Ronald G. Cadle

411 total citations
8 papers, 251 citations indexed

About

Ronald G. Cadle is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Ronald G. Cadle has authored 8 papers receiving a total of 251 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 2 papers in Surgery and 2 papers in Molecular Biology. Recurrent topics in Ronald G. Cadle's work include Connective tissue disorders research (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genetic and rare skin diseases. (2 papers). Ronald G. Cadle is often cited by papers focused on Connective tissue disorders research (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genetic and rare skin diseases. (2 papers). Ronald G. Cadle collaborates with scholars based in United States and Canada. Ronald G. Cadle's co-authors include Bryan D. Hall, Clair A. Francomano, Harry C. Dietz, Reed E. Pyeritz, Ada Hamosh, Deborah A. Meyers, J.C. Schwartz, Maimon M. Cohen, Colleen A. Morris and Mahin Golabi and has published in prestigious journals such as Journal of Bone and Joint Surgery, Human Molecular Genetics and Genomics.

In The Last Decade

Ronald G. Cadle

8 papers receiving 242 citations

Peers

Countries citing papers authored by Ronald G. Cadle

Since Specialization

Citations

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

Fields of papers citing papers by Ronald G. Cadle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ronald G. Cadle. 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 Ronald G. Cadle. The network helps show where Ronald G. Cadle may publish in the future.

Co-authorship network of co-authors of Ronald G. Cadle

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

#	Work	Indexed citations
1	Phakomatosis pigmentovascularis: Implications for severity with special reference to Mongolian spots associated with Sturge–Weber and Klippel–Trenaunay syndromes 2008 ·American Journal of Medical Genetics Part A ·Bryan D. Hall, Ronald G. Cadle, (unknown), Carolyn Bay	4
2	Phakomatosis pigmentovascularis: Implications for severity with special reference to Mongolian spots associated with Sturge–Weber and Klippel–Trenaunay syndromes 2007 ·American Journal of Medical Genetics Part A ·Bryan D. Hall, Ronald G. Cadle, (unknown), Carolyn Bay	18
3	X-linked mental retardation with variable stature, head circumference, and testicular volume linked to Xq12-q21 1999 ·American Journal of Medical Genetics ·Fatima Abidi, Bryan D. Hall, Ronald G. Cadle, Gerald L. Feldman, Herbert A. Lubs, (unknown), J. Fernando Arena, Roger E. Stevenson, Charles E. Schwartz	13
4	Renpenning syndrome evidence for pericentric location of the gene in two families, including the original Renpenning family 1994 ·American Journal of Medical Genetics Part A ·C. Schwartz, (unknown), Alice Gibson, Ronald G. Cadle, J. Fernando Arena, (unknown), Brad Hall, (unknown), Roger E. Stevenson	3
5	Substitution of a cysteine residue in a non-calcium binding, EGF-like domain of fibrillin segregates with the Marfan syndrome in a large kindred 1994 ·Human Molecular Genetics ·Linda Piersall, Harry C. Dietz, Bryan D. Hall, Ronald G. Cadle, Reed E. Pyeritz, Clair A. Francomano, Iain McIntosh	9
6	Beare‐Stevenson cutis gyrata syndrome 1992 ·American Journal of Medical Genetics ·Bryan D. Hall, Ronald G. Cadle, Mahin Golabi, Colleen A. Morris, Maimon M. Cohen	51
7	The Marfan syndrome locus: Confirmation of assignment to chromosome 15 and identification of tightly linked markers at 15q15-q21.3 1991 ·Genomics ·Harry C. Dietz, Reed E. Pyeritz, Bryan D. Hall, Ronald G. Cadle, Ada Hamosh, J.C. Schwartz, Deborah A. Meyers, Clair A. Francomano	127
8	Tarsal and carpal coalition and symphalangism of the Fuhrmann type. Report of a family. 1985 ·Journal of Bone and Joint Surgery ·(unknown), (unknown), Ronald G. Cadle, Bertil Hall	26

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.

Explore authors with similar magnitude of impact