Newcastle University

University / College


Location: Newcastle upon Tyne, United Kingdom (GB) GB

ISNI: 0000000104627212

ROR: https://ror.org/01kj2bm70

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

From
To

Abstract

Journal

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries (2022) Skoric-Milosavljevic D, Tadros R, Bosada FM, Tessadori F, Van Weerd JH, Woudstra O, Tjong FVY, et al. Journal article Test–retest precision and longitudinal cartilage thickness loss in the IMI-APPROACH cohort (2022) Wirth W, Maschek S, Marijnissen AC, Lalande A, Blanco FJ, Berenbaum F, van de Stadt LA, et al. Journal article Observations of root growth in stratified soils at the microscopic scale: Insights from micro-computed tomography (2022) Nadimi S, Kemp N, Angelidakis V, Luli S Conference contribution, Abstract of lecture Three-dimensional Particle Shape Acquisition, Characterisation, Classification, and Simplification (2022) Angelidakis V, Nadimi S Conference contribution, Abstract of a poster Nano-scale characterisation of particulate iron pyrite morphology in shale (2022) Angelidakis V, Nadimi S, Garum M, Hassanpour, A Journal article Elongation, flatness and compactness indices to characterise particle form (2022) Angelidakis V, Nadimi S, Utili S Journal article, Original article Standard intensities of transcranial alternating current stimulation over the motor cortex do not entrain corticospinal inputs to motor neurons (2022) Ibanez J, Zicher B, Brown KE, Rocchi L, Casolo A, Del Vecchio A, Spampinato D, et al. Journal article Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseases (2022) Wopperer F, Knaup K, Stanzick KJ, Schneider K, Jobst-Schwan T, Ekici AB, Uebe S, et al. Journal article A phase II, randomized, open-label, 52-week study of seladelpar in patients with primary biliary cholangitis (2022) Bowlus CL, Galambos MR, Aspinall RJ, Hirschfield GM, Jones DE, Dörffel Y, Gordon SC, et al. Journal article SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile (2022) Al-Jawahiri R, Foroutan A, Kerkhof J, McConkey H, Levy M, Haghshenas S, Rooney K, et al. Journal article