Karen Leung

693 citations
11 papers · 466 indexed · h-index 8
Topics
Genomic variations and chromosomal abnormalities (4 papers)Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers)Genetic Syndromes and Imprinting (2 papers)
Partner nations
United StatesCanadaJapan

In The Last Decade

Karen Leung

11 papers receiving 449 citations

Peers

Karen Leung
Comparison fields: 5 of 66
  • Molecular Biology 283
  • Genetics 237
  • Cognitive Neuroscience 55
  • Cancer Research 38
  • Oncology 35
Replace Ewa Bocian with:
Ewa Bocian Poland
Shachar Sherman Israel
Hayk Barseghyan United States
Jungyoon Choi South Korea
Oz Pomp United States
Gemma Buck United Kingdom
Veronika Akopian United States
Sergey Kupriyanov United States
Christina Galonska United States
Jeffrey J. Schrick United States
Karen Leung relative to Ewa Bocian Poland Ewa Bocian's profile →
Citations per field
00.5×1.5×1.8×
Ewa Bocian · 1×
Citations per year

Countries citing papers authored by Karen Leung

Since Specialization
Citations

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

Fields of papers citing papers by Karen Leung

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen Leung

This figure shows the co-authorship network connecting the top 25 collaborators of Karen Leung. A scholar is included among the top collaborators of Karen Leung based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Karen Leung. Karen Leung is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

11 of 11 papers shown
#WorkIndexed citations
1 5
2 52
3 2
4 91
5 59
6 11
7 13
8 59
9 107
10 65
11 2

About Karen Leung

Karen Leung is a scholar working on Structural Biology, Genetics and Genetics, having authored 11 papers that have together received 466 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Structural Biology (24 citations), Genetics (237 citations) and Molecular Biology (283 citations). Karen Leung has collaborated with scholars based in United States, Canada and Japan. Frequent co-authors include Janine M. LaSalle, Roxanne O. Vallero, Barbara Panning, David Wu, Amber Hogart, N. Carolyn Schanen, Amanda J. DuBose, James L. Resnick, Elizabeth A. Smith and Keith W. Dunaway. Their work appears in journals such as Blood, Biophysical Journal and Cell stem cell.

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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026