Tartu University Hospital

Hospital


Location: Tartu, Estonia (EE) EE

ISNI: 0000000105857044

ROR: https://ror.org/01dm91j21

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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Unpublished / Preprint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

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To

Abstract

Journal

GAB1::ABL1 fusions define a distinctive soft tissue neoplasm, with variable perineurial differentiation, and a predilection for children and young adults (2023) Agaimy A, Perret R, Demicco EG, Gross J, Liu YJ, Azmani R, Engelmann C, et al. Journal article Transcriptome-wide association study of coronary artery disease identifies novel susceptibility genes (2022) Li L, Chen Z, Von Scheidt M, Li S, Steiner A, Gueldener U, Koplev S, et al. Journal article Publisher Correction: Transcriptome-wide association study of coronary artery disease identifies novel susceptibility genes (Basic Research in Cardiology, (2022), 117, 1, (6), 10.1007/s00395-022-00917-8) (2022) Li L, Chen Z, Von Scheidt M, Li S, Steiner A, Gueldener U, Koplev S, et al. Journal article, Erratum A randomized trial of a transglutaminase 2 inhibitor for celiac disease (2021) Schuppan D, Mäki M, Lundin KE, Isola J, Friesing-Sosnik T, Taavela J, Popp A, et al. Journal article Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype (2021) Zanoni P, Steindl K, Sengupta D, Joset P, Bahr A, Sticht H, Lang-Muritano M, et al. Journal article CTCF variants in 31 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum (2019) Konrad E, Nardini N, Blyth M, Prescott K, Bouman AM, Brilstra EH, Caliebe A, et al. Conference contribution CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum (2019) Konrad E, Nardini N, Caliebe A, Nagel I, Young D, Horvath G, Santoro SL, et al. Journal article