Henry H. Heng

15.5k total citations · 5 hit papers
202 papers, 11.8k citations indexed

About

Henry H. Heng is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Henry H. Heng has authored 202 papers receiving a total of 11.8k indexed citations (citations by other indexed papers that have themselves been cited), including 135 papers in Molecular Biology, 72 papers in Genetics and 39 papers in Cancer Research. Recurrent topics in Henry H. Heng's work include Genomic variations and chromosomal abnormalities (42 papers), Cancer Genomics and Diagnostics (35 papers) and Genomics and Chromatin Dynamics (32 papers). Henry H. Heng is often cited by papers focused on Genomic variations and chromosomal abnormalities (42 papers), Cancer Genomics and Diagnostics (35 papers) and Genomics and Chromatin Dynamics (32 papers). Henry H. Heng collaborates with scholars based in United States, Canada and Germany. Henry H. Heng's co-authors include Lap‐Chee Tsui, Brian F. O’Dowd, Tuan Nguyen, Christine J. Ye, Stephen W. Scherer, L.-C. Tsui, Joshua B. Stevens, Xiaomei Shi, Steven W. Bremer and Susan R. George and has published in prestigious journals such as Proceedings of the National Academy of Sciences, JAMA and Journal of Biological Chemistry.

In The Last Decade

Henry H. Heng

199 papers receiving 11.6k citations

Hit Papers

A human gene that shows identity with the gene encoding t... 1992 2026 2003 2014 1993 1993 1997 1996 1992 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Henry H. Heng United States 60 7.0k 2.9k 1.7k 1.3k 1.2k 202 11.8k
Jay A. Tischfield United States 59 6.8k 1.0× 2.1k 0.7× 1.0k 0.6× 1.1k 0.8× 1.9k 1.6× 258 12.2k
Masatoshi Hagiwara Japan 62 11.6k 1.7× 1.5k 0.5× 1.1k 0.7× 1.5k 1.1× 2.3k 1.9× 301 16.4k
Michael F. Seldin United States 73 8.3k 1.2× 4.0k 1.4× 1.6k 0.9× 1.2k 0.9× 1.2k 0.9× 281 17.6k
William F. Dove United States 51 7.0k 1.0× 3.1k 1.1× 1.5k 0.9× 597 0.5× 483 0.4× 176 12.6k
David W. Rose United States 58 14.8k 2.1× 5.6k 1.9× 2.2k 1.3× 1.0k 0.8× 1.4k 1.1× 91 19.5k
En Li United States 57 17.0k 2.4× 4.7k 1.6× 1.4k 0.8× 2.5k 1.9× 1.7k 1.4× 119 22.4k
John R. Walker United States 52 6.9k 1.0× 1.3k 0.4× 807 0.5× 925 0.7× 1.4k 1.1× 121 11.9k
Francesco Cecconi Italy 57 10.2k 1.5× 797 0.3× 1.6k 1.0× 2.3k 1.7× 1.5k 1.2× 176 17.3k
James Douglas Engel United States 72 14.5k 2.1× 2.6k 0.9× 1.2k 0.7× 1.4k 1.1× 555 0.5× 225 19.0k
Patrick Matthias Switzerland 52 9.3k 1.3× 1.7k 0.6× 1.7k 1.0× 963 0.7× 836 0.7× 109 13.6k

Countries citing papers authored by Henry H. Heng

Since Specialization
Citations

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

Fields of papers citing papers by Henry H. Heng

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Henry H. Heng. 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 Henry H. Heng. The network helps show where Henry H. Heng may publish in the future.

