Richard C. Juberg
- Developmental Biology top 10%
- Congenital limb and hand anomalies 5
- Genetics top 10%
- Genomic variations and chromosomal abnormalities 12
- Dermatoglyphics and Human Traits 4
- Genetic Syndromes and Imprinting 3
-
- Prenatal Screening and Diagnostics 11
- Assisted Reproductive Technology and Twin Pregnancy 4
- Anatomy top 5%
-
- Urological Disorders and Treatments 4
-
- Chromosomal and Genetic Variations 4
- Co-authors
- Philip N. MowreyJames R. HaywardRichard E. StallardJuan J. GershanikAlison JonesEnid F. GilbertCarlos F. GonzalezKeith S. Henley
- Journals
- Journal of Medical Genetics (5 papers)The Journal of Pediatrics (4 papers)PEDIATRICS (4 papers)
- Partner nations
- United StatesUnited Kingdom
In The Last Decade
Richard C. Juberg
43 papers receiving 563 citations
Peers
Comparison fields: 5 of 78
- Developmental Biology 29
- Genetics 335
- Pediatrics, Perinatology and Child Health 198
- Anatomy 7
- Urology 22
Countries citing papers authored by Richard C. Juberg
This map shows the geographic impact of Richard C. Juberg'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 Richard C. Juberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Richard C. Juberg more than expected).
Fields of papers citing papers by Richard C. Juberg
This network shows the impact of papers produced by Richard C. Juberg. 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 Richard C. Juberg. The network helps show where Richard C. Juberg may publish in the future.
Co-authorship network
The 22 scholars most cited alongside Richard C. Juberg, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 1 | |
| 2 | 1990 | 7 | |
| 3 | 1989 | 4 | |
| 4 | 1987 | 6 | |
| 5 | 1984 | 7 | |
| 6 | 1983 | 73 | |
| 7 | 1983 | 16 | |
| 8 | 1981 | 19 | |
| 9 | A new form of X-linked mental retardation with growth retardation, deafness, and microgenitalism. | 1980 | 26 |
| 10 | Familial occurrence of Wilms' tumor: nephroblastoma in one of monozygous twins and in another sibling. | 1975 | 21 |
| 11 | 1973 | 7 | |
| 12 | Making the family history relevant. | 1972 | 1 |
| 13 | 1971 | 57 | |
| 14 | Blood group gene frequencies in an Amish deme of Northern Indiana: comparison with other Amish demes. | 1971 | 5 |
| 15 | Consanguineous marriages in West Virginia. | 1970 | 1 |
| 16 | 1970 | 10 | |
| 17 | 1969 | 31 | |
| 18 | 1969 | 15 | |
| 19 | 1966 | 43 | |
| 20 | 1966 | 3 |
About Richard C. Juberg
Richard C. Juberg is a scholar working on Developmental Biology, Genetics, Anatomy, Urology and Pediatrics, Perinatology and Child Health, having authored 45 papers that have together received 617 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (11 papers), Congenital limb and hand anomalies (5 papers), Dermatoglyphics and Human Traits (4 papers), Assisted Reproductive Technology and Twin Pregnancy (4 papers), Urological Disorders and Treatments (4 papers), Chromosomal and Genetic Variations (4 papers) and Genetic Syndromes and Imprinting (3 papers). The work is most often cited by research in Developmental Biology (29 citations), Genetics (335 citations), Pediatrics, Perinatology and Child Health (198 citations), Anatomy (7 citations) and Urology (22 citations). Richard C. Juberg has collaborated with scholars based in United States and United Kingdom. Frequent co-authors include Philip N. Mowrey, James R. Hayward, Richard E. Stallard, Juan J. Gershanik, Alison Jones, Enid F. Gilbert, Carlos F. Gonzalez, Keith S. Henley, H. Warner Kloepfer and Harold A. Oberman. Their work appears in journals such as Journal of Medical Genetics, The Journal of Pediatrics, PEDIATRICS, American Journal of Physical Anthropology and Human Genetics.
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.