Huw R Morris

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nicholas w woodUCLDirección de correo verificada de ucl.ac.uk
Yoav Ben-ShlomoUniversity of BristolDirección de correo verificada de bristol.ac.uk
David J BurnProfessor of Movement Disorder Neurology, Newcastle UniversityDirección de correo verificada de ncl.ac.uk
Andrew SingletonNational Institute on AgingDirección de correo verificada de mail.nih.gov
Professor Tamas ReveszEmeritus Professor of Neuropathology, UCL Queen Square Institute of Neurology, Univ Coll LondonDirección de correo verificada de ucl.ac.uk
Thomas FoltynieSenior Lecturer, UCL Institute of NeurologyDirección de correo verificada de ucl.ac.uk
Roger A BarkerUniversity of CambridgeDirección de correo verificada de cam.ac.uk
Mike A. NallsFounder/consultant with Data Tecnica International + Data science lead at NIH’s Center for AlzheimerDirección de correo verificada de mail.nih.gov
Martin RossorProfessor Emeritus and Principal Research Associate at University College LondonDirección de correo verificada de ucl.ac.uk
Henry HouldenProf NeurogeneticsDirección de correo verificada de ucl.ac.uk
Manuela MX TanOslo University hospitalDirección de correo verificada de medisin.uio.no
Michele HuNuffield Department Clinical Neurosciences, University of OxfordDirección de correo verificada de ndcn.ox.ac.uk
Nin Bajaj MA, FRCP, PhDConsultant neurologistDirección de correo verificada de nhs.net
Peter HeutinkAlectorDirección de correo verificada de alector.com
Anette SchragUniversity College LondonDirección de correo verificada de doctors.org.uk
Steven LubbeAssistant Professor of Neurology and Genetic MedicineDirección de correo verificada de northwestern.edu
Adrian WaiteResearch Associate at Cardiff University, School of BiosciencesDirección de correo verificada de cf.ac.uk
Thomas GasserProfessor of NeurologyDirección de correo verificada de uni-tuebingen.de
Rohan de SilvaProfessor of Molecular Neuroscience, UCL Queen Square Institute of NeurologyDirección de correo verificada de ucl.ac.uk
Kailash BhatiaProfessor of Clinical Neurology, Institute of Neurology, UCL, Queen Square, London WC1N 3BG,Dirección de correo verificada de ucl.ac.uk

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Huw R Morris

UCL Queen Square Institute of Neurology

Dirección de correo verificada de ucl.ac.uk

Parkinson disease psp als ftd genetics


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ... Neuron, 2011	4833	2011
Clinical diagnosis of progressive supranuclear palsy: the movement disorder society criteria GU Höglinger, G Respondek, M Stamelou, C Kurz, KA Josephs, AE Lang, ... Movement disorders 32 (6), 853-864, 2017	1859	2017
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... The Lancet Neurology 18 (12), 1091-1102, 2019	1722	2019
Neurological and neuropsychiatric complications of COVID-19 in 153 patients: a UK-wide surveillance study A Varatharaj, N Thomas, MA Ellul, NWS Davies, TA Pollak, EL Tenorio, ... The Lancet Psychiatry 7 (10), 875-882, 2020	1575	2020
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018	1409	2018
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ... The Lancet Neurology 11 (4), 323-330, 2012	1353	2012
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. MA Nalls, V Plagnol, DG Hernandez, M Sharma, UM Sheerin, M Saad, ... Lancet 377 (9766), 641, 2011	1015	2011
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy GU Höglinger, NM Melhem, DW Dickson, PMA Sleiman, LS Wang, L Klei, ... Nature genetics 43 (7), 699-705, 2011	646	2011
Differentiation of atypical parkinsonian syndromes with routine MRI A Schrag, CD Good, K Miszkiel, HR Morris, CJ Mathias, AJ Lees, ... Neurology 54 (3), 697-697, 2000	515	2000
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype H Houlden, M Baker, HR Morris, N MacDonald, S Pickering–Brown, ... Neurology 56 (12), 1702-1706, 2001	489	2001
100,000 genomes pilot on rare-disease diagnosis in health care—preliminary report 100,000 Genomes Project Pilot Investigators New England Journal of Medicine 385 (20), 1868-1880, 2021	427	2021
Visual dysfunction in Parkinson’s disease RS Weil, AE Schrag, JD Warren, SJ Crutch, AJ Lees, HR Morris Brain 139 (11), 2827-2843, 2016	423	2016
Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ... The American Journal of Human Genetics 98 (3), 500-513, 2016	419	2016
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ... Brain 140 (12), 3191-3203, 2017	405	2017
Frontotemporal dementia and its subtypes: a genome-wide association study R Ferrari, DG Hernandez, MA Nalls, JD Rohrer, A Ramasamy, JBJ Kwok, ... The Lancet Neurology 13 (7), 686-699, 2014	404	2014
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ... Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014	386	2014
Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion AJ Waite, D Bäumer, S East, J Neal, HR Morris, O Ansorge, DJ Blake Neurobiology of aging 35 (7), 1779. e5-1779. e13, 2014	339	2014
The prevalence of progressive supranuclear palsy (Steele–Richardson–Olszewski syndrome) in the UK U Nath, Y Ben-Shlomo, RG Thomson, HR Morris, NW Wood, AJ Lees, ... Brain 124 (7), 1438-1449, 2001	318	2001
Parkinson's disease age at onset genome‐wide association study: defining heritability, genetic loci, and α‐synuclein mechanisms C Blauwendraat, K Heilbron, CL Vallerga, S Bandres‐Ciga, R Von Coelln, ... Movement Disorders 34 (6), 866-875, 2019	306	2019
Genome-wide pleiotropy between Parkinson disease and autoimmune diseases A Witoelar, IE Jansen, Y Wang, RS Desikan, JR Gibbs, C Blauwendraat, ... JAMA neurology 74 (7), 780-792, 2017	289	2017

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