Bethan E. Hoskins

4.3k total citations
20 papers, 2.4k citations indexed

About

Bethan E. Hoskins is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Bethan E. Hoskins has authored 20 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Genetics and 4 papers in Nephrology. Recurrent topics in Bethan E. Hoskins's work include Genetic and Kidney Cyst Diseases (11 papers), Genetic Syndromes and Imprinting (10 papers) and Hedgehog Signaling Pathway Studies (6 papers). Bethan E. Hoskins is often cited by papers focused on Genetic and Kidney Cyst Diseases (11 papers), Genetic Syndromes and Imprinting (10 papers) and Hedgehog Signaling Pathway Studies (6 papers). Bethan E. Hoskins collaborates with scholars based in United States, United Kingdom and Germany. Bethan E. Hoskins's co-authors include Philip L. Beales, Nicholas Katsanis, José L. Badano, Erica R. Eichers, Stephen J. Ansley, Richard A. Lewis, Carmen C. Leitch, James R. Lupski, Peter Scambler and Alison Ross and has published in prestigious journals such as Nature, Science and Nature Genetics.

In The Last Decade

Bethan E. Hoskins

20 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bethan E. Hoskins United States 16 1.7k 1.6k 358 274 209 20 2.4k
Noel Murcia United States 12 2.5k 1.5× 2.4k 1.5× 123 0.3× 390 1.4× 350 1.7× 16 3.3k
David J. Bunyan United Kingdom 23 991 0.6× 979 0.6× 188 0.5× 108 0.4× 304 1.5× 60 2.0k
Yoav Segal United States 22 1.1k 0.6× 845 0.5× 174 0.5× 200 0.7× 371 1.8× 40 1.9k
David Geneviève France 24 1.3k 0.8× 1.1k 0.7× 65 0.2× 233 0.9× 136 0.7× 80 2.3k
Israela Lerer Israel 29 1.2k 0.7× 972 0.6× 68 0.2× 108 0.4× 237 1.1× 77 2.5k
Elena Torban Canada 23 1.4k 0.8× 438 0.3× 231 0.6× 319 1.2× 66 0.3× 43 1.8k
Yoko Kurotaki Japan 13 856 0.5× 603 0.4× 429 1.2× 111 0.4× 123 0.6× 16 1.5k
Tatjana Levi United States 9 1.9k 1.1× 534 0.3× 480 1.3× 88 0.3× 124 0.6× 9 3.0k
Koji Muroya Japan 28 1.9k 1.1× 1.9k 1.2× 93 0.3× 47 0.2× 62 0.3× 119 3.1k
Dieter Kotzot Austria 29 1.3k 0.8× 1.9k 1.2× 99 0.3× 65 0.2× 104 0.5× 100 2.9k

Countries citing papers authored by Bethan E. Hoskins

Since Specialization
Citations

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

Fields of papers citing papers by Bethan E. Hoskins

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bethan E. Hoskins. 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 Bethan E. Hoskins. The network helps show where Bethan E. Hoskins may publish in the future.

