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 10
- Ocular Disorders and Treatments 3
- Craniofacial Disorders and Treatments 2
- Co-authors
- Thomas B. Friedman (16 shared papers)Robert J. Morell (12 shared papers)John T. Hinnant (3 shared papers)George W. Nace (1 shared paper)Christina M. Richards (1 shared paper)Yong Liang (3 shared papers)Thomas D. Barber (2 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)Human Mutation (2 papers)Genetics (2 papers)
- Partner nations
- United StatesIndonesiaGhana
In The Last Decade
James H. Asher
32 papers receiving 875 citations
Peers
Comparison fields: 5 of 92
- Sensory Systems 234
- Cell Biology 200
- Genetics 307
- Neurology 66
- Molecular Biology 471
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 33 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 | 57 | |
| 7 | Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes. | 1994 | 54 |
| 8 | 1990 | 48 | |
| 9 | 1998 | 47 | |
| 10 | Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q. | 1991 | 35 |
| 11 | 1995 | 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 | 8 |
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 33 papers that have together received 914 indexed citations. Recurring topics across this work include melanin and skin pigmentation (9 papers), Hearing, Cochlea, Tinnitus, Genetics (6 papers), Biochemical Analysis and Sensing Techniques (4 papers), RNA regulation and disease (4 papers), Genomics and Chromatin Dynamics (3 papers), Cancer-related molecular mechanisms research (3 papers), Ocular Disorders and Treatments (3 papers) and Craniofacial Disorders and Treatments (2 papers). The work is most often cited by research in Sensory Systems (234 citations), Cell Biology (200 citations), Genetics (307 citations), Neurology (66 citations) and Molecular Biology (471 citations). James H. Asher has collaborated with scholars based in United States, Indonesia and Ghana. Frequent co-authors include Thomas B. Friedman, Robert J. Morell, John T. Hinnant, George W. Nace, Christina M. Richards, Yong Liang, Thomas D. Barber, 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, Human Mutation and Genetics.
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.