Publications by authors named "Jason Hehir"

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ITPR1 Deletion in a Patient With Sensory Ataxic Neuropathy and Sjögren Syndrome.
Saif Haddad, Roy Poh, Jason Hehir, James M Polke, Julian Blake

J Peripher Nerv Syst· December 2025

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Parkinson's families project: a UK-wide study of early onset and familial Parkinson's disease.
Clodagh Towns, Zih-Hua Fang, Manuela M X Tan, Simona Jasaityte, Theresa M Schmaderer, Jason Hehir

NPJ Parkinsons Dis· October 2024

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Assessing the relationship between monoallelic PRKN mutations and Parkinson's risk.
Steven J Lubbe, Bernabe I Bustos, Jing Hu, Dimitri Krainc, Theresita Joseph, Jason Hehir

Hum Mol Genet· March 2021

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Ambroxol for the Treatment of Patients With Parkinson Disease With and Without Glucocerebrosidase Gene Mutations: A Nonrandomized, Noncontrolled Trial.
Stephen Mullin, Laura Smith, Katherine Lee, Gayle D'Souza, Philip Woodgate, Jason Hehir

JAMA Neurol· April 2020

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Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study.
Manuela M X Tan, Naveed Malek, Michael A Lawton, Leon Hubbard, Alan M Pittman, Jason Hehir

Brain· September 2019

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Analysis of the genetic variability in Parkinson's disease from Southern Spain.
Sara Bandrés-Ciga, Niccolò Emmanuele Mencacci, Raquel Durán, Francisco Javier Barrero, Francisco Escamilla-Sevilla, Jason Hehir

Neurobiol Aging· January 2016

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A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations.
Eleanna Kara, Aoife P Kiely, Christos Proukakis, Nicola Giffin, Seth Love, Jason Hehir

JAMA Neurol· September 2014

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C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies.
Davina J Hensman Moss, Mark Poulter, Jon Beck, Jason Hehir, James M Polke

Neurology· January 2014

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