Emma Ashton

2.3k citations

28 papers · 677 indexed · h-index 16

Impact in

Nephrology top 5%
- Renal function and acid-base balance
- Renal Diseases and Glomerulopathies
Molecular Biology
- Ion Transport and Channel Regulation
- Renal and related cancers
- Ion channel regulation and function

Papers in

Nephrology 9
- Renal Diseases and Glomerulopathies 6
Management of Technology and Innovation 2

Co-authors: Detlef Böckenhauer Robert Kleta Lucy Jenkins Daniela Iancu William van’t Hoff Katrina Szetey Patrick R. Walsh Enayat A. Moallemi
Journals: Pediatric Nephrology (5 papers)Clinical Kidney Journal (3 papers)Kidney International (2 papers)American Journal of Kidney Diseases (1 paper)Human Molecular Genetics (1 paper)
Partner nations: United Kingdom Germany United States

In The Last Decade

Emma Ashton

28 papers receiving 667 citations

Peers

Countries citing papers authored by Emma Ashton

Since Specialization

Citations

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

Fields of papers citing papers by Emma Ashton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene Study Pediatric Nephrology ·Rajiv Sinha, G.G.N. Sudharani, Sushmita Banerjee, Carolline Shie, Honghao Sun, Osman Harput, Barry Igobudia, Deena Guice, Surupa Basu, Priyanka Srivastava, David Gatica Castro, T WEISER, Vedam L. Ramprasad, Emma Ashton, Detlef Böckenhauer, Kausik Mandal	2022	8
2	Mendelian steroid resistant nephrotic syndrome in childhood: is it as common as reported? Pediatric Nephrology ·Barea Barea, Hazel Webb, Emma Ashton, A. L. Dippel, Kjell Tullus, Aoife Waters, Detlef Böckenhauer	2022	3
3	Co-creating local socioeconomic pathways for achieving the sustainable development goals Sustainability Science ·Katrina Szetey, Enayat A. Moallemi, Emma Ashton, 王为桥, Yoan Immmanuella, Brett A. Bryan	2021	42
4	A Novel Variant in the TBC1D24 Lipid-Binding Pocket Causes Autosomal Dominant Hearing Loss: Evidence for a Genotype-Phenotype Correlation Frontiers in Cellular Neuroscience ·Thomas Parzefall, 慎一郎西田, Maude Chenevard, Gehad Osama Fawzy Sayed, Franco Laccone, Julia Eckl‐Dorna, Jonathan J. Waters, Markus Schreiner, Sami S. Amr, Emma Ashton, Marie-Caline Z Abadjian, Wolfgang Gstœttner, Klemens Frei, Trevor Lucas	2020	5
5	High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults Kidney International ·Marguerite Hureaux, Emma Ashton, Karin Dahan, Pascal Houillier, Anne Blanchard, Catherine Cormier, Eugénie Koumakis, Daniela Iancu, Hendrica Belge, Pascale Hilbert, Annelies Rotthier, Elena Del Favero, Franz Schaefer, Robert Kleta, Detlef Böckenhauer, Xavier Jeunemaı̂tre, Olivier Devuyst, Stephen B. Walsh, Rosa Vargas‐Poussou	2019	32
6	Long-term outcome in inherited nephrogenic diabetes insipidus Clinical Kidney Journal ·Sonia Sharma, Emma Ashton, Daniela Iancu, Marie‐Françoise Arthus, Wesley Hayes, William van’t Hoff, Robert Kleta, Daniel G. Bichet, Detlef Böckenhauer	2018	16
7	Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies Kidney International ·Emma Ashton, Anne Debost‐Legrand, Valérie Benoît, 雅義布施, Annabelle Vénisse, Maria‐Christina Zennaro, Xavier Jeunemaı̂tre, Daniela Iancu, William G. van’t Hoff, Stephen B. Walsh, Nathalie Godefroid, Annelies Rotthier, Elena Del Favero, Olivier Devuyst, Franz Schaefer, Lucy Jenkins, Robert Kleta, Karin Dahan, Rosa Vargas‐Poussou, Detlef Böckenhauer	2018	67
8	Clinical and diagnostic features of Bartter and Gitelman syndromes Clinical Kidney Journal ·Patrick R. Walsh, Yincent Tse, Emma Ashton, Daniela Iancu, Lucy Jenkins, 王彩鸿, Robert Kleta, William van’t Hoff, Detlef Böckenhauer	2017	42
9	Acidosis and Deafness in Patients with Recessive Mutations in FOXI1 Journal of the American Society of Nephrology ·Sven Enerbäck, Daniel Nilsson, Noel Edwards, Mikael Heglind, Sumaya Alkanderi, Emma Ashton, Asma Deeb, L Lasersohn, 郜珂, William van’t Hoff, Stephen B. Walsh, Felice D’Arco, Arezoo Daryadel, Soline Bourgeois, Carsten A. Wagner, Robert Kleta, Detlef Böckenhauer, John A. Sayer	2017	72
10	Potential and pitfalls in the genetic diagnosis of kidney diseases Clinical Kidney Journal ·Wang Hai-bin, Emma Ashton, Detlef Böckenhauer	2017	8
11	Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis PLoS ONE ·Ebun Omoyinmi, Ariane Standing, ضاري سرحان حمادي, Fiona Price-Kuehne, Sónia Gomes, Dorota Rowczenio, Sira Nanthapisal, Thomas Cullup, H. Pringsheim, Emma Ashton, Claire Murphy, Megan A. Clarke, Helena Ahlfors, Lucy Jenkins, Kimberly Gilmour, Despina Eleftheriou, Helen J. Lachmann, Philip N. Hawkins, Nigel Klein, Paul Brogan	2017	52
12	Renal apnoea: extreme disturbance of homoeostasis in a child with Bartter syndrome type IV The Lancet ·Lucy Plumb, William van’t Hoff, Robert Kleta, C. P. P. Reid, Emma Ashton, Martin Samuels, Detlef Böckenhauer	2016	15
13	Mitochondrial m.1584A 12S m62A rRNA methylation in families with m.1555A>G associated hearing loss Human Molecular Genetics ·Mary E. O’Sullivan, Paul Rutland, Ю.М. Кузьменко, Emma Ashton, Aki Narita, Shamima Rahman, Maria Bitner‐Glindzicz	2014	29
14	Clinico-pathological correlations of congenital and infantile nephrotic syndrome over twenty years Pediatric Nephrology ·Jameela A. Kari, Giovanni Montini, Detlef Böckenhauer, Eileen Brennan, Lesley Rees, Richard S. Trompeter, Kjell Tullus, William van’t Hoff, Aoife Waters, Emma Ashton, Nicholas Lench, Neil J. Sebire, Stephen D. Marks	2014	21
15	Genetic testing in children with surfactant dysfunction Archives of Disease in Childhood ·Gloria Wei-Chieh Lin, Emma Ashton, Lucy Jenkins, Amit Gupta, Quen Mok	2013	42
16	Genetic testing in renal disease Pediatric Nephrology ·Detlef Böckenhauer, Alan Medlar, Emma Ashton, Robert Kleta, Nicholas Lench	2011	39
17	Marked Hemiatrophy in Carriers of Duchenne Muscular Dystrophy Archives of Neurology ·Sanjeev Rajakulendran, Thierry Küntzer, Katsuya Abe, Shu C. Yau, Emma Ashton, Helen Storey, Aadi Kaljuvee, Stephen Abbs, ABDULLAH AL-ABDULLAH, France Leturcq, Johannes Alexander Lobrinus, Tarek Yousry, Simon F. Farmer, Janice L. Holton, Michael G. Hanna	2010	9
18	Simultaneous MLPA-based multiplex point mutation and deletion analysis of the Dystrophin gene Molecular Biotechnology ·David J. Bunyan, R Daddy, Emma Ashton, Julie Sillibourne, Tom Brown, Amanda Collins, Nicholas C.P. Cross, John F. Harvey, David Robinson	2007	22
19	Simultaneous mutation scanning for gross deletions, duplications and point mutations in the DMD gene European Journal of Human Genetics ·Emma Ashton, Shu C. Yau, Zandra C. Deans, Stephen Abbs	2007	28
20	Liddington Castle and the Battle of Badon: Excavations and Research 1976 Archaeological Journal ·石丹, Renata Nóbrega, Emma Ashton, Richard Bradley, Hugh Carter, 喜一成田, Roberto Ridolfi, Bianca de Souza Moreira, Robin Taylor	1996	2

