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MR/L501554/1

Funded outputs count: 22
Funder award ID: MR/L501554/1
OpenAlex ID: G503224829
Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease
2018 · Cornelis Blauwendraat, Xylena Reed, et al. · JAMA Neurology · 84
Mendelian randomization study shows no causal relationship between circulating urate levels and Parkinson's disease
2018 · Demis A. Kia, Alastair J. Noyce, et al. · Annals of Neurology · 58
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Analysis of shared heritability in common disorders of the brain
2018 · Verneri Anttila, Brendan Bulik-Sullivan, et al. · Science · 1,915
Stratification of candidate genes for Parkinson’s disease using weighted protein-protein interaction network analysis
2018 · Raffaele Ferrari, Demis A. Kia, et al. · BMC Genomics · 39
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Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2
2018 · Erik Boot, Nancy J. Butcher, et al. · Neurology · 49
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Features of GBA-associated Parkinson’s disease at presentation in the UK Tracking Parkinson’s study
2018 · Naveed Malek, Rimona S Weil, et al. · Journal of Neurology Neurosurgery & Psychiatry · 133
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Establishing the role of rare coding variants in known Parkinson's disease risk loci
2017 · Iris E. Jansen, J. Raphael Gibbs, et al. · Neurobiology of Aging · 18
Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study
2017 · Alastair J. Noyce, Demis A. Kia, et al. · PLoS Medicine · 175
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NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
2017 · Cornelis Blauwendraat, Faraz Faghri, et al. · Neurobiology of Aging · 142
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Additional rare variant analysis in Parkinson’s disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
2016 · Steven J. Lubbe, Valentina Escott-Price, et al. · Human Molecular Genetics · 61
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A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies
2016 · Corneliu A. Bodea, Benjamin M. Neale, et al. · The American Journal of Human Genetics · 20
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Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data
2016 · Kin Y Mok, Una Sheerin, et al. · The Lancet Neurology · 92
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Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
2016 · Suzanne Lesage, Valérie Drouet, et al. · The American Journal of Human Genetics · 434
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Is the MC1R variant p.R160W associated with Parkinson's?
2015 · Steven J. Lubbe, Valentina Escott‐Price, et al. · Annals of Neurology · 19
A systematic screening to identifyde novomutations causing sporadic early-onset Parkinson's disease
2015 · Celia Kun-Rodrigues, Christos Ganos, et al. · Human Molecular Genetics · 44
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A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia
2015 · Niccolo E. Mencacci, Ignacio Rubio-Agusti, et al. · The American Journal of Human Genetics · 145
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Mutations in HPCA Cause Autosomal-Recessive Primary Isolated Dystonia
2015 · Gavin Charlesworth, Plamena R. Angelova, et al. · The American Journal of Human Genetics · 102
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Polygenic risk of P arkinson disease is correlated with disease age at onset
2015 · Valentina Escott‐Price, Mike A. Nalls, et al. · Annals of Neurology · 135
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Reply: Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers
2014 · Niccolo E. Mencacci, Alan M. Pittman, et al. · Brain · 6
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NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
2014 · Mike A. Nalls, Jose Bras, et al. · Neurobiology of Aging · 98
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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
2014 · Mike A Nalls, 23andMe, et al. · Nature Genetics · 1,888
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Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers
2014 · Niccolò E. Mencacci, Ioannis U. Isaias, et al. · Brain · 201
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