Whole genome sequencing for diagnosis of neurological repeat expansion disorders
Kristina Ibáñez(Queen Mary University of London), Denise Perry(Illumina (United States)), James M. Polke(National Hospital for Neurology and Neurosurgery), Dimitris Polychronopoulos(Genomics England), Anna C. Need(University of Pavia), Thomas T. Warner(King's College London), Ana Lisa Taylor Tavares(University of Leeds), Egor Dolzhenko(Illumina (United States)), Mary M. Reilly(National Hospital for Neurology and Neurosurgery), Lara Menzies(Great Ormond Street Hospital), Louise C. Daugherty(University of Cambridge), Tanner Hagelstrom(Illumina (United States)), Liana Santos(National Hospital for Neurology and Neurosurgery), James Davison(Great Ormond Street Hospital for Children NHS Foundation Trust), Katherine R. Smith(Murdoch Children's Research Institute), Loukas Moutsianas(Genomics England), Isabella Sheikh(National Hospital for Neurology and Neurosurgery), Elisabeth Rosser(Great Ormond Street Hospital), Jonathan M. Schott(UK Dementia Research Institute), Dalia Kasperavičiūtė(University of Leeds), Matilde Laurá(National Hospital for Neurology and Neurosurgery), Kelly Eggleton, Ellen M. McDonagh(Wellcome Sanger Institute), Pietro Fratta, Jana Vandrovcová(Texas Tech University), Paola Giunti(National Hospital for Neurology and Neurosurgery), Helen Brittain(Great Ormond Street Hospital), Nicholas Wood(National Hospital for Neurology and Neurosurgery), Zerin Hyder(University of Manchester), Antonio Rueda Martin(Genomics England), Anette Schrag(National Hospital for Neurology and Neurosurgery), David Bourn(Centre for Life), Meriel McEntagart(St George's, University of London), Richard Festenstein(Imperial College London), Heather Angus‐Leppan(Queen Mary University of London), Robert Robinson(National Health Service), Christine Patch(Wellcome Connecting Science), Huw R. Morris(University College London), Robyn Labrum(National Hospital for Neurology and Neurosurgery), Stephen Abbs(Guy's Hospital), Ellen Thomas(Imperial College Healthcare NHS Trust), Emma L. Baple(University of Exeter), Francesca Faravelli, Viraj Deshpande(Illumina (United States)), Kailash P. Bhatia(National Hospital for Neurology and Neurosurgery), Robin Howard(National Hospital for Neurology and Neurosurgery), L.V. Prasad Korlipara(Centre for Movement Disorders), Ghareesa Almheiri(University College London), Dorota Pasko(University of Exeter), Philip Twiss(NIHR Research Delivery Network)
Cited by 7
Related Papers
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
|Nature|2011|2.8k
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria
|Movement Disorders|2017|2.3k
Large recurrent microdeletions associated with schizophrenia
|Nature|2008|1.8k