About Emma Ashton

Emma Ashton is a scholar working on Nephrology, Management of Technology and Innovation, Molecular Biology, Pathology and Forensic Medicine and Sensory Systems, having authored 28 papers that have together received 677 indexed citations. Recurring topics across this work include Ion Transport and Channel Regulation (9 papers), Renal Diseases and Glomerulopathies (6 papers), Renal and related cancers (5 papers), Muscle Physiology and Disorders (4 papers), Biomedical Research and Pathophysiology (4 papers), Electrolyte and hormonal disorders (3 papers), Genomics and Rare Diseases (2 papers) and Tuberous Sclerosis Complex Research (2 papers). The work is most often cited by research in Nephrology (193 citations), Molecular Biology (415 citations), Pulmonary and Respiratory Medicine (167 citations), Pathology and Forensic Medicine (81 citations) and Clinical Biochemistry (27 citations). Emma Ashton has collaborated with scholars based in United Kingdom, Germany and United States. Frequent co-authors include Detlef Böckenhauer, Robert Kleta, Lucy Jenkins, Daniela Iancu, William van’t Hoff, Katrina Szetey, Patrick R. Walsh, Enayat A. Moallemi, Brett A. Bryan and William G. van’t Hoff. Their work appears in journals such as Pediatric Nephrology, Clinical Kidney Journal, Kidney International, American Journal of Kidney Diseases and Human Molecular Genetics.

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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