James H. Asher
Impact in
- Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics
- Cell Biology top 10%
- melanin and skin pigmentation
Papers in
-
- RNA regulation and disease 4
- Genomics and Chromatin Dynamics 3
- Genetics 11
- Ocular Disorders and Treatments 4
- Evolution and Genetic Dynamics 2
- Co-authors
- Thomas B. Friedman (17 shared papers)Robert J. Morell (12 shared papers)John T. Hinnant (3 shared papers)Christina M. Richards (1 shared paper)George W. Nace (1 shared paper)Thomas D. Barber (2 shared papers)Yong Liang (3 shared papers)James L. Weber (1 shared paper)
- Journals
- Human Molecular Genetics (5 papers)Journal of Medical Genetics (4 papers)Journal of Experimental Zoology (3 papers)Genetics (2 papers)Human Mutation (2 papers)
- Partner nations
- United StatesIndonesiaSouth Africa
In The Last Decade
James H. Asher
32 papers receiving 879 citations
Peers
Comparison fields: 5 of 90
- Sensory Systems 227
- Cell Biology 183
- Genetics 296
- Neurology 58
- Molecular Biology 423
Countries citing papers authored by James H. Asher
This map shows the geographic impact of James H. Asher'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 James H. Asher with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites James H. Asher more than expected).
Fields of papers citing papers by James H. Asher
This network shows the impact of papers produced by James H. Asher. 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 James H. Asher. The network helps show where James H. Asher may publish in the future.
Co-authors
The 25 scholars most cited alongside James H. Asher, 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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1995 | 165 | |
| 2 | 1992 | 73 | |
| 3 | 1970 | 71 | |
| 4 | 1997 | 68 | |
| 5 | 1970 | 64 | |
| 6 | 1996 | 58 | |
| 7 | Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes. | 1994 | 54 |
| 8 | 1990 | 48 | |
| 9 | 1998 | 47 | |
| 10 | 1995 | 35 | |
| 11 | Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q. | 1991 | 35 |
| 12 | 1996 | 32 | |
| 13 | 1971 | 31 | |
| 14 | 1993 | 20 | |
| 15 | 1998 | 18 | |
| 16 | 1997 | 15 | |
| 17 | 1995 | 10 | |
| 18 | 1997 | 8 | |
| 19 | 1997 | 8 | |
| 20 | 1983 | 7 |
About James H. Asher
James H. Asher is a scholar working on Molecular Biology, Genetics, Cell Biology, Sensory Systems and Nutrition and Dietetics, having authored 32 papers that have together received 913 indexed citations. Recurring topics across this work include melanin and skin pigmentation (9 papers), Hearing, Cochlea, Tinnitus, Genetics (5 papers), Biochemical Analysis and Sensing Techniques (4 papers), Ocular Disorders and Treatments (4 papers), RNA regulation and disease (4 papers), Genomics and Chromatin Dynamics (3 papers), Cancer-related molecular mechanisms research (3 papers) and Evolution and Genetic Dynamics (2 papers). The work is most often cited by research in Sensory Systems (227 citations), Cell Biology (183 citations), Genetics (296 citations), Neurology (58 citations) and Molecular Biology (423 citations). James H. Asher has collaborated with scholars based in United States, Indonesia and South Africa. Frequent co-authors include Thomas B. Friedman, Robert J. Morell, John T. Hinnant, Christina M. Richards, George W. Nace, Thomas D. Barber, Yong Liang, James L. Weber, Sukarti Moeljopawiro and Annemarie Sommer. Their work appears in journals such as Human Molecular Genetics, Journal of Medical Genetics, Journal of Experimental Zoology, Genetics and Human Mutation.
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.