Walter E. Nance
Impact in
- Sensory Systems top 0.02%
- Hearing, Cochlea, Tinnitus, Genetics
- Genetics top 1%
- Genetic Associations and Epidemiology
- Congenital Ear and Nasal Anomalies
- Genomic variations and chromosomal abnormalities
Papers in
-
- Hearing, Cochlea, Tinnitus, Genetics 57
- Genetics 93
- Genetic Associations and Epidemiology 48
- Genomic variations and chromosomal abnormalities 14
- Congenital Ear and Nasal Anomalies 11
- Genomics and Rare Diseases 9
- Co-authors
- Cynthia Casson Morton (9 shared papers)Linda A. Corey (23 shared papers)Arti Pandya (32 shared papers)Joe C. Christian (9 shared papers)KATHLEEN SHAVER ARNOS (17 shared papers)Per Minor Magnus (10 shared papers)P. Michael Conneally (3 shared papers)Joann A. Boughman (4 shared papers)
- Journals
- Clinical Genetics (19 papers)Journal of Medical Genetics (10 papers)Science (9 papers)The American Journal of Human Genetics (7 papers)Human Genetics (7 papers)
- Partner nations
- United StatesUnited KingdomNorway
In The Last Decade
Walter E. Nance
259 papers receiving 11k citations
Walter E. Nance's Hit Papers
Peers
Comparison fields: 5 of 148
- Sensory Systems 4.4k
- Genetics 2.2k
- Developmental Biology 149
- Genetics 578
- Pediatrics, Perinatology and Child Health 846
Countries citing papers authored by Walter E. Nance
This map shows the geographic impact of Walter 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 Walter 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 Walter E. Nance more than expected).
Fields of papers citing papers by Walter E. Nance
This network shows the impact of papers produced by Walter 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 Walter E. Nance. The network helps show where Walter E. Nance may publish in the future.
Co-authors
The 25 scholars most cited alongside Walter 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 265 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Newborn Hearing Screening — A Silent Revolution Hit paper breakdown → | 2006 | 1331 |
| 2 | Genetic Factors in Determining Bone Mass Hit paper breakdown → | 1973 | 495 |
| 3 | 2001 | 467 | |
| 4 | 1993 | 384 | |
| 5 | 1985 | 279 | |
| 6 | Population genetic studies of retinitis pigmentosa. | 1980 | 274 |
| 7 | 2005 | 272 | |
| 8 | 2003 | 271 | |
| 9 | 2003 | 254 | |
| 10 | 2005 | 218 | |
| 11 | 2003 | 177 | |
| 12 | 2002 | 162 | |
| 13 | 1976 | 153 | |
| 14 | 2002 | 143 | |
| 15 | 2003 | 140 | |
| 16 | 2009 | 133 | |
| 17 | 1981 | 127 | |
| 18 | 1991 | 123 | |
| 19 | 2005 | 122 | |
| 20 | 1997 | 118 |
About Walter E. Nance
Walter E. Nance is a scholar working on Sensory Systems, Genetics, Pediatrics, Perinatology and Child Health, Genetics and Clinical Biochemistry, having authored 265 papers that have together received 12k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (57 papers), Genetic Associations and Epidemiology (48 papers), Assisted Reproductive Technology and Twin Pregnancy (29 papers), Metabolism and Genetic Disorders (14 papers), Genomic variations and chromosomal abnormalities (14 papers), Congenital Ear and Nasal Anomalies (11 papers), Retinal Development and Disorders (10 papers) and Genomics and Rare Diseases (9 papers). The work is most often cited by research in Sensory Systems (4.4k citations), Genetics (2.2k citations), Developmental Biology (149 citations), Genetics (578 citations) and Pediatrics, Perinatology and Child Health (846 citations). Walter E. Nance has collaborated with scholars based in United States, United Kingdom and Norway. Frequent co-authors include Cynthia Casson Morton, Linda A. Corey, Arti Pandya, Joe C. Christian, KATHLEEN SHAVER ARNOS, Per Minor Magnus, P. Michael Conneally, Joann A. Boughman, C. Conrad Johnston and David M. Smith. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, Science, The American Journal of Human Genetics and Human 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.