Christopher D. Elzinga
Impact in
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- Hereditary Neurological Disorders
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- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 4
- BRCA gene mutations in cancer 3
- Genomics and Rare Diseases 1
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- Prenatal Screening and Diagnostics 1
- Co-authors
- Izabela Karbassi (1 shared paper)Zhenyuan Wang (1 shared paper)James R. Lupski (1 shared paper)Sat Dev Batish (1 shared paper)Corey D. Braastad (2 shared papers)Joseph J Higgins (1 shared paper)Malgorzata Jaremko (1 shared paper)Carol A. Hoffman (1 shared paper)
- Journals
- PLoS ONE (3 papers)Human Mutation (2 papers)BioMed Research International (1 paper)Molecular Genetics & Genomic Medicine (1 paper)
- Partner nations
- United StatesFrance
In The Last Decade
Christopher D. Elzinga
7 papers receiving 320 citations
Peers
Comparison fields: 5 of 39
- Cellular and Molecular Neuroscience 122
- Genetics 121
- Pediatrics, Perinatology and Child Health 18
- Cancer Research 11
- Neurology 9
Countries citing papers authored by Christopher D. Elzinga
This map shows the geographic impact of Christopher D. Elzinga'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 D. Elzinga with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher D. Elzinga more than expected).
Fields of papers citing papers by Christopher D. Elzinga
This network shows the impact of papers produced by Christopher D. Elzinga. 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 D. Elzinga. The network helps show where Christopher D. Elzinga may publish in the future.
Co-authors
The 25 scholars most cited alongside Christopher D. Elzinga, 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 | 2014 | 152 | |
| 2 | 2015 | 60 | |
| 3 | 2016 | 51 | |
| 4 | 2015 | 36 | |
| 5 | 2017 | 14 | |
| 6 | 2021 | 7 | |
| 7 | 2020 | 6 |
About Christopher D. Elzinga
Christopher D. Elzinga is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Hematology, Cellular and Molecular Neuroscience and Nuclear Energy and Engineering, having authored 7 papers that have together received 326 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (3 papers), Prenatal Screening and Diagnostics (1 paper), Acute Myeloid Leukemia Research (1 paper), Hereditary Neurological Disorders (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (122 citations), Genetics (121 citations), Pediatrics, Perinatology and Child Health (18 citations), Cancer Research (11 citations) and Neurology (9 citations). Christopher D. Elzinga has collaborated with scholars based in United States and France. Frequent co-authors include Izabela Karbassi, Zhenyuan Wang, James R. Lupski, Sat Dev Batish, Corey D. Braastad, Joseph J Higgins, Malgorzata Jaremko, Carol A. Hoffman, Weimin Sun and David A. Ross. Their work appears in journals such as PLoS ONE, Human Mutation, BioMed Research International and Molecular Genetics & Genomic Medicine.
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.