Hungshu Wang

653 total citations
10 papers, 400 citations indexed

About

Hungshu Wang is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hungshu Wang has authored 10 papers receiving a total of 400 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hungshu Wang's work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (4 papers) and Chromosomal and Genetic Variations (4 papers). Hungshu Wang is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (4 papers) and Chromosomal and Genetic Variations (4 papers). Hungshu Wang collaborates with scholars based in Canada, Taiwan and France. Hungshu Wang's co-authors include Gerald J. Goldenberg, Gordon W. Blair, Bradley N. White, Jeanette J. A. Holden, Michael J. Higgins, John Roder, Tina Haliotis, Alasdair G. W. Hunter, Philip Wyatt and Dagmar K. Kalousek and has published in prestigious journals such as Human Genetics, Chromosoma and American Journal of Medical Genetics.

In The Last Decade

Hungshu Wang

10 papers receiving 384 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hungshu Wang Canada 8 238 179 163 90 59 10 400
Hideaki Chiyo Japan 14 196 0.8× 101 0.6× 216 1.3× 69 0.8× 41 0.7× 24 430
Steven Schonberg United States 13 147 0.6× 111 0.6× 247 1.5× 39 0.4× 20 0.3× 19 422
R.N. Simmers Australia 9 158 0.7× 70 0.4× 205 1.3× 31 0.3× 31 0.5× 10 389
Osamu Miyoshi Japan 11 116 0.5× 74 0.4× 176 1.1× 37 0.4× 23 0.4× 22 278
Hélène Moirot France 9 119 0.5× 59 0.3× 76 0.5× 45 0.5× 20 0.3× 13 198
N.J. Barton United Kingdom 7 303 1.3× 51 0.3× 264 1.6× 77 0.9× 39 0.7× 10 453
Shun‐Ping Chang Taiwan 10 94 0.4× 89 0.5× 96 0.6× 33 0.4× 47 0.8× 41 278
M. Murer‐Orlando United Kingdom 11 118 0.5× 43 0.2× 200 1.2× 68 0.8× 14 0.2× 19 294
Nadja Kokalj-Vokač Slovenia 11 176 0.7× 51 0.3× 276 1.7× 73 0.8× 13 0.2× 19 406
J. Stamberg United States 12 158 0.7× 65 0.4× 151 0.9× 78 0.9× 15 0.3× 17 329

Countries citing papers authored by Hungshu Wang

Since Specialization
Citations

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

Fields of papers citing papers by Hungshu Wang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hungshu Wang

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

All Works

10 of 10 papers shown
1.
Winsor, E.J.T., Darrell J. Tomkins, Dagmar K. Kalousek, et al.. (1999). Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT). Prenatal Diagnosis. 19(7). 620–627. 19 indexed citations
2.
Hsu, Lillian Y. F., Richard L. Neu, Daniel L. Van Dyke, et al.. (1997). RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS. Prenatal Diagnosis. 17(3). 201–242. 143 indexed citations
3.
Rajcan‐Separovic, Evica, Hungshu Wang, Marsha Speevak, et al.. (1995). Identification of the origin of double minutes in normal human cells by laser-based chromosome microdissection approach. Human Genetics. 96(1). 39–43. 14 indexed citations
4.
Wang, Hungshu, et al.. (1994). Minute chromatin structures in cells of amniotic fluid—an interpretative dilemma. Prenatal Diagnosis. 14(9). 868–872. 3 indexed citations
5.
Wang, Hungshu, et al.. (1993). VACTERL with hydrocephalus: Spontaneous chromosome breakage and rearrangement in a family showing apparent sex‐linked recessive inheritance. American Journal of Medical Genetics. 47(1). 114–117. 27 indexed citations
6.
Wang, Hungshu, et al.. (1993). Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis. American Journal of Medical Genetics. 46(5). 559–562. 12 indexed citations
7.
Goldenberg, Gerald J., Hungshu Wang, & Gordon W. Blair. (1986). Resistance to adriamycin: relationship of cytotoxicity to drug uptake and DNA single- and double-strand breakage in cloned cell lines of adriamycin-sensitive and -resistant P388 leukemia.. PubMed. 46(6). 2978–83. 66 indexed citations
8.
Higgins, Michael J., Hungshu Wang, Tina Haliotis, et al.. (1985). Organization of a repetitive human 1.8 kb KpnI sequence localized in the heterochromatin of chromosome 15. Chromosoma. 93(1). 77–86. 102 indexed citations
9.
Holden, Jeanette J. A., Hungshu Wang, Bradley N. White, & John M. Opitz. (1984). The fragile‐X syndrome, IV. Progress towards the identification of linked restriction fragment length variants (RFLVs). American Journal of Medical Genetics. 17(1). 259–273. 8 indexed citations
10.
Wang, Hungshu & Alasdair G. W. Hunter. (1979). A supernumerary “G” like chromosome originating from a maternal 13;15 translocation in a nondysmorphic, retarded girl. Clinical Genetics. 15(3). 273–277. 6 indexed citations

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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2026