Huw R Morris

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nicholas w woodUCLEmail yang diverifikasi di ucl.ac.uk
Yoav Ben-ShlomoUniversity of BristolEmail yang diverifikasi di bristol.ac.uk
David J BurnProfessor of Movement Disorder Neurology, Newcastle UniversityEmail yang diverifikasi di ncl.ac.uk
Andrew SingletonNational Institute on AgingEmail yang diverifikasi di mail.nih.gov
Professor Tamas ReveszEmeritus Professor of Neuropathology, UCL Queen Square Institute of Neurology, Univ Coll LondonEmail yang diverifikasi di ucl.ac.uk
Thomas FoltynieSenior Lecturer, UCL Institute of NeurologyEmail yang diverifikasi di ucl.ac.uk
Roger A BarkerUniversity of CambridgeEmail yang diverifikasi di cam.ac.uk
Mike A. NallsFounder/consultant with Data Tecnica International + Data science lead at NIH’s Center for AlzheimerEmail yang diverifikasi di mail.nih.gov
Henry HouldenProf NeurogeneticsEmail yang diverifikasi di ucl.ac.uk
Michele HuNuffield Department Clinical Neurosciences, University of OxfordEmail yang diverifikasi di ndcn.ox.ac.uk
Martin RossorProfessor Emeritus and Principal Research Associate at University College LondonEmail yang diverifikasi di ucl.ac.uk
Manuela MX TanOslo University hospitalEmail yang diverifikasi di medisin.uio.no
Nin Bajaj MA, FRCP, PhDConsultant neurologistEmail yang diverifikasi di nhs.net
Peter HeutinkAlectorEmail yang diverifikasi di alector.com
Anette SchragUniversity College LondonEmail yang diverifikasi di doctors.org.uk
Steven LubbeAssistant Professor of Neurology and Genetic MedicineEmail yang diverifikasi di northwestern.edu
Kailash BhatiaProfessor of Clinical Neurology, Institute of Neurology, UCL, Queen Square, London WC1N 3BG,Email yang diverifikasi di ucl.ac.uk
Adrian WaiteResearch Associate at Cardiff University, School of BiosciencesEmail yang diverifikasi di cf.ac.uk
Thomas GasserProfessor of NeurologyEmail yang diverifikasi di uni-tuebingen.de
Rohan de SilvaProfessor of Molecular Neuroscience, UCL Queen Square Institute of NeurologyEmail yang diverifikasi di ucl.ac.uk

Ikuti

Huw R Morris

UCL Queen Square Institute of Neurology

Email yang diverifikasi di ucl.ac.uk

Parkinson disease psp als ftd genetics


Judul Urutkan menurut kutipan Urutkan menurut tahun Urutkan menurut judul	Dikutip oleh Dikutip oleh	Tahun
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	4905	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	1934	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	1836	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	1608	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	1454	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	1376	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	1021	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	652	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	516	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	494	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	480	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	436	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	435	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	414	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	413	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	388	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	343	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	326	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	315	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	299	2017

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