HH Ropers
About
In The Last Decade
HH Ropers
10 papers receiving 172 citations
Peers
Comparison fields: 5 of 40
- Molecular Biology 138
- Genetics 115
- Epidemiology 56
- Pediatrics, Perinatology and Child Health 21
- Pulmonary and Respiratory Medicine 14
Countries citing papers authored by HH Ropers
This map shows the geographic impact of HH Ropers'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 HH Ropers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites HH Ropers more than expected).
Fields of papers citing papers by HH Ropers
This network shows the impact of papers produced by HH Ropers. 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 HH Ropers. The network helps show where HH Ropers may publish in the future.
Co-authorship network of co-authors of HH Ropers
This figure shows the co-authorship network connecting the top 25 collaborators of HH Ropers. A scholar is included among the top collaborators of HH Ropers 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 HH Ropers. HH Ropers is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 40 | |
| 2 | 86 | |
| 3 | 15 | |
| 4 | 10 | |
| 5 | Severe X-linked mental retardation caused by mutations in the gene for the thyroid hormone transporter MCT8 | 10 |
| 6 | A defect of midline development, Opitz syndrome, is due to mutations in a novel RING finger gene on Xp22 | 1 |
| 7 | Cloning of candidate genes for X-linked mental retardation by use of chromosome aberrations | 1 |
| 8 | Norrie's disease: delineation of carriers among daughters of obligate carriers by linkage analysis. | 9 |
| 9 | H-Y antigen in human X-autosome translocations. | 1 |
| 10 | Exclusion of the C3 gene from the 19q133 to 19qter region by Southern analysis of human-rodent somatic cell hybrids, employing a cloned genomic C3 gene fragment. | 1 |
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.