Bethan E. Hoskins

4.3k citations

20 papers · 2.4k · h-index 16

Impact in

Genetics top 1%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
Nephrology top 2%
- Renal Diseases and Glomerulopathies

Papers in

Molecular Biology 14
- Hedgehog Signaling Pathway Studies 6
- Renal and related cancers 6
Genetics 11
- Genetic and Kidney Cyst Diseases 11
- Genetic Syndromes and Imprinting 10

Co-authors: Philip L. Beales (8 shared papers)Nicholas Katsanis (6 shared papers)José L. Badano (4 shared papers)Erica R. Eichers (4 shared papers)Stephen J. Ansley (4 shared papers)Richard A. Lewis (3 shared papers)James R. Lupski (3 shared papers)Carmen C. Leitch (3 shared papers)
Journals: Nephrology Dialysis Transplantation (3 papers)Nature Genetics (2 papers)The American Journal of Human Genetics (2 papers)European Journal of Human Genetics (2 papers)Kidney International (2 papers)
Partner nations: United States United Kingdom Germany

In The Last Decade

Bethan E. Hoskins

20 papers receiving 2.4k citations

Peers

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-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome Nature ·Stephen J. Ansley, José L. Badano, Oliver E. Blacque, Josephine Hill, Bethan E. Hoskins, Carmen C. Leitch, Jun Chul Kim, Alison Ross, Erica R. Eichers, Tanya M. Teslovich, Allan K. Mah, Robert Johnsen, John C. Cavender, Richard A. Lewis, Michel R. Leroux, Philip L. Beales, Nicholas Katsanis	2003	495
2	Triallelic Inheritance in Bardet-Biedl Syndrome, a Mendelian Recessive Disorder Science ·Nicholas Katsanis, Stephen J. Ansley, José L. Badano, Erica R. Eichers, Richard A. Lewis, Bethan E. Hoskins, Peter Scambler, William S. Davidson, Philip L. Beales, James R. Lupski	2001	438
3	The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression Nature Genetics ·Jun Chul Kim, José L. Badano, Sonja Sibold, Muneer A. Esmail, Josephine Hill, Bethan E. Hoskins, Carmen C. Leitch, Kerrie Venner, Stephen J. Ansley, Alison Ross, Michel R. Leroux, Nicholas Katsanis, Philip L. Beales	2004	329
4	Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse Nature Genetics ·Heather Kulaga, Carmen C. Leitch, Erica R. Eichers, José L. Badano, Alysa Lesemann, Bethan E. Hoskins, James R. Lupski, Philip L. Beales, Randall R. Reed, Nicholas Katsanis	2004	270
5	Transcription Factor SIX5 Is Mutated in Patients with Branchio-Oto-Renal Syndrome The American Journal of Human Genetics ·Bethan E. Hoskins, Carl H. Cramer, Derek Silvius, Dan Zou, Richard M. Raymond, Dana J. Orten, William J. Kimberling, Richard J. Smith, Dominique Weil, Christine Petit, Edgar A. Otto, Pin-Xian Xu, Friedhelm Hildebrandt	2007	137
6	Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders Kidney International ·K Hasselbacher, Roger C. Wiggins, Verena Matejas, Bernward Hinkes, Bettina E. Mucha, Bethan E. Hoskins, Fatih Özaltın, Gudrun Nürnberg, C. Becker, Daniela Hangan, Martina Pohl, Eberhard Kuwertz-Bröking, Martin Griebel, Valerié Schumacher, Brigitte Royer‐Pokora, Ayşı̇n Bakkaloğlu, Peter Nürnberg, Martin Zenker, Friedhelm Hildebrandt	2006	136
7	Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS) Nephrology Dialysis Transplantation ·Rasheed Gbadegesin, Bernward Hinkes, Bethan E. Hoskins, Christopher N. Vlangos, Saskia F. Heeringa, J. Liu, C Loirat, Fatih Özaltın, S. Hashmi, Francis Ulmer, Roxana Cleper, Robert B. Ettenger, Corinne Antignac, Roger C. Wiggins, Martin Zenker, Friedhelm Hildebrandt	2007	99
8	BBS4 Is a Minor Contributor to Bardet-Biedl Syndrome and May Also Participate in Triallelic Inheritance The American Journal of Human Genetics ·Nicholas Katsanis, Erica R. Eichers, Stephen J. Ansley, Richard A. Lewis, Hülya Kayserili, Bethan E. Hoskins, Peter Scambler, Philip L. Beales, James R. Lupski	2002	90
9	Mutations in the Wilms' Tumor 1 Gene Cause Isolated Steroid Resistant Nephrotic Syndrome and Occur in Exons 8 and 9 Pediatric Research ·Bettina E. Mucha, Fatih Özaltın, Bernward Hinkes, K Hasselbacher, Rainer Ruf, Michael Schultheiß, Daniela Hangan, Bethan E. Hoskins, Anne Schulze Everding, Radovan Bogdanović, Thomas Seeman, Bernd Höppe, Friedhelm Hildebrandt	2006	88
10	Risk Factors for Severe Renal Disease in Bardet–Biedl Syndrome Journal of the American Society of Nephrology ·Elizabeth Forsythe, Kathryn Sparks, Sunayna Best, Sarah Borrows, Bethan E. Hoskins, Ataf Sabir, Timothy Barrett, Denise Williams, Shehla Mohammed, David Goldsmith, David V. Milford, Detlef Böckenhauer, Lukas Foggensteiner, Philip L. Beales	2016	74
