D A McCullough
About
In The Last Decade
D A McCullough
13 papers receiving 900 citations
Peers
Comparison fields: 5 of 58
- Molecular Biology 859
- Clinical Biochemistry 439
- Ophthalmology 71
- Genetics 65
- Cellular and Molecular Neuroscience 54
Countries citing papers authored by D A McCullough
This map shows the geographic impact of D A McCullough'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 D A McCullough with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D A McCullough more than expected).
Fields of papers citing papers by D A McCullough
This network shows the impact of papers produced by D A McCullough. 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 D A McCullough. The network helps show where D A McCullough may publish in the future.
Co-authorship network of co-authors of D A McCullough
This figure shows the co-authorship network connecting the top 25 collaborators of D A McCullough. A scholar is included among the top collaborators of D A McCullough 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 D A McCullough. D A McCullough is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | 10 | |
| 3 | 90 | |
| 4 | 6 | |
| 5 | 140 | |
| 6 | 102 | |
| 7 | 5 | |
| 8 | Molecular genetic analysis of a sporadic case of Leber hereditary optic neuropathy. | 19 |
| 9 | Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees. | 315 |
| 10 | Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation. | 195 |
| 11 | An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 gene. | 27 |
| 12 | 17 | |
| 13 | 3 | |
| 14 | Proceedings: Inhibition of constrictor responses if the rabbit ear artery by a mixture of oxytetracycline and ascorbic acid. | 0 |
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.