Sewerin S, Aurnhammer C, Skubic C, et al. Mechanisms of pathogenicity and the quest for genetic modifiers of kidney disease in branchiootorenal syndrome. Clinical kidney journal. 2024;17(1):sfad260. doi:10.1093/ckj/sfad260
Publications
Kagerer SM, Awasthi S, Ripke S, et al. Polygenic risk for Alzheimer’s disease is associated with neuroaxonal damage before onset of clinical symptoms. Alzheimer’s & dementia (Amsterdam, Netherlands). 2024;16(1):e12504. doi:10.1002/dad2.12504
Ho PC, Yu WH, Tee BL, et al. Asian Cohort for Alzheimer’s Disease (ACAD) pilot study on genetic and non-genetic risk factors for Alzheimer’s disease among Asian Americans and Canadians. Alzheimer’s & dementia : the journal of the Alzheimer’s Association. 2024. doi:10.1002/alz.13611
Zhu QM, Hsu YHH, Lassen FH, et al. Protein interaction networks in the vasculature prioritize genes and pathways underlying coronary artery disease. Communications biology. 2024;7(1):87. doi:10.1038/s42003-023-05705-1
Zhao J, Cato LD, Arora UP, et al. Inherited blood cancer predisposition through altered transcription elongation. Cell. 2024. doi:10.1016/j.cell.2023.12.016
Seligowski A V, Grewal SS, Abohashem S, et al. PTSD increases risk for major adverse cardiovascular events through neural and cardio-inflammatory pathways. Brain, behavior, and immunity. 2024;117:149-154. doi:10.1016/j.bbi.2024.01.006
Lindelöf L, Rantapää-Dahlqvist S, Lundtoft C, et al. A survey of ficolin-3 activity in Systemic Lupus Erythematosus reveals a link to hematological disease manifestations and autoantibody profile. Journal of autoimmunity. 2024;143:103166. doi:10.1016/j.jaut.2023.103166
Youssef O, Loukola A, Zidi-Mouaffak YHS, et al. High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases. Laboratory investigation; a journal of technical methods and pathology. 2024:100325. doi:10.1016/j.labinv.2024.100325
Perdyan A, JÄ…kalski M, Horbacz M, Beheshti A, Mieczkowski J. Chromosomal positioning and epigenetic architecture influence DNA methylation patterns triggered by galactic cosmic radiation. Scientific reports. 2024;14(1):1324. doi:10.1038/s41598-024-51756-7
Chen S, Francioli LC, Goodrich JK, et al. Author Correction: A genomic mutational constraint map using variation in 76,156 human genomes. Nature. 2024. doi:10.1038/s41586-024-07050-7