Stuart Schwartz

17.7k citations

197 papers · 11.0k indexed · 3 hit papers · h-index 49

Genetics top 0.05%
- Genomic variations and chromosomal abnormalities 102
- Genetic Syndromes and Imprinting 30
- Genetics and Neurodevelopmental Disorders 12
Pediatrics, Perinatology and Child Health top 0.2%
- Prenatal Screening and Diagnostics 63
Molecular Biology top 1%
- Genomics and Chromatin Dynamics 22
- Congenital heart defects research 12
- DNA Repair Mechanisms 10
Plant Science top 0.5%
- Chromosomal and Genetic Variations 59
Cancer Research top 2%

Co-authors: Suzanne B. Cassidy Evan E. Eichler Daniel J. Driscoll Jennifer Miller Robert D. Nicholls Jeffrey A. Bailey Royden A. Clark Rhea U. Vallente
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: Prenatal Diagnosis (13 papers)The American Journal of Human Genetics (12 papers)Genetics in Medicine (8 papers)
Partner nations: United States Canada Italy

In The Last Decade

Stuart Schwartz

191 papers receiving 10.6k citations

Hit Papers

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Peers

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

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.

Border = papers with Stuart Schwartz Line = papers co-authored together Stuart Schwartz links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Utilization of a SNP microarray to detect uniparental disomy: Implications and outcomes Genetics in Medicine ·Alexandra Arreola,Gloria Haskell,Inder Gadi,Andrea Penton,Stuart Schwartz	2024	0
2	Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes Prenatal Diagnosis ·G.H. LeFevre,Gloria Haskell,Alexandra Arreola,Christine M. Riordan,Inder Gadi,Andrea Penton,Peter Papenhausen,Stuart Schwartz	2024	0
3	Uniparental disomy of multiple chromosomes in two cases with a complex phenotype American Journal of Medical Genetics Part A ·Katarzyna Polonis,Luciana Cristante Izar,Gülin TÜRK,S. Navin Sellaraju,Ph. Letellier,Noorazizah Mohamad Ali,Stuart Schwartz,Christina Grant,Linda Hasadsri,Ross Rowsey,Nicole L. Hoppman	2023	3
4	Navigating choice in the face of uncertainty: using a theory informed qualitative approach to identifying potential patient barriers and enablers to participating in an early phase chimeric antigen receptor T (CAR-T) cell therapy trial BMJ Open ·Kim Ji Soo,Manoj M. Lalu,曹冬如,Madison Foster,Natasha Kekre,Dean Fergusson,В. К. Пьянзин,Harold Atkins,Kednapa Thavorn,Joshua Montroy,Stuart Schwartz,Robert A. Holt,Raewyn Broady,Justin Presseau	2021	11
5	Clinical significance and mechanisms associated with segmental UPD Molecular Cytogenetics ·Peter Papenhausen,Teodosio Juan Chávez Campos,فرزانه فیضی,كرفاح ليلى,Stuart Schwartz,Andrea Penton	2021	6
6	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 ·Madison Foster,Dean Fergusson,В. К. Пьянзин,Justin Presseau,Natasha Kekre,Stuart Schwartz,Kim Ji Soo,曹冬如,L. Di Feo,Harold Atkins,Kednapa Thavorn,Joshua Montroy,Robert A. Holt,Zarah Monfaredi,Manoj M. Lalu	2020	12
7	Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Darrel Waggoner,Karen E. Wain,Adrian M. Dubuc,Laura K. Conlin,Scott E. Hickey,Allen N. Lamb,Christa Lese Martin,Cynthia C. Morton,Kristen Rasmussen,Jane L. Schuette,Stuart Schwartz,David T. Miller	2018	46
8	Punctuated duplication seeding events during the evolution of human chromosome 2p11 Genome Research ·Julie E. Horvath,Cassandra Gulden,Rhea U. Vallente,Ruzaini Izyan Ruslan,Mario Ventura,John D. McPherson,Tina Graves,Richard K. Wilson,Stuart Schwartz,Mariano Rocchi,Evan E. Eichler	2005	29
9	BAC microarray analysis of 15q11–q13 rearrangements and the impact of segmental duplications Journal of Medical Genetics ·Devin P. Locke,Richard Segraves,Robert D. Nicholls,Stuart Schwartz,D. Pinkel,Donna G. Albertson,Evan E. Eichler	2004	79
