Nancy Wang
Impact in
Papers in
- Genetics 21
- Genomic variations and chromosomal abnormalities 13
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
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- Ovarian cancer diagnosis and treatment 8
- Co-authors
- David Lee Bronson (2 shared papers)Elwin E. Fraley (2 shared papers)Thuluvancheri K. Mohandas (1 shared paper)R.T. Taggart (1 shared paper)Pauline Hsiao Yen (1 shared paper)Larry J. Shapiro (1 shared paper)Jia Xu (8 shared papers)Robert N. Shoffner (6 shared papers)
- Journals
- Mutation research. Fundamental and molecular mechanisms of mutagenesis (3 papers)Cancer Genetics and Cytogenetics (19 papers)Leukemia Research (2 papers)Genes Chromosomes and Cancer (2 papers)Pediatric and Developmental Pathology (2 papers)
- Partner nations
- United StatesChinaSweden
In The Last Decade
Nancy Wang
70 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 78
- Genetics 455
- Oncology 318
- Otorhinolaryngology 60
- Reproductive Medicine 110
- Cancer Research 138
Countries citing papers authored by Nancy Wang
This map shows the geographic impact of Nancy 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 Nancy Wang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nancy Wang more than expected).
Fields of papers citing papers by Nancy Wang
This network shows the impact of papers produced by Nancy 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 Nancy Wang. The network helps show where Nancy Wang may publish in the future.
Co-authors
The 25 scholars most cited alongside Nancy Wang, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 71 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1987 | 245 | |
| 2 | Nonrandom abnormalities in chromosome 1 in human testicular cancers. | 1980 | 140 |
| 3 | 2005 | 115 | |
| 4 | 1984 | 104 | |
| 5 | 2004 | 82 | |
| 6 | 1986 | 81 | |
| 7 | 1982 | 80 | |
| 8 | 1986 | 70 | |
| 9 | 2003 | 62 | |
| 10 | 1997 | 44 | |
| 11 | 2009 | 39 | |
| 12 | Characterization of high- and low-metastatic clones derived from a methylcholanthrene-induced murine fibrosarcoma. | 1982 | 38 |
| 13 | Cytogenetic evidence for premeiotic transformation of human testicular cancers. | 1981 | 36 |
| 14 | 1987 | 31 | |
| 15 | 1996 | 31 | |
| 16 | 1974 | 30 | |
| 17 | 1989 | 30 | |
| 18 | 1995 | 29 | |
| 19 | 2013 | 29 | |
| 20 | 2001 | 26 |
About Nancy Wang
Nancy Wang is a scholar working on Genetics, Reproductive Medicine, Hematology, Cancer Research and Oncology, having authored 71 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Ovarian cancer diagnosis and treatment (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Acute Myeloid Leukemia Research (6 papers), Carcinogens and Genotoxicity Assessment (6 papers), Testicular diseases and treatments (4 papers), Chromosomal and Genetic Variations (4 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Genetics (455 citations), Oncology (318 citations), Otorhinolaryngology (60 citations), Reproductive Medicine (110 citations) and Cancer Research (138 citations). Nancy Wang has collaborated with scholars based in United States, China and Sweden. Frequent co-authors include David Lee Bronson, Elwin E. Fraley, Thuluvancheri K. Mohandas, R.T. Taggart, Pauline Hsiao Yen, Larry J. Shapiro, Jia Xu, Robert N. Shoffner, Edward Cedrone and Joan Wennstrom Bennett. Their work appears in journals such as Mutation research. Fundamental and molecular mechanisms of mutagenesis, Cancer Genetics and Cytogenetics, Leukemia Research, Genes Chromosomes and Cancer and Pediatric and Developmental Pathology.
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.