Publications by authors named "Tom Warner"

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Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's Disease.
Lara M Lange, Zih-Hua Fang, Laurel Screven, Ai Huey Tan, Roy N Alcalay, Tom Warner

Mov Disord· October 2025

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Intronic FGF14 GAA repeat expansions impact progression and survival in multiple system atrophy.
Viorica Chelban, David Pellerin, Nirosen Vijiaratnam, Hamin Lee, Yen Yee Goh, Tom Warner

Brain· September 2025

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Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's Disease.
Lara M Lange, Zih-Hua Fang, Laurel Screven, Ai Huey Tan, Roy N Alcalay, Tom Warner

medRxiv· July 2025

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High-speed odor sensing using miniaturized electronic nose.
Nik Dennler, Damien Drix, Tom P A Warner, Shavika Rastogi, Cecilia Della Casa

Sci Adv· November 2024

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Author Correction: Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes.
Kurt Farrell, Jack Humphrey, Timothy Chang, Yi Zhao, Yuk Yee Leung, Tom T Warner

Nat Commun· November 2024

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Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes.
Kurt Farrell, Jack Humphrey, Timothy Chang, Yi Zhao, Yuk Yee Leung, Tom T Warner

Nat Commun· September 2024

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Mutations in alpha-B-crystallin cause autosomal dominant axonal Charcot-Marie-Tooth disease with congenital cataracts.
Andrea Cortese, Riccardo Currò, Riccardo Ronco, Julian Blake, Alex M Rossor, Tom Warner

Eur J Neurol· January 2024

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Differential LRRK2 signalling and gene expression in WT-LRRK2 and G2019S-LRRK2 mouse microglia treated with zymosan and MLi2.
Iqra Nazish, Adamantios Mamais, Anna Mallach, Conceicao Bettencourt, Alice Kaganovich, Tom Warner

bioRxiv· September 2023

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The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy.
Gregor K Wenning, Iva Stankovic, Luca Vignatelli, Alessandra Fanciulli, Giovanna Calandra-Buonaura, Tom Warner

Mov Disord· June 2022

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Coupling of Mouse Olfactory Bulb Projection Neurons to Fluctuating Odor Pulses.
Debanjan Dasgupta, Tom P A Warner, Andrew Erskine, Andreas T Schaefer

J Neurosci· May 2022

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Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An Update.
Lara M Lange, Paulina Gonzalez-Latapi, Rajasumi Rajalingam, Marina A J Tijssen, Darius Ebrahimi-Fakhari, Tom Warner

Mov Disord· May 2022

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jULIEs: nanostructured polytrodes for low traumatic extracellular recordings and stimulation in the mammalian brain.
Romeo R Racz, Mihaly Kollo, Gabriella Racz, Ciprian Bulz, Tobias Ackels, Tom Warner

J Neural Eng· February 2022

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Fast odour dynamics are encoded in the olfactory system and guide behaviour.
Tobias Ackels, Andrew Erskine, Debanjan Dasgupta, Alina Cristina Marin, Tom P A Warner

Nature· May 2021

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Opicapone Efficacy and Tolerability in Parkinson's Disease Patients Reporting Insufficient Benefit/Failure of Entacapone.
Petr Vokurka, Andrew Barron, Sheetal Sumaria, Lindsey Stockford, Paul Jarman, Tom Warner

Mov Disord Clin Pract· November 2020

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Optical observation of needles in upward lightning flashes.
Marcelo M F Saba, Amanda R de Paiva, Luke C Concollato, Tom A Warner, Carina Schumann

Sci Rep· October 2020

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The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy.
Edwin Jabbari, John Woodside, Manuela M X Tan, Nicola Pavese, Oliver Bandmann, Tom T Warner

Mov Disord· September 2019

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On the Triggering Mechanisms of Upward Lightning.
Carina Schumann, Marcelo M F Saba, Tom A Warner, Marco A S Ferro, John H Helsdon

Sci Rep· July 2019

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Verbal adynamia in parkinsonian syndromes: behavioral correlates and neuroanatomical substrate.
Nadia K Magdalinou, Hannah L Golden, Jennifer M Nicholas, Pirada Witoonpanich, Catherine J Mummery, Tom T Warner

Neurocase· August 2018

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Genetic and phenotypic characterization of complex hereditary spastic paraplegia.
Eleanna Kara, Arianna Tucci, Claudia Manzoni, David S Lynch, Marilena Elpidorou, Tom Warner

Brain· July 2016

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Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data.
Kin Y Mok, Una Sheerin, Javier Simón-Sánchez, Afnan Salaka, Lucy Chester, Tom T Warner

Lancet Neurol· May 2016

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The clinical and genetic heterogeneity of paroxysmal dyskinesias.
Alice R Gardiner, Fatima Jaffer, Russell C Dale, Robyn Labrum, Roberto Erro, Tom Warner

Brain· December 2015

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DRD1 rare variants associated with tardive-like dystonia: a pilot pathway sequencing study in dystonia.
Justus L Groen, Katja Ritz, Tom T Warner, Frank Baas, Marina A J Tijssen

Parkinsonism Relat Disord· July 2014

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PRRT2-related disorders: further PKD and ICCA cases and review of the literature.
Felicitas Becker, Julian Schubert, Pasquale Striano, Anna-Kaisa Anttonen, Elina Liukkonen, Tom Warner

J Neurol· May 2013

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PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.
Alice R Gardiner, Kailash P Bhatia, Maria Stamelou, Russell C Dale, Manju A Kurian, Tom Warner

Neurology· November 2012

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Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration.
Maria K Tsaousidou, Karim Ouahchi, Tom T Warner, Yi Yang, Michael A Simpson

Am J Hum Genet· February 2008

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