James H. Asher

1.2k total citations
33 papers, 914 citations indexed

About

James H. Asher is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, James H. Asher has authored 33 papers receiving a total of 914 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 9 papers in Cell Biology. Recurrent topics in James H. Asher's work include melanin and skin pigmentation (9 papers), Hearing, Cochlea, Tinnitus, Genetics (6 papers) and RNA regulation and disease (4 papers). James H. Asher is often cited by papers focused on melanin and skin pigmentation (9 papers), Hearing, Cochlea, Tinnitus, Genetics (6 papers) and RNA regulation and disease (4 papers). James H. Asher collaborates with scholars based in United States, Indonesia and South Africa. James H. Asher's co-authors include Thomas B. Friedman, Robert J. Morell, John T. Hinnant, George W. Nace, Christina M. Richards, Thomas D. Barber, Yong Liang, James L. Weber, Sukarti Moeljopawiro and Annemarie Sommer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Genetics.

In The Last Decade

James H. Asher

32 papers receiving 875 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
James H. Asher United States 16 471 307 234 200 93 33 914
Kathleen E. Whitlock United States 19 446 0.9× 224 0.7× 277 1.2× 284 1.4× 86 0.9× 38 1.2k
Frances Hannan United States 17 751 1.6× 307 1.0× 119 0.5× 246 1.2× 51 0.5× 21 1.8k
M. S. Deol United Kingdom 26 754 1.6× 363 1.2× 733 3.1× 181 0.9× 161 1.7× 51 1.7k
Sarah B. Emery United States 15 546 1.2× 307 1.0× 243 1.0× 85 0.4× 30 0.3× 23 954
Kwanghyuk Lee United States 16 566 1.2× 183 0.6× 310 1.3× 66 0.3× 47 0.5× 39 1.0k
Edmund J. Koundakjian United States 8 739 1.6× 344 1.1× 313 1.3× 254 1.3× 27 0.3× 8 1.1k
Pamela J. Lanford United States 10 821 1.7× 117 0.4× 693 3.0× 238 1.2× 42 0.5× 14 1.4k
Anabel Varela United Kingdom 5 1.0k 2.2× 120 0.4× 772 3.3× 267 1.3× 58 0.6× 5 1.4k
Jo Begbie United Kingdom 18 1.2k 2.5× 284 0.9× 155 0.7× 170 0.8× 31 0.3× 28 1.5k
Claudius F. Kratochwil Germany 18 454 1.0× 361 1.2× 49 0.2× 188 0.9× 52 0.6× 38 1.1k

Countries citing papers authored by James H. Asher

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of James H. Asher

This figure shows the co-authorship network connecting the top 25 collaborators of James H. Asher. A scholar is included among the top collaborators of James H. Asher 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 James H. Asher. James H. Asher 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
1.
Ramirez, Daniel, et al.. (2025). CANDID-CNS: AI Unlocks Stereochemistry and Beyond Rule of 5 to Predict CNS Penetration of Small Molecules. Journal of Chemical Information and Modeling. 65(23). 12918–12928. 1 indexed citations
2.
DeStefano, Anita L., L. Adrienne Cupples, Kathleen S. Arnos, et al.. (1998). Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations. Human Genetics. 102(5). 499–506. 47 indexed citations
3.
Morell, Robert J., et al.. (1997). Apparent Digenic Inheritance of Waardenburg Syndrome Type 2 (WS2) and Autosomal Recessive Ocular Albinism (AROA). Human Molecular Genetics. 6(5). 659–664. 68 indexed citations
4.
Liang, Yong, Hong Chen, James H. Asher, Chia‐Cheng Chang, & Thomas B. Friedman. (1997). Human inner ear OCP2 cDNA maps to 5q22-5q35.2 with related sequences on chromosomes 4p16.2-4p14, 5p13-5q22, 7pter-q22, 10 and 12p13-12qter. Gene. 184(2). 163–167. 8 indexed citations
5.
Morell, Robert J., et al.. (1997). Three Mutations in the Paired Homeodomain of <i>PAX3That </i>Cause Waardenburg Syndrome Type 1. Human Heredity. 47(1). 38–41. 8 indexed citations
6.
Innis, Jeffrey W., James H. Asher, Yong Liang, et al.. (1997). Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia. American Journal of Medical Genetics. 71(3). 292–297. 1 indexed citations
7.
8.
Asher, James H., Annemarie Sommer, Robert J. Morell, & Thomas B. Friedman. (1996). Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndrome. Human Mutation. 7(1). 30–35. 57 indexed citations
9.
Morell, Robert J., Yong Liang, James H. Asher, et al.. (1995). Analysis of short tandem repeat (STR) allele frequency distributions in a Balinese population. Human Molecular Genetics. 4(1). 85–91. 10 indexed citations
10.
Liang, Yong, et al.. (1995). A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17. Nature Genetics. 9(1). 86–91. 165 indexed citations
11.
Farrer, Lindsay A., Kathleen S. Arnos, James H. Asher, et al.. (1994). Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes.. PubMed. 55(4). 728–37. 54 indexed citations
12.
Morell, Robert J., Thomas B. Friedman, & James H. Asher. (1993). A plus-one frameshift mutation in PAX3 alters the entire deduced amino acid sequence of the paired box in a Waardenburg syndrome type 1 (WS1) family. Human Molecular Genetics. 2(9). 1487–1488. 20 indexed citations
13.
Barber, Thomas D., et al.. (1993). A highly informative dinucleotide repeat polymorphism at the D2S211 locus linked to ALPP, FN1 and TNP1. Human Molecular Genetics. 2(1). 88–88. 5 indexed citations
14.
15.
Asher, James H., Robert J. Morell, & Thomas B. Friedman. (1991). Confirmation of the Location of a Waardenburg Syndrome Type I Mutation on Human Chromosome 2qa. Annals of the New York Academy of Sciences. 630(1). 295–297. 2 indexed citations
16.
Asher, James H., et al.. (1991). Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.. PubMed. 48(1). 43–52. 35 indexed citations
17.
Gergerich, Rose C., James H. Asher, & D.C. Ramsdell. (1983). A Comparison of Some Serological and Biological Properties of Seven Isolates of Tobacco Ringspot Virus. Journal of Phytopathology. 107(4). 298–300. 1 indexed citations
18.
Asher, James H., et al.. (1982). The primary ultrastructural defect caused by anophthalmic white (Wh) in the Syrian hamster.. Proceedings of the National Academy of Sciences. 79(14). 4371–4375. 5 indexed citations
19.
Asher, James H., et al.. (1971). The Genetic Structure and Evolutionary Fate of Parthenogenetic Amphibian Populations as Determined by Markovian Analysis. American Zoologist. 11(2). 381–398. 31 indexed citations
20.
Asher, James H.. (1970). PARTHENOGENESIS AND GENETIC VARIABILITY. II. ONE-LOCUS MODELS FOR VARIOUS DIPLOID POPULATIONS. Genetics. 66(2). 369–391. 64 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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