CE Schwartz
Impact in
- Immunology and Allergy top 10%
- Cell Adhesion Molecules Research
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
Papers in
-
- Ubiquitin and proteasome pathways 4
- Congenital heart defects research 3
- RNA regulation and disease 3
- Epigenetics and DNA Methylation 2
- Genetics 15
- Genetics and Neurodevelopmental Disorders 13
- Genomic variations and chromosomal abnormalities 2
- Genomics and Rare Diseases 2
- Co-authors
- Roger E. Stevenson (5 shared papers)Maria Giuseppina Miano (1 shared paper)JC Murray (1 shared paper)Mark H. Skolnick (3 shared papers)K. Nguyen (1 shared paper)Curtis L. Atkin (1 shared paper)Lisa A. Cannon (1 shared paper)Sandra J. Hasstedt (1 shared paper)
- Journals
- Clinical Genetics (5 papers)Journal of Medical Genetics (4 papers)Human Genetics (1 paper)Journal of Psychosomatic Research (1 paper)Cytogenetic and Genome Research (1 paper)
- Partner nations
- United StatesFranceBelgium
In The Last Decade
CE Schwartz
21 papers receiving 602 citations
Peers
Comparison fields: 5 of 56
- Immunology and Allergy 75
- Genetics 340
- Hematology 54
- Molecular Biology 344
- Developmental Neuroscience 19
Countries citing papers authored by CE Schwartz
This map shows the geographic impact of CE 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 CE Schwartz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites CE Schwartz more than expected).
Fields of papers citing papers by CE Schwartz
This network shows the impact of papers produced by CE 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 CE Schwartz. The network helps show where CE Schwartz may publish in the future.
Co-authors
The 25 scholars most cited alongside CE 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mapping of Alport syndrome to the long arm of the X chromosome. | 1988 | 95 |
| 2 | 1999 | 89 | |
| 3 | 2007 | 83 | |
| 4 | 2002 | 61 | |
| 5 | 2010 | 40 | |
| 6 | OPD-spectrum Disorders Clinical Collaborative Group. Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans | 2003 | 34 |
| 7 | 2002 | 33 | |
| 8 | Hereditary thrombosis in a Utah kindred is caused by a dysfunctional antithrombin III gene. | 1985 | 27 |
| 9 | 2006 | 25 | |
| 10 | 1997 | 25 | |
| 11 | 2002 | 23 | |
| 12 | 1993 | 21 | |
| 13 | Relationships between the human pepsinogen DNA and protein polymorphisms. | 1986 | 20 |
| 14 | 2002 | 14 | |
| 15 | 1998 | 8 | |
| 16 | 2000 | 8 | |
| 17 | 2009 | 5 | |
| 18 | 1989 | 2 | |
| 19 | High prevalence of SLC6A8 deficiency, a novel X-linked mental retardation syndrome | 2005 | 1 |
| 20 | Maternal expressed emotion and parental affective disorder : risk for childhood depressive disorder, substance abuse or conduct disorder | 1990 | 1 |
About CE Schwartz
CE Schwartz is a scholar working on Molecular Biology, Genetics, Surgery, Pediatrics, Perinatology and Child Health and Oncology, having authored 22 papers that have together received 616 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (13 papers), Ubiquitin and proteasome pathways (4 papers), Congenital heart defects research (3 papers), RNA regulation and disease (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Epigenetics and DNA Methylation (2 papers), Genomics and Rare Diseases (2 papers) and Peptidase Inhibition and Analysis (2 papers). The work is most often cited by research in Immunology and Allergy (75 citations), Genetics (340 citations), Hematology (54 citations), Molecular Biology (344 citations) and Developmental Neuroscience (19 citations). CE Schwartz has collaborated with scholars based in United States, France and Belgium. Frequent co-authors include Roger E. Stevenson, Maria Giuseppina Miano, JC Murray, Mark H. Skolnick, K. Nguyen, Curtis L. Atkin, Lisa A. Cannon, Sandra J. Hasstedt, L.A. Menlove and Arnold L. Christianson. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, Human Genetics, Journal of Psychosomatic Research and Cytogenetic and Genome Research.
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.