Nance We
Impact in
- Sensory Systems top 10%
- Hearing, Cochlea, Tinnitus, Genetics
-
- Assisted Reproductive Technology and Twin Pregnancy
- Birth, Development, and Health
- Prenatal Screening and Diagnostics
Papers in
-
- Mitochondrial Function and Pathology 2
-
- Assisted Reproductive Technology and Twin Pregnancy 6
- Birth, Development, and Health 3
- Co-authors
- Irene A. Uchida (1 shared paper)David Bixler (3 shared papers)Mette Warburg (1 shared paper)Ann T. Sweeney (2 shared papers)j. c. christian (1 shared paper)RE Harris (1 shared paper)Mustafa Tekin (2 shared papers)Witkop Cj (2 shared papers)
- Journals
- Clinical Genetics (3 papers)The American Journal of Human Genetics (1 paper)PubMed (33 papers)Twin Research (2 papers)
- Partner nations
- United StatesGermanyTürkiye
In The Last Decade
Nance We
38 papers receiving 485 citations
Peers
Comparison fields: 5 of 82
- Sensory Systems 43
- Pediatrics, Perinatology and Child Health 122
- Genetics 176
- Developmental Biology 9
- Cell Biology 54
Countries citing papers authored by Nance We
This map shows the geographic impact of Nance We'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 Nance We with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nance We more than expected).
Fields of papers citing papers by Nance We
This network shows the impact of papers produced by Nance We. 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 Nance We. The network helps show where Nance We may publish in the future.
Co-authors
The 25 scholars most cited alongside Nance We, 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 39 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Congenital X-linked cataract, dental anomalies and brachymetacarpalia. | 1974 | 59 |
| 2 | TURNER'S SYNDROME, TWINNING, AND AN UNUSUAL VARIANT OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE. | 1964 | 52 |
| 3 | Do twin Lyons have larger spots? | 1990 | 47 |
| 4 | 2008 | 44 | |
| 5 | Effects of chorion type on variation in cord blood cholesterol of monozygotic twins. | 1976 | 41 |
| 6 | Malformations unique to the twinning process. | 1981 | 28 |
| 7 | Evidence for autosomal recessive inheritance of the syndrome of renal tubular acidosis with deafness. | 1971 | 21 |
| 8 | 1998 | 20 | |
| 9 | 2001 | 18 | |
| 10 | Human blood pressure and the ABO blood group system: an apparent association. | 1965 | 17 |
| 11 | Genetic studies of ocular albinism in a large Virginia kindred. | 1984 | 16 |
| 12 | 2007 | 13 | |
| 13 | One X and four hypotheses: response to Lehrke's "A Theory of X-Linkage of Major Intellectual Traits. | 1972 | 12 |
| 14 | Blood pressure studies on monozygotic twins and their families. | 1978 | 12 |
| 15 | Classification of albinism in man. | 1971 | 12 |
| 16 | 1998 | 11 | |
| 17 | The role of twin studies in human quantitative genetics. | 1979 | 11 |
| 18 | Quantitative studies of glucose-6-phosphate dehydrogenase. | 1977 | 10 |
| 19 | The genetic analysis of profound prelingual deafness. | 1980 | 10 |
| 20 | Anencephaly and spina bifida: an etiologic hypothesis. | 1971 | 9 |
About Nance We
Nance We is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health, Experimental and Cognitive Psychology, Genetics and Clinical Biochemistry, having authored 39 papers that have together received 541 indexed citations. Recurring topics across this work include Cognitive Abilities and Testing (6 papers), Assisted Reproductive Technology and Twin Pregnancy (6 papers), Metabolism and Genetic Disorders (4 papers), melanin and skin pigmentation (3 papers), Birth, Development, and Health (3 papers), Demographic Trends and Gender Preferences (2 papers), Mitochondrial Function and Pathology (2 papers) and Genetic Mapping and Diversity in Plants and Animals (2 papers). The work is most often cited by research in Sensory Systems (43 citations), Pediatrics, Perinatology and Child Health (122 citations), Genetics (176 citations), Developmental Biology (9 citations) and Cell Biology (54 citations). Nance We has collaborated with scholars based in United States, Germany and Türkiye. Frequent co-authors include Irene A. Uchida, David Bixler, Mette Warburg, Ann T. Sweeney, j. c. christian, RE Harris, Mustafa Tekin, Witkop Cj, H. Krieger and E Tunçbilek. Their work appears in journals such as Clinical Genetics, The American Journal of Human Genetics, PubMed and Twin Research.
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.