Christopher McCaskill
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 20
- Genomic variations and chromosomal abnormalities 16
- Genetic Syndromes and Imprinting 11
- Genomics and Rare Diseases 2
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- Prenatal Screening and Diagnostics 14
- Co-authors
- Lisa G. Shaffer (19 shared papers)Sue Ann Berend (9 shared papers)Frank Greenberg (2 shared papers)V. Reid Sutton (2 shared papers)Stuart K. Shapira (1 shared paper)Hope Northrup (1 shared paper)F.F.B. Elder (1 shared paper)Julie R. Korenberg (1 shared paper)
- Journals
- The American Journal of Human Genetics (7 papers)Prenatal Diagnosis (3 papers)Human Genetics (1 paper)Australasian Emergency Nursing Journal (1 paper)American Journal of Medical Genetics (9 papers)
- Partner nations
- United StatesNetherlandsMexico
In The Last Decade
Christopher McCaskill
21 papers receiving 720 citations
Peers
Comparison fields: 5 of 57
- Genetics 672
- Pediatrics, Perinatology and Child Health 397
- Developmental Biology 21
- Molecular Biology 296
- Genetics 39
Countries citing papers authored by Christopher McCaskill
This map shows the geographic impact of Christopher McCaskill'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 McCaskill with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher McCaskill more than expected).
Fields of papers citing papers by Christopher McCaskill
This network shows the impact of papers produced by Christopher McCaskill. 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 McCaskill. The network helps show where Christopher McCaskill may publish in the future.
Co-authors
The 25 scholars most cited alongside Christopher McCaskill, 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 | 1997 | 201 | |
| 2 | 2000 | 73 | |
| 3 | 2002 | 67 | |
| 4 | 2000 | 65 | |
| 5 | 1996 | 50 | |
| 6 | 1998 | 43 | |
| 7 | 1993 | 42 | |
| 8 | 1999 | 40 | |
| 9 | 1995 | 36 | |
| 10 | 1996 | 33 | |
| 11 | 2002 | 31 | |
| 12 | 2002 | 31 | |
| 13 | 2002 | 28 | |
| 14 | 1996 | 22 | |
| 15 | 2000 | 22 | |
| 16 | 1998 | 17 | |
| 17 | 1993 | 9 | |
| 18 | 2003 | 7 | |
| 19 | 1998 | 4 | |
| 20 | 1997 | 2 |
About Christopher McCaskill
Christopher McCaskill is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Genetics, having authored 22 papers that have together received 825 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (14 papers), Genetic Syndromes and Imprinting (11 papers), Chromosomal and Genetic Variations (5 papers), Congenital heart defects research (2 papers), Genomics and Rare Diseases (2 papers), Advanced biosensing and bioanalysis techniques (1 paper) and LGBTQ Health, Identity, and Policy (1 paper). The work is most often cited by research in Genetics (672 citations), Pediatrics, Perinatology and Child Health (397 citations), Developmental Biology (21 citations), Molecular Biology (296 citations) and Genetics (39 citations). Christopher McCaskill has collaborated with scholars based in United States, Netherlands and Mexico. Frequent co-authors include Lisa G. Shaffer, Sue Ann Berend, Frank Greenberg, V. Reid Sutton, Stuart K. Shapira, Hope Northrup, F.F.B. Elder, Julie R. Korenberg, Aimee S. Spikes and Lorraine Potocki. Their work appears in journals such as The American Journal of Human Genetics, Prenatal Diagnosis, Human Genetics, Australasian Emergency Nursing Journal and American Journal of Medical 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.