Stuart Schwartz

17.7k total citations · 3 hit papers
197 papers, 11.0k citations indexed

About

Stuart Schwartz is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Stuart Schwartz has authored 197 papers receiving a total of 11.0k indexed citations (citations by other indexed papers that have themselves been cited), including 124 papers in Genetics, 77 papers in Molecular Biology and 63 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Stuart Schwartz's work include Genomic variations and chromosomal abnormalities (102 papers), Prenatal Screening and Diagnostics (63 papers) and Chromosomal and Genetic Variations (59 papers). Stuart Schwartz is often cited by papers focused on Genomic variations and chromosomal abnormalities (102 papers), Prenatal Screening and Diagnostics (63 papers) and Chromosomal and Genetic Variations (59 papers). Stuart Schwartz collaborates with scholars based in United States, Canada and Italy. Stuart Schwartz's 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 Donna G. Albertson and has published in prestigious journals such as Nature, Science and Nature Genetics.

In The Last Decade

Stuart Schwartz

191 papers receiving 10.6k citations

Hit Papers

Prader-Willi syndrome 2002 2026 2010 2018 2012 2002 2005 250 500 750 1000
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Prader-Willi syndrome
    2012 1.0k citations Stuart Schwartz et al. Genetics in Medicine profile →
  2. Recent Segmental Duplications in the Human Genome
    2002 958 citations Jeffrey A. Bailey, Rhea U. Vallente et al. profile →
  3. Segmental Duplications and Copy-Number Variation in the Human Genome
    2005 678 citations Devin P. Locke, Jeffrey A. Bailey et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Stuart Schwartz United States 49 7.3k 5.7k 2.7k 2.3k 706 197 11.0k
Paweł Stankiewicz United States 50 6.2k 0.9× 5.0k 0.9× 2.2k 0.8× 1.4k 0.6× 676 1.0× 198 9.2k
P. Pearson Netherlands 55 4.7k 0.6× 6.3k 1.1× 1.4k 0.5× 901 0.4× 338 0.5× 209 10.7k
Chad A. Shaw United States 65 5.7k 0.8× 7.7k 1.3× 1.2k 0.5× 1.4k 0.6× 471 0.7× 193 13.9k
Christine M. Distèche United States 67 6.9k 0.9× 10.6k 1.8× 2.3k 0.9× 833 0.4× 375 0.5× 226 17.3k
Douglas R. Higgs United Kingdom 83 5.4k 0.7× 13.1k 2.3× 1.9k 0.7× 2.1k 0.9× 396 0.6× 323 21.4k
Sau Wai Cheung United States 47 5.6k 0.8× 3.8k 0.7× 1.2k 0.5× 2.2k 1.0× 299 0.4× 181 7.9k
Ethylin Wang Jabs United States 58 7.9k 1.1× 8.6k 1.5× 644 0.2× 696 0.3× 660 0.9× 243 14.7k
Norio Niikawa Japan 52 4.9k 0.7× 5.2k 0.9× 672 0.3× 2.1k 0.9× 344 0.5× 306 9.3k
Bernhard Horsthemke Germany 57 6.7k 0.9× 8.2k 1.4× 493 0.2× 3.3k 1.4× 461 0.7× 222 12.9k
Lisenka E.L.M. Vissers Netherlands 39 5.1k 0.7× 3.6k 0.6× 790 0.3× 943 0.4× 638 0.9× 98 7.7k

