Robin Schwartz
Impact in
- Genetics top 5%
- Connective tissue disorders research
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Dermatological and Skeletal Disorders
- Immunology and Allergy top 10%
- Cell Adhesion Molecules Research
Papers in
- Genetics 14
- Connective tissue disorders research 7
- Genomic variations and chromosomal abnormalities 4
- BRCA gene mutations in cancer 3
- Dermatological and Skeletal Disorders 2
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- RNA Research and Splicing 2
- Co-authors
- Petros Tsipouras (12 shared papers)Peter H. Byers (2 shared papers)B J Starman (1 shared paper)Jeffrey Bonadio (1 shared paper)Francesco Ramirez (5 shared papers)Dominique Weil (2 shared papers)Talia Donenberg (1 shared paper)Karina L. Brierley (1 shared paper)
- Journals
- Journal of Medical Genetics (2 papers)Human Genetics (2 papers)Cytogenetic and Genome Research (2 papers)Genomics (2 papers)Current Opinion in Pediatrics (1 paper)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Robin Schwartz
22 papers receiving 530 citations
Peers
Comparison fields: 5 of 73
- Genetics 379
- Immunology and Allergy 46
- Rheumatology 109
- Cancer Research 48
- Molecular Biology 188
Countries citing papers authored by Robin Schwartz
This map shows the geographic impact of Robin 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 Robin Schwartz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robin Schwartz more than expected).
Fields of papers citing papers by Robin Schwartz
This network shows the impact of papers produced by Robin 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 Robin Schwartz. The network helps show where Robin Schwartz may publish in the future.
Co-authors
The 25 scholars most cited alongside Robin Schwartz, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Perinatal lethal osteogenesis imperfecta (OI type II): a biochemically heterogeneous disorder usually due to new mutations in the genes for type I collagen. | 1988 | 181 |
| 2 | Errors in delivery of cancer genetics services: implications for practice. | 2010 | 79 |
| 3 | 1986 | 56 | |
| 4 | 1989 | 40 | |
| 5 | 2000 | 33 | |
| 6 | Use of molecular haplotypes specific for the human pro alpha 2(I) collagen gene in linkage analysis of the mild autosomal dominant forms of osteogenesis imperfecta. | 1986 | 33 |
| 7 | 1990 | 19 | |
| 8 | 1988 | 18 | |
| 9 | 2011 | 16 | |
| 10 | 1984 | 14 | |
| 11 | 1987 | 10 | |
| 12 | 1988 | 9 | |
| 13 | 1981 | 9 | |
| 14 | 1989 | 8 | |
| 15 | 1978 | 8 | |
| 16 | 1990 | 6 | |
| 17 | 1988 | 3 | |
| 18 | 1993 | 3 | |
| 19 | Mild osteogenesis imperfecta is not always associated with defects in type i collagen and it is not always inherited as a dominant trait | 1988 | 3 |
| 20 | 2008 | 2 |
About Robin Schwartz
Robin Schwartz is a scholar working on Genetics, Molecular Biology, Oncology, Immunology and Allergy and Genetics, having authored 23 papers that have together received 553 indexed citations. Recurring topics across this work include Connective tissue disorders research (7 papers), Cell Adhesion Molecules Research (4 papers), Genomic variations and chromosomal abnormalities (4 papers), BRCA gene mutations in cancer (3 papers), RNA Research and Splicing (2 papers), Dermatological and Skeletal Disorders (2 papers), Bone health and treatments (2 papers) and Bone and Dental Protein Studies (2 papers). The work is most often cited by research in Genetics (379 citations), Immunology and Allergy (46 citations), Rheumatology (109 citations), Cancer Research (48 citations) and Molecular Biology (188 citations). Robin Schwartz has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Petros Tsipouras, Peter H. Byers, B J Starman, Jeffrey Bonadio, Francesco Ramirez, Dominique Weil, Talia Donenberg, Karina L. Brierley, Kristen M. Shannon and Ellen Matloff. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, Cytogenetic and Genome Research, Genomics and Current Opinion in Pediatrics.
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.