Stuart Schwartz
Impact in
- Genetics top 0.05%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 122
- Genomic variations and chromosomal abnormalities 100
- Genetic Syndromes and Imprinting 30
- Genetics and Neurodevelopmental Disorders 11
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- Genomics and Chromatin Dynamics 21
- Congenital heart defects research 12
- DNA Repair Mechanisms 9
- Co-authors
- Suzanne B. Cassidy (16 shared papers)Evan E. Eichler (13 shared papers)Daniel J. Driscoll (6 shared papers)Jennifer Miller (2 shared papers)Robert D. Nicholls (9 shared papers)Jeffrey A. Bailey (3 shared papers)Royden A. Clark (3 shared papers)Rhea U. Vallente (3 shared papers)
- Journals
- Prenatal Diagnosis (13 papers)The American Journal of Human Genetics (12 papers)Genetics in Medicine (8 papers)Human Genetics (6 papers)Genomics (4 papers)
- Partner nations
- United StatesCanadaGermany
In The Last Decade
Stuart Schwartz
192 papers receiving 11.1k citations
Stuart Schwartz's Hit Papers
Peers
Comparison fields: 5 of 155
- Genetics 7.4k
- Pediatrics, Perinatology and Child Health 2.0k
- Molecular Biology 5.3k
- Plant Science 2.5k
- Cancer Research 622
Countries citing papers authored by Stuart Schwartz
This map shows the geographic impact of Stuart 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 Stuart Schwartz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stuart Schwartz more than expected).
Fields of papers citing papers by Stuart Schwartz
This network shows the impact of papers produced by Stuart 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 Stuart Schwartz. The network helps show where Stuart Schwartz may publish in the future.
Co-authors
The 25 scholars most cited alongside Stuart 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 200 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Prader-Willi syndrome Hit paper breakdown → | 2012 | 1077 |
| 2 | Recent Segmental Duplications in the Human Genome Hit paper breakdown → | 2002 | 1004 |
| 3 | Segmental Duplications and Copy-Number Variation in the Human Genome Hit paper breakdown → | 2005 | 736 |
| 4 | 1995 | 491 | |
| 5 | 1999 | 473 | |
| 6 | 2006 | 453 | |
| 7 | 2001 | 339 | |
| 8 | 1997 | 300 | |
| 9 | 2006 | 240 | |
| 10 | 2002 | 234 | |
| 11 | 2000 | 220 | |
| 12 | 1999 | 216 | |
| 13 | CWR22: the first human prostate cancer xenograft with strongly androgen-dependent and relapsed strains both in vivo and in soft agar. | 1996 | 212 |
| 14 | CWR22: androgen-dependent xenograft model derived from a primary human prostatic carcinoma. | 1994 | 198 |
| 15 | 1995 | 196 | |
| 16 | 2011 | 190 | |
| 17 | 1997 | 183 | |
| 18 | 2004 | 160 | |
| 19 | 1998 | 139 | |
| 20 | 2002 | 134 |
About Stuart Schwartz
Stuart Schwartz is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 200 papers that have together received 11.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (100 papers), Prenatal Screening and Diagnostics (61 papers), Chromosomal and Genetic Variations (56 papers), Genetic Syndromes and Imprinting (30 papers), Genomics and Chromatin Dynamics (21 papers), Congenital heart defects research (12 papers), Genetics and Neurodevelopmental Disorders (11 papers) and DNA Repair Mechanisms (9 papers). The work is most often cited by research in Genetics (7.4k citations), Pediatrics, Perinatology and Child Health (2.0k citations), Molecular Biology (5.3k citations), Plant Science (2.5k citations) and Cancer Research (622 citations). Stuart Schwartz has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include Suzanne B. Cassidy, Evan E. Eichler, Daniel J. Driscoll, Jennifer Miller, Robert D. Nicholls, Jeffrey A. Bailey, Royden A. Clark, Rhea U. Vallente, Beth A. Sullivan and Shauna Heeger. Their work appears in journals such as Prenatal Diagnosis, The American Journal of Human Genetics, Genetics in Medicine, Human Genetics and Genomics.
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.