Charles E. Schwartz
Impact in
- Genetics top 0.1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Molecular Biology top 0.5%
- Epigenetics and DNA Methylation
- Congenital heart defects research
- RNA modifications and cancer
Papers in
-
- Congenital heart defects research 35
- Epigenetics and DNA Methylation 33
- RNA modifications and cancer 31
- Ubiquitin and proteasome pathways 22
- Genetics 193
- Genetics and Neurodevelopmental Disorders 151
- Genomic variations and chromosomal abnormalities 41
- Genomics and Rare Diseases 21
- Co-authors
- Roger E. Stevenson (86 shared papers)Herbert A. Lubs (30 shared papers)Cindy Skinner (42 shared papers)Anand K. Srivastava (8 shared papers)Melanie May (22 shared papers)Giovanni Neri (13 shared papers)Robert M. Plenge (4 shared papers)Richard J. Simensen (23 shared papers)
- Journals
- European Journal of Human Genetics (13 papers)Human Molecular Genetics (13 papers)The American Journal of Human Genetics (11 papers)Journal of Medical Genetics (11 papers)Clinical Genetics (8 papers)
- Partner nations
- United StatesCanadaAustralia
In The Last Decade
Charles E. Schwartz
315 papers receiving 12.8k citations
Charles E. Schwartz's Hit Papers
Peers
Comparison fields: 5 of 165
- Genetics 6.3k
- Molecular Biology 7.6k
- Cognitive Neuroscience 1.7k
- Cell Biology 1.3k
- Developmental Biology 156
Countries citing papers authored by Charles E. Schwartz
This map shows the geographic impact of Charles E. 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 Charles E. Schwartz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Charles E. Schwartz more than expected).
Fields of papers citing papers by Charles E. Schwartz
This network shows the impact of papers produced by Charles E. 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 Charles E. Schwartz. The network helps show where Charles E. Schwartz may publish in the future.
Co-authors
The 25 scholars most cited alongside Charles E. 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 319 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | AGTR2 Mutations in X-Linked Mental Retardation Hit paper breakdown → | 2002 | 521 |
| 2 | 1991 | 331 | |
| 3 | 2003 | 297 | |
| 4 | 2005 | 287 | |
| 5 | 1994 | 238 | |
| 6 | 2006 | 229 | |
| 7 | 2006 | 219 | |
| 8 | 1997 | 214 | |
| 9 | 1996 | 199 | |
| 10 | 1996 | 189 | |
| 11 | 2008 | 186 | |
| 12 | 2002 | 177 | |
| 13 | 2012 | 176 | |
| 14 | 2012 | 166 | |
| 15 | 2013 | 160 | |
| 16 | 2004 | 159 | |
| 17 | 2014 | 157 | |
| 18 | 1994 | 153 | |
| 19 | 2007 | 152 | |
| 20 | 1992 | 152 |
About Charles E. Schwartz
Charles E. Schwartz is a scholar working on Molecular Biology, Genetics, Cognitive Neuroscience, Surgery and Genetics, having authored 319 papers that have together received 13.0k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (151 papers), Genomic variations and chromosomal abnormalities (41 papers), Autism Spectrum Disorder Research (38 papers), Congenital heart defects research (35 papers), Epigenetics and DNA Methylation (33 papers), RNA modifications and cancer (31 papers), Ubiquitin and proteasome pathways (22 papers) and Genomics and Rare Diseases (21 papers). The work is most often cited by research in Genetics (6.3k citations), Molecular Biology (7.6k citations), Cognitive Neuroscience (1.7k citations), Cell Biology (1.3k citations) and Developmental Biology (156 citations). Charles E. Schwartz has collaborated with scholars based in United States, Canada and Australia. Frequent co-authors include Roger E. Stevenson, Herbert A. Lubs, Cindy Skinner, Anand K. Srivastava, Melanie May, Giovanni Neri, Robert M. Plenge, Richard J. Simensen, Huntington F. Willard and Michael J. Friez. Their work appears in journals such as European Journal of Human Genetics, Human Molecular Genetics, The American Journal of Human Genetics, Journal of Medical Genetics and Clinical 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.