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Molecular Neurodegeneration|August 16, 2024
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsyHui Wang, Timothy S Chang, Beth A Dombroski, et al.Medrxiv : the Preprint Server for Health Sciences|March 11, 2024
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub-haplotypesHui Wang, Timothy S Chang, Beth A Dombroski, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|October 13, 2022
Overall survival in the OlympiA phase III trial of adjuvant olaparib in patients with germline pathogenic variants in BRCA1/2 and high-risk, early breast cancerC E Geyer, J E Garber, R D Gelber, et al.Movement Disorders : Official Journal of the Movement Disorder Society|March 8, 2025
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal CellsHui Wang, Timothy S Chang, Beth A Dombroski, et al.Human Molecular Genetics|June 6, 2014
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degenerationRinki Ratnapriya, Xiaowei Zhan, Robert N Fariss, et al.Nature Genetics|March 5, 2013
Seven new loci associated with age-related macular degenerationLars G Fritsche, Wei Chen, Matthew Schu, et al.Nature Neuroscience|June 8, 2021
Baseline brain function in the preadolescents of the ABCD StudyB Chaarani, S Hahn, N Allgaier, et al.Pageof 229