10	Human Artificial Chromosomes with Alpha Satellite-Based De Novo Centromeres Show Increased Frequency of Nondisjunction and Anaphase Lag Molecular and Cellular Biology ·M. Katharine Rudd,Robert W. Mays,Stuart Schwartz,Huntington F. Willard	2003	49
11	Human-Specific Duplication and Mosaic Transcripts: The Recent Paralogous Structure of Chromosome 22 The American Journal of Human Genetics ·Jeffrey A. Bailey,Leonard Bertain,Luigi Viggiano,Doriana Misceo,А. Ицхокин,Nicoletta Archidiacono,Stuart Schwartz,Mariano Rocchi,Evan E. Eichler	2002	123
12	Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski−/− mice Nature Genetics ·Clemencia Colmenares,Heidi A. Heilstedt,Lisa G. Shaffer,Stuart Schwartz,Michael Berk,Jeffrey C. Murray,Ed Stavnezer	2001	102
13	Maternal Folate Polymorphisms and the Etiology of Human Nondisjunction The American Journal of Human Genetics ·Terry Hassold,Lindsay C. Burrage,E. Ricky Chan,LuAnn Judis,Stuart Schwartz,S. Jill James,Patricia A. Jacobs,N. Simon Thomas	2001	58
14	Structure of Chromosomal Duplicons and their Role in Mediating Human Genomic Disorders Genome Research ·Yonggang Ji,Evan E. Eichler,Stuart Schwartz,Robert D. Nicholls	2000	196
15	Chromosome Breakage Hotspots and Delineation of the Critical Region for the 9p-Deletion Syndrome The American Journal of Human Genetics ·Laurie A. Christ,Carol A. Crowe,Mark A. Micale,Jeffrey M. Conroy,Stuart Schwartz	1999	74
16	Chromosome number and structure both are markedly stable in RER colorectal cancers and are not destabilized by mutation of p53 Oncogene ·James R. Eshleman,Graham Casey,А. В. Кочубей,W. David Sedwick,Sandra E. Swinler,Martina Veigl,James K. V. Willson,Stuart Schwartz,Sanford D. Markowitz	1998	106
17	Human chromosomes: Manual of basic techniques The American Journal of Human Genetics ·Stuart Schwartz	1991	2
18	Ataxia-telangiectasia: Genetics, neuropathology, and immunology of a degenerative disease of childhood. The American Journal of Human Genetics ·Stuart Schwartz	1987	106
19	Analysis of translocations observed in three different populations Cytogenetic and Genome Research ·Stuart Schwartz,Catherine G. Palmer,Philip L. H. Yu,Joann A. Boughman,Maimon M. Cohen	1986	2
20	Analysis of translocations observed in three different populations Cytogenetic and Genome Research ·Stuart Schwartz,Catherine G. Palmer,Philip L. H. Yu,Joann A. Boughman,Maimon M. Cohen	1986	2

About Stuart Schwartz

Stuart Schwartz is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Plant Science, Molecular Biology and Developmental Biology, having authored 197 papers that have together received 11.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (102 papers), Prenatal Screening and Diagnostics (63 papers), Chromosomal and Genetic Variations (59 papers), Genetic Syndromes and Imprinting (30 papers), Genomics and Chromatin Dynamics (22 papers), Congenital heart defects research (12 papers), Genetics and Neurodevelopmental Disorders (12 papers) and DNA Repair Mechanisms (10 papers). The work is most often cited by research in Genetics (7.3k citations), Pediatrics, Perinatology and Child Health (2.3k citations), Molecular Biology (5.7k citations), Plant Science (2.7k citations) and Cancer Research (667 citations). Stuart Schwartz has collaborated with scholars based in United States, Canada and Italy. 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 Donna G. Albertson. Their work appears in journals such as Prenatal Diagnosis, The American Journal of Human Genetics, Genetics in Medicine, Cytogenetic and Genome Research and Human Genetics.

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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