Barbara Ploplis

1.0k total citations
7 papers, 713 citations indexed

About

Barbara Ploplis is a scholar working on Molecular Biology, Sensory Systems and Neurology. According to data from OpenAlex, Barbara Ploplis has authored 7 papers receiving a total of 713 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Sensory Systems and 2 papers in Neurology. Recurrent topics in Barbara Ploplis's work include Hearing, Cochlea, Tinnitus, Genetics (3 papers), Cancer-related molecular mechanisms research (2 papers) and RNA regulation and disease (2 papers). Barbara Ploplis is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (3 papers), Cancer-related molecular mechanisms research (2 papers) and RNA regulation and disease (2 papers). Barbara Ploplis collaborates with scholars based in United States, Pakistan and Japan. Barbara Ploplis's co-authors include Atsushi Watanabe, Kazuhisa Takeda, Masayoshi Tachibana, Edward R. Wilcox, Sheikh Riazuddin, Thomas B. Friedman, Robert J. Morell, Tamar Ben‐Yosef, Doris K. Wu and Andrew J. Griffith and has published in prestigious journals such as Cell, Nature Genetics and Human Molecular Genetics.

In The Last Decade

Barbara Ploplis

7 papers receiving 702 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Barbara Ploplis United States 6 455 268 231 178 92 7 713
Tenesha N. Smith United States 7 534 1.2× 351 1.3× 456 2.0× 87 0.5× 60 0.7× 7 857
Magdalena Beneyto Spain 18 738 1.6× 116 0.4× 328 1.4× 107 0.6× 22 0.2× 48 965
Denise M. Hoover United States 6 381 0.8× 92 0.3× 313 1.4× 121 0.7× 43 0.5× 7 562
Xuezhong Liu United States 11 461 1.0× 87 0.3× 350 1.5× 107 0.6× 35 0.4× 14 659
Lingyun Mei China 14 315 0.7× 107 0.4× 223 1.0× 159 0.9× 48 0.5× 61 531
Mohamed Drira Tunisia 12 431 0.9× 192 0.7× 517 2.2× 50 0.3× 33 0.4× 16 779
Eeva‐Marja Sankila Finland 18 811 1.8× 115 0.4× 345 1.5× 141 0.8× 26 0.3× 38 1.1k
Mirjam W.J. Luijendijk Netherlands 9 345 0.8× 88 0.3× 257 1.1× 78 0.4× 24 0.3× 10 579
Sigrid Wayne United States 11 344 0.8× 115 0.4× 364 1.6× 36 0.2× 26 0.3× 19 543
Laurence Jonard France 15 379 0.8× 135 0.5× 301 1.3× 44 0.2× 29 0.3× 36 742

Countries citing papers authored by Barbara Ploplis

Since Specialization
Citations

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

Fields of papers citing papers by Barbara Ploplis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Ploplis

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

All Works

7 of 7 papers shown
1.
Ahmed, Zubair M., Saima Riazuddin, Terry‐Lynn Young, et al.. (2004). Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan. BMC Medical Genetics. 5(1). 24–24. 28 indexed citations
2.
Wilcox, Edward R., Sadaf Naz, Saima Riazuddin, et al.. (2001). Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29. Cell. 104(1). 165–172. 344 indexed citations
3.
Watanabe, Atsushi, Kazuhisa Takeda, Barbara Ploplis, & Masayoshi Tachibana. (1998). Epistatic relationship between Waardenburg Syndrome genes MITF and PAX3. Nature Genetics. 18(3). 283–286. 220 indexed citations
4.
Tachibana, M., Nobuhisa Iwata, Atsushi Watanabe, et al.. (1996). Assignment of the gene for a ubiquitin-conjugating enzyme (UBE2I) to human chromosome band 16p13.3 by in situ hybridization. Cytogenetic and Genome Research. 75(4). 222–223. 4 indexed citations
5.
Jain, Pawan Kumar, Kunihiro Fukushima, Dilip Deshmukh, et al.. (1995). A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus. Human Molecular Genetics. 4(12). 2391–2394. 51 indexed citations
6.
Lalwani, Anil K., et al.. (1994). A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.. PubMed. 55(4). 685–94. 45 indexed citations
7.
Wilcox, Edward R., Marcelo N. Rivolta, Barbara Ploplis, S. Brian Potterf, & Jörgen Fex. (1992). The PAX3 gene is mapped to human chromosome 2 together with a highly informative CA dinucleotide repeat. Human Molecular Genetics. 1(3). 215–215. 21 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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