Wellcome Trust Sanger Institute - Genome Research Limited

GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways (2019) López-Isac E, Acosta-Herrera M, Kerick M, Assassi S, Satpathy AT, Granja J, Mumbach MR, et al. Journal article A cellular census of human lungs identifies novel cell states in health and in asthma (2019) Braga FAV, Kar G, Berg M, Carpaij OA, Polanski K, Simon LM, Brouwer S, et al. Journal article De novo missense variants in RHOBTB2 cause a developmental and epileptic encephalopathy in humans, and altered levels cause neurological defects in Drosophila (2019) Straub J, Konrad E, Grüner J, Toutain A, Bok LA, Cho MT, Crawford HP, et al. Conference contribution Exploring the complex etiology of oncogenic fusions in childhood cancer (2019) Anderson ND, De Borja R, Young MD, Fuligni F, Rosic A, Roberts ND, Pillay N, et al. Conference contribution The human lung cell atlas: A high-resolution reference map of the human lung in health and disease (2019) Schiller HB, Montoro DT, Simon LM, Rawlins EL, Meyer KB, Strunz M, Braga FAV, et al. Journal article, Review article Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors (2018) Anderson ND, De Borja R, Young MD, Fuligni F, Rosic A, Roberts ND, Hajjar S, et al. Journal article Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation (2018) Teumer A, Chaker L, Groeneweg S, Li Y, Di Munno C, Barbieri C, Schultheiss UT, et al. Journal article UTX-mediated enhancer and chromatin remodeling suppresses myeloid leukemogenesis through noncatalytic inverse regulation of ETS and GATA programs (2018) Gozdecka M, Meduri E, Mazan M, Tzelepis K, Dudek M, Knights AJ, Pardo M, et al. Journal article Glutaminolysis is a metabolic dependency in FLT3ITD acute myeloid leukemia unmasked by FLT3 tyrosine kinase inhibition (2018) Gallipoli P, Giotopoulos G, Tzelepis K, Costa ASH, Vohra S, Medina-Perez P, Basheer F, et al. Journal article De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder (2018) Gregor A, Sadleir LG, Asadollahi R, Azzarello-Burri S, Battaglia A, Ousager LB, Boonsawat P, et al. Journal article