia Oliver Spain
Stefanie Dukowic‐Schulze United States
Hisato Okuizumi Japan
Andrew J. Tock United Kingdom
Željka Pezer Croatia
Cláudia Martinho Germany
Fanny Cheung relative to Aiko Iwata‐Otsubo United States Aiko Iwata‐Otsubo's profile →
Citations per field
00.5×1.5×2.5×
Aiko Iwata‐Otsubo · 1×
Citations per year

Countries citing papers authored by Fanny Cheung

Since Specialization
Citations

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

Fields of papers citing papers by Fanny Cheung

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fanny Cheung. 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 Fanny Cheung. The network helps show where Fanny Cheung may publish in the future.

Co-authors

The 23 scholars most cited alongside Fanny Cheung, 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 Fanny Cheung Line = papers co-authored together Fanny Cheung links everyone, so they are left out of the graph.

All Works

6 of 6 papers shown
#Work
1 2004214
2 201078
3 200770
4 201141
5 201221
6 20196

About Fanny Cheung

Fanny Cheung is a scholar working on Plant Science, Molecular Biology, Genetics, Neurology and Epidemiology, having authored 6 papers that have together received 430 indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (4 papers), Genomics and Chromatin Dynamics (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Parkinson's Disease Mechanisms and Treatments (1 paper), Neurological disorders and treatments (1 paper) and Autophagy in Disease and Therapy (1 paper). The work is most often cited by research in Plant Science (274 citations), Genetics (135 citations), Molecular Biology (320 citations), Cell Biology (51 citations) and Endocrinology (5 citations). Fanny Cheung has collaborated with scholars based in United States, Netherlands and Switzerland. Frequent co-authors include Peter E. Warburton, Gary Benson, Dan Hasson, Alicia Alonso, Andreas G. Ladurner, Bernhard Radlwimmer, Björn Fritz, Kinya Yoda, György Abrusán and J.J.M. Engelen. Their work appears in journals such as Chromosoma, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Genome biology, Human Genetics and Genome 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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