University Medical Centre Utrecht (UMC Utrecht)

Hospital


Location: Utrecht, Netherlands (NL) NL

ISNI: 0000000090126352

ROR: https://ror.org/0575yy874

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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Unpublished / Preprint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

Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis. (2022) Kerick M, Acosta-Herrera M, Pilar Simeon-Aznar C, Luis Callejas J, Assassi S, Proudman SM, Nikpour M, 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 Brain Structure in Acutely Underweight and Partially Weight-Restored Individuals With Anorexia Nervosa: A Coordinated Analysis by the ENIGMA Eating Disorders Working Group (2022) Walton E, Bernardoni F, Batury VL, Bahnsen K, Larivière S, Abbate-Daga G, Andres-Perpiña S, et al. Journal article Phase Ib/II Trial of Ribociclib in Combination with Binimetinib in Patients with NRAS-mutant Melanoma. (2022) Schuler M, Zimmer L, Kim KB, Sosman JA, Ascierto PA, Postow MA, De Vos FY, et al. Journal article Loss-of-function variants in SRRM2 cause a neurodevelopmental disorder (2022) Cuinat S, Nizon M, Isidor B, Stegmann A, van Jaarsveld RH, van Gassen KL, van der Smagt JJ, et al. Journal article Kidney Transplantation After Rescue Allocation-the Eurotransplant Experience: A Retrospective Multicenter Outcome Analysis. (2022) Assfalg V, Miller G, Stocker F, Van Meel M, Groenevelt T, Tieken I, Ankerst D, et al. Journal article Cervical Lymph Node Metastases from Central Nervous System Tumors: A Systematic Review (2022) Coca-Pelaz A, Bishop JA, Zidar N, Agaimy A, Mello Santiago Gebrim EM, Mondin V, Cohen O, et al. Journal article, Review article DNA methylation-based classification of malformations of cortical development in the human brain (2022) Jabari S, Kobow K, Pieper T, Hartlieb T, Kudernatsch M, Polster T, Bien CG, et al. Journal article De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability (2021) Schalk A, Cousin MA, Challman TD, Wain KE, Powis Z, Minks K, Trimouille A, et al. Journal article Coding practice in national and regional kidney biopsy registries (2021) Dendooven A, Peetermans H, Helbert M, Nguyen TQ, Marcussen N, Nagata M, Gesualdo L, et al. Journal article