Christopher C. Glenn
Impact in
- Genetics top 2%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 12
- Genetic Syndromes and Imprinting 12
- Genetics and Neurodevelopmental Disorders 1
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- Epigenetics and DNA Methylation 9
- Co-authors
- Daniel J. Driscoll (11 shared papers)Robert D. Nicholls (7 shared papers)M T Jong (4 shared papers)Shinji Saitoh (5 shared papers)Charles A. Williams (3 shared papers)Todd A. Gray (1 shared paper)Yazhong Ji (1 shared paper)Urvashi Surti (1 shared paper)
- Journals
- Human Molecular Genetics (3 papers)Prenatal Diagnosis (2 papers)Journal of Neurochemistry (1 paper)Journal of Neurotrauma (1 paper)Genomics (1 paper)
- Partner nations
- United StatesJapanGermany
In The Last Decade
Christopher C. Glenn
14 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 54
- Genetics 892
- Pediatrics, Perinatology and Child Health 417
- Molecular Biology 751
- Neurology 61
- Reproductive Medicine 30
Countries citing papers authored by Christopher C. Glenn
This map shows the geographic impact of Christopher C. Glenn'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 Christopher C. Glenn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher C. Glenn more than expected).
Fields of papers citing papers by Christopher C. Glenn
This network shows the impact of papers produced by Christopher C. Glenn. 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 Christopher C. Glenn. The network helps show where Christopher C. Glenn may publish in the future.
Co-authors
The 25 scholars most cited alongside Christopher C. Glenn, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene. | 1996 | 185 |
| 2 | 1999 | 184 | |
| 3 | 1992 | 165 | |
| 4 | 1993 | 132 | |
| 5 | 1997 | 115 | |
| 6 | 1993 | 110 | |
| 7 | 2000 | 83 | |
| 8 | 1997 | 76 | |
| 9 | 2002 | 31 | |
| 10 | Familial cryptic translocation resulting in Angelman syndrome:implications for imprinting or location of the Angelman gene? | 1996 | 23 |
| 11 | 2000 | 18 | |
| 12 | 1997 | 3 | |
| 13 | Molecular pathogenesis of Prader-Willi syndrome | 1996 | 2 |
| 14 | 2000 | 2 |
About Christopher C. Glenn
Christopher C. Glenn is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Epidemiology and Neurology, having authored 14 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (12 papers), Epigenetics and DNA Methylation (9 papers), Prenatal Screening and Diagnostics (5 papers), Genetics and Neurodevelopmental Disorders (1 paper), Blood properties and coagulation (1 paper), Traumatic Brain Injury and Neurovascular Disturbances (1 paper), Cerebral Palsy and Movement Disorders (1 paper) and Traumatic Brain Injury Research (1 paper). The work is most often cited by research in Genetics (892 citations), Pediatrics, Perinatology and Child Health (417 citations), Molecular Biology (751 citations), Neurology (61 citations) and Reproductive Medicine (30 citations). Christopher C. Glenn has collaborated with scholars based in United States, Japan and Germany. Frequent co-authors include Daniel J. Driscoll, Robert D. Nicholls, M T Jong, Shinji Saitoh, Charles A. Williams, Todd A. Gray, Yazhong Ji, Urvashi Surti, Roberto T. Zori and Michael F. Waters. Their work appears in journals such as Human Molecular Genetics, Prenatal Diagnosis, Journal of Neurochemistry, Journal of Neurotrauma 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.