Marcia Schwartz
- Co-authors
- William SoferHans JörnvallRobert J. DesnickStuart SchwartzMaimon M. CohenRichard M. CantorMartin E. GoldmanK. Lund Ayaz
- Topics
- Genomic variations and chromosomal abnormalities (8 papers)Chromosomal and Genetic Variations (5 papers)Prenatal Screening and Diagnostics (3 papers)
- Partner nations
- United StatesDenmarkSweden
In The Last Decade
Marcia Schwartz
24 papers receiving 682 citations
Peers
Comparison fields: 5 of 75
- Molecular Biology 283
- Genetics 188
- Physiology 181
- Epidemiology 95
- Pediatrics, Perinatology and Child Health 90
Countries citing papers authored by Marcia Schwartz
This map shows the geographic impact of Marcia Schwartz'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 Marcia Schwartz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marcia Schwartz more than expected).
Fields of papers citing papers by Marcia Schwartz
This network shows the impact of papers produced by Marcia Schwartz. 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 Marcia Schwartz. The network helps show where Marcia Schwartz may publish in the future.
Co-authorship network of co-authors of Marcia Schwartz
This figure shows the co-authorship network connecting the top 25 collaborators of Marcia Schwartz. A scholar is included among the top collaborators of Marcia Schwartz based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marcia Schwartz. Marcia Schwartz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 17 | |
| 2 | 45 | |
| 3 | [Adrenogenital syndrome--molecular biology and prenatal diagnosis]. | 1 |
| 4 | 7 | |
| 5 | 1 | |
| 6 | 24 | |
| 7 | 14 | |
| 8 | 2 | |
| 9 | 44 | |
| 10 | 21 | |
| 11 | 25 | |
| 12 | 15 | |
| 13 | 11 | |
| 14 | 79 | |
| 15 | Inherited X-chromosome inverted tandem duplication in a male traced to a grandparental mitotic error. | 26 |
| 16 | 2 | |
| 17 | 26 | |
| 18 | 2 | |
| 19 | 62 | |
| 20 | 47 |
About Marcia Schwartz
Marcia Schwartz is a scholar working on Genetics, Hematology and Cellular and Molecular Neuroscience, having authored 24 papers that have together received 718 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (5 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Clinical Biochemistry (53 citations), Physiology (181 citations) and Genetics (188 citations). Marcia Schwartz has collaborated with scholars based in United States, Denmark and Sweden. Frequent co-authors include William Sofer, Hans Jörnvall, Robert J. Desnick, Stuart Schwartz, Maimon M. Cohen, Richard M. Cantor, Martin E. Goldman, K. Lund Ayaz, William Krivit and Margaret M. McGovern. Their work appears in journals such as Nature, New England Journal of Medicine and Journal of the American College of Cardiology.
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.