Jayne Houghton - Concepedia

Author

Jayne Houghton

Also Known As

Houghton, Jayne A. L., J Houghton, J. A. L. Houghton, J. Houghton, Jayne AL Houghton, Jayne A L Houghton, Jayne A. Houghton, Jayne A. L. Houghton, Jayne A.L. Houghton, Jayne AL Houghton

Publications

2.4K

Citations

H-Index

Concepts

All Affiliations

University of Exeter Royal Devon & Exeter NHS Foundation Trust University College London Great Ormond Street Hospital Genomics (United Kingdom)

About

Jayne Houghton is an author at University of Exeter specializing in medicine, diabetes, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	518
2	Diabetes	4	4	205
3	Health Sciences	1	1	136
4	Public Health	1	1	14
5	Cell Biology	1	1	29

Jayne Houghton

Publications

Citations

H-Index

Page 1

	Year	Citations
The effect of early, comprehensive genomic testing on clinical care in neonatal diabetes: an international cohort study Elisa De Franco, Sarah E. Flanagan, Jayne Houghton, The Lancet	2015	338
Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis Michael N. Weedon, Inês Cebola, Ann‐Marie Patch, Nature Genetics Developmental BiologyPancreatic CancerGeneticsMolecular GeneticsRecessive Mutations	2013	313
Improved genetic testing for monogenic diabetes using targeted next-generation sequencing Sian Ellard, Hana Lango Allen, Elisa De Franco, Diabetologia	2013	307
Analysis of Transcription Factors Key for Mouse Pancreatic Development Establishes NKX2-2 and MNX1 Mutations as Causes of Neonatal Diabetes in Man Sarah E. Flanagan, Elisa De Franco, Hana Lango Allen, Cell Metabolism	2014	144
SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion Francis H. Sansbury, Sarah E. Flanagan, Jayne Houghton, Diabetologia Insulin ResistanceMetabolic SyndromeHuman Insulin SecretionInsulin SignalingDevelopmental Biology	2012	136
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 Hüseyin Demirbilek, Ved Bhushan Arya, Mehmet Nuri Özbek, European Journal of Endocrinology	2015	66
The Common p.R114W <i>HNF4A</i> Mutation Causes a Distinct Clinical Subtype of Monogenic Diabetes Thomas W. Laver, Kevin Colclough, Maggie Shepherd, Diabetes	2016	57
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 Daphne Yau, Thomas W. Laver, Antonia Dastamani, PLoS ONE	2020	57
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinism Matthew N. Wakeling, Nick Owens, Jessica R. Hopkinson, Nature Genetics	2022	57
A type 1 diabetes genetic risk score can discriminate monogenic autoimmunity with diabetes from early-onset clustering of polygenic autoimmunity with diabetes Matthew B. Johnson, Kashyap Patel, Elisa De Franco, Diabetologia	2018	49

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