11	Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis Kidney International ·Pawaree Saisawat, Velibor Tasić, Virginia Vega-Warner, Elijah O. Kehinde, Barbara Günther, Rannar Airik, Jeffrey W. Innis, Bethan E. Hoskins, Julia Hoefele, Edgar A. Otto, Friedhelm Hildebrandt	2011	65
12	Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome Nephrology Dialysis Transplantation ·Saskia F. Heeringa, Christopher N. Vlangos, Gil Chernin, Bernward Hinkes, Rasheed Gbadegesin, J. Liu, Bethan E. Hoskins, Fatih Özaltın, Friedhelm Hildebrandt, (unknown)	2008	56
13	Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum Scientific Reports ·Maleeha Maria, Ideke J.C. Lamers, Miriam Schmidts, Muhammad Ajmal, Sulman Jaffar, Ehsan Ullah, Bilal Mustafa, Shakeel Ahmad, Katia Nazmutdinova, Bethan E. Hoskins, Erwin van Wijk, Linda Koster‐Kamphuis, Muhammad Imran Khan, Phil Beales, Frans P.M. Cremers, Ronald Roepman, Maleeha Azam, Heleen H. Arts, Raheel Qamar	2016	31
14	Arrayed primer extension technology simplifies mutation detection in Bardet–Biedl and Alström syndrome European Journal of Human Genetics ·Inés Pereiro, Bethan E. Hoskins, Jan D. Marshall, Gayle B. Collin, Jürgen Κ. Naggert, Teresa Piñeiro-Gallego, Eneli Oitmaa, Nicholas Katsanis, Diana Valverde, Philip L. Beales	2010	31
15	Identification of BRAF as a new interactor of PLCε1, the protein mutated in nephrotic syndrome type 3 American Journal of Physiology-Renal Physiology ·Hassan Chaı̈b, Bethan E. Hoskins, Shazia Ashraf, Meera Goyal, Roger C. Wiggins, Friedhelm Hildebrandt	2007	26
16	Genetic predictors of cardiovascular morbidity in Bardet–Biedl syndrome Clinical Genetics ·Elisabeth Forsythe, Kristie M Sparks, Bethan E. Hoskins, Emmanouil Bagkeris, Barbara McGowan, Paul Carroll, M. S. B. Huda, S. Mujahid, Christopher J. Peters, Timothy Barrett, Shehla Mohammed, Phillip Beales	2014	26
17	Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT) Pediatric Nephrology ·Matthias T. F. Wolf, Bethan E. Hoskins, Bodo B. Beck, Bernd Höppe, Velibor Tasić, Edgar A. Otto, Friedhelm Hildebrandt	2008	13
18	Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24 Nephrology Dialysis Transplantation ·Shazia Ashraf, Bethan E. Hoskins, H. Chaib, Julia Hoefele, Andreas Pasch, Pawaree Saisawat, F. K. Trefz, Hans-Walter Hacker, Gudrun Nuernberg, Peter Nüernberg, Edgar A. Otto, Friedhelm Hildebrandt	2009	12
19	Evaluation of multiplex capillary heteroduplex analysis: A rapid and sensitive mutation screening technique Human Mutation ·Bethan E. Hoskins, Anita Thorn, Peter Scambler, Philip L. Beales	2003	11
20	Biallelic P4HTM variants associated with HIDEA syndrome and mitochondrial respiratory chain complex I deficiency European Journal of Human Genetics ·Eleanor Hay, Louise C. Wilson, Bethan E. Hoskins, Martin Samuels, Pinki Munot, Shamima Rahman	2021	5

About Bethan E. Hoskins

Bethan E. Hoskins is a scholar working on Molecular Biology, Genetics, Nephrology, Urology and Pulmonary and Respiratory Medicine, having authored 20 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (11 papers), Genetic Syndromes and Imprinting (10 papers), Hedgehog Signaling Pathway Studies (6 papers), Renal and related cancers (6 papers), Renal Diseases and Glomerulopathies (4 papers), Urological Disorders and Treatments (3 papers), Chronic Kidney Disease and Diabetes (2 papers) and Renal cell carcinoma treatment (2 papers). The work is most often cited by research in Genetics (1.6k citations), Nephrology (358 citations), Molecular Biology (1.7k citations), Aging (37 citations) and Sensory Systems (90 citations). Bethan E. Hoskins has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Philip L. Beales, Nicholas Katsanis, José L. Badano, Erica R. Eichers, Stephen J. Ansley, Richard A. Lewis, James R. Lupski, Carmen C. Leitch, Peter Scambler and Alison Ross. Their work appears in journals such as Nephrology Dialysis Transplantation, Nature Genetics, The American Journal of Human Genetics, European Journal of Human Genetics and Kidney International.

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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