Huw R Morris
University College London
H-index: 82
Europe-United Kingdom
Top articles of Huw R Morris
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
The pathogenesis of Parkinson's disease | Huw R Morris Maria Grazia Spillantini Carolyn M Sue Caroline H Williams-Gray | 2024/1/20 | |
Genotype–phenotype correlation in PRKN-associated Parkinson’s disease | npj Parkinson's Disease | Poornima Jayadev Menon Sara Sambin Baptiste Criniere-Boizet Thomas Courtin Christelle Tesson | 2024/3/29 |
Evaluation of cerebrospinal fluid alpha-synuclein seed amplification assay in PSP and CBS | medRxiv | David Vaughan Riona Fumi Marte Theilmann Jensen Tatiana Georgiades Lesley Wu | 2024 |
Motor Complications in Parkinson's Disease: Results from 3343 Patients Followed for up to 12 Years | Movement Disorders Clinical Practice | Sacha E Gandhi Tanja Zerenner Anahita Nodehi Michael A Lawton Vicky Marshall | 2024/3/19 |
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1 | medRxiv | Pilar Alvarez Jerez Peter A Wild Crea Dan Ramos Emil K Gustavsson Mandy Radefeldt | 2024 |
Association of Structural Forms of 17q21. 31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub-haplotypes | medRxiv | Hui Wang Timothy S Chang Beth A Dombroski Po-Liang Cheng Ya-Qin Si | 2024/2/28 |
A pathogenic variant in RAB32 causes autosomal dominant Parkinsons disease and activates LRRK2 kinase | medRxiv | Emil K Gustavsson Jordan Follett Joanne Trinh Sandeep K Barodia Raquel Real | 2024 |
Frequency and outcomes of gastrostomy insertion in a longitudinal cohort study of atypical parkinsonism | European Journal of Neurology | Christopher Kobylecki Viorica Chelban Yee Yen Goh Emilia Michou Riona Fumi | 2024/2/26 |
Loss-of-function SMPD1 gene variant in Progressive Supranuclear Palsy-Richardson Syndrome patients of Chinese ancestry | Journal of Movement Disorders | Shen-Yang Lim Ai Huey Tan Jia Nee Foo Yi Jayne Tan Elaine GY Chew | 2024/1/31 |
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses | The Lancet Neurology | Emil K Gustavsson Jordan Follett Joanne Trinh Sandeep K Barodia Raquel Real | 2024/4/10 |
Cohort profile: ADAMS project: a genetic Association study in individuals from Diverse Ancestral backgrounds with Multiple Sclerosis based in the UK | BMJ Open | Benjamin M Jacobs Luisa Schalk Angie Dunne Antonio Scalfari Ashwini Nandoskar | 2023 |
Uncovering spatiotemporal patterns of atrophy in progressive supranuclear palsy using unsupervised machine learning | Brain communications | William J Scotton Cameron Shand Emily Todd Martina Bocchetta David M Cash | 2023/4/1 |
Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) | npj Parkinson's Disease | Lara M Lange Micol Avenali Melina Ellis Anastasia Illarionova Ignacio J Keller Sarmiento | 2023/6/27 |
Association between the LRP1B and APOE loci and the development of Parkinson’s disease dementia | Brain | Raquel Real Alejandro Martinez-Carrasco Regina H Reynolds Michael A Lawton Manuela MX Tan | 2023/5/2 |
Large-scale rare variant burden testing in Parkinson's disease | Brain | Mary B Makarious Julie Lake Vanessa Pitz Allen Ye Fu Joseph L Guidubaldi | 2023/11 |
Obituary for Dr. John C. Steele, 1934–2022 | Movement Disorders Clinical Practice | Huw R Morris Andrew J Lees | 2023/1 |
MAPT‐Associated Familial Progressive Supranuclear Palsy with Typical Corticobasal Degeneration Neuropathology: A Clinicopathological Report | Movement Disorders Clinical Practice | Patrick W Cullinane Riona Fumi Marte Theilmann Jensen Edwin Jabbari Thomas T Warner | 2023/4 |
Clinical features and changing patterns of neurodegenerative disorders on Guam | John C Steele John Hardy Katrina Gwinn-Hardy Patrick McGeer Huw Morris | 2023/6/26 | |
Prioritization of drug targets for neurodegenerative diseases by integrating genetic and proteomic data from brain and blood | Biological psychiatry | Yi-Jun Ge Ya-Nan Ou Yue-Ting Deng Bang-Sheng Wu Liu Yang | 2023/5/1 |
Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2) | npj Parkinson's Disease | Clodagh Towns Madeleine Richer Simona Jasaityte Eleanor J Stafford Julie Joubert | 2023/9/12 |
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