Specialist multidisciplinary input maximises rare disease diagnoses from whole genome sequencing
William L. Macken(Princess Anne Hospital), Augusto Rendon(University of Cambridge), Matthew A. Brown(Translational Research Institute), Tim Hubbard(King's College London), Anna C. Need(University of Pavia), J. Pullinger, Chiara Pizzamiglio(National Hospital for Neurology and Neurosurgery), Federico Minneci(University College London), Nirupa Murugaesu(University of Pavia), L. Lahnstein(University of Cambridge), Melis Kayikci(Jackson Laboratory), Rebecca Ellmers, Mariana Buongermino Pereira(Genomics England), C. R. Boustred(Jackson Laboratory), Yogen Patel, A. Lakey, I. U. S. Leong(Genomics England), John N. Griffin(Yale University), Loukas Moutsianas(Genomics England), Athanasios Kousathanas(Jackson Laboratory), Dalia Kasperavičiūtė(University of Leeds), Adam Giess(Jackson Laboratory), Marta Bleda(University of Cambridge), Michael Mueller(Genomics England), Kelly Eggleton, Peter O’Donovan(Genomics England), Prabhu Arumugam(Jackson Laboratory), Micol Falabella(National Hospital for Neurology and Neurosurgery), Helen Brittain(Great Ormond Street Hospital), S. E. A. Leigh(Queen Mary University of London), Angela Hamblin(Genomics England), T. Rahim(University of Pavia), G. C. Chan(Jackson Laboratory), R. Jackson(Genomics England), Caroline McKittrick(National Hospital for Neurology and Neurosurgery), F. Maleady-Crowe(Genomics England), Meriel McEntagart(St George's, University of London), Mark J. Caulfield(Queen Mary University of London), J. Louise Jones(Queen Mary University of London), Christine Patch(Wellcome Connecting Science), Robyn Labrum(National Hospital for Neurology and Neurosurgery), Fabrice Lopez(Genomics England), Jonathon Mitchell(Oakland University), John C. Ambrose(Jackson Laboratory), Cathy E. Woodward(University College London), D. Perez-Gil(Queen Mary University of London), Chris A. Odhams(University of Pavia), Shirley Henderson(Genomics England), R. Bevers(Maastricht University)
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