Stuart A. Holmes

1.0k total citations
16 papers, 776 citations indexed

About

Stuart A. Holmes is a scholar working on Molecular Biology, Cell Biology and Nutrition and Dietetics. According to data from OpenAlex, Stuart A. Holmes has authored 16 papers receiving a total of 776 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Cell Biology and 6 papers in Nutrition and Dietetics. Recurrent topics in Stuart A. Holmes's work include melanin and skin pigmentation (10 papers), RNA regulation and disease (7 papers) and Biochemical Analysis and Sensing Techniques (6 papers). Stuart A. Holmes is often cited by papers focused on melanin and skin pigmentation (10 papers), RNA regulation and disease (7 papers) and Biochemical Analysis and Sensing Techniques (6 papers). Stuart A. Holmes collaborates with scholars based in United States, Canada and Switzerland. Stuart A. Holmes's co-authors include Richard A. Spritz, Lutz B. Giebel, Elizabeth A. Craig, Charles M. Nicolet, Margaret Werner‐Washburne, Rhonda E. Schnur, Kazuyoshi Fukai, Peter Beighton, David Curtis and Raj Ramesar and has published in prestigious journals such as Science, Nature Genetics and Molecular and Cellular Biology.

In The Last Decade

Stuart A. Holmes

16 papers receiving 758 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stuart A. Holmes United States	13	490	371	171	107	88	16	776
Bailin Tu United States	8	239 0.5×	306 0.8×	166 1.0×	157 1.5×	85 1.0×	14	562
Tsuneto Kushimoto United States	10	427 0.9×	653 1.8×	332 1.9×	79 0.7×	201 2.3×	12	831
Kathleen M. Strunk United States	16	853 1.7×	747 2.0×	517 3.0×	110 1.0×	149 1.7×	18	1.2k
Darren J. Smit Australia	16	351 0.7×	492 1.3×	250 1.5×	89 0.8×	241 2.7×	24	827
Linh Le United States	8	270 0.6×	263 0.7×	81 0.5×	90 0.8×	51 0.6×	13	547
Brenda Watt United States	8	593 1.2×	290 0.8×	90 0.5×	39 0.4×	38 0.4×	9	860
Gayle A. Shinder Canada	9	383 0.8×	88 0.2×	9 0.1×	127 1.2×	65 0.7×	14	716
Caterina Valetti Italy	13	668 1.4×	707 1.9×	73 0.4×	227 2.1×	10 0.1×	14	1.1k
Emma Martínez‐Alonso Spain	14	286 0.6×	350 0.9×	54 0.3×	34 0.3×	16 0.2×	24	566
A. Dipasquale United States	9	326 0.7×	256 0.7×	38 0.2×	29 0.3×	36 0.4×	10	589

Countries citing papers authored by Stuart A. Holmes

Since Specialization

Citations

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

Fields of papers citing papers by Stuart A. Holmes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stuart A. Holmes. 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 Stuart A. Holmes. The network helps show where Stuart A. Holmes may publish in the future.

Co-authorship network of co-authors of Stuart A. Holmes

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

All Works

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16 of 16 papers shown

Spritz, Richard A., Jangsuk Oh, Kazuyoshi Fukai, et al.. (1997). Novel mutations of the tyrosinase (TYR) gene in type I oculocutaneous albinism (OCA1). Human Mutation. 10(2). 171–174. 45 indexed citations

Spritz, Richard A., Jangsuk Oh, Stuart A. Holmes, et al.. (1997). Novel mutations of the tyrosinase (TYR) gene in type I oculocutaneous albinism (OCA1). Human Mutation. 10(2). 171–174. 5 indexed citations

Schnur, Rhonda E., et al.. (1996). Type I Oculocutaneous Albinism Associated with a Full-Length Deletion of the Tyrosinase Gene. Journal of Investigative Dermatology. 106(5). 1137–1140. 19 indexed citations

Holmes, Stuart A., et al.. (1995). DNA‐based carrier detection and prenatal diagnosis of tyrosinase‐negative oculocutaneous albinism (OCA1A). Prenatal Diagnosis. 15(4). 345–349. 5 indexed citations

Holmes, Stuart A., Chris Bennett, L A Brueton, et al.. (1995). Novel mutations and deletions of the KIT (steel factor receptor) gene in human piebaldism.. PubMed. 56(1). 58–66. 71 indexed citations

Holmes, Stuart A., et al.. (1995). Autosomal recessive ocular albinism associated with a functionally significant tyrosinase gene polymorphism. Nature Genetics. 9(1). 92–95. 57 indexed citations

Lee, Seung‐Taek, Sang Kyu Park, Kyoung Hwa Lee, Stuart A. Holmes, & Richard A. Spritz. (1995). A Non-radioactive Method for Simultaneous Detection of Single-strand Conformation Polymorphisms (SSCPs) and Heteroduplexes. Molecules and Cells. 5(6). 668–672. 25 indexed citations

Spritz, Richard A., Kazuyoshi Fukai, Stuart A. Holmes, & J. Luande. (1995). Frequent intragenic deletion of the P gene in Tanzanian patients with type II oculocutaneous albinism (OCA2).. PubMed. 56(6). 1320–3. 42 indexed citations

Spritz, Richard A., et al.. (1993). A recurrent deletion in the KIT (mast/stem cell growth factor receptor) proto-oncogene is a frequent cause of human piebaldism. Human Molecular Genetics. 2(9). 1499–1500. 15 indexed citations

10.

Spritz, Richard A., Stuart A. Holmes, Peter Itin, & Wolfgang Küster. (1993). Novel Mutations of the KIT (Mast/Stem Cell Growth Factor Receptor) Proto-Oncogene in Human Piebaldism. Journal of Investigative Dermatology. 101(1). 22–25. 34 indexed citations

11.

Tripathi, R. K., Sarah Bundey, Sara Droetto, et al.. (1993). Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA).. PubMed. 53(6). 1173–9. 32 indexed citations

12.

Spritz, Richard A., Lutz B. Giebel, & Stuart A. Holmes. (1992). Reply to Fleischman. The American Journal of Human Genetics. 51(3). 678. 1 indexed citations

13.

Spritz, Richard A., Stuart A. Holmes, Raj Ramesar, et al.. (1992). Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism.. PubMed. 51(5). 1058–65. 72 indexed citations

14.

Spritz, Richard A., Lutz B. Giebel, & Stuart A. Holmes. (1992). Dominant negative and loss of function mutations of the c-kit (mast/stem cell growth factor receptor) proto-oncogene in human piebaldism.. PubMed. 50(2). 261–9. 122 indexed citations

15.

Craig, Elizabeth A., et al.. (1989). SSC1, an Essential Member of the Yeast HSP70 Multigene Family, Encodes a Mitochondrial Protein. Molecular and Cellular Biology. 9(7). 3000–3008. 212 indexed citations

16.

Sato, Gordon, Toby G. Rossman, Leon M. Edelstein, Stuart A. Holmes, & V. Buonassisi. (1965). Phenotypic Alterations in Adrenal Tumor Cultures. Science. 148(3678). 1733–1734. 19 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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