Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics
| dc.contributor.author | Nho, K. | |
| dc.contributor.author | Corneveaux, J. J. | |
| dc.contributor.author | Kim, S. | |
| dc.contributor.author | Lin, H. | |
| dc.contributor.author | Risacher, S. L. | |
| dc.contributor.author | Shen, L. | |
| dc.contributor.author | Swaminathan, S. | |
| dc.contributor.author | Ramanan, V. K. | |
| dc.contributor.author | Liu, Y. | |
| dc.contributor.author | Foroud, T. | |
| dc.contributor.author | Inlow, M. H. | |
| dc.contributor.author | Siniard, A. L. | |
| dc.contributor.author | Reiman, R. A. | |
| dc.contributor.author | Aisen, P. S. | |
| dc.contributor.author | Petersen, R. C. | |
| dc.contributor.author | Green, R. C. | |
| dc.contributor.author | Jack, C. R. | |
| dc.contributor.author | Weiner, M. W. | |
| dc.contributor.author | Baldwin, C. T. | |
| dc.contributor.author | Lunetta, K. | |
| dc.contributor.author | Farrer, L. A. | |
| dc.contributor.author | Multi-Institutional Research on Alzheimer Genetic Epidemiology (MIRAGE) Study | |
| dc.contributor.author | Furney, S. J. | |
| dc.contributor.author | Lovestone, S. | |
| dc.contributor.author | Simmons, A. | |
| dc.contributor.author | Mecocci, P. | |
| dc.contributor.author | Vellas, B. | |
| dc.contributor.author | Tsolaki, M. | |
| dc.contributor.author | Kloszewska, I. | |
| dc.contributor.author | Soininen, H. | |
| dc.contributor.author | AddNeuroMed Consortium | |
| dc.contributor.author | McDonald, B. C. | |
| dc.contributor.author | Farlow, M. R. | |
| dc.contributor.author | Ghetti, B. | |
| dc.contributor.author | Indiana Memory and Aging Study | |
| dc.contributor.author | Huentelman, M. J. | |
| dc.contributor.author | Saykin, A. J. | |
| dc.contributor.author | Alzheimer's Disease Neuroimaging Initiative (ADNI) | |
| dc.contributor.department | Radiology and Imaging Sciences, School of Medicine | |
| dc.date.accessioned | 2025-05-06T12:41:18Z | |
| dc.date.available | 2025-05-06T12:41:18Z | |
| dc.date.issued | 2013 | |
| dc.eprint.version | Author's manuscript | |
| dc.identifier.citation | Nho K, Corneveaux JJ, Kim S, et al. Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics. Mol Psychiatry. 2013;18(7):739. doi:10.1038/mp.2013.81 | |
| dc.identifier.uri | https://hdl.handle.net/1805/47800 | |
| dc.language.iso | en_US | |
| dc.publisher | Springer Nature | |
| dc.relation.isversionof | 10.1038/mp.2013.81 | |
| dc.relation.journal | Molecular Psychiatry | |
| dc.rights | Publisher Policy | |
| dc.source | PMC | |
| dc.subject | Cognitive dysfunction | |
| dc.subject | Atrophy | |
| dc.subject | Exome | |
| dc.subject | Hippocampus | |
| dc.subject | Neuroimaging | |
| dc.title | Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics | |
| dc.type | Article |