Jayne Houghton

2.5k total citations
59 papers, 1.5k citations indexed

About

Jayne Houghton is a scholar working on Endocrinology, Diabetes and Metabolism, Surgery and Genetics. According to data from OpenAlex, Jayne Houghton has authored 59 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Endocrinology, Diabetes and Metabolism, 31 papers in Surgery and 24 papers in Genetics. Recurrent topics in Jayne Houghton's work include Hyperglycemia and glycemic control in critically ill and hospitalized patients (31 papers), Pancreatic function and diabetes (30 papers) and Diabetes and associated disorders (17 papers). Jayne Houghton is often cited by papers focused on Hyperglycemia and glycemic control in critically ill and hospitalized patients (31 papers), Pancreatic function and diabetes (30 papers) and Diabetes and associated disorders (17 papers). Jayne Houghton collaborates with scholars based in United Kingdom, Türkiye and India. Jayne Houghton's co-authors include Sarah E. Flanagan, Sian Ellard, Andrew T. Hattersley, Elisa De Franco, Hana Lango Allen, Richard Caswell, Deborah Mackay, Michael N. Weedon, I. Karen Temple and Maggie Shepherd and has published in prestigious journals such as The Lancet, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Jayne Houghton

55 papers receiving 1.5k citations

Peers

Countries citing papers authored by Jayne Houghton

Since Specialization

Citations

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

Fields of papers citing papers by Jayne Houghton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jayne Houghton

