C. E. Blank
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
Papers in
- Genetics 21
- Genomic variations and chromosomal abnormalities 11
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Dermatoglyphics and Human Traits 3
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- Sexual Differentiation and Disorders 3
- Co-authors
- C. J. Dewhurst (5 shared papers)R.R. Gordon (2 shared papers)John Lorber (2 shared papers)A. M. Potter (2 shared papers)C. E. Ford (1 shared paper)E.P. Evans (1 shared paper)R.S.K. Chaganti (1 shared paper)Paul R. Heath (1 shared paper)
- Journals
- Journal of Medical Genetics (11 papers)The Lancet (6 papers)Clinical Genetics (4 papers)Annals of Human Genetics (3 papers)Human Genetics (2 papers)
- Partner nations
- United KingdomIndiaUnited States
In The Last Decade
C. E. Blank
38 papers receiving 999 citations
Peers
Comparison fields: 5 of 85
- Developmental Biology 74
- Genetics 763
- Pediatrics, Perinatology and Child Health 253
- Reproductive Medicine 74
- Molecular Biology 438
Countries citing papers authored by C. E. Blank
This map shows the geographic impact of C. E. Blank'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 C. E. Blank with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. E. Blank more than expected).
Fields of papers citing papers by C. E. Blank
This network shows the impact of papers produced by C. E. Blank. 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 C. E. Blank. The network helps show where C. E. Blank may publish in the future.
Co-authors
The 25 scholars most cited alongside C. E. Blank, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 39 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1959 | 240 | |
| 2 | 1978 | 232 | |
| 3 | 1966 | 99 | |
| 4 | 1962 | 54 | |
| 5 | 1962 | 50 | |
| 6 | 1970 | 42 | |
| 7 | 1960 | 37 | |
| 8 | 1978 | 36 | |
| 9 | 1960 | 36 | |
| 10 | 1961 | 28 | |
| 11 | 1975 | 25 | |
| 12 | 1963 | 23 | |
| 13 | 1992 | 22 | |
| 14 | 1985 | 21 | |
| 15 | 1987 | 20 | |
| 16 | 1984 | 20 | |
| 17 | 1972 | 18 | |
| 18 | 1966 | 17 | |
| 19 | 1969 | 17 | |
| 20 | 1984 | 16 |
About C. E. Blank
C. E. Blank is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Developmental Biology and Plant Science, having authored 39 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (5 papers), Sexual Differentiation and Disorders (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Congenital limb and hand anomalies (3 papers), Chromosomal and Genetic Variations (3 papers), Dermatoglyphics and Human Traits (3 papers) and Neurological diseases and metabolism (2 papers). The work is most often cited by research in Developmental Biology (74 citations), Genetics (763 citations), Pediatrics, Perinatology and Child Health (253 citations), Reproductive Medicine (74 citations) and Molecular Biology (438 citations). C. E. Blank has collaborated with scholars based in United Kingdom, India and United States. Frequent co-authors include C. J. Dewhurst, R.R. Gordon, John Lorber, A. M. Potter, C. E. Ford, E.P. Evans, R.S.K. Chaganti, Paul R. Heath, Barbara A. Smith and Diana Curtis. Their work appears in journals such as Journal of Medical Genetics, The Lancet, Clinical Genetics, Annals of Human Genetics 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.