Sara Kaffe
Impact in
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- Prenatal Screening and Diagnostics
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Connective tissue disorders research
Papers in
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- Prenatal Screening and Diagnostics 15
- Fetal and Pediatric Neurological Disorders 2
- Pediatric Urology and Nephrology Studies 2
- Genetics 18
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 4
- Co-authors
- Kurt Hirschhorn (16 shared papers)Lillian Y. F. Hsu (9 shared papers)Theresa E. Perlis (3 shared papers)Philip D. Cotter (2 shared papers)Darwin J. Prockop (1 shared paper)Leslie D. McCurdy (1 shared paper)Judith P. Willner (1 shared paper)Lynn Godmilow (3 shared papers)
- Journals
- Prenatal Diagnosis (6 papers)Journal of Medical Genetics (4 papers)Clinical Genetics (3 papers)The Lancet (2 papers)Human Genetics (1 paper)
- Partner nations
- United StatesIsraelFinland
In The Last Decade
Sara Kaffe
30 papers receiving 781 citations
Peers
Comparison fields: 5 of 62
- Pediatrics, Perinatology and Child Health 451
- Genetics 595
- Developmental Biology 21
- Genetics 50
- Urology 24
Countries citing papers authored by Sara Kaffe
This map shows the geographic impact of Sara Kaffe'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 Sara Kaffe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sara Kaffe more than expected).
Fields of papers citing papers by Sara Kaffe
This network shows the impact of papers produced by Sara Kaffe. 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 Sara Kaffe. The network helps show where Sara Kaffe may publish in the future.
Co-authors
The 25 scholars most cited alongside Sara Kaffe, 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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 135 | |
| 2 | 1997 | 93 | |
| 3 | 1991 | 89 | |
| 4 | 1984 | 65 | |
| 5 | 1998 | 59 | |
| 6 | 2003 | 55 | |
| 7 | 1987 | 52 | |
| 8 | 2001 | 38 | |
| 9 | 1977 | 36 | |
| 10 | 1982 | 33 | |
| 11 | 1977 | 31 | |
| 12 | 1994 | 30 | |
| 13 | Prenatal diagnosis of bilateral renal agenesis. | 1977 | 28 |
| 14 | 1984 | 28 | |
| 15 | 1978 | 22 | |
| 16 | Variable cell-mediated immune defects in a family with `Candida endocrinopathy syndrome' | 1975 | 21 |
| 17 | 1978 | 18 | |
| 18 | 1974 | 16 | |
| 19 | 1988 | 14 | |
| 20 | 1974 | 10 |
About Sara Kaffe
Sara Kaffe is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Surgery, Molecular Biology and Cancer Research, having authored 32 papers that have together received 918 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (12 papers), Congenital Anomalies and Fetal Surgery (5 papers), Genetic Syndromes and Imprinting (4 papers), Chromosomal and Genetic Variations (3 papers), Immunodeficiency and Autoimmune Disorders (2 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Pediatric Urology and Nephrology Studies (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (451 citations), Genetics (595 citations), Developmental Biology (21 citations), Genetics (50 citations) and Urology (24 citations). Sara Kaffe has collaborated with scholars based in United States, Israel and Finland. Frequent co-authors include Kurt Hirschhorn, Lillian Y. F. Hsu, Theresa E. Perlis, Philip D. Cotter, Darwin J. Prockop, Leslie D. McCurdy, Judith P. Willner, Lynn Godmilow, Teresa M. Dunn and Nataline B. Kardon. Their work appears in journals such as Prenatal Diagnosis, Journal of Medical Genetics, Clinical Genetics, The Lancet 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.