Paulette Barahona

827 total citations
14 papers, 148 citations indexed

About

Paulette Barahona is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Paulette Barahona has authored 14 papers receiving a total of 148 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Paulette Barahona's work include Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Fetal and Pediatric Neurological Disorders (3 papers). Paulette Barahona is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Fetal and Pediatric Neurological Disorders (3 papers). Paulette Barahona collaborates with scholars based in Australia, United States and France. Paulette Barahona's co-authors include Fergus Scott, Louise Carey, Andrew McLennan, W.D. Greville, Don Leigh, Yvonne Tay, Isidore Rigoutsos, Peter Dröge, Paul G. Ekert and Carel Pretorius and has published in prestigious journals such as Cancer Research, Clinical Chemistry and European Journal of Cancer.

In The Last Decade

Paulette Barahona

12 papers receiving 133 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paulette Barahona Australia 6 88 74 36 21 20 14 148
Olga Shamardina United Kingdom 3 129 1.5× 32 0.4× 56 1.6× 8 0.4× 27 1.4× 3 192
Aurélie Coussement France 7 67 0.8× 38 0.5× 40 1.1× 33 1.6× 6 0.3× 16 141
Ulrik Kristoffer Stoltze Denmark 8 55 0.6× 39 0.5× 73 2.0× 6 0.3× 15 0.8× 19 137
Myrthe van den Born Netherlands 7 38 0.4× 30 0.4× 29 0.8× 41 2.0× 5 0.3× 12 160
Guillaume Jedraszak France 7 62 0.7× 28 0.4× 53 1.5× 8 0.4× 3 0.1× 26 147
Brian D. Kuchinka Canada 7 162 1.8× 151 2.0× 84 2.3× 16 0.8× 3 0.1× 8 237
Nakamichi Saito Japan 6 47 0.5× 30 0.4× 71 2.0× 47 2.2× 7 0.3× 12 147
Zhenjun Yang China 6 146 1.7× 139 1.9× 59 1.6× 27 1.3× 2 0.1× 6 221
Zita Halász Hungary 8 164 1.9× 12 0.2× 131 3.6× 20 1.0× 16 0.8× 20 267
Elham Al Mardawi Saudi Arabia 4 93 1.1× 29 0.4× 92 2.6× 14 0.7× 2 0.1× 5 153

Countries citing papers authored by Paulette Barahona

Since Specialization
Citations

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

Fields of papers citing papers by Paulette Barahona

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paulette Barahona

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

All Works

14 of 14 papers shown
1.
Brown, Lauren M., Antoine de Weck, Thomas Robertson, et al.. (2025). A novel TRKB-activating internal tandem duplication characterizes a new mechanism of receptor tyrosine kinase activation. npj Precision Oncology. 9(1). 137–137.
2.
Mayoh, Chelsea, Marie Wong, Paul G. Ekert, et al.. (2024). Novel paediatric case of a spinal high-grade astrocytoma with piloid features in a patient with Noonan Syndrome. npj Precision Oncology. 8(1). 236–236. 1 indexed citations
3.
Mayoh, Chelsea, Paulette Barahona, Loretta M. S. Lau, et al.. (2024). Abstract B014: Increasing the clinical utility of transcriptome analysis in high-risk childhood precision oncology. Cancer Research. 84(17_Supplement). B014–B014.
4.
Geoerger, Birgit, Lynley V. Marshall, Karsten Nysom, et al.. (2023). Afatinib in paediatric patients with recurrent/refractory ErbB-dysregulated tumours: Results of a phase I/expansion trial. European Journal of Cancer. 188. 8–19. 3 indexed citations
5.
Pretorius, Carel, Paulette Barahona, Jim McGill, et al.. (2023). Feasibility of Targeted Next-Generation DNA Sequencing for Expanding Population Newborn Screening. Clinical Chemistry. 69(8). 890–900. 5 indexed citations
6.
Shum, Bennett O. V., et al.. (2023). Technical feasibility of newborn screening for spinal muscular atrophy by next-generation DNA sequencing. Frontiers in Genetics. 14. 1095600–1095600. 10 indexed citations
7.
Shum, Bennett O. V., Rasa Ruseckaite, Natalie A. Twine, et al.. (2022). The inequity of targeted cystic fibrosis reproductive carrier screening tests in Australia. Prenatal Diagnosis. 43(1). 109–116. 2 indexed citations
8.
Lau, Loretta M. S., Paulette Barahona, Marie Wong, et al.. (2021). Efficacy of MEK inhibition in a recurrent malignant peripheral nerve sheath tumor. npj Precision Oncology. 5(1). 9–9. 21 indexed citations
9.
Howlett, Meegan, Chelsea Mayoh, Marie Wong, et al.. (2020). A Novel Orthotopic Patient-Derived Xenograft Model of Radiation-Induced Glioma Following Medulloblastoma. Cancers. 12(10). 2937–2937. 4 indexed citations
10.
Carey, Louise, et al.. (2014). Prenatal diagnosis of chromosomal mosaicism in over 1600 cases using array comparative genomic hybridization as a first line test. Prenatal Diagnosis. 34(5). 478–486. 38 indexed citations
11.
Scott, Fergus, et al.. (2013). OP17.08: Prenatal diagnosis using combined qf‐PCR and array CGH analysis as a first line test: results from over 1000 consecutive cases. Ultrasound in Obstetrics and Gynecology. 42(s1). 97–97. 3 indexed citations
12.
13.
Tay, Yvonne, et al.. (2009). Insights into the Regulation of a Common Variant of HMGA2 Associated with Human Height During Embryonic Development. Stem Cell Reviews and Reports. 5(4). 328–333. 15 indexed citations
14.
Barahona, Paulette, et al.. (1997). Effect of oviductal secretions and cells on fertilizing ability of goat spermatozoa in vitro. Theriogenology. 47(1). 331–331. 3 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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