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Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families
Carlos Cruchaga, Sumitra Chakraverty, Kevin Mayo, Francesco L.M. Vallania, Robi D. Mitra, Kelley Faber, Jennifer Williamson, Tom Bird, Ramon Diaz-Arrastia, Tatiana M. Foroud, Bradley F. Boeve, Neill R. Graff-Radford, Pamela St. Jean, Michael Lawson, Margaret G. Ehm, Richard Mayeux, Alison M. Goate, the NIA-LOAD - NCRAD Family Study Consortium for the NIA-LOAD - NCRAD Family Study Consortium
- Bursky Center for Human Immunology & Immunotherapy Programs (CHiiPs)
- Roy and Diana Vagelos Division of Biology & Biomedical Sciences (DBBS)
- Institute of Clinical and Translational Sciences (ICTS)
- McDonnell Genome Institute (MGI)
- NeuroGenomics and Informatics Center
- COVID-19 Researchers
- Department of Genetics
- Edison Family Center for Genome Sciences & Systems Biology
- DBBS - Neurosciences
- DBBS - Human and Statistical Genetics
- DBBS - Biomedical Informatics and Data Science
- DBBS - Molecular Genetics and Genomics
- DBBS - Computational and Systems Biology
- Hope Center for Neurological Disorders
- Intellectual and Developmental Disabilities Research Center (IDDRC)
- Division of Basic Science Research
Research output: Contribution to journal › Article › peer-review
255
Scopus
citations