Andrea Penton

1.3k total citations
17 papers, 1.1k citations indexed

About

Andrea Penton is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Andrea Penton has authored 17 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Andrea Penton's work include Developmental Biology and Gene Regulation (7 papers), Prenatal Screening and Diagnostics (5 papers) and Hippo pathway signaling and YAP/TAZ (4 papers). Andrea Penton is often cited by papers focused on Developmental Biology and Gene Regulation (7 papers), Prenatal Screening and Diagnostics (5 papers) and Hippo pathway signaling and YAP/TAZ (4 papers). Andrea Penton collaborates with scholars based in United States, Australia and Germany. Andrea Penton's co-authors include F. Michael Hoffmann, Laura D. Leonard, Nancy B. Spinner, Roel Nusse, Andreas Wodarz, Liliana Attisano, Joan Massagué, J.Aaron Cassill, Jeffrey L. Wrana and Yijing Chen and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Andrea Penton

14 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Andrea Penton United States	11	886	289	190	120	70	17	1.1k
Veit Riechmann Germany	14	926 1.0×	419 1.4×	134 0.7×	136 1.1×	122 1.7×	23	1.2k
Alan Jian Zhu China	15	919 1.0×	378 1.3×	126 0.7×	172 1.4×	71 1.0×	26	1.3k
Marcel Wehrli United States	11	1.2k 1.4×	359 1.2×	185 1.0×	190 1.6×	96 1.4×	14	1.4k
Alexandre Djiane France	16	1.1k 1.2×	586 2.0×	185 1.0×	141 1.2×	81 1.2×	21	1.4k
Jocelyn A. McDonald United States	16	539 0.6×	435 1.5×	232 1.2×	57 0.5×	81 1.2×	26	883
Marian B. Wilkin United Kingdom	14	787 0.9×	285 1.0×	157 0.8×	105 0.9×	104 1.5×	16	981
Eugene Buff United States	9	825 0.9×	458 1.6×	188 1.0×	122 1.0×	119 1.7×	11	989
Adam Cliffe Singapore	11	761 0.9×	387 1.3×	109 0.6×	76 0.6×	66 0.9×	18	1.1k
Maria Langegger Germany	8	712 0.8×	494 1.7×	98 0.5×	87 0.7×	50 0.7×	8	1.0k
Kazuya Hori Japan	14	954 1.1×	291 1.0×	121 0.6×	72 0.6×	109 1.6×	19	1.2k

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-authorship network of co-authors of Andrea Penton

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

All Works

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17 of 17 papers shown

Arreola, Alexandra, Gloria Haskell, Inder Gadi, Andrea Penton, & Stuart Schwartz. (2024). Utilization of a SNP microarray to detect uniparental disomy: Implications and outcomes. Genetics in Medicine. 26(12). 101275–101275.

Haskell, Gloria, Alexandra Arreola, Christine M. Riordan, et al.. (2024). Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes. Prenatal Diagnosis. 44(5). 586–594.

Penton, Andrea, Peter Papenhausen, Stuart Schwartz, Tuan A. Vu, & Gloria Haskell. (2024). P140: A rare phenomenon: Double trisomy rescue detected during clinical SNP microarray testing*. SHILAP Revista de lepidopterología. 2. 101037–101037.

Papenhausen, Peter, et al.. (2021). Clinical significance and mechanisms associated with segmental UPD. Molecular Cytogenetics. 14(1). 38–38. 6 indexed citations

Penton, Andrea, Peter Papenhausen, Stuart Schwartz, & James Tepperberg. (2018). 35. Runs of homozygosity (ROH) reveal that segmental-UPD is associated with the repair of genomic imbalance. Cancer Genetics. 224-225. 64–64. 1 indexed citations

Yelavarthi, Krishna K., Golder N. Wilson, Luis Rohena, et al.. (2015). Partial monosomy of 11q22.2q22.3 including the SDHD gene in individuals with developmental delay. American Journal of Medical Genetics Part A. 167(4). 695–700. 2 indexed citations

Penton, Andrea, Laura D. Leonard, & Nancy B. Spinner. (2012). Notch signaling in human development and disease. Seminars in Cell and Developmental Biology. 23(4). 450–457. 252 indexed citations

Hoopfer, Eric D., et al.. (2008). Genomic Analysis of Drosophila Neuronal Remodeling: A Role for the RNA-Binding Protein Boule as a Negative Regulator of Axon Pruning. Journal of Neuroscience. 28(24). 6092–6103. 43 indexed citations

Penton, Andrea, Pierre Billuart, Ethan K. Scott, et al.. (2003). A mosaic genetic screen for genes necessary forDrosophilamushroom body neuronal morphogenesis. Development. 130(6). 1203–1213. 85 indexed citations

10.

Penton, Andrea, Andreas Wodarz, & Roel Nusse. (2002). A Mutational Analysis of dishevelled in Drosophila Defines Novel Domains in the Dishevelled Protein as Well as Novel Suppressing Alleles of axin. Genetics. 161(2). 747–762. 97 indexed citations

11.

Horsfield, Julia A., et al.. (1998). decapentaplegic is required for arrest in G1 phase during Drosophila eye development. Development. 125(24). 5069–5078. 76 indexed citations

12.

Penton, Andrea, Scott B. Selleck, & F. Michael Hoffmann. (1997). Regulation of Cell Cycle Synchronization by decapentaplegic During Drosophila Eye Development. Science. 275(5297). 203–206. 75 indexed citations

13.

Burgess, Diane, Andrea Penton, Pamela Dunsmuir, & Hugo K. Dooner. (1997). Molecular cloning and characterization of ADP-glucose pyrophosphorylase cDNA clones isolated from pea cotyledons. Plant Molecular Biology. 33(3). 431–444. 31 indexed citations

14.

Singer, Matthew A., Andrea Penton, Vern Twombly, F. Michael Hoffmann, & William M Gelbart. (1997). Signaling through both type I DPP receptors is required for anterior-posterior patterning of the entire Drosophila wing. Development. 124(1). 79–89. 71 indexed citations

15.

Penton, Andrea & F. Michael Hoffmann. (1996). Decapentaplegic restricts the domain of wingless during Drosophila limb patterning. Nature. 382(6587). 162–165. 92 indexed citations

16.

Penton, Andrea, Yijing Chen, Karen Staehling-Hampton, et al.. (1994). Identification of two bone morphogenetic protein type I receptors in Drosophila and evidence that Brk25D is a decapentaplegic receptor. Cell. 78(2). 239–250. 231 indexed citations

17.

Heberlein, Ulrike, et al.. (1994). The C-terminus of the homeodomain is required for functional specificity of the Drosophila rough gene. Mechanisms of Development. 48(1). 35–49. 19 indexed citations

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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