C. M. Conn
Impact in
-
- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
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- Prenatal Screening and Diagnostics 5
- Assisted Reproductive Technology and Twin Pregnancy 2
- Genetics 2
- Genomic variations and chromosomal abnormalities 2
- Genetic Syndromes and Imprinting 1
- Co-authors
- Joy Delhanty (5 shared papers)Robert Winston (3 shared papers)Joyce Harper (3 shared papers)J. Cozzi (3 shared papers)M.J.W. Faed (1 shared paper)S. Cupisti (1 shared paper)Katherine Whalley (1 shared paper)Joseph L. Mills (1 shared paper)
- Journals
- Human Genetics (2 papers)Journal of Medical Genetics (1 paper)Prenatal Diagnosis (1 paper)Human Reproduction (1 paper)
- Partner nations
- United KingdomGermany
In The Last Decade
C. M. Conn
5 papers receiving 286 citations
Peers
Comparison fields: 5 of 21
- Pediatrics, Perinatology and Child Health 272
- Genetics 213
- Developmental Biology 8
- Public Health, Environmental and Occupational Health 71
- Reproductive Medicine 18
Countries citing papers authored by C. M. Conn
This map shows the geographic impact of C. M. Conn'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 C. M. Conn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. M. Conn more than expected).
Fields of papers citing papers by C. M. Conn
This network shows the impact of papers produced by C. M. Conn. 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 C. M. Conn. The network helps show where C. M. Conn may publish in the future.
Co-authors
The 11 scholars most cited alongside C. M. Conn, 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 | 1998 | 141 | |
| 2 | 2003 | 70 | |
| 3 | 1999 | 62 | |
| 4 | 1999 | 47 | |
| 5 | 1997 | 2 |
About C. M. Conn
C. M. Conn is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Surgery, Public Health, Environmental and Occupational Health and Plant Science, having authored 5 papers that have together received 322 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Assisted Reproductive Technology and Twin Pregnancy (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Reproductive Biology and Fertility (1 paper), Congenital Anomalies and Fetal Surgery (1 paper), Genetic Syndromes and Imprinting (1 paper) and Chromosomal and Genetic Variations (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (272 citations), Genetics (213 citations), Developmental Biology (8 citations), Public Health, Environmental and Occupational Health (71 citations) and Reproductive Medicine (18 citations). C. M. Conn has collaborated with scholars based in United Kingdom and Germany. Frequent co-authors include Joy Delhanty, Robert Winston, Joyce Harper, J. Cozzi, M.J.W. Faed, S. Cupisti, Katherine Whalley, Joseph L. Mills, E. Fragouli and Peter Farndon. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Prenatal Diagnosis and Human Reproduction.
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.