W. E. Nance
Impact in
- Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
-
- Birth, Development, and Health
- Assisted Reproductive Technology and Twin Pregnancy
Papers in
- Genetics 12
- Dermatoglyphics and Human Traits 3
- Genetic Associations and Epidemiology 3
- Genomic variations and chromosomal abnormalities 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Birth, Development, and Health 5
- Prenatal Screening and Diagnostics 3
- Co-authors
- Per Magnus (7 shared papers)K. Berg (5 shared papers)Linda A. Corey (8 shared papers)Kyung-Won Kang (2 shared papers)T Bjerkedal (2 shared papers)Arti Pandya (3 shared papers)J.C. Christian (1 shared paper)Marit Hornberg Solaas (3 shared papers)
- Journals
- Clinical Genetics (3 papers)Human Heredity (2 papers)Behavior Genetics (2 papers)Journal of Medical Genetics (2 papers)American Journal of Hypertension (1 paper)
- Partner nations
- United StatesNorwayUnited Kingdom
In The Last Decade
W. E. Nance
30 papers receiving 807 citations
Peers
Comparison fields: 5 of 91
- Sensory Systems 94
- Pediatrics, Perinatology and Child Health 218
- Experimental and Cognitive Psychology 112
- Genetics 219
- Obstetrics and Gynecology 50
Countries citing papers authored by W. E. Nance
This map shows the geographic impact of W. E. Nance'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 W. E. Nance with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites W. E. Nance more than expected).
Fields of papers citing papers by W. E. Nance
This network shows the impact of papers produced by W. E. Nance. 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 W. E. Nance. The network helps show where W. E. Nance may publish in the future.
Co-authors
The 25 scholars most cited alongside W. E. Nance, 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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 115 | |
| 2 | 1979 | 85 | |
| 3 | 1984 | 84 | |
| 4 | 1991 | 82 | |
| 5 | 2008 | 62 | |
| 6 | 2000 | 47 | |
| 7 | 1975 | 46 | |
| 8 | Chromosome polymorphism and twin zygosity. | 1977 | 37 |
| 9 | 1981 | 34 | |
| 10 | 1985 | 34 | |
| 11 | 1979 | 31 | |
| 12 | 1976 | 29 | |
| 13 | Aphidicolin-inducible common fragile-site expression: results from a population survey of twins. | 1992 | 24 |
| 14 | 1988 | 23 | |
| 15 | Sampling from a skewed population distribution as exemplified by estimation of the creatine kinase upper reference limit. | 1984 | 23 |
| 16 | 1990 | 22 | |
| 17 | 1989 | 17 | |
| 18 | 1985 | 14 | |
| 19 | 1985 | 13 | |
| 20 | 1969 | 11 |
About W. E. Nance
W. E. Nance is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Experimental and Cognitive Psychology and Surgery, having authored 32 papers that have together received 877 indexed citations. Recurring topics across this work include Birth, Development, and Health (5 papers), Cognitive Abilities and Testing (4 papers), Dermatoglyphics and Human Traits (3 papers), Prenatal Screening and Diagnostics (3 papers), Genetic Associations and Epidemiology (3 papers), Demographic Trends and Gender Preferences (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Sensory Systems (94 citations), Pediatrics, Perinatology and Child Health (218 citations), Experimental and Cognitive Psychology (112 citations), Genetics (219 citations) and Obstetrics and Gynecology (50 citations). W. E. Nance has collaborated with scholars based in United States, Norway and United Kingdom. Frequent co-authors include Per Magnus, K. Berg, Linda A. Corey, Kyung-Won Kang, T Bjerkedal, Arti Pandya, J.C. Christian, Marit Hornberg Solaas, Nathan Fischel‐Ghodsian and X.-J. Xia. Their work appears in journals such as Clinical Genetics, Human Heredity, Behavior Genetics, Journal of Medical Genetics and American Journal of Hypertension.
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.