Researcher
Benjamin O'Callaghan
UCL Queen Square Institute of Neurology,University College London
Statistics
19 papers found
All papers authored by Benjamin O'Callaghan
Refreshing results…
,
Noemi Esteras ,
Noemi Esteras Gallego,
Marc P. M. Soutar ,
Benjamin O’Callaghan ,
Helene Plun-Favreau
KAT8 compound inhibition inhibits the initial steps of PINK1-dependant mitophagy
Download from doi.org
,
John Hardy,
Helene Plun-Favreau
PINK1: From Parkinson’s disease to mitophagy and back again
Download from doi.org
,
Daniela Melandri ,
Benjamin O’Callaghan ,
Emily Annuario ,
Amy E. Monaghan ,
Natalie J. Welsh ,
Karishma D’Sa,
Sebastian Guelfi ,
David Zhang ,
Alan Pittman ,
Daniah Trabzuni ,
Anouk H. A. Verboven ,
Kylie S. Pan ,
Demis A. Kia,
Magda Bictash
and 14 other authors
Upload
,
Emily Annuario,
Amy Monaghan,
Natalie Welsh,
Karishma D'Sa,
Sebastian Guelfi,
David Zhang,
Alan Pittman,
Daniah Trabzuni,
Anouk Verboven,
Kylie S. Pan,
Demis A. Kia,
Magda Bictash
and 14 other authors
Tabular Data for figures of Soutar et al. 2022
Upload
,
Stephanie Efthymiou,
Perumal Varalakshmi,
Naveen Benakappa,
Henry Houlden,
Balasubramaniem Ashokkumar
Download from onlinelibrary.wiley.com
,
Benjamin O’Callaghan ,
Enrico Bugiardini ,
Emer O’Connor,
Jana Vandrovcova,
Indran Davagnanam ,
Varinder Alg,
Stephen Bonner,
Daniel Walsh ,
Diederik Bulters ,
Neil Kitchen,
Martin M. Brown,
Joan Grieve,
David J. Werring,
Henry Houlden
ANGPTL6 genetic variants are an underlying cause of familial intracranial aneurysms
Upload
,
Timo Greiner ,
Lucia G. Sivilotti
The Startle disease mutation, α1S270T, predicts shortening of glycinergic synaptic currents
Download from api.wiley.com
,
John H. Livingston,
John McKinley,
Bernardett Kalmar,
Reza Maroofian,
Gary Hotton
and 74 other authors
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification
Upload
,
Amy E. Monaghan,
Natalie J. Welsh ,
David Zhang,
Alan Pittman,
Daniah Trabzuni,
Emily Annuario,
Kylie S. Pan,
Daniela Melandri ,
Karishma D'Sa,
Sebastian Guelfi,
Nicholas W. Wood,
Andrew B. Singleton,
Demis A. Kia
and 12 other authors
Upload
,
Rahul Phadke,
Enrico Bugiardini,
Richa Sud,
Samuel McCall,
Michael G. Hanna,
Hanne Poulsen,
Roope Männikkö
and 1 other authors
A novelATP1A2mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms
UploadMissing publications? Search for publications with a matching author name.