Denise Williams

4.7k citations
38 papers · 1.6k indexed · h-index 18
Topics
Prenatal Screening and Diagnostics (17 papers)Fetal and Pediatric Neurological Disorders (12 papers)Genomic variations and chromosomal abnormalities (8 papers)

In The Last Decade

Denise Williams

38 papers receiving 1.5k citations

Peers

Denise Williams
Comparison fields: 5 of 124
  • Genetics 704
  • Pediatrics, Perinatology and Child Health 574
  • Molecular Biology 461
  • Physiology 311
  • Surgery 235
Replace Yukio Tsunoda with:
Yukio Tsunoda Japan
Mojtaba Rezazadeh Valojerdi Iran
Julia F. Charles United States
Don A. Baldwin United States
Wade Bushman United States
Tomohito Hayashi Japan
Wei Si China
Franklin D. West United States
Nicola Bernabò Italy
Isao Narama Japan
Denise Williams relative to Yukio Tsunoda Japan Yukio Tsunoda's profile →
Citations per field
00.5×10×17.3×
Yukio Tsunoda · 1×
Citations per year

Countries citing papers authored by Denise Williams

Since Specialization
Citations

This map shows the geographic impact of Denise Williams'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 Denise Williams with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Denise Williams more than expected).

Fields of papers citing papers by Denise Williams

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Denise Williams. 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 Denise Williams. The network helps show where Denise Williams may publish in the future.

Co-authorship network of co-authors of Denise Williams

This figure shows the co-authorship network connecting the top 25 collaborators of Denise Williams. A scholar is included among the top collaborators of Denise Williams 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 Denise Williams. Denise Williams is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
#WorkIndexed citations
1 2
2 5
3 12
4 29
5 18
6 20
7 6
8 4
9 74
10 30
11 80
12 23
13 3
14 46
15 18
16 34
17 233
18 161
19 15
20 135

About Denise Williams

Denise Williams is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Genetics, having authored 38 papers that have together received 1.6k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (17 papers), Fetal and Pediatric Neurological Disorders (12 papers) and Genomic variations and chromosomal abnormalities (8 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (574 citations), Genetics (704 citations) and Aging (32 citations). Denise Williams has collaborated with scholars based in United Kingdom, France and United States. Frequent co-authors include Chiaki Mukai, A. Kuipers, Mark D. Kilby, Danielle I. Young, Marian F. Young, Dominic McMullan, Sarah Hillman, Eamonn R. Maher, Stephanie Allen and Fiona S. Togneri. Their work appears in journals such as Diabetes, Journal of the American Society of Nephrology and The American Journal of 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026