W E Nance

2.2k total citations
48 papers, 1.4k citations indexed

About

W E Nance is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, W E Nance has authored 48 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 15 papers in Genetics and 11 papers in Cell Biology. Recurrent topics in W E Nance's work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), Biotin and Related Studies (4 papers) and melanin and skin pigmentation (4 papers). W E Nance is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (6 papers), Biotin and Related Studies (4 papers) and melanin and skin pigmentation (4 papers). W E Nance collaborates with scholars based in United States, United Kingdom and Norway. W E Nance's co-authors include Joann A. Boughman, P. M. Conneally, Linda A. Corey, Carl J. Witkop, Heun Y. Yune, David Bixler, Freeman McConnell, J.A. Brown, Cynthia C. Morton and A Sweeney and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Circulation.

In The Last Decade

W E Nance

48 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
W E Nance United States	21	613	323	228	183	165	48	1.4k
Mary Z. Pelias United States	17	536 0.9×	238 0.7×	68 0.3×	99 0.5×	375 2.3×	35	1.1k
Theo Peters Netherlands	25	1.4k 2.3×	464 1.4×	135 0.6×	401 2.2×	417 2.5×	74	2.4k
Mette Warburg Denmark	29	1.1k 1.8×	1.1k 3.5×	211 0.9×	212 1.2×	53 0.3×	92	2.5k
Sandra L. H. Davenport United States	21	869 1.4×	341 1.1×	326 1.4×	131 0.7×	507 3.1×	35	2.0k
Uppala Radhakrishna United States	25	1.0k 1.7×	758 2.3×	252 1.1×	67 0.4×	80 0.5×	81	2.1k
Hanne Jensen Denmark	25	576 0.9×	167 0.5×	176 0.8×	72 0.4×	45 0.3×	107	2.0k
Mohnish Suri United Kingdom	24	1.2k 2.0×	736 2.3×	200 0.9×	260 1.4×	158 1.0×	82	2.2k
Lisa A. Schimmenti United States	27	1.6k 2.6×	736 2.3×	184 0.8×	306 1.7×	230 1.4×	106	2.7k
Barbara F. Crandall United States	25	704 1.1×	719 2.2×	245 1.1×	98 0.5×	69 0.4×	88	2.0k
Vazken M. Der Kaloustian Canada	29	1.5k 2.4×	958 3.0×	336 1.5×	223 1.2×	30 0.2×	121	2.7k

Countries citing papers authored by W E Nance

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of W E Nance

This figure shows the co-authorship network connecting the top 25 collaborators of W E Nance. A scholar is included among the top collaborators of W E Nance based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with W E Nance. W E Nance is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Jacobson, Samuel G., et al.. (2003). USH1C: a rare cause of USH1 in a non‐Acadian population and a founder effect of the Acadian allele. Clinical Genetics. 63(2). 150–153. 19 indexed citations

Blanton, Susan H., Maria Bitner‐Glindzicz, Arti Pandya, et al.. (2001). Haplotype analysis of the USH1D locus and genotype–phenotype correlations. Clinical Genetics. 60(1). 58–62. 17 indexed citations

Tekin, Mustafa, et al.. (2001). Waardenburg syndrome type 3 (Klein–Waardenburg syndrome) segregating with a heterozygous deletion in the paired box domain of PAX3: a simple variant or a true syndrome?. Clinical Genetics. 60(4). 301–304. 23 indexed citations

Nance, W E, et al.. (2000). Is Assortative Mating the Cause for the High Frequency of Connexin 26 (Cx 26) Deafness?. Genetics in Medicine. 2(1). 64–64. 2 indexed citations

Pomponio, Robert J., Jeanne Hymes, Arti Pandya, et al.. (1998). Prenatal diagnosis of heterozygosity for biotinidase deficiency by enzymatic and molecular analyses. Prenatal Diagnosis. 18(2). 117–122. 6 indexed citations

Pandya, Arti, et al.. (1997). Implications of Molecular Diagnostic Testing in Families with Hereditary Pancreatitis. Genetic Testing. 1(3). 207–211. 4 indexed citations

Pandya, Arti, et al.. (1996). Linkage Studies in a Large Kindred with Hereditary Pancreatitis Confirms Mapping of the Gene to a 16-cM Region on 7q. Genomics. 38(2). 227–230. 78 indexed citations

Weber, Frederick, et al.. (1995). Waardenburg syndrome and gastric stasis in adults.. PubMed. 122(4). 279–80. 4 indexed citations

Nance, W E. (1993). 1992 American Society of Human Genetics presidential address: back to the future.. PubMed. 53(1). 6–15. 11 indexed citations

10.

Corey, Linda A., K Berg, Marit Hornberg Solaas, & W E Nance. (1992). The epidemiology of pregnancy complications and outcome in a Norwegian twin population.. PubMed. 80(6). 989–94. 33 indexed citations

11.

Stevens, C A, Kathleen S. Arnos, Joann Bodurtha, et al.. (1991). Ascertainment of Families with Hereditary Deafness for Linkage Studies. Annals of the New York Academy of Sciences. 630(1). 293–294. 2 indexed citations

12.

Bodurtha, Joann, et al.. (1991). Genetic and environmental contributions to cholesterol and its subfractions in 11-year-old twins. The Medical College of Virginia Twin Study.. Arteriosclerosis and Thrombosis A Journal of Vascular Biology. 11(4). 844–850. 16 indexed citations

13.

Weissbecker, Karen, et al.. (1989). An automated procedure for measuring biotinidase activity in serum.. Clinical Chemistry. 35(5). 831–833. 10 indexed citations

14.

Heath, Andrew C., L. J. Eaves, W E Nance, & Linda A. Corey. (1987). Social inequality and assortative mating: Cause or consequence?. Behavior Genetics. 17(1). 9–17. 26 indexed citations

15.

Boughman, Joann A., P. M. Conneally, & W E Nance. (1980). Population genetic studies of retinitis pigmentosa.. PubMed. 32(2). 223–35. 247 indexed citations

16.

Heiberg, Astrid Nøklebye, et al.. (1980). Myofascial Pain Dysfunction (MPD) Syndrome in twins. Community Dentistry And Oral Epidemiology. 8(8). 434–436. 18 indexed citations

17.

Melnick, Michael, David Bixler, Kenneth R. Silk, Heun Y. Yune, & W E Nance. (1975). Autosomal dominant branchiootorenal dysplasia.. PubMed. 11(5). 121–8. 65 indexed citations

18.

Witkop, Carl J., et al.. (1970). Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity.. PubMed. 22(1). 55–74. 57 indexed citations

19.

Nance, W E, et al.. (1969). Genetic linkage studies in a Negro kindred with Norrie's disease.. PubMed. 21(5). 423–9. 14 indexed citations

20.

Nance, W E, et al.. (1968). Neurologic aspects of typical and atypical Down's syndrome.. PubMed. 18(3). 305–6. 1 indexed citations

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.

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