University of Manchester

University / College


Location: Manchester, United Kingdom (GB) GB

ISNI: 0000000121662407

ROR: https://ror.org/027m9bs27

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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Unpublished / Preprint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

Electronic Structures of Group III–V Element Haeckelite Compounds: A Novel Family of Semiconductors, Dirac Semimetals, and Topological Insulators (2022) Khazaei M, Ranjbar A, Kang YG, Liang Y, Khaledialidusti R, Bae S, Raebiger H, et al. Journal article Guest Editorial Special Issue on Next Generation Multiple Access-Part II (2022) Liu Y, Zhang S, Ding Z, Schober R, Al-Dhahir N, Hossain E, Shen X Journal article, Editorial A gamma-ray pulsar timing array constrains the nanohertz gravitational wave background (2022) Ajello M, Atwood WB, Baldini L, Ballet J, Barbiellini G, Bastieri D, Bellazzini R, et al. Journal article 2022 EULAR points to consider for remote care in rheumatic and musculoskeletal diseases (2022) De Thurah A, Bosch P, Marques A, Meissner Y, Mukhtyar CB, Knitza J, Najm A, et al. Journal article Genome-wide and transcriptome-wide association studies of mammographic density phenotypes reveal novel loci (2022) Chen H, Fan S, Stone J, Thompson DJ, Douglas J, Li S, Scott C, et al. Journal article Reconfigurable Intelligent Surface-Aided Multi-User Networks: Interplay Between NOMA and RIS (2022) Liu Y, Mu X, Liu X, Di Renzo M, Ding Z, Schober R Journal article Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group (2022) Bakhuizen JJ, Hanson H, Van De Tuin K, Lalloo F, Tischkowitz M, Wadt K, Doergeloh BB, et al. Conference contribution Common RUNX3 missense variant contributes to psoriatic arthritis by modifying differentiation of CD8(+) T-cells (2022) Kerker I, Löhr S, Uebe S, Popp B, Vasileiou G, Bowes J, Kirchner P, et al. Conference contribution A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness (2022) Issler N, Afonso S, Weissman I, Jordan K, Cebrian-Serrano A, Meindl K, Dahlke E, et al. Journal article Special Issue on Next Generation Multiple Access-Part I (2022) Liu Y, Zhang S, Ding Z, Schober R, Al-Dhahir N, Hossain E, Shen X Journal article, Editorial