W E Nance

2.2k citations
51 papers · 1.5k · h-index 22

Impact in

Papers in

    • Epigenetics and DNA Methylation 3
    • Genomic variations and chromosomal abnormalities 4
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
    • Hemoglobinopathies and Related Disorders 3

W E Nance

51 papers receiving 1.4k citations

Peers

W E Nance
Comparison fields: 5 of 111
  • Sensory Systems 165
  • Cell Biology 204
  • Genetics 323
  • Ophthalmology 85
  • Pediatrics, Perinatology and Child Health 178
Replace Mary Z. Pelias with:
Mary Z. Pelias United States
Sulman Basit Saudi Arabia
Mordechai Shohat Israel
Michal Sagi Israel
Mette Warburg Denmark
Mohnish Suri United Kingdom
Vazken M. Der Kaloustian Lebanon
Klaus Kjaer Denmark
Sandra L. H. Davenport United States
Barbara F. Crandall United States
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Citations per field
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Citations per year

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-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.

Border = papers with W E Nance Line = papers co-authored together W E Nance links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 51 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Population genetic studies of retinitis pigmentosa.
1980266
2
X-linked mixed deafness with congenital fixation of the stapedial footplate and perilymphatic gusher.
197197
3 196489
4 199679
5
Autosomal dominant branchiootorenal dysplasia.
197572
6 197865
7
Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity.
197064
8 198348
9 196345
10
A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia.
198042
11
A causal analysis of birth weight in the offspring of monozygotic twins.
198340
12
Amish albinism: a distinctive autosomal recessive phenotype.
197039
13 197138
14
The epidemiology of pregnancy complications and outcome in a Norwegian twin population.
199235
15 199234
16 197333
17
Nucleolar organizer region variants as a risk factor for Down syndrome.
198533
18 198428
19 198726
20 200124

About W E Nance

W E Nance is a scholar working on Molecular Biology, Genetics, Cell Biology, Surgery and Pediatrics, Perinatology and Child Health, having authored 51 papers that have together received 1.5k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), Biotin and Related Studies (5 papers), Cognitive Abilities and Testing (4 papers), melanin and skin pigmentation (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Epigenetics and DNA Methylation (3 papers) and Hemoglobinopathies and Related Disorders (3 papers). The work is most often cited by research in Sensory Systems (165 citations), Cell Biology (204 citations), Genetics (323 citations), Ophthalmology (85 citations) and Pediatrics, Perinatology and Child Health (178 citations). W E Nance has collaborated with scholars based in United States, United Kingdom and Norway. Frequent co-authors include P. M. Conneally, Joann A. Boughman, Linda A. Corey, Carl J. Witkop, Heun Y. Yune, David Bixler, Freeman McConnell, Cynthia C. Morton, J.A. Brown and O. Smithies. Their work appears in journals such as Clinical Genetics, Clinical Chemistry, Cold Spring Harbor Symposia on Quantitative Biology, Circulation and Journal of Inherited Metabolic Disease.

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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