Minghong Ward

4.0k total citations · 1 hit paper
5 papers, 711 citations indexed

About

Minghong Ward is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Minghong Ward has authored 5 papers receiving a total of 711 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Clinical Biochemistry. Recurrent topics in Minghong Ward's work include Genomics and Rare Diseases (2 papers), RNA and protein synthesis mechanisms (2 papers) and Genomics and Phylogenetic Studies (2 papers). Minghong Ward is often cited by papers focused on Genomics and Rare Diseases (2 papers), RNA and protein synthesis mechanisms (2 papers) and Genomics and Phylogenetic Studies (2 papers). Minghong Ward collaborates with scholars based in United States. Minghong Ward's co-authors include Stephen T. Sherry, Karl Sirotkin, Lon Phan, Lewis Y. Geer, Aron Marchler‐Bauer, Jiyao Wang, Christopher J. Lanczycki, Renata C. Geer, Philippe Youkharibache and Dachuan Zhang and has published in prestigious journals such as Bioinformatics, Genome Research and Human Mutation.

In The Last Decade

Minghong Ward

4 papers receiving 696 citations

Hit Papers

dbSNP—Database for Single Nucleotide Polymorphisms and Ot... 1999 2026 2008 2017 1999 100 200 300 400 500

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Minghong Ward United States 4 449 224 115 54 48 5 711
Mirko Francesconi Spain 15 508 1.1× 103 0.5× 105 0.9× 70 1.3× 38 0.8× 24 788
Lai Hong Wong Canada 9 563 1.3× 320 1.4× 88 0.8× 63 1.2× 53 1.1× 17 898
Christiana Spyrou United Kingdom 8 680 1.5× 218 1.0× 88 0.8× 97 1.8× 49 1.0× 8 809
Hyun‐Jun Nam South Korea 9 501 1.1× 223 1.0× 49 0.4× 52 1.0× 38 0.8× 15 763
Guido van Mierlo Netherlands 14 950 2.1× 184 0.8× 82 0.7× 78 1.4× 65 1.4× 28 1.1k
Stephanie L. Chissoe United States 14 390 0.9× 191 0.9× 53 0.5× 55 1.0× 53 1.1× 20 698
Karin Klinga‐Levan Sweden 17 531 1.2× 211 0.9× 241 2.1× 133 2.5× 57 1.2× 54 768
Naohiro Hori Japan 13 634 1.4× 171 0.8× 70 0.6× 54 1.0× 56 1.2× 29 836
Keun‐Cheol Kim South Korea 16 569 1.3× 85 0.4× 104 0.9× 113 2.1× 54 1.1× 38 784

Countries citing papers authored by Minghong Ward

Since Specialization
Citations

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

Fields of papers citing papers by Minghong Ward

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Minghong Ward

This figure shows the co-authorship network connecting the top 25 collaborators of Minghong Ward. A scholar is included among the top collaborators of Minghong Ward 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 Minghong Ward. Minghong Ward is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

5 of 5 papers shown
1.
Ward, Minghong, J. S. Bloom, Mike Feolo, et al.. (2025). P604: Advancing genomic research: Enhancing dbGaP interoperability with FHIR APIs. Genetics in Medicine Open. 3. 102452–102452.
2.
Wang, Jiyao, Philippe Youkharibache, Dachuan Zhang, et al.. (2019). iCn3D, a web-based 3D viewer for sharing 1D/2D/3D representations of biomolecular structures. Bioinformatics. 36(1). 131–135. 127 indexed citations
3.
Phan, Lon, et al.. (2014). The Database of Short Genetic Variation (dbSNP). 16 indexed citations
4.
Sherry, Stephen T., Minghong Ward, & Karl Sirotkin. (2000). Use of molecular variation in the NCBI dbSNP database. Human Mutation. 15(1). 68–75. 38 indexed citations
5.
Sherry, Stephen T., Minghong Ward, & Karl Sirotkin. (1999). dbSNP—Database for Single Nucleotide Polymorphisms and Other Classes of Minor Genetic Variation. Genome Research. 9(8). 677–679. 530 indexed citations breakdown →

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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