Rina Schmidt
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Dermatoglyphics and Human Traits
Papers in
- Genetics 13
- Genomic variations and chromosomal abnormalities 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- 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)Hanna Dar (6 shared papers)Harold M. Nitowsky (6 shared papers)Ichiro Sekine (1 shared paper)M Pajewski (2 shared papers)M Rosenblatt (2 shared papers)Lydia Eviatar (1 shared paper)
- Journals
- Journal of Medical Genetics (6 papers)Pediatric Research (2 papers)PEDIATRICS (2 papers)Clinical Genetics (2 papers)American Journal of Obstetrics and Gynecology (1 paper)
- Partner nations
- United StatesIsraelDenmark
In The Last Decade
Rina Schmidt
18 papers receiving 405 citations
Peers
Comparison fields: 5 of 57
- Developmental Biology 40
- Genetics 263
- Pediatrics, Perinatology and Child Health 111
- Genetics 34
- Hematology 31
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 | 82 |
| 2 | 1966 | 77 | |
| 3 | 1981 | 36 | |
| 4 | 1975 | 36 | |
| 5 | 1977 | 35 | |
| 6 | 1976 | 30 | |
| 7 | 1978 | 29 | |
| 8 | 1999 | 28 | |
| 9 | 1976 | 24 | |
| 10 | 1987 | 22 | |
| 11 | 1978 | 13 | |
| 12 | 1981 | 12 | |
| 13 | 1977 | 11 | |
| 14 | 1972 | 10 | |
| 15 | 1972 | 9 | |
| 16 | 1976 | 8 | |
| 17 | 1966 | 1 | |
| 18 | 1974 | 1 | |
| 19 | 1984 | 0 | |
| 20 | [THE MUSCULI LUMBRICALES OF THE HUMAN FOOT]. | 1963 | 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 464 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (5 papers), Congenital limb and hand anomalies (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Cancer-related Molecular Pathways (2 papers), Hedgehog Signaling Pathway Studies (2 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Developmental Biology (40 citations), Genetics (263 citations), Pediatrics, Perinatology and Child Health (111 citations), Genetics (34 citations) and Hematology (31 citations). Rina Schmidt has collaborated with scholars based in United States, Israel and Denmark. Frequent co-authors include Arthur Falek, George A. Jervis, Hanna Dar, Harold M. Nitowsky, Ichiro Sekine, M Pajewski, M Rosenblatt, Lydia Eviatar, Marty Kwok‐Shing Wong and F H Allen. Their work appears in journals such as Journal of Medical Genetics, Pediatric Research, PEDIATRICS, Clinical Genetics and American Journal of Obstetrics and Gynecology.
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.