Co-authorship network of co-authors of Bethan E. Hoskins

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

All Works

20 of 20 papers shown
1.
Wilson, Louise C., et al.. (2021). Biallelic P4HTM variants associated with HIDEA syndrome and mitochondrial respiratory chain complex I deficiency. European Journal of Human Genetics. 29(10). 1536–1541. 5 indexed citations
2.
Lamers, Ideke J.C., Miriam Schmidts, Muhammad Ajmal, et al.. (2016). Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum. Scientific Reports. 6(1). 34764–34764. 31 indexed citations
3.
Forsythe, Elizabeth, Sunayna Best, Bethan E. Hoskins, et al.. (2016). Risk Factors for Severe Renal Disease in Bardet–Biedl Syndrome. Journal of the American Society of Nephrology. 28(3). 963–970. 74 indexed citations
4.
Hoskins, Bethan E., Emmanouil Bagkeris, Barbara McGowan, et al.. (2014). Genetic predictors of cardiovascular morbidity in Bardet–Biedl syndrome. Clinical Genetics. 87(4). 343–349. 26 indexed citations
5.
Saisawat, Pawaree, Velibor Tasić, Virginia Vega-Warner, et al.. (2011). Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis. Kidney International. 81(2). 196–200. 65 indexed citations
6.
Hoskins, Bethan E., Jan D. Marshall, Gayle B. Collin, et al.. (2010). Arrayed primer extension technology simplifies mutation detection in Bardet–Biedl and Alström syndrome. European Journal of Human Genetics. 19(4). 485–488. 31 indexed citations
7.
Ashraf, Shazia, Bethan E. Hoskins, H. Chaib, et al.. (2009). Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24. Nephrology Dialysis Transplantation. 25(5). 1496–1501. 12 indexed citations
8.
Wolf, Matthias T. F., Bethan E. Hoskins, Bodo B. Beck, et al.. (2008). Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT). Pediatric Nephrology. 24(1). 55–60. 13 indexed citations
9.
Heeringa, Saskia F., Christopher N. Vlangos, Gil Chernin, et al.. (2008). Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome. Nephrology Dialysis Transplantation. 23(11). 3527–3533. 56 indexed citations
10.
Hoskins, Bethan E., Carl H. Cramer, Derek Silvius, et al.. (2007). Transcription Factor SIX5 Is Mutated in Patients with Branchio-Oto-Renal Syndrome. The American Journal of Human Genetics. 80(4). 800–804. 137 indexed citations
11.
Gbadegesin, Rasheed, Bernward Hinkes, Bethan E. Hoskins, et al.. (2007). Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS). Nephrology Dialysis Transplantation. 23(4). 1291–1297. 99 indexed citations
12.
Chaı̈b, Hassan, Bethan E. Hoskins, Shazia Ashraf, et al.. (2007). Identification of BRAF as a new interactor of PLCε1, the protein mutated in nephrotic syndrome type 3. American Journal of Physiology-Renal Physiology. 294(1). F93–F99. 26 indexed citations
13.
Mucha, Bettina E., Fatih Özaltın, Bernward Hinkes, et al.. (2006). Mutations in the Wilms' Tumor 1 Gene Cause Isolated Steroid Resistant Nephrotic Syndrome and Occur in Exons 8 and 9. Pediatric Research. 59(2). 325–331. 88 indexed citations
14.
Hasselbacher, K, Roger C. Wiggins, Verena Matejas, et al.. (2006). Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders. Kidney International. 70(6). 1008–1012. 136 indexed citations
15.
Kim, Jun Chul, José L. Badano, Muneer A. Esmail, et al.. (2004). The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression. Nature Genetics. 36(5). 462–470. 329 indexed citations
16.
Kulaga, Heather, Carmen C. Leitch, Erica R. Eichers, et al.. (2004). Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse. Nature Genetics. 36(9). 994–998. 270 indexed citations
17.
Ansley, Stephen J., José L. Badano, Oliver E. Blacque, et al.. (2003). Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome. Nature. 425(6958). 628–633. 495 indexed citations
18.
Hoskins, Bethan E., et al.. (2003). Evaluation of multiplex capillary heteroduplex analysis: A rapid and sensitive mutation screening technique. Human Mutation. 22(2). 151–157. 11 indexed citations
19.
Katsanis, Nicholas, Erica R. Eichers, Stephen J. Ansley, et al.. (2002). BBS4 Is a Minor Contributor to Bardet-Biedl Syndrome and May Also Participate in Triallelic Inheritance. The American Journal of Human Genetics. 71(1). 22–29. 90 indexed citations
20.
Katsanis, Nicholas, Stephen J. Ansley, José L. Badano, et al.. (2001). Triallelic Inheritance in Bardet-Biedl Syndrome, a Mendelian Recessive Disorder. Science. 293(5538). 2256–2259. 438 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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