This map shows the geographic impact of Witkop Cj'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 Witkop Cj with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Witkop Cj more than expected).
This network shows the impact of papers produced by Witkop Cj. 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 Witkop Cj. The network helps show where Witkop Cj may publish in the future.
Co-authorship network of co-authors of Witkop Cj
This figure shows the co-authorship network connecting the top 25 collaborators of Witkop Cj.
A scholar is included among the top collaborators of Witkop Cj 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 Witkop Cj. Witkop Cj is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Cj, Witkop, et al.. (1989). Prepubertal diagnosis of Klinefelter syndrome in a patient with taurodontic teeth.. PubMed. 11(3). 224–6.4 indexed citations
Cj, Witkop, et al.. (1982). Optic and otic neurologic abnormalities in oculocutaneous and ocular albinism.. PubMed. 18(6). 299–318.20 indexed citations
5.
Cj, Witkop, et al.. (1982). Hereditary mucoepithelial dysplasia, a disease of gap junction and desmosome formation.. PubMed. 18(6). 493–511.3 indexed citations
6.
Cj, Witkop. (1980). Disorders affecting cellular communications in oral tissues: gap junctions.. PubMed. 16(2). 197–209.1 indexed citations
7.
Cj, Witkop. (1979). Depigmentations of the general and oral tissues and their genetic foundations.. PubMed. 16(4). 330–43.16 indexed citations
8.
Cj, Witkop, et al.. (1977). [Globodontia--a new familial tooth abnormality].. PubMed. 32(2). 194–6.2 indexed citations
Rj, Gorlin, et al.. (1975). Malformation syndromes. A selected miscellany.. PubMed. 11(2). 39–50.56 indexed citations
13.
Jg, White, et al.. (1975). Proceedings: Differences in platelet storage pool deficiency (SPD) of Hermansky Pudlak syndrome (HPS) and non-albinos (NA).. PubMed. 34(1). 360–1.4 indexed citations
14.
We, Nance, et al.. (1971). Genetic and biochemical evidence for two forms of oculocutaneous albinism in man.. PubMed. 7(3). 125–8.8 indexed citations
Cj, Witkop. (1968). Gardner's syndrome and other osteognathodermal disorders with defects in parathyroid functions.. PubMed. 26(10). 639–42.3 indexed citations
17.
Cj, Witkop, et al.. (1966). Medical and dental findings in the Brandywine isolate.. PubMed. 3(4). 382–403.34 indexed citations
18.
Cj, Witkop, et al.. (1965). The frequency of discolored teeth showing yellow fluorescence under ultra-violet light.. PubMed. 2(2). 81–7.8 indexed citations
19.
Cj, Witkop, et al.. (1960). Hereditary benign intraepithelial dyskeratosis. II. Oral manifestations and hereditary transmission.. PubMed. 70. 696–711.29 indexed citations
20.
Cj, Witkop, et al.. (1956). A study of hereditary defects occurring in a racial isolate residing in Southern Maryland; special report.. PubMed. 12(2). 29–33.2 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.