Matthew Benger
University of Cambridge
18 Papers
9 Citations
Matthew Benger is an academic researcher from University of Cambridge. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 4, co-authored 9 publications. Previous affiliations of Matthew Benger include Imperial College London.
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Papers
Cerebral venous sinus thrombosis and thrombocytopenia after COVID-19 vaccination - A report of two UK cases.
Puja Mehta,Puja Mehta,Sean Apap Mangion,Matthew Benger,Biba R. Stanton,Julia Czuprynska,Roopen Arya,László Sztriha +7 more
TL;DR: In this article, the authors describe the cases of two young males who developed severe thrombocytopenia and fatal cerebral venous sinus Thrombosis following the first dose of Vaxzevria.
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Autism spectrum disorder: prospects for treatment using gene therapy
TL;DR: Despite a number of outstanding challenges, gene therapy has excellent potential to address cognitive dysfunction in ASD, and the first preclinical studies in monogenic ASD, involving both gene replacement and silencing are highlighted.
Deep learning to automate the labelling of head MRI datasets for computer vision applications.
David A. Wood,Sina Kafiabadi,Aisha Al Busaidi,Emily Guilhem,Jeremy Lynch,Matthew Townend,Antanas Montvila,Antanas Montvila,Martin Kiik,Juveria Siddiqui,Naveen Gadapa,Matthew Benger,Asif Mazumder,Gareth J. Barker,Sebastian Ourselin,James H. Cole,James H. Cole,Thomas C. Booth,Thomas C. Booth +18 more
TL;DR: In this paper, a deep learning model was used to derive labels from neuroradiology reports and assign these to the corresponding examinations, overcoming a bottleneck to computer vision model development.
Prognostic indicators and outcomes of hospitalised COVID-19 patients with neurological disease: An individual patient data meta-analysis
Bhagteshwar Singh,Suzannah Lant,Sofia Cividini,J. W. S. Cattrall,Lynsey Goodwin,Laura A Benjamin,Benedict D Michael,Ayaz Khawaja,Aline de Moura Brasil Matos,Walid Alkeridy,Andrea Pilotto,Durjoy Lahiri,Rebecca Rawlinson,S. Mhlanga,Evelyn C Lopez,Brendan F Sargent,Anushri Somasundaran,Arina Tamborska,Glynn W Webb,Komal Younas,Yaqub Al Sami,Heavenna Babu,Tristan Banks,Francesco Cavallieri,M. Cohen,Emma Davies,Shalley Dhar,Anna Fajardo Modol,Hamzah Z. Farooq,Jeffrey Harte,Samuel Hey,Albert Joseph,D. Karthikappallil,Daniel Kassahun,G. Lipunga,Rachel Mason,Thomas Hosker Minton,Gabrielle Mond,J. Poxon,Sophie Rabas,Germander Soothill,Marialuisa Zedde,Konstantin Yenkoyan,Bruce J. Brew,Erika W. Contini,Lucette A. Cysique,Xin Zhang,Pietro Maggi,Vincent Van Pesch,Jerome R. Lechien,Sven Saussez,Alex Heyse,Maria Lucia Brito Ferreira,Cristiane Nascimento Soares,Isabel Elicer,Laura Eugenín-von Bernhardi,Waleng Ñancupil Reyes,Rong Yin,Mohammed Azab,Foad Abd-Allah,A. Elkady,Simon Escalard,Jean-Christophe Corvol,Cécile Delorme,Pierre Tattevin,Kévin Bigaut,Norbert Lorenz,Daniel Hornuss,Jonas A. Hosp,Siegbert Rieg,Dirk Wagner,Benjamin Knier,Paul Lingor,Andrea Sylvia Winkler,A. Sharifi-Razavi,Shima T. Moein,SeyedAhmad SeyedAlinaghi,Saeidreza Jamalimoghadamsiahkali,Mauro Morassi,Alessandro Padovani,Marcello Giunta,Ilenia Libri,Simone Beretta,Sabrina Ravaglia,Matteo Foschi,Paolo Calabresi,Guido Primiano,Serenella Servidei,Nicola Biagio Mercuri,Claudio Liguori,Mariangela Pierantozzi,Loredana Sarmati,Federica Boso,Silvia Garazzino,Sara Mariotto,Kimani N Patrick,Oana Costache,Alexander Pincherle,Frederikus A. Klok,Roger M. Meza,Verónica Cabreira,Sofia R. Valdoleiros,Vanessa Oliveira,Igor Kaimovsky,Alla Guekht,Jasmin Jiemin Koh,E. Fernández Díaz,José María Barrios-López,Cristina Guijarro-Castro,Álvaro Beltrán-Corbellini,Javier Martínez‐Poles,A.M. Diezma-Martín,María Isabel Morales-Casado,S. García García,Gautier Breville,Matteo Coen,Marjolaine Uginet,Raphaël Bernard-Valnet,Renaud Du Pasquier,Yildiz Kaya,Loay H. Abdelnour,Claire M Rice,Hamish Morrison,Sylviane Defres,Saif Huda,Noelle Enright,Jane Hassell,Lucio D'Anna,Matthew Benger,László Sztriha,Eamon P. Raith,Krishna Chinthapalli,Ross Nortley,Ross Paterson,Arvind Chandratheva,David J. Werring,Samir Dervisevic,Kirsty Harkness,Ashwin Pinto,Dinesh V Jillella,Scott R. Beach,Kulothungan Gunasekaran,Ivan Rocha Ferreira da Silva,Krishna Nalleballe,Jon M Santoro,Tyler Scullen,Lora Kahn,Carla Kim,Kiran T. Thakur,Rajan B. Jain,Thirugnanam Umapathi,Timothy R Nicholson,James J. Sejvar,Eva Maria Hodel,Catrin Tudur Smith,Tom Solomon +155 more
TL;DR: The spectrum of neurological disease in hospitalised COVID-19 patients is described; clinical outcomes are characterised; factors associated with a poor outcome are investigated; and preliminary data suggest these may differ according to WHO regions and country income levels.
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The Interaction of Genetic Mutations in PARK2 and FA2H Causes a Novel Phenotype in a Case of Childhood-Onset Movement Disorder.
TL;DR: A second homozygous mutation in the FA2H gene, implicated in Hereditary spastic paraplegia, was revealed, appearing to have contributed to the novel phenotype observed, and highlighting a potential interaction between the two mutated genes.