Helen M. Stuart

1.4k total citations
16 papers, 362 citations indexed

About

Helen M. Stuart is a scholar working on Urology, Molecular Biology and Nephrology. According to data from OpenAlex, Helen M. Stuart has authored 16 papers receiving a total of 362 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Urology, 4 papers in Molecular Biology and 3 papers in Nephrology. Recurrent topics in Helen M. Stuart's work include Urological Disorders and Treatments (5 papers), Urinary Bladder and Prostate Research (4 papers) and Pediatric Urology and Nephrology Studies (3 papers). Helen M. Stuart is often cited by papers focused on Urological Disorders and Treatments (5 papers), Urinary Bladder and Prostate Research (4 papers) and Pediatric Urology and Nephrology Studies (3 papers). Helen M. Stuart collaborates with scholars based in United Kingdom, Malaysia and China. Helen M. Stuart's co-authors include N. Ridley, Rachel Lennon, Adrian S. Woolf, William G. Newman, Emma Hilton, Neil Roberts, Edward A. McKenzie, Michael J. Randles, Raphaël Thuret and Jill Urquhart and has published in prestigious journals such as Journal of Clinical Oncology, Scientific Reports and Kidney International.

In The Last Decade

Helen M. Stuart

15 papers receiving 348 citations

Peers

Countries citing papers authored by Helen M. Stuart

Since Specialization

Citations

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

Fields of papers citing papers by Helen M. Stuart

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Helen M. Stuart. 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 Helen M. Stuart. The network helps show where Helen M. Stuart may publish in the future.

Co-authorship network of co-authors of Helen M. Stuart

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

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Detection of Alport gene variants in children and young people with persistent haematuria 2024 ·Pediatric Nephrology ·(unknown), Tomohiko Yamamura, Mohan Shenoy, Helen M. Stuart, Rachel Lennon	1
2	Predicting congenital renal tract malformation genes using machine learning 2023 ·Scientific Reports ·M. Shahjahan Kabir, Helen M. Stuart, Filipa M. Lopes, Elisavet Fotiou, Bernard Keavney, Andrew J. Doig, Adrian S. Woolf, Kathryn E. Hentges	1
3	Early B-cell Factor 3–Related Genetic Disease Can Mimic Urofacial Syndrome 2020 ·Kidney International Reports ·(unknown), Glenda M. Beaman, Keng Wee Teik, (unknown), John A. Sayer, Heather J. Cordell, Huw B. Thomas, K Wood, Helen M. Stuart, Adrian S. Woolf, William G. Newman	7
4	A homozygous missense variant in CHRM3 associated with familial urinary bladder disease 2019 ·Clinical Genetics ·Glenda M. Beaman, (unknown), Keng Wee Teik, Jill Urquhart, (unknown), James O’Sullivan, Sanjeev S. Bhaskar, K Wood, Huw B. Thomas, Raymond T. O’Keefe, Adrian S. Woolf, Helen M. Stuart, William G. Newman	9
5	Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladder 2019 ·Kidney International ·Neil Roberts, Emma Hilton, Filipa M. Lopes, Subir Singh, Michael J. Randles, Natalie J. Gardiner, (unknown), Riccardo Coletta, (unknown), Robert J. Hall, Wyatt W. Yue, Franz Schaefer, Stefanie Weber, Roger Henriksson, Helen M. Stuart, Håkan Hedman, William G. Newman, Adrian S. Woolf	28
6	22q11.2 duplications in a UK cohort with bladder exstrophy–epispadias complex 2019 ·American Journal of Medical Genetics Part A ·Glenda M. Beaman, Adrian S. Woolf, Raimondo M. Cervellione, (unknown), Imran Mushtaq, Jill Urquhart, Helen M. Stuart, William G. Newman	9
7	Genetic testing in steroid-resistant nephrotic syndrome: why, who, when and how? 2017 ·Pediatric Nephrology ·(unknown), Helen M. Stuart, Rachel Lennon	98
8	Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease 2015 ·Pediatric Nephrology ·Rachel Lennon, Helen M. Stuart, Agnieszka Bierżyńska, Michael J. Randles, Bronwyn Kerr, (unknown), Gauri Batra, J. M. H. Campbell, Helen Storey, Frances Flinter, Ania Koziell, Gavin I. Welsh, Moin A. Saleem, Nicholas J.A. Webb, Adrian S. Woolf	33
9	Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus 2014 ·Human Molecular Genetics ·Neil Roberts, Adrian S. Woolf, Helen M. Stuart, Raphaël Thuret, Edward A. McKenzie, William G. Newman, Emma Hilton	22
10	Genetics of human congenital urinary bladder disease 2013 ·Pediatric Nephrology ·Adrian S. Woolf, Helen M. Stuart, William G. Newman	11
11	Urofacial syndrome: a genetic and congenital disease of aberrant urinary bladder innervation 2013 ·Pediatric Nephrology ·Adrian S. Woolf, Helen M. Stuart, Neil Roberts, Edward A. McKenzie, Emma Hilton, William G. Newman	17
12	Utilizing a collaborative working model to optimize molecular analysis of solid tumors in the Cancer Research UK's Stratified Medicine Programme. 2013 ·Journal of Clinical Oncology ·Ian Walker, Fiona MacDonald, Helen M. Stuart, Rachel Butler, (unknown), Celia Brown, (unknown), David González de Castro, Lisa A. Thompson, S. Lillis, (unknown), (unknown), (unknown), (unknown), (unknown), Brendan O’Sullivan, Philippe Tanière, Mike Griffiths, Peter Johnson, (unknown)	5
13	Determining the pathogenicity of patient-derived TSC2 mutations by functional characterization and clinical evidence 2011 ·European Journal of Human Genetics ·Elaine A. Dunlop, (unknown), Stephen C. Land, (unknown), (unknown), Helen M. Stuart, Shane McKee, (unknown), Anand Saggar, (unknown), Ana Medeira, Helen Kingston, Julian R. Sampson, D. M. Davies, Andrew R. Tee	9
14	Partial Molar Volumes from High-Temperature Lattice Parameters of Iron–Carbon Austenites 1970 ·Metal Science Journal ·N. Ridley, Helen M. Stuart	57
15	Lattice parameters and Curie-point anomalies of iron-cobalt alloys 1969 ·Journal of Physics D Applied Physics ·Helen M. Stuart, N. Ridley	18
16	Lattice parameter anomalies at the Curie point of pure iron 1968 ·Journal of Physics D Applied Physics ·N. Ridley, Helen M. Stuart	37

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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