C. E. Blank
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Genetics top 5%
- 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
- Congenital Ear and Nasal Anomalies 2
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- Prenatal Screening and Diagnostics 5
- Co-authors
- C. J. Dewhurst (5 shared papers)R.R. Gordon (2 shared papers)John Lorber (2 shared papers)Anthony M. Potter (2 shared papers)E.P. Evans (1 shared paper)Diana Curtis (4 shared papers)R.S.K. Chaganti (1 shared paper)Charles Edmund Ford (1 shared paper)
- Journals
- Journal of Medical Genetics (11 papers)The Lancet (7 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 1.0k citations
Peers
Comparison fields: 5 of 86
- Developmental Biology 75
- Genetics 779
- Pediatrics, Perinatology and Child Health 256
- Reproductive Medicine 74
- Molecular Biology 440
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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1959 | 247 | |
| 2 | 1978 | 234 | |
| 3 | 1966 | 98 | |
| 4 | 1962 | 55 | |
| 5 | 1962 | 52 | |
| 6 | 1970 | 41 | |
| 7 | 1960 | 37 | |
| 8 | 1978 | 36 | |
| 9 | 1960 | 36 | |
| 10 | 1961 | 28 | |
| 11 | 1992 | 27 | |
| 12 | 1975 | 26 | |
| 13 | 1963 | 23 | |
| 14 | 1985 | 22 | |
| 15 | 1987 | 22 | |
| 16 | 1984 | 21 | |
| 17 | 1972 | 18 | |
| 18 | 1966 | 17 | |
| 19 | 1969 | 17 | |
| 20 | 1984 | 17 |
About C. E. Blank
C. E. Blank is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Developmental Biology, Molecular Biology and Neurology, having authored 40 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), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Sexual Differentiation and Disorders (3 papers), Dermatoglyphics and Human Traits (3 papers), Congenital limb and hand anomalies (3 papers), Chromosomal and Genetic Variations (3 papers) and Congenital Ear and Nasal Anomalies (2 papers). The work is most often cited by research in Developmental Biology (75 citations), Genetics (779 citations), Pediatrics, Perinatology and Child Health (256 citations), Reproductive Medicine (74 citations) and Molecular Biology (440 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, Anthony M. Potter, E.P. Evans, Diana Curtis, R.S.K. Chaganti, Charles Edmund Ford, Paul Roy Heath and Beatrice L. Griffiths. 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.