Martina Owens

1.7k total citations
17 papers, 310 citations indexed

About

Martina Owens is a scholar working on Genetics, Epidemiology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Martina Owens has authored 17 papers receiving a total of 310 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Epidemiology and 5 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Martina Owens's work include Neuroendocrine Tumor Research Advances (7 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Martina Owens is often cited by papers focused on Neuroendocrine Tumor Research Advances (7 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Martina Owens collaborates with scholars based in United Kingdom, Belgium and Denmark. Martina Owens's co-authors include Sian Ellard, Lorna W. Harries, Andrew T. Hattersley, Emma L. Edghill, Richard Caswell, Bijay Vaidya, Coralie Bingham, Karen Stals, Richard A. Oram and Karen Moore and has published in prestigious journals such as Scientific Reports, Diabetologia and Nephrology Dialysis Transplantation.

In The Last Decade

Martina Owens

17 papers receiving 304 citations

Peers

Countries citing papers authored by Martina Owens

Since Specialization

Citations

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

Fields of papers citing papers by Martina Owens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martina Owens

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

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Medullary Thyroid Cancer Risk and Mortality in Carriers of Incidentally Identified MEN2A RET Variants 2025 ·JAMA Network Open ·(unknown), Uyenlinh L. Mirshahi, Katherine S. Ruth, (unknown), (unknown), (unknown), Caroline F. Wright, Bijay Vaidya, Martina Owens, David J. Carey, Kashyap Patel	1
2	TECPR2‐related hereditary sensory and autonomic neuropathy in two siblings from Palestine 2024 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), James Fasham, (unknown), (unknown), (unknown), Adam C. Gunning, (unknown), (unknown), (unknown), (unknown), Martina Owens, (unknown), Peter D. Turnpenny, (unknown), Emma L. Baple, Andrew H. Crosby, Lettie E. Rawlins	2
3	Penetrance of MEN2A-causing RET mutations in clinically unselected population is very low - important implications for clinical practice 2023 ·Endocrine Abstracts ·(unknown), Katherine S. Ruth, Martina Owens, Bijay Vaidya, Kashyap Patel	1
4	Multiple endocrine neoplasia type 2A syndrome presenting with corneal nerve thickening 2023 ·QJM ·(unknown), (unknown), Harry Roberts, (unknown), Christopher Moudiotis, Martina Owens, (unknown), J. A. Smith, Bijay Vaidya	1
5	Assessing the clinical utility of protein structural analysis in genomic variant classification: experiences from a diagnostic laboratory 2022 ·Genome Medicine ·Richard Caswell, Adam C. Gunning, Martina Owens, Sian Ellard, Caroline F. Wright	13
6	A practical guide to genetic testing in endocrinology 2021 ·Clinical Endocrinology ·Louise Izatt, Martina Owens, Heather Pierce, Sarah Wilcox, Soo‐Mi Park	1
7	AIP variant causing familial prolactinoma 2020 ·Pituitary ·David Carty, (unknown), Russell Drummond, Rebecca Ward, Kesson Magid, David Collier, Martina Owens, Márta Korbonits	10
8	Diagnostic RET genetic testing in 1,058 index patients: A UK centre perspective 2020 ·Clinical Endocrinology ·Jonathan Fussey, Joel Smith, (unknown), Christopher Bowles, Sian Ellard, Bijay Vaidya, Martina Owens	6
9	Using Structural Analysis In Silico to Assess the Impact of Missense Variants in MEN1 2019 ·Journal of the Endocrine Society ·Richard Caswell, Martina Owens, Adam C. Gunning, Sian Ellard, Caroline F. Wright	13
10	Pitfalls of haplotype phasing from amplicon-based long-read sequencing 2016 ·Scientific Reports ·Thomas W. Laver, Richard Caswell, Karen Moore, Jérémie Poschmann, Matthew B. Johnson, Martina Owens, Sian Ellard, Konrad Paszkiewicz, Michael N. Weedon	55
11	Novel LMNA mutations cause an aggressive atypical neonatal progeria without progerin accumulation 2016 ·Journal of Medical Genetics ·Clara Soria‐Valles, Dido Carrero, Elisabeth Gabau, Gloria Velasco, Vı́ctor Quesada, Clea Bárcena, (unknown), Karen Fieggen, (unknown), Martina Owens, Diana Puente, Òscar Asensio, Bart Loeys, Ana Beatriz Alvarez Pérez, Valérie Benoît, Wim Wuyts, Nicolas Lévy, Raoul C. M. Hennekam, Annachiara De Sandre‐Giovannoli, Carlos López-Otı́n	13
12	ESR2 mutations in RET mutation-negative familial medullary thyroid carcinoma 2016 ·Endocrine Abstracts ·(unknown), Donato Iacovazzo, Maria Alevizaki, William D. Foulkes, Francesca Lugli, Maralyn Druce, Pinaki Dutta, Mary Dang, Plamena Gabrovska, Patrick J. Morrison, Martina Owens, Sian Ellard, Julian R. Sampson, (unknown), Márta Korbonits	1
13	SOS1 frameshift mutations cause pure mucosal neuroma syndrome, a clinical phenotype distinct from multiple endocrine neoplasia type 2B 2015 ·Clinical Endocrinology ·Martina Owens, Emma Kivuva, Anthony Quinn, Paul Brennan, Richard Caswell, Hana Lango Allen, Bijay Vaidya, Sian Ellard	10
14	A prospective study of brachytelephalangic chondrodysplasia punctata: identification of arylsulfatase E mutations, functional analysis of novel missense alleles, and determination of potential phenocopies 2013 ·Genetics in Medicine ·(unknown), Graeme Nimmo, (unknown), Carolyn Tysoe, Martina Owens, Sherri J. Bale, Nancy Braverman	14
15	Hepatocyte nuclear factor-1 gene deletions--a common cause of renal disease 2007 ·Nephrology Dialysis Transplantation ·Emma L. Edghill, Richard A. Oram, Martina Owens, Karen Stals, Lorna W. Harries, Andrew T. Hattersley, Sian Ellard, Coralie Bingham	82
16	Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the young 2007 ·Diabetologia ·Sian Ellard, (unknown), Emma L. Edghill, Martina Owens, Louise Ambye, (unknown), (unknown), M. Strachan, Amanda Stride, Betül Ersoy, Hans Eiberg, Oluf Pedersen, Maggie Shepherd, Torben Hansen, Lorna W. Harries, Andrew T. Hattersley	56
17	Analysis of gross deletions in the MEN1 gene in patients with multiple endocrine neoplasia type 1 2007 ·Clinical Endocrinology ·Martina Owens, Sian Ellard, Bijay Vaidya	31

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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