Publications by authors named "Peter Noons"

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Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non-syndromic sagittal and metopic craniosynostosis.
Isaac S Walton, Emma McCann, Astrid Weber, Jenny E V Morton, Peter Noons

J Anat· December 2024

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Regulatory elements in (7q21.3) locus contribute to genetic control of coronal nonsyndromic craniosynostosis and bone density-related traits.
Paola Nicoletti, Samreen Zafer, Lital Matok, Inbar Irron, Meidva Patrick, Peter Noons

Genet Med Open· May 2024

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Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetrance.
Rebecca S Tooze, Kerry A Miller, Sigrid M A Swagemakers, Eduardo Calpena, Simon J McGowan, Peter Noons

Genet Med· September 2023

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Psychological Adjustment in Apert Syndrome: Parent and Young Person Perspectives.
Jennifer Netherton, Jo Horton, Nicola M Stock, Rachel Shaw, Peter Noons

Cleft Palate Craniofac J· April 2023

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ERF-related craniosynostosis and surgical management in the paediatric cohort.
Fardad T Afshari, Pasquale Gallo, Ahad Shafi, Jaime Grant, Amy Drew, Peter Noons

Childs Nerv Syst· April 2023

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Posterior Calvarial Distraction in older paediatric population: single centre paediatric neurosurgery craniofacial unit outcomes.
Fardad T Afshari, Pasquale Gallo, Guirish A Solanki, Jaime Grant, Peter Noons

Childs Nerv Syst· July 2022

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A Simple Method for Eye Protection During Prone Positioning for Craniofacial Surgery.
Jaime Grant, Peter Noons, Edmund D Carver, Martin J Evans, Nicholas White

Cleft Palate Craniofac J· March 2022

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A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis.
Cristina M Justice, Araceli Cuellar, Krithi Bala, Jeremy A Sabourin, Michael L Cunningham, Peter Noons

Hum Genet· August 2020

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ERF-related craniosynostosis: The phenotypic and developmental profile of a new craniosynostosis syndrome.
Graeme E Glass, Justine O'Hara, Natalie Canham, Deirdre Cilliers, David Dunaway, Peter Noons

Am J Med Genet A· April 2019

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Diagnostic value of exome and whole genome sequencing in craniosynostosis.
Kerry A Miller, Stephen R F Twigg, Simon J McGowan, Julie M Phipps, Aimée L Fenwick, Peter Noons

J Med Genet· April 2017

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The Quality of Life in Adult Patients With Syndromic Craniosynostosis From Their Perspective.
Mark S Lloyd, Anuradha Venugopal, Johan Horton, Desiderio Rodrigues, Hiroshi Nishikawa, Peter Noons

J Craniofac Surg· September 2016

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Isolated Unilateral Frontosphenoidal Suture Synostosis in Six Patients: Lessons Learned in Diagnosis and Treatment.
Mark Sheldon Lloyd, Desi Rodrigues, Hiroshi Nishikawa, Nicholas White, Gurish Solanki, Peter Noons

J Craniofac Surg· June 2016

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Empowerment of Parents of Children With Craniosynostosis by Objective Scoring of Patient Information Websites.
Mark Sheldon Lloyd, Kirsten Lafferty, Johan Horton, Peter Noons, Stephen Dover

J Craniofac Surg· June 2016

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The increase of metopic synostosis: a pan-European observation.
Jacques van der Meulen, Rene van der Hulst, Leon van Adrichem, Eric Arnaud, David Chin-Shong, Peter Noons

J Craniofac Surg· March 2009

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Posterior calvarial vault expansion using distraction osteogenesis.
Nicholas White, Martin Evans, M Stephen Dover, Peter Noons, Guirish Solanki

Childs Nerv Syst· February 2009

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