Chung, J., Sun, X., Schmidt, M. A., Song, Y. E., Grunin, M., Palmer, E. L., Bush, W. S., Naj, A. C., Rajabli, F., Hamilton‐Nelson, K. L., Zhang, X., Leung, Y. Y., Wang, L., Mayeux, R., Schellenberg, G. D., Vance, M. A., Haines, J. L., Farrer, L. A., Kunkle, B. W., & Martin, E. R. (2023). Variants near X‐Chromosome Genes NLGN4X and PTCHD1 are Significantly Associated with Alzheimer’s Disease Risk. Alzheimer’s & Dementia, 19(S1). Portico. https://doi.org/10.1002/alz.067117
Columbia Affiliation:
Subjects:
Genomic Studies and Association Analyses
(OpenAlex Topic)
Epigenetic Modifications and Their Functional Implications
(OpenAlex Topic)
Molecular Basis of Rett Syndrome and Related Disorders
(OpenAlex Topic)
Publication Type:
Article
Unique ID:
10.1002/alz.067117
DOI:
Journal:
Publication Date:
Data Source:
OpenAlex
Source Link: