Holly A.F. Stessman

8.7k citations
33 papers · 1.3k indexed · 1 hit paper · h-index 15
Topics
Genetics and Neurodevelopmental Disorders (9 papers)Multiple Myeloma Research and Treatments (7 papers)Protein Degradation and Inhibitors (7 papers)

In The Last Decade

Holly A.F. Stessman

28 papers receiving 1.3k citations

Hit Papers

Excess of rare, inherited truncating mutations in autism20152026201820222015100200300

Peers

Holly A.F. Stessman
Comparison fields: 5 of 89
  • Genetics 824
  • Molecular Biology 714
  • Cognitive Neuroscience 464
  • Hematology 98
  • Cellular and Molecular Neuroscience 82
Replace Ryan M. Teague with:
Ryan M. Teague United States
Seda S. Tolu United States
Francesca Ariani Italy
Kiran K. Mantripragada United Kingdom
Niklas Krumm United States
Masaaki Nishiyama Japan
Ragnheiður Fossdal Iceland
James M. Stafford United States
Yeun Jun Chung South Korea
Katherine Lachlan United Kingdom
Holly A.F. Stessman relative to Ryan M. Teague United States Ryan M. Teague's profile →
Citations per field
00.5×
Ryan M. Teague · 1×
Citations per year

Countries citing papers authored by Holly A.F. Stessman

Since Specialization
Citations

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

Fields of papers citing papers by Holly A.F. Stessman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Holly A.F. Stessman. 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 Holly A.F. Stessman. The network helps show where Holly A.F. Stessman may publish in the future.

Co-authorship network of co-authors of Holly A.F. Stessman

This figure shows the co-authorship network connecting the top 25 collaborators of Holly A.F. Stessman. A scholar is included among the top collaborators of Holly A.F. Stessman 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 Holly A.F. Stessman. Holly A.F. Stessman 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 0
2 1
3 0
4 2
5 23
6 3
7 22
8 166
9 17
10 5
11 14
12 120
13 15
14
Excess of rare, inherited truncating mutations in autismbreakdown →
345
15 144
16 15
17 223
18 5
19 62
20 15

About Holly A.F. Stessman

Holly A.F. Stessman is a scholar working on Hematology, Genetics and Clinical Biochemistry, having authored 33 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Multiple Myeloma Research and Treatments (7 papers) and Protein Degradation and Inhibitors (7 papers). The work is most often cited by research in Genetics (824 citations), Cognitive Neuroscience (464 citations) and Molecular Biology (714 citations). Holly A.F. Stessman has collaborated with scholars based in United States, Poland and Israel. Frequent co-authors include Evan E. Eichler, Raphael Bernier, Kali Witherspoon, Laura Vives, Carl Baker, Tychele N. Turner, Bradley P. Coe, Niklas Krumm, Suzanne M. Leal and Archana N. Raja. Their work appears in journals such as Cell, Nucleic Acids Research and Nature Communications.

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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