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Characterization of congenital hyperinsulinism in Argentina: Clinical features, genetic findings, and treatment outcomes 2025 ·PLoS ONE ·(unknown), (unknown), Juan Cáceres, Guillermo Alonso, (unknown), (unknown), Adriana Flores, (unknown), (unknown), Jayne Houghton, (unknown), Sabrina Martín, Sarah E. Flanagan, (unknown)	0
2	Large copy number variants are an important cause of congenital hyperinsulinism that should be screened for during routine testing 2025 ·Frontiers in Endocrinology ·Sarah E. Flanagan, (unknown), Jonna M. E. Männistö, James T. Bennett, (unknown), Matthew B. Johnson, Matthew N. Wakeling, Jayne Houghton, Thomas W. Laver	0
3	Comprehensive clinical and molecular characterization with long-term outcomes in 40 patients with congenital hyperinsulinism 2025 ·Endocrine ·Zehra Yavaş Abalı, Firdevs Baş, Jayne Houghton, Saygın Abalı, (unknown), (unknown), Ayça Dilruba Aslanger, (unknown), (unknown), Mehmet Yücesoy, Sarah E. Flanagan, Şükran Poyrazoğlu, Rüveyde Bundak, Feyza Darendelıler	0
4	Congenital hyperinsulinism in the Ukraine: a 10-year national study 2024 ·Frontiers in Endocrinology ·Evgenia Globa, (unknown), Michael Bau Mortensen, Jayne Houghton, Anne Lerberg Nielsen, Sönke Detlefsen, Sarah E. Flanagan	1
5	Widening the phenotypic spectrum caused by pathogenic PDX1 variants in individuals with neonatal diabetes 2024 ·BMJ Open Diabetes Research & Care ·Nicola Jeffery, (unknown), Jayne Houghton, Evgenia Globa, Matthew N. Wakeling, Sarah E. Flanagan, Andrew T. Hattersley, Kashyap Patel, Elisa De Franco	1
6	Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements 2024 ·European Journal of Human Genetics ·Thomas W. Laver, Matthew N. Wakeling, Richard Caswell, (unknown), Daphne Yau, Jonna M. E. Männistö, Jayne Houghton, (unknown), Michael N. Weedon, Vrinda Saraff, Melanie Kershaw, Engela Honey, Nuala Murphy, Dinesh Giri, (unknown), (unknown), Indraneel Banerjee, (unknown), Nick Owens, Sarah E. Flanagan	2
7	FOXP3 TSDR Measurement Could Assist Variant Classification and Diagnosis of IPEX Syndrome 2023 ·Journal of Clinical Immunology ·Rebecca C. Wyatt, Sven Olek, Elisa De Franco, (unknown), Kashyap Patel, Jayne Houghton, Steffi Walter, (unknown), Rosa Bacchetta, Andrew T. Hattersley, Sarah E. Flanagan, Matthew B. Johnson	8
8	Bringing precision medicine to the management of pregnancy in women with glucokinase-MODY: a study of diagnostic accuracy and feasibility of non-invasive prenatal testing 2023 ·Diabetologia ·Alice E. Hughes, Jayne Houghton, (unknown), Ali Chakera, Gill Spyer, Maggie Shepherd, Sarah E. Flanagan, Andrew T. Hattersley	4
9	Increased referrals for congenital hyperinsulinism genetic testing in children with trisomy 21 reflects the high burden of non‐genetic risk factors in this group 2022 ·Pediatric Diabetes ·(unknown), Thomas W. Laver, Jayne Houghton, Jonna M. E. Männistö, (unknown), Stephen Brearey, (unknown), Antonia Dastamani, (unknown), Nuala Murphy, Birgit Rami‐Merhar, (unknown), Hanna Huopio, Indraneel Banerjee, Matthew B. Johnson, Sarah E. Flanagan	6
10	Hyperinsulinemic Hypoglycemia Diagnosed in Childhood Can Be Monogenic 2022 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), (unknown), Jayne Houghton, (unknown), Navoda Atapattu, Matthew B. Johnson, Kashyap Patel, Thomas W. Laver, Sarah E. Flanagan	7
11	Birth weight and diazoxide unresponsiveness strongly predict the likelihood of congenital hyperinsulinism due to a mutation in ABCC8 or KCNJ11\n 2021 ·Europe PMC (PubMed Central) ·(unknown), Daphne Yau, (unknown), Thomas W. Laver, Jayne Houghton, Beverley M. Shields, Sarah E. Flanagan, Kashyap Patel	7
12	Genetic Testing Access and Results for Patients with Congenital Hyperinsulinism as Conducted through the CHI and University of Exeter Partnership 2021 ·(unknown), Jayne Houghton, (unknown), Sarah E. Flanagan, (unknown)	1
13	Heterozygous Insulin Receptor (INSR) Mutation Associated with Neonatal Hyperinsulinemic Hypoglycaemia and Familial Diabetes Mellitus: Case Series 2020 ·Journal of Clinical Research in Pediatric Endocrinology ·(unknown), Nicola Foulds, Sarah Ehtisham, Syed Haris Ahmed, Jayne Houghton, Kevin Colclough, Mohammed Didi, Sarah E. Flanagan, Senthil Senniappan	12
14	Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389 2020 ·PLoS ONE ·Daphne Yau, Thomas W. Laver, Antonia Dastamani, Senthil Senniappan, Jayne Houghton, M Guftar Shaikh, Tim Cheetham, Talat Mushtaq, Ritika R. Kapoor, Tabitha Randell, Sian Ellard, Pratik Shah, Indraneel Banerjee, Sarah E. Flanagan	38
15	Comprehensive screening shows that mutations in the known syndromic genes are rare in infants presenting with hyperinsulinaemic hypoglycaemia 2018 ·Clinical Endocrinology ·Thomas W. Laver, Matthew N. Wakeling, (unknown), Jayne Houghton, Khalid Hussain, Sian Ellard, Sarah E. Flanagan	7
16	Neonatal Diabetes Mellitus Caused by a Novel GLIS3 Mutation in Twins 2018 ·(unknown), (unknown), (unknown), Clari Felszer, (unknown), (unknown), Sarah E. Flanagan, Jayne Houghton, Yardena Rakover	1
17	A successful transition to sulfonylurea treatment in male infant with neonatal diabetes caused by the novel abcc8 gene mutation and three years follow-up 2017 ·Diabetes Research and Clinical Practice ·(unknown), (unknown), Andrew T. Hattersley, Sian Ellard, Jayne Houghton, Dragana Obreht, (unknown), (unknown), (unknown)	7
18	Neonatal Diabetes - Experience from a Single Centre in Sri Lanka 2015 ·Navoda Atapattu, (unknown), (unknown), (unknown), (unknown), Andrew T. Hattersley, Sian Ellard, Sarah E. Flanagan, Jayne Houghton, Khalid Hussain	1
19	Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations 2015 ·European Journal of Endocrinology ·Hüseyin Demirbilek, Ved Bhushan Arya, Mehmet Nuri Özbek, Jayne Houghton, (unknown), Melek Akar, Selahattin Tekeş, (unknown), Deborah Mackay, Sarah E. Flanagan, Andrew T. Hattersley, Sian Ellard, Khalid Hussain	49
20	Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis 2013 ·Nature Genetics ·Michael N. Weedon, Inês Cebola, Ann‐Marie Patch, Sarah E. Flanagan, Elisa De Franco, Richard Caswell, Santiago A. Rodríguez‐Seguí, Charles Shaw‐Smith, (unknown), Hana Lango Allen, Jayne Houghton, Christian L. Roth, Rongrong Chen, Khalid Hussain, Phil Marsh, Ludovic Vallier, Anna Murray, Sian Ellard, Jorge Ferrer, Andrew T. Hattersley	191

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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