Georgia Katsoula

ORCID: 0000-0001-9611-9281
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Osteoarthritis Treatment and Mechanisms
  • Cancer-related molecular mechanisms research
  • Inflammatory mediators and NSAID effects
  • Cytokine Signaling Pathways and Interactions
  • Genetic Associations and Epidemiology
  • RNA Research and Splicing
  • Pancreatic function and diabetes
  • Immune Response and Inflammation
  • Diet, Metabolism, and Disease
  • Bioinformatics and Genomic Networks
  • Diabetes and associated disorders
  • Metabolomics and Mass Spectrometry Studies
  • NF-κB Signaling Pathways
  • Digestive system and related health
  • Cell Adhesion Molecules Research

Technical University of Munich
2021-2025

Helmholtz Zentrum München
2020-2025

Klinikum rechts der Isar
2024-2025

Genomics (United Kingdom)
2024

Multimorbidity is a rising public health challenge with important implications for management and policy. The most common multimorbidity pattern the combination of cardiometabolic osteoarticular diseases. Here, we study genetic underpinning comorbidity between type 2 diabetes osteoarthritis. We find genome-wide correlation two diseases robust evidence association-signal colocalization at 18 genomic regions. integrate multi-omics functional information to resolve colocalizing signals identify...

10.1016/j.ajhg.2023.06.010 article EN cc-by The American Journal of Human Genetics 2023-07-10

Osteoarthritis is a complex disease with huge public health burden. Genome-wide association studies (GWAS) have identified hundreds of osteoarthritis-associated sequence variants, but the effector genes underpinning these signals remain largely elusive. Understanding chromosome organisation in three-dimensional (3D) space essential for identifying long-range contacts between distant genomic features (e.g., and regulatory elements), tissue-specific manner. Here, we generate first whole genome...

10.1136/ard-2023-224945 article EN cc-by Annals of the Rheumatic Diseases 2024-03-13

Abstract Osteoarthritis is a prevalent joint disease and major cause of disability worldwide with no curative therapy. Development disease-modifying therapies requires better understanding the molecular mechanisms underpinning disease. A hallmark osteoarthritis cartilage degradation. To define events characterizing at whole transcriptome level, we performed deep RNA sequencing in paired samples low- high-osteoarthritis grade knee derived from 124 patients undergoing total replacement. We...

10.1093/hmg/ddac017 article EN cc-by Human Molecular Genetics 2022-01-25

Osteoarthritis (OA) is a joint disease featuring cartilage breakdown and chronic pain. Although age trauma are prominently associated with OA occurrence, the trigger signaling pathways propagating their pathogenic aspects ill defined. Following long-term catabolic activity traumatic breakdown, debris accumulates can Toll-like receptors (TLRs). Here we show that TLR2 stimulation suppressed expression of matrix proteins induced an inflammatory phenotype in human chondrocytes. Further, impaired...