Countries citing papers authored by Stuart Schwartz

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Stuart Schwartz

This figure shows the co-authorship network connecting the top 25 collaborators of Stuart Schwartz. A scholar is included among the top collaborators of Stuart 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 Stuart Schwartz. Stuart Schwartz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Arreola, Alexandra, Gloria Haskell, Inder Gadi, Andrea Penton, & Stuart Schwartz. (2024). Utilization of a SNP microarray to detect uniparental disomy: Implications and outcomes. Genetics in Medicine. 26(12). 101275–101275.
2.
Haskell, Gloria, Alexandra Arreola, Christine M. Riordan, et al.. (2024). Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes. Prenatal Diagnosis. 44(5). 586–594.
3.
Polonis, Katarzyna, Stuart Schwartz, Christina Grant, et al.. (2023). Uniparental disomy of multiple chromosomes in two cases with a complex phenotype. American Journal of Medical Genetics Part A. 191(7). 1978–1983. 3 indexed citations
4.
5.
Papenhausen, Peter, et al.. (2021). Clinical significance and mechanisms associated with segmental UPD. Molecular Cytogenetics. 14(1). 38–38. 6 indexed citations
6.
Foster, Madison, Dean Fergusson, Justin Presseau, et al.. (2020). Partnering with patients to get better outcomes with chimeric antigen receptor T-cell therapy: towards engagement of patients in early phase trials. Research Involvement and Engagement. 6(1). 61–61. 12 indexed citations
7.
8.
Horvath, Julie E., Cassandra Gulden, Rhea U. Vallente, et al.. (2005). Punctuated duplication seeding events during the evolution of human chromosome 2p11. Genome Research. 15(7). 914–927. 29 indexed citations
9.
Locke, Devin P., Richard Segraves, Robert D. Nicholls, et al.. (2004). BAC microarray analysis of 15q11–q13 rearrangements and the impact of segmental duplications. Journal of Medical Genetics. 41(3). 175–182. 79 indexed citations
10.
Rudd, M. Katharine, Robert W. Mays, Stuart Schwartz, & Huntington F. Willard. (2003). Human Artificial Chromosomes with Alpha Satellite-Based De Novo Centromeres Show Increased Frequency of Nondisjunction and Anaphase Lag. Molecular and Cellular Biology. 23(21). 7689–7697. 49 indexed citations
11.
Bailey, Jeffrey A., Luigi Viggiano, Doriana Misceo, et al.. (2002). Human-Specific Duplication and Mosaic Transcripts: The Recent Paralogous Structure of Chromosome 22. The American Journal of Human Genetics. 70(1). 83–100. 123 indexed citations
12.
Colmenares, Clemencia, Heidi A. Heilstedt, Lisa G. Shaffer, et al.. (2001). Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski−/− mice. Nature Genetics. 30(1). 106–109. 102 indexed citations
13.
Hassold, Terry, Lindsay C. Burrage, E. Ricky Chan, et al.. (2001). Maternal Folate Polymorphisms and the Etiology of Human Nondisjunction. The American Journal of Human Genetics. 69(2). 434–439. 58 indexed citations
14.
Ji, Yonggang, Evan E. Eichler, Stuart Schwartz, & Robert D. Nicholls. (2000). Structure of Chromosomal Duplicons and their Role in Mediating Human Genomic Disorders. Genome Research. 10(5). 597–610. 196 indexed citations
15.
Christ, Laurie A., Carol A. Crowe, Mark A. Micale, Jeffrey M. Conroy, & Stuart Schwartz. (1999). Chromosome Breakage Hotspots and Delineation of the Critical Region for the 9p-Deletion Syndrome. The American Journal of Human Genetics. 65(5). 1387–1395. 74 indexed citations
16.
Eshleman, James R., Graham Casey, W. David Sedwick, et al.. (1998). Chromosome number and structure both are markedly stable in RER colorectal cancers and are not destabilized by mutation of p53. Oncogene. 17(6). 719–725. 106 indexed citations
17.
Schwartz, Stuart. (1991). Human chromosomes: Manual of basic techniques. The American Journal of Human Genetics. 48(1). 172–173. 2 indexed citations
18.
Schwartz, Stuart. (1987). Ataxia-telangiectasia: Genetics, neuropathology, and immunology of a degenerative disease of childhood.. The American Journal of Human Genetics. 41(1). 79–80. 106 indexed citations
19.
Schwartz, Stuart, Catherine G. Palmer, Philip L. H. Yu, Joann A. Boughman, & Maimon M. Cohen. (1986). Analysis of translocations observed in three different populations. Cytogenetic and Genome Research. 42(1-2). 42–52. 2 indexed citations
20.
Schwartz, Stuart, Catherine G. Palmer, Philip L. H. Yu, Joann A. Boughman, & Maimon M. Cohen. (1986). Analysis of translocations observed in three different populations. Cytogenetic and Genome Research. 42(1-2). 53–56. 2 indexed citations

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.

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