F Char
- Genetics top 10%
- Connective tissue disorders research 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
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- Tracheal and airway disorders 3
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- Metabolism and Genetic Disorders 4
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- Protein Tyrosine Phosphatases 4
- RNA modifications and cancer 4
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- Congenital Heart Disease Studies 3
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- Sperm and Testicular Function 3
F Char
28 papers receiving 451 citations
Peers
Comparison fields: 5 of 67
- Genetics 215
- Developmental Biology 13
- Cardiology and Cardiovascular Medicine 107
- Pulmonary and Respiratory Medicine 152
- Pediatrics, Perinatology and Child Health 77
Countries citing papers authored by F Char
This map shows the geographic impact of F Char'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 F Char with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F Char more than expected).
Fields of papers citing papers by F Char
This network shows the impact of papers produced by F Char. 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 F Char. The network helps show where F Char may publish in the future.
Co-authorship network
The 25 scholars most cited alongside F Char, 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 | Chromosome 13 long arm interstitial deletion associated with features of Noonan phenotype. | 1987 | 10 |
| 2 | 1987 | 107 | |
| 3 | 1985 | 18 | |
| 4 | A photographic study: the natural history of Prader-Willi syndrome. | 1984 | 3 |
| 5 | 1980 | 5 | |
| 6 | Problems in counseling the epileptic mother. | 1979 | 2 |
| 7 | 1978 | 10 | |
| 8 | Possible etiologic mechanisms of the short stature in the Noonan syndrome. | 1976 | 11 |
| 9 | Abdominal aortic aneurysmectomy in a 17-year-old patient with Ehlers-Danlos syndrome: case report and review of the literature. | 1973 | 39 |
| 10 | 1972 | 43 | |
| 11 | The otopalatodigital (OPD) syndrome: (conductive deafness, cleft palate and anomaly of digits). | 1971 | 2 |
| 12 | A prospectus on the prevention of aortic rupture in the Marfan syndrome with data on survivorship without treatment. | 1971 | 65 |
| 13 | 1971 | 3 | |
| 14 | Frontonasal dysplasia with cutis aplasia congenita. | 1971 | 3 |
| 15 | Cleft lip/palate in the Waardenburg syndrome. | 1971 | 2 |
| 16 | 1970 | 5 | |
| 17 | 1970 | 29 | |
| 18 | Congenital coronary artery fistula. Communication of the left coronary artery with the left atrium. | 1966 | 2 |
| 19 | 1959 | 20 | |
| 20 | 1958 | 33 |
About F Char
F Char is a scholar working on Clinical Biochemistry, Developmental Biology, Genetics, Reproductive Medicine and Pulmonary and Respiratory Medicine, having authored 28 papers that have together received 492 indexed citations. Recurring topics across this work include Connective tissue disorders research (5 papers), Metabolism and Genetic Disorders (4 papers), Protein Tyrosine Phosphatases (4 papers), RNA modifications and cancer (4 papers), Congenital Heart Disease Studies (3 papers), Sperm and Testicular Function (3 papers), Tracheal and airway disorders (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). The work is most often cited by research in Genetics (215 citations), Developmental Biology (13 citations), Cardiology and Cardiovascular Medicine (107 citations), Pulmonary and Respiratory Medicine (152 citations) and Pediatrics, Perinatology and Child Health (77 citations). F Char has collaborated with scholars based in United States and China. Frequent co-authors include William B. Horton, McKusick Va, Paul Adams, Emilie H. Mules, Ray C. Anderson, G. Doyne Williams, Digamber S. Borgaonkar, John C. Carey, Glenn V. Dalrymple and Susanne M. Gollin. Their work appears in journals such as Clinical Genetics, JAMA, Journal of Pediatric Ophthalmology & Strabismus, The Annals of Thoracic Surgery and The Lancet.
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.