Marianne L. Seto

770 citations
13 papers · 618 indexed · h-index 13
  • Genetics top 10%
    • Craniofacial Disorders and Treatments 9
    • Cleft Lip and Palate Research 6
    • Connective tissue disorders research 5
    • Congenital Ear and Nasal Anomalies 1
    • Congenital limb and hand anomalies 1
    • dental development and anomalies 3
    • Fibroblast Growth Factor Research 2
    • Bone Metabolism and Diseases 2
    • Craniofacial Disorders and Treatments 9
    • Cleft Lip and Palate Research 6
    • Connective tissue disorders research 5
    • Congenital Ear and Nasal Anomalies 1

Marianne L. Seto

13 papers receiving 606 citations

Peers

Marianne L. Seto
Comparison fields: 5 of 59
  • Genetics 338
  • Developmental Biology 20
  • Molecular Biology 422
  • Cell Biology 42
  • Genetics 27
Replace Meredith P. O'Rourke with:
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M Le Merrer France
Gabriele Gillessen-Kaesbach Germany
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Olivier Pichon France
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Marianne L. Seto relative to Meredith P. O'Rourke Australia Meredith P. O'Rourke's profile →
Citations per field
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Meredith P. O'Rourke · 1×
Citations per year

Countries citing papers authored by Marianne L. Seto

Since Specialization
Citations

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

Fields of papers citing papers by Marianne L. Seto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marianne L. Seto. 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 Marianne L. Seto. The network helps show where Marianne L. Seto may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Marianne L. Seto, 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 Marianne L. Seto Line = papers co-authored together Marianne L. Seto links everyone, so they are left out of the graph.

All Works

13 of 13 papers shown
#Work
1 201189
2 200916
3 200856
4 200782
5 200636
6 200659
7 200543
8 200493
9 200217
10 200116
11 200129
12 199761
13 199721

About Marianne L. Seto

Marianne L. Seto is a scholar working on Developmental Biology, Genetics and Molecular Biology, having authored 13 papers that have together received 618 indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (9 papers), Cleft Lip and Palate Research (6 papers), Connective tissue disorders research (5 papers), dental development and anomalies (3 papers), Fibroblast Growth Factor Research (2 papers), Bone Metabolism and Diseases (2 papers), Congenital Ear and Nasal Anomalies (1 paper) and Congenital limb and hand anomalies (1 paper). The work is most often cited by research in Genetics (338 citations), Developmental Biology (20 citations) and Molecular Biology (422 citations). Marianne L. Seto has collaborated with scholars based in United States. Frequent co-authors include Michael L. Cunningham, Jeong Kyo Yoon, Yong-Ri Jin, Xiang Han, Richard G. Ellenbogen, Anne Hing, Craig A. MacArthur, Joseph S. Gruss, Mark P. Hudson and Avery H. Weiss. Their work appears in journals such as Journal of Biological Chemistry, Birth Defects Research Part A Clinical and Molecular Teratology, The Cleft Palate-Craniofacial Journal, Plastic & Reconstructive Surgery and BMC Developmental Biology.

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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