Co-authorship network of co-authors of Henry H. Heng

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

All Works

20 of 20 papers shown
2.
Kasperski, Andrzej & Henry H. Heng. (2024). The Digital World of Cytogenetic and Cytogenomic Web Resources. Methods in molecular biology. 2825. 361–391. 1 indexed citations
3.
Yang, Zhao, Qi Chen, Jie‐Mei Wang, et al.. (2024). Inhalation exposure to airborne PM2.5 attenuates hepatic metabolic pathways through S-nitrosylation of the primary ER stress sensor. American Journal of Physiology-Cell Physiology. 328(1). C212–C226. 1 indexed citations
4.
Heng, Henry H., et al.. (2023). Challenges and Opportunities for Clinical Cytogenetics in the 21st Century. Genes. 14(2). 493–493. 14 indexed citations
5.
Horne, Steven D., et al.. (2014). Stress, genomic adaptation, and the evolutionary trade-off. Frontiers in Genetics. 5. 92–92. 63 indexed citations
6.
Abdallah, Batoul Y., Steven D. Horne, Markku Kurkinen, et al.. (2013). Ovarian cancer evolution through stochastic genome alterations: defining the genomic role in ovarian cancer. Systems Biology in Reproductive Medicine. 60(1). 2–13. 10 indexed citations
7.
Stevens, Joshua B., Liu G, Batoul Y. Abdallah, et al.. (2013). Unstable genomes elevate transcriptome dynamics. International Journal of Cancer. 134(9). 2074–2087. 30 indexed citations
8.
Stevens, Joshua B., Batoul Y. Abdallah, Guiming Liu, et al.. (2011). Diverse system stresses: common mechanisms of chromosome fragmentation. Cell Death and Disease. 2(6). e178–e178. 56 indexed citations
9.
Piechocki, Marie P., et al.. (2008). DNA Vaccination Controls Her-2+ Tumors that Are Refractory to Targeted Therapies. Cancer Research. 68(18). 7502–7511. 24 indexed citations
10.
Heng, Henry H., Joshua B. Stevens, Steven W. Bremer, et al.. (2006). Stochastic cancer progression driven by non‐clonal chromosome aberrations. Journal of Cellular Physiology. 208(2). 461–472. 123 indexed citations
11.
Heng, Henry H., et al.. (2005). Characterization of three pairs of prostate cells lines derived from tumor and adjacent normal tissues. Cancer Research. 65. 462–462. 2 indexed citations
12.
Heng, Henry H., et al.. (2003). FISH Detection on DAPI-Banded Chromosomes. Humana Press eBooks. 33. 35–50. 7 indexed citations
13.
Claudio, Jaime O., et al.. (1999). Cloning and Expression Analysis of a Novel WD Repeat Gene, WDR3, Mapping to 1p12–p13. Genomics. 59(1). 85–89. 13 indexed citations
14.
Liu, Lide, Lina Wang, Hong Peng Jia, et al.. (1998). Structure and mapping of the human β-defensin HBD-2 gene and its expression at sites of inflammation. Gene. 222(2). 237–244. 213 indexed citations
15.
Motoyama, Jun, Henry H. Heng, Michael A. Crackower, et al.. (1998). Overlapping and non-overlapping Ptch2 expression with Shh during mouse embryogenesis. Mechanisms of Development. 78(1-2). 81–84. 60 indexed citations
16.
Vadnal, Robert, et al.. (1998). Human chromosomal localization of a gene for inositol monophosphatase by fluorescence in situ hybridization. Neuroreport. 9(4). 683–685. 4 indexed citations
17.
Heng, Henry H., Robert Lowsky, Yi Xu, et al.. (1997). Cloning, Expression, and Chromosomal Localization to 11p12-13 of a Human LIM/HOMEOBOX Gene, hLim-1. DNA and Cell Biology. 16(6). 671–678. 20 indexed citations
18.
Barron‐Casella, Emily, et al.. (1995). Sequence Analysis and Chromosomal Localization of Human Cap Z. Journal of Biological Chemistry. 270(37). 21472–21479. 51 indexed citations
19.
Leung, Irene, et al.. (1994). MLK-3: identification of a widely-expressed protein kinase bearing an SH3 domain and a leucine zipper-basic region domain.. PubMed. 9(6). 1745–50. 84 indexed citations
20.
Heng, Henry H., et al.. (1988). Effects of pingyanymycin on chromosomes: A possible structural basis for chromosome aberration. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 199(1). 199–205. 26 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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