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Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|July 18, 2024
A Damaging COL6A3 Variant Alters the MIR31HG-Regulated Response of Chondrocytes in Neocartilage Organoids to Hyperphysiologic Mechanical LoadingNiek Gc Bloks, Zainab Harissa, Giorgia Mazzini, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|December 1, 2020
RNA Sequencing Reveals Interacting Key Determinants of Osteoarthritis Acting in Subchondral Bone and Articular Cartilage: Identification of IL11 and CHADL as Attractive Treatment TargetsMargo Tuerlings, Marcella van Hoolwerff, Evelyn Houtman, et al.
Rheumatology (Oxford, England)|May 9, 2022
Identification and functional characterization of imbalanced osteoarthritis-associated fibronectin splice variantsMarcella van Hoolwerff, Margo Tuerlings, Imke J L Wijnen, et al.
Annals of the Rheumatic Diseases|October 15, 2020
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify WNT9A as novel osteoarthritis geneCindy Germaine Boer, Michelle S Yau, Sarah J Rice, et al.
Annals of the Rheumatic Diseases|December 4, 2018
RNA sequencing data integration reveals an miRNA interactome of osteoarthritis cartilageRodrigo Coutinho de Almeida, Yolande F M Ramos, Ahmed Mahfouz, et al.
Experimental Dermatology|January 4, 2021
Genetic variability of immune-related lncRNAs: polymorphisms in LINC-PINT and LY86-AS1 are associated with pemphigus foliaceus susceptibilityAmanda Salviano-Silva, Ticiana Della Justina Farias, Valéria Bumiller-Bini, et al.
Frontiers in Immunology|December 24, 2021
Circulating miRNAs as Potential Biomarkers for Celiac Disease DevelopmentIneke L Tan, Rodrigo Coutinho de Almeida, Rutger Modderman, et al.
Nature Genetics|November 8, 2011
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac diseaseGosia Trynka, Karen A Hunt, Nicholas A Bockett, et al.
Cell|August 27, 2021
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populationsCindy G Boer, Konstantinos Hatzikotoulas, Lorraine Southam, et al.
Nature Communications|January 30, 2024
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implicationsRosalie B T M Sterenborg, Inga Steinbrenner, Yong Li, et al.
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