Andrea Penton

1.3k citations
17 papers · 1.1k · h-index 11

Impact in

    • Hippo pathway signaling and YAP/TAZ
    • Developmental Biology and Gene Regulation
    • Wnt/β-catenin signaling in development and cancer
    • TGF-β signaling in diseases
    • Cancer-related gene regulation
    • Hedgehog Signaling Pathway Studies

Papers in

    • Developmental Biology and Gene Regulation 7
    • Wnt/β-catenin signaling in development and cancer 3
    • TGF-β signaling in diseases 2
    • Cancer-related gene regulation 2
    • Genetic Syndromes and Imprinting 3
    • Genomic variations and chromosomal abnormalities 3

Andrea Penton

14 papers receiving 1.1k citations

Peers

Andrea Penton
Comparison fields: 5 of 85
  • Cell Biology 289
  • Molecular Biology 886
  • Aging 20
  • Cellular and Molecular Neuroscience 190
  • Genetics 120
Replace Marian B. Wilkin with:
Marian B. Wilkin United Kingdom
Adam Cliffe Singapore
Jianwu Bai United States
Kazuya Hori Japan
Alexandre Djiane France
Eugene Buff United States
Jacinta Caddy Australia
Liang Schweizer United States
Petra Pandur Germany
Vern Twombly United States
Andrea Penton relative to Marian B. Wilkin United Kingdom Marian B. Wilkin's profile →
Citations per field
00.5×1.5×
Marian B. Wilkin · 1×
Citations per year

Countries citing papers authored by Andrea Penton

Since Specialization
Citations

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

Fields of papers citing papers by Andrea Penton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

17 of 17 papers shown
#Work
1 2012252
2 1994231
3 200297
4 199692
5 200385
6 199876
7 199775
8 199771
9 200843
10 199731
11 199419
12 20216
13 20152
14 20181
15 20240
16 20240
17 20240

About Andrea Penton

Andrea Penton is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cell Biology and Cellular and Molecular Neuroscience, having authored 17 papers that have together received 1.1k indexed citations. Recurring topics across this work include Developmental Biology and Gene Regulation (7 papers), Prenatal Screening and Diagnostics (5 papers), Hippo pathway signaling and YAP/TAZ (4 papers), Wnt/β-catenin signaling in development and cancer (3 papers), Genetic Syndromes and Imprinting (3 papers), Genomic variations and chromosomal abnormalities (3 papers), TGF-β signaling in diseases (2 papers) and Cancer-related gene regulation (2 papers). The work is most often cited by research in Cell Biology (289 citations), Molecular Biology (886 citations), Aging (20 citations), Cellular and Molecular Neuroscience (190 citations) and Genetics (120 citations). Andrea Penton has collaborated with scholars based in United States, Netherlands and Japan. Frequent co-authors include F. Michael Hoffmann, Laura D. Leonard, Nancy B. Spinner, Andreas Wodarz, Roel Nusse, J.Aaron Cassill, Joan Massagué, Jeffrey L. Wrana, János Szidonya and Yijing Chen. Their work appears in journals such as Development, Journal of Neuroscience, Seminars in Cell and Developmental Biology, Molecular Cytogenetics and Genetics in Medicine.

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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