The impact of clinical genome sequencing in a global population with suspected rare genetic disease
Authors: Erin Thorpe; Taylor Williams; Chad Shaw; Evgenii Chekalin; Julia Ortega; Keisha Robinson; Jason Button; Marilyn C Jones; Miguel Del Campo; Donald Basel; Julie McCarrier; Laura Davis Keppen; Erin Royer; Romina Foster-Bonds; Milagros M Duenas-Roque; Nora Urraca; Kerri Bosfield; Chester W Brown; Holly Lydigsen; Henry J Mroczkowski; Jewell Ward; Fabio Sirchia; Elisa Giorgio; Keith Vaux; Hildegard Peña Salguero; Aimé Lumaka; Gerrye Mubungu; Prince Makay 17, 17, 17, 18, 19, 20, 21, 21, 22, 22, 23, 24, Marwan Shinawi 25, Pilar Magoulas 26, Duncan Henry 27, Kate Gibson 28, Samuel Wiafe 29, Parul Jayakar 30, Daria Salyakina 30, Diane Masser-Frye 31, Arturo Serize 32, Jorge E Perez 32, Alan Taylor 33, Shruti Shenbagam 33, Ahmad Abou Tayoun 34, Alka Malhotra 1, Maren Bennett 1, Vani Rajan 35, James Avecilla 1, Andrew Warren 1, Max Arseneault 1, Tasha Kalista 1, Ali Crawford 1, Subramanian S Ajay 1, Denise L Perry 1, John Belmont 2, Ryan J Taft; Mamy Ngole; Prosper Tshilobo Lukusa; Adeline Vanderver; Kayla Muirhead; Omar Sherbini; Melissa D Lah; Katelynn Anderson; Jeny Bazalar-Montoya; Richard S Rodriguez; Mario Cornejo-Olivas; Karina Milla-Neyra
Collaborators: Al Jalila Children's Specialty Hospital; Baylor College of Medicine; Children's Hospital of Philadelphia; Illumina Inc; Indiana University School of Medicine; Medical College of Wisconsin; Mohammed Bin Rashid University; Rady Children's Hospital San Diego; Rare Genomics Institute (RG); Texas Children's Hospital; Washington University School of Medicine, St. Louis Children’s Hospital