Publications by authors named "Alan Mighell"

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Burden of hereditary enamel disorders.
Guilherme H S Bomfim, Geneviève Dupont, Timothy Wright, Alan Mighell, Rodrigo S Lacruz

Trends Mol Med· July 2025

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Genetic Screening of a Nonsyndromic Amelogenesis Imperfecta Patient Cohort Using a Custom smMIP Reagent for Selective Enrichment of Target Loci.
Ummey Hany, Christopher M Watson, Lu Liu, Georgios Nikolopoulos, Claire E L Smith, Alan J Mighell

Hum Mutat· July 2025

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Authors' response to the commentary by Kivela on Hany (2024).
Alan J Mighell, Chris Inglehearn

J Med Genet· December 2024

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Biallelic variants in Plexin B2 () cause amelogenesis imperfecta, hearing loss and intellectual disability.
Claire E L Smith, Virginie Laugel-Haushalter, Ummey Hany, Sunayna Best, Rachel L Taylor, Alan J Mighell

J Med Genet· June 2024

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Heterozygous variants are a frequent cause of amelogenesis imperfecta.
Ummey Hany, Christopher M Watson, Lu Liu, Claire E L Smith, Asmaa Harfoush, Alan J Mighell

J Med Genet· March 2024

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Review of 1.75 million referrals over 34 months identifies the disruptive impact of the SARS-CoV-2 pandemic on oral surgery care in England: a service evaluation.
Richard J Moore, Iain Pretty, Gail V A Douglas, Alan J Mighell

Br Dent J· February 2023

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The changing face of a dental school: a Leeds perspective.
Alan J Mighell

Br Dent J· October 2022

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An evaluation of referrer factors for 98,671 referrals made to the West Yorkshire oral surgery managed clinical network over a three-year period.
Richard J Moore, Iain Pretty, Gail Douglas, Alan J Mighell

Br Dent J· March 2022

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Efficacy and safety of a novel mucoadhesive clobetasol patch for treatment of erosive oral lichen planus: A phase 2 randomized clinical trial.
Michael T Brennan, Lars Siim Madsen, Deborah P Saunders, Joel J Napenas, Christine McCreary, Alan Mighell

J Oral Pathol Med· January 2022

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Implementation of biopsychosocial supported self-management for chronic primary oro-facial pain including temporomandibular disorders: A theory, person and evidence-based approach.
Vishal R Aggarwal, Jianhua Wu, Frank Fox, Daniel Howdon, Elspeth Guthrie, Alan Mighell

J Oral Rehabil· October 2021

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Spectrum of pathogenic variants and founder effects in amelogenesis imperfecta associated with MMP20.
Georgios Nikolopoulos, Claire E L Smith, James A Poulter, Gina Murillo, Sandra Silva, Alan J Mighell

Hum Mutat· May 2021

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Dry mouth diagnosis and saliva substitutes-A review from a textural perspective.
Jing Hu, Efren Andablo-Reyes, Alan Mighell, Sue Pavitt, Anwesha Sarkar

J Texture Stud· April 2021

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Salivary lubricity (ex vivo) enhances upon moderate exercise: A pilot study.
Mark Hopkins, Christine Boesch, Matthew Lansdall, Conor Mullen, Alan Mighell

Arch Oral Biol· August 2020

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A missense variant in specificity protein 6 (SP6) is associated with amelogenesis imperfecta.
Claire E L Smith, Laura L E Whitehouse, James A Poulter, Laura Wilkinson Hewitt, Fatima Nadat, Alan J Mighell

Hum Mol Genet· June 2020

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A missense mutation of Leu74Pro of OGR1 found in familial amelogenesis imperfecta actually causes the loss of the pH-sensing mechanism.
Koichi Sato, Chihiro Mogi, Alan J Mighell, Fumikazu Okajima

Biochem Biophys Res Commun· June 2020

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New missense variants in RELT causing hypomineralised amelogenesis imperfecta.
Georgios Nikolopoulos, Claire E L Smith, Steven J Brookes, Mohammed E El-Asrag, Catriona J Brown, Alan J Mighell

Clin Genet· May 2020

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Novel DLX3 variants in amelogenesis imperfecta with attenuated tricho-dento-osseous syndrome.
Laura L E Whitehouse, Claire E L Smith, James A Poulter, Catriona J Brown, Anesha Patel, Alan J Mighell

Oral Dis· January 2019

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Dentin dysplasia: diagnostic challenges.
Ahmed Alhilou, Hannah P Beddis, Alan J Mighell, Kathryn Durey

BMJ Case Rep· June 2018

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Defects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfecta.
Claire El Smith, Laura LE Whitehouse, James A Poulter, Steven J Brookes, Peter F Day, Alan J Mighell

Eur J Hum Genet· August 2017

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Amelogenesis Imperfecta; Genes, Proteins, and Pathways.
Claire E L Smith, James A Poulter, Agne Antanaviciute, Jennifer Kirkham, Steven J Brookes, Alan J Mighell

Front Physiol· June 2017

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Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress.
Steven J Brookes, Martin J Barron, Claire E L Smith, James A Poulter, Alan J Mighell

Hum Mol Genet· May 2017

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A Fourth Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities.
Claire E L Smith, Jennifer Kirkham, Peter F Day, Francesca Soldani, Esther J McDerra, Alan J Mighell

Front Physiol· May 2017

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Spectrum of PEX1 and PEX6 variants in Heimler syndrome.
Claire E L Smith, James A Poulter, Alex V Levin, Jenina E Capasso, Susan Price, Alan J Mighell

Eur J Hum Genet· November 2016

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Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta.
David A Parry, Claire E L Smith, Walid El-Sayed, James A Poulter, Roger C Shore, Alan J Mighell

Am J Hum Genet· October 2016

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Deletion of amelotin exons 3-6 is associated with amelogenesis imperfecta.
Claire E L Smith, Gina Murillo, Steven J Brookes, James A Poulter, Sandra Silva, Alan J Mighell

Hum Mol Genet· August 2016

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