Ruth McGowan

3.5k total citations
43 papers, 677 citations indexed

About

Ruth McGowan is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Ruth McGowan has authored 43 papers receiving a total of 677 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 18 papers in Genetics and 10 papers in Surgery. Recurrent topics in Ruth McGowan's work include Sexual Differentiation and Disorders (16 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers) and Urological Disorders and Treatments (10 papers). Ruth McGowan is often cited by papers focused on Sexual Differentiation and Disorders (16 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers) and Urological Disorders and Treatments (10 papers). Ruth McGowan collaborates with scholars based in United Kingdom, United States and Spain. Ruth McGowan's co-authors include S. Faisal Ahmed, Carmen Sapienza, Alan C. Peterson, Robert M. Campbell, Edward S. Tobias, Angela Lucas-Herald, Andreas Kyriakou, Nils Krone, Jill P. Pell and Sally‐Ann Cooper and has published in prestigious journals such as Genes & Development, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Ruth McGowan

41 papers receiving 636 citations

Peers

Countries citing papers authored by Ruth McGowan

Since Specialization

Citations

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

Fields of papers citing papers by Ruth McGowan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruth McGowan

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Should Scotland provide genome-wide sequencing for the diagnosis of rare developmental disorders? A cost-effectiveness analysis 2024 ·The European Journal of Health Economics ·Michael Abbott, Mandy Ryan, Rodolfo Hernández, Lynda McKenzie, Sebastian Heidenreich, Lynne J. Hocking, Caroline Clark, Morad Ansari, David Moore, Anne Lampe, Ruth McGowan, Jonathan Berg, Zosia Miedzybrodzka	0
2	SEC31A may be associated with pituitary hormone deficiency and gonadal dysgenesis 2024 ·Endocrine ·Edward S. Tobias, Angela Lucas-Herald, (unknown), Augusto C. Montezano, Francisco J. Rios, Lívia L. Camargo, Graham Hamilton, (unknown), Louise A Diver, Nicola Williams, Pawel Herzyk, Rhian M. Touyz, Andy Greenfield, Ruth McGowan, S Faisal Ahmed	1
3	Outcomes of patients with Juvenile Polyposis-Hereditary Haemorrhagic Telangiectasia caused by pathogenic SMAD4 variants in a pan-Scotland cohort 2024 ·European Journal of Human Genetics ·(unknown), Ruth McGowan, Philip Greene, Wayne Lam, (unknown), Jonathan Berg	0
4	Childhood Hypertrophic Cardiomyopathy Caused by Beta-Myosin Heavy Chain Variants Is Associated With a More Obstructive but Less Arrhythmogenic Phenotype Than Myosin-Binding Protein C Disease 2023 ·Circulation Genomic and Precision Medicine ·Gabrielle Norrish, (unknown), Ella Field, (unknown), (unknown), Karen McLeod, Ruth McGowan, Elena Cervi, Juan Pablo Kaski	1
5	Expanding the phenotypic spectrum of Chromosome 16p13.11 microduplication: A multicentric analysis of 206 patients 2023 ·European Journal of Medical Genetics ·(unknown), (unknown), (unknown), (unknown), Karen Low, Ramya Nair, Francis H. Sansbury, Lettie E. Rawlins, Jenny Carmichael, (unknown), (unknown), (unknown), (unknown), Mary Callaghan, Catherine H Mercer, Ruth McGowan, Leema Robert, Hannah Titheradge, Swati Naik	2
6	Gonadal Function in Boys with Bilateral Undescended Testes 2023 ·Journal of the Endocrine Society ·Angela Lucas-Herald, (unknown), (unknown), (unknown), (unknown), Jane McNeilly, Timothy Bradnock, (unknown), (unknown), (unknown), Stuart O’Toole, Ruth McGowan, S. Faisal Ahmed	3