10.1073/pnas.2207993120 article EN cc-by Proceedings of the National Academy of Sciences 2023-07-10
Konstantinos Hatzikotoulas Lorraine Southam Lilja Stefánsdóttir Cindy G. Boer Merry‐Lynn McDonald and 95 more J. Patrick Pett Young‐Chan Park Margo Tuerlings Rick Mulders Andrei Barysenka Ana Luiza Arruda Vinicius Tragante Alison Rocco Norbert Bittner Shibo Chen Susanne Horn Vinodh Srinivasasainagendra Ken To Georgia Katsoula Peter Kreitmaier Amabel Tenghe Arthur Gilly Liubov Arbeeva Lane G. Chen Agathe de Pins Daniel Dochtermann Cecilie Henkel Jonas Höijer Shuji Ito Penelope A. Lind Bitota Lukusa-Sawalena Aye Ko Ko Minn Marina Mola-Caminal Akira Narita Chelsea Nguyen Ene Reimann Micah Silberstein Anne Heidi Skogholt Hemant K. Tiwari Michelle S. Yau Ming Yue Wei Zhao Jin Zhou George Alexiadis Karina Banasik Søren Brunak Archie Campbell Jackson T S Cheung Joseph Dowsett Tariq Faquih Jessica D. Faul Lijiang Fei Anne Marie Fenstad Takamitsu Funayama Maiken E. Gabrielsen Chinatsu Gocho Kirill Gromov Thomas Hansen Georgi Hudjashov Þorvaldur Ingvarsson Jessica Johnson Helgi Jónsson Saori Kakehi Juha Karjalainen Elisa Kasbohm Susanna Lemmelä Kuang Lin Xiaoxi Liu M. Loef Massimo Mangino Daniel L. McCartney Iona Y. Millwood Joshua Richman Mary B. Roberts Kathleen A. Ryan Dino Samartzis Manu Shivakumar Søren Thorgaard Skou Sachiyo Sugimoto Ken Suzuki Hiroshi Takuwa Maris Teder‐Laving Laurent F. Thomas Kohei Tomizuka Constance Turman Stefan Weiß Tian Wu Eleni Zengini Yanfei Zhang Manuel A. R. Ferreira George C. Babis Aris Baras Tyler Barker David J. Carey Kathryn S.E. Cheah Zhengming Chen Jason Pui Yin Cheung Mark Daly Renée de Mutsert Charles B. Eaton

Abstract Osteoarthritis is the third most rapidly growing health condition associated with disability, after dementia and diabetes 1 . By 2050, total number of patients osteoarthritis estimated to reach billion worldwide 2 As no disease-modifying treatments exist for osteoarthritis, a better understanding disease aetiopathology urgently needed. Here we perform genome-wide association study meta-analyses across up 489,975 cases 1,472,094 controls, establishing 962 independent associations,...

10.1038/s41586-025-08771-z article EN cc-by Nature 2025-04-09

<h3>Background:</h3> Osteoarthritis (OA) is a complex disease with huge public health burden. Genome-wide association studies (GWAS) have identified hundreds of osteoarthritis-associated DNA sequence variants, but the effector genes underpinning these signals remain largely elusive. Understanding chromosome organization in 3D space essential for identifying long-range contacts between distant genomic features (e.g., and regulatory elements), tissue-specific manner. <h3>Objectives:</h3> Our...

10.1136/annrheumdis-2024-eular.491 article EN 2024-06-01

Translational efforts in osteoarthritis are hampered by a gap our understanding of disease processes at the molecular level. Here, we present evidence pronounced transcriptional changes high- and low-disease-grade cartilage tissue, pointing to embryonic involved progression. We identify shared programs between cell populations human fetal limb, increases pre-hypertrophic chondrocytes' low-grade osteoblastic signatures high-grade tissue. find that genetic risk signals enriched six gene...

10.1016/j.ajhg.2024.10.019 article EN cc-by-nc-nd The American Journal of Human Genetics 2024-11-22

Osteoarthritis, a whole-joint degenerative disorder, is major public health burden that affects nearly 600 million individuals worldwide. Molecular profiling of relevant tissues crucial for understanding the biological mechanisms underlying disease development. We present first comprehensive map transcriptional regulation disease-relevant primary from knee osteoarthritis patients: macroscopically intact (low-grade, N=263) and degenerated (high-grade, N=216) cartilage, synovium (N=278), fat...

10.1101/2024.12.04.24318411 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2024-12-05

Abstract Multimorbidity is a rising public health challenge with important implications for management and policy. The most common multimorbidity pattern the combination of cardiometabolic osteoarticular diseases. Here, we study genetic underpinning comorbidity between type 2 diabetes osteoarthritis. We find genome-wide correlation two diseases, robust evidence association signal colocalization at 18 genomic regions. integrate multi-omics functional information to resolve colocalizing...

10.1101/2023.03.28.23287861 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2023-03-29
Coming Soon ...