K. Fried
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 30
- Genomic variations and chromosomal abnormalities 13
- Genomics and Rare Diseases 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
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- Metabolism and Genetic Disorders 4
- Co-authors
- G Mundel (10 shared papers)Sarit Kaufman (2 shared papers)Yehuda Matoth (1 shared paper)Alan E H Emery (1 shared paper)Nelly Zilber (1 shared paper)Amos D. Korczyn (1 shared paper)Milton Alter (1 shared paper)Esther Kahana (1 shared paper)
- Journals
- Clinical Genetics (21 papers)Journal of Medical Genetics (14 papers)Human Heredity (4 papers)Journal of Intellectual Disability Research (2 papers)The Lancet (1 paper)
- Partner nations
- IsraelUnited KingdomUnited States
In The Last Decade
K. Fried
55 papers receiving 784 citations
Peers
Comparison fields: 5 of 59
- Developmental Biology 63
- Genetics 350
- Pediatrics, Perinatology and Child Health 104
- Genetics 69
- Clinical Biochemistry 29
Countries citing papers authored by K. Fried
This map shows the geographic impact of K. Fried'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 K. Fried with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K. Fried more than expected).
Fields of papers citing papers by K. Fried
This network shows the impact of papers produced by K. Fried. 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 K. Fried. The network helps show where K. Fried may publish in the future.
Co-authors
The 25 scholars most cited alongside K. Fried, 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 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1984 | 71 | |
| 2 | 1972 | 61 | |
| 3 | Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim. | 1977 | 54 |
| 4 | 1971 | 50 | |
| 5 | Chronic Gaucher's disease; clinical observations on 34 patients. | 1965 | 40 |
| 6 | 1975 | 40 | |
| 7 | 1980 | 40 | |
| 8 | 1971 | 34 | |
| 9 | 1972 | 32 | |
| 10 | 1977 | 27 | |
| 11 | Some effects on the offspring of uncle-niece marriage in the Moroccan Jewish community in Jerusalem. | 1974 | 24 |
| 12 | 1975 | 21 | |
| 13 | 1981 | 21 | |
| 14 | 1973 | 19 | |
| 15 | 1978 | 19 | |
| 16 | 1993 | 19 | |
| 17 | 1970 | 18 | |
| 18 | 1980 | 18 | |
| 19 | 1977 | 17 | |
| 20 | 1962 | 16 |
About K. Fried
K. Fried is a scholar working on Genetics, Clinical Biochemistry, Developmental Biology, Pediatrics, Perinatology and Child Health and Genetics, having authored 57 papers that have together received 905 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Lysosomal Storage Disorders Research (5 papers), Genomics and Rare Diseases (4 papers), Metabolism and Genetic Disorders (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Down syndrome and intellectual disability research (3 papers), Genetic Neurodegenerative Diseases (3 papers) and Genetic factors in colorectal cancer (3 papers). The work is most often cited by research in Developmental Biology (63 citations), Genetics (350 citations), Pediatrics, Perinatology and Child Health (104 citations), Genetics (69 citations) and Clinical Biochemistry (29 citations). K. Fried has collaborated with scholars based in Israel, United Kingdom and United States. Frequent co-authors include G Mundel, Sarit Kaufman, Yehuda Matoth, Alan E H Emery, Nelly Zilber, Amos D. Korczyn, Milton Alter, Esther Kahana, Rachel Krikler and A.M. Davies. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, Human Heredity, Journal of Intellectual Disability Research 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.