7	Thioredoxin Reductase 2 Variant as a Cause of Micropenis, Undescended Testis, and Selective Glucocorticoid Deficiency 2023 ·Hormone Research in Paediatrics ·(unknown), Angela Lucas-Herald, Martin McMillan, Rathi Prasad, Louise Metherell, Ruth McGowan, Edward S. Tobias, S. Faisal Ahmed	2
8	The Use of Genetics for Reaching a Diagnosis in XY DSD 2022 ·Sexual Development ·S. Faisal Ahmed, (unknown), Rafael Loch Batista, Sorahia Domenice, Nathália Lisboa Gomes, Ruth McGowan, (unknown), Berenice B. Mendonça	9
9	Clinical and Genetic Evaluation of People with or at Risk of Hereditary ATTR Amyloidosis: An Expert Opinion and Consensus on Best Practice in Ireland and the UK 2022 ·Advances in Therapy ·Julian D. Gillmore, Mary M. Reilly, Caroline Coats, Robert Cooper, Helen Cox, Mark Coyne, Andrew Green, Ruth McGowan, William E. Moody, Philip N. Hawkins	19
10	Cardiac myosin binding protein-C variants in paediatric-onset hypertrophic cardiomyopathy: natural history and clinical outcomes 2021 ·Journal of Medical Genetics ·Ella Field, Gabrielle Norrish, (unknown), (unknown), Marcos Cicerchia, Juan Pablo Ochoa, Petros Syrris, Karen McLeod, Ruth McGowan, (unknown), Luís R. Lopes, Elena Cervi, Juan Pablo Kaski	10
11	Birth incidence, deaths and hospitalisations of children and young people with Down syndrome, 1990–2015: birth cohort study 2020 ·BMJ Open ·Laura Anne Hughes-McCormack, Ruth McGowan, Jill P. Pell, Daniel Mackay, Angela Henderson, Lisa O’Leary, Sally‐Ann Cooper	25
12	Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life 2018 ·Journal of Clinical Research in Pediatric Endocrinology ·Filiz Çizmecioğlu, Jeremy Jones, Wendy F. Paterson, (unknown), (unknown), Ruth McGowan, M Guftar Shaikh, Malcolm Donaldson	19
13	DNA copy number variations are important in the complex genetic architecture of müllerian disorders 2015 ·Fertility and Sterility ·Ruth McGowan, Graham Tydeman, David N. Shapiro, (unknown), Norma Morrison, Susan Logan, Adam Balen, S. Faisal Ahmed, Miriam Deeny, John Tolmie, Edward S. Tobias	21
14	46,XX testicular disorder of sex development 2014 ·ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) ·S. Faisal Ahmed, Angela Lucas-Herald, Ruth McGowan, Edward S. Tobias	4
15	Results of Duchenne muscular dystrophy family screening in practice: leaks rather than cascades? 2012 ·Clinical Genetics ·Ruth McGowan, (unknown), Sarah J. Ross, Susan Holloway, Shelagh Joss, D.E. Wilcox, Simon Holden, John Tolmie, Cheryl Longman	6
16	Clinical features and respiratory complications in Myhre syndrome 2011 ·European Journal of Medical Genetics ·Ruth McGowan, (unknown), P.M. McHenry, Alexander Cooke, (unknown), Wee Teik Keng, Victoria Murday, Margo Whiteford, Frederik G. Dikkers, (unknown), Ton van Essen, John Tolmie	24
17	Factors That Influence the Decision to Perform a Karyotype in Suspected Disorders of Sex Development: Lessons from the Scottish Genital Anomaly Network Register 2011 ·Sexual Development ·Martina Rodie, Ruth McGowan, Amalia Mayo, Paula Midgley, Chris Driver, (unknown), David Young, S. Faisal Ahmed	19
18	X‐linked VACTERL with hydrocephalus syndrome: Further delineation of the phenotype caused by FANCB mutations 2011 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Ruth McGowan, Sulekha Rajagopalan, Alasdair G. W. Hunter, Jacques L. Michaud, Kate Gibson, Jeremy Robertson, (unknown), Stephen Abbs, Simon Holden	30
19	Novel features in auriculo-condylar syndrome 2010 ·Clinical Dysmorphology ·Ruth McGowan, Victoria Murday, Esther Kinning, (unknown), David Koppel, Margo Whiteford	6
20	Depression of follicle stimulating hormone in bulls injected with follicular fluid 1988 ·Theriogenology ·Ruth McGowan, G.H. Kiracofe, D. J. Bolt	5

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.

Explore authors with similar magnitude of impact