Rina Schmidt
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 13
- Genomic variations and chromosomal abnormalities 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genetic Syndromes and Imprinting 2
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- Hedgehog Signaling Pathway Studies 2
- Co-authors
- Arthur Falek (2 shared papers)George A. Jervis (2 shared papers)Harold M. Nitowsky (6 shared papers)Hanna Dar (6 shared papers)Ichiro Sekine (1 shared paper)Marty Kwok‐Shing Wong (1 shared paper)Lydia Eviatar (1 shared paper)M Rosenblatt (2 shared papers)
- Journals
- Journal of Medical Genetics (6 papers)Pediatric Research (2 papers)Clinical Genetics (2 papers)PEDIATRICS (2 papers)JAMA (1 paper)
- Partner nations
- United StatesIsraelUnited Kingdom
In The Last Decade
Rina Schmidt
18 papers receiving 391 citations
Peers
Comparison fields: 5 of 58
- Developmental Biology 39
- Genetics 257
- Pediatrics, Perinatology and Child Health 109
- Genetics 32
- Anatomy 4
Countries citing papers authored by Rina Schmidt
This map shows the geographic impact of Rina Schmidt'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 Rina Schmidt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rina Schmidt more than expected).
Fields of papers citing papers by Rina Schmidt
This network shows the impact of papers produced by Rina Schmidt. 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 Rina Schmidt. The network helps show where Rina Schmidt may publish in the future.
Co-authors
The 25 scholars most cited alongside Rina Schmidt, 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 | Familial de Lange syndrome with chromosome abnormalities. | 1966 | 80 |
| 2 | 1966 | 72 | |
| 3 | 1981 | 35 | |
| 4 | 1975 | 35 | |
| 5 | 1977 | 34 | |
| 6 | 1978 | 28 | |
| 7 | 1976 | 27 | |
| 8 | 1987 | 22 | |
| 9 | 1976 | 21 | |
| 10 | 1999 | 13 | |
| 11 | 1978 | 12 | |
| 12 | 1981 | 11 | |
| 13 | 1977 | 11 | |
| 14 | 1972 | 10 | |
| 15 | 1972 | 9 | |
| 16 | 1976 | 8 | |
| 17 | 1966 | 1 | |
| 18 | 1974 | 1 | |
| 19 | [THE MUSCULI LUMBRICALES OF THE HUMAN FOOT]. | 1963 | 0 |
| 20 | 1984 | 0 |
About Rina Schmidt
Rina Schmidt is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Developmental Biology and Oncology, having authored 20 papers that have together received 430 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Congenital limb and hand anomalies (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Hedgehog Signaling Pathway Studies (2 papers), Chromosomal and Genetic Variations (2 papers), Genetic Syndromes and Imprinting (2 papers) and Cancer-related Molecular Pathways (2 papers). The work is most often cited by research in Developmental Biology (39 citations), Genetics (257 citations), Pediatrics, Perinatology and Child Health (109 citations), Genetics (32 citations) and Anatomy (4 citations). Rina Schmidt has collaborated with scholars based in United States, Israel and United Kingdom. Frequent co-authors include Arthur Falek, George A. Jervis, Harold M. Nitowsky, Hanna Dar, Ichiro Sekine, Marty Kwok‐Shing Wong, Lydia Eviatar, M Rosenblatt, M Pajewski and Gerald S. Golden. Their work appears in journals such as Journal of Medical Genetics, Pediatric Research, Clinical Genetics, PEDIATRICS and JAMA.
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.