University College London (UCL)

Multimodal analysis of cell-free DNA whole-genome sequencing for pediatric cancers with low mutational burden (2021) Peneder P, Stütz AM, Surdez D, Krumbholz M, Semper S, Chicard M, Sheffield NC, et al. Journal article Oral Anticoagulants in the Oldest Old with Recent Stroke and Atrial Fibrillation (2021) Polymeris AA, Macha K, Paciaroni M, Wilson D, Koga M, Cappellari M, Schaedelin S, et al. Journal article Standardized measurement of coronary inflammation using cardiovascular computed tomography: integration in clinical care as a prognostic medical device (2021) Oikonomou EK, Antonopoulos AS, Schottlander D, Marwan M, Mathers C, Tomlins P, Siddique M, et al. Journal article Providing care for older adults in the Emergency Department: expert clinical recommendations from the European Task Force on Geriatric Emergency Medicine (2021) Lucke JA, Mooijaart SP, Heeren P, Singler K, Mcnamara R, Gilbert T, Nickel CH, et al. Journal article An efficient and combined placental T1-ADC acquisition in pregnancies with and without pre-eclampsia (2021) Hutter J, Ho A, Jackson LH, Slator PJ, Chappell LC, Hajnal JV, Rutherford MA Journal article, Original article Priming of Frames and Slots in Bilingual Children’s Code-Mixing: A Usage-Based Approach (2021) Quick AE, Gaskins D, Frick M Journal article Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss (2021) Richard EM, Bakhtiari S, Marsh AP, Kaiyrzhanov R, Wagner M, Shetty S, Pagnozzi A, et al. Journal article Application of win ratio methodology in the Global SYMPLICITY Registry for patients with atrial fibrillation or obstructive sleep apnea (2021) Mahfoud F, Mancia G, Ukena C, Schmieder R, Narkiewicz K, Ruilope L, Schlaich M, et al. Conference contribution EARLY CHILDHOOD HEIGHT-ADJUSTED TOTAL KIDNEY VOLUME AS A RISK MARKER OF KIDNEY SURVIVAL IN AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE (ARPKD) (2021) Burgmaier K, Kilian S, Arbeiter K, Atmis B, Buescher A, Derichs U, Dursun I, et al. Conference contribution The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype (2021) Averdunk L, Sticht H, Surowy H, Luedecke HJ, Koch-Hogrebe M, Alsaif HS, Kahrizi K, et al. Journal article