Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics.
| Τίτλος | Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics. |
| Publication Type | Journal Article |
| Year of Publication | 2013 |
| Authors | Nho, K., Corneveaux J. J., Kim S., Lin H., Risacher S. L., Shen L., Swaminathan S., Ramanan V. K., Liu Y., Foroud T., Inlow M. H., Siniard A. L., Reiman R. A., Aisen P. S., Petersen R. C., Green R. C., Jack C. R., Weiner M. W., Baldwin C. T., Lunetta K., Farrer L. A., Furney S. J., Lovestone S., Simmons A., Mecocci P., Vellas B., Tsolaki M., Kloszewska I., Soininen H., McDonald B. C., Farlow M. R., Ghetti B., Huentelman M. J., & Saykin A. J. |
| Corporate Authors | Multi-Institutional Research on Alzheimer Genetic Epidemiology(MIRAGE) Study, AddNeuroMed Consortium, Indiana Memory and Aging Study, & Alzheimer's Disease Neuroimaging Initiative(ADNI) |
| Journal | Mol Psychiatry |
| Volume | 18 |
| Issue | 7 |
| Pagination | 739 |
| Date Published | 2013 Jul |
| ISSN | 1476-5578 |
| Λέξεις κλειδιά | Atrophy, Exome, Genome-Wide Association Study, Hippocampus, Humans, Mild Cognitive Impairment, Neuroimaging |
| DOI | 10.1038/mp.2013.81 |
| Alternate Journal | Mol. Psychiatry |
| PubMed ID | 23787478 |
| PubMed Central ID | PMC3777293 |
| Grant List | K99 LM011384 / LM / NLM NIH HHS / United States P30 AG010133 / AG / NIA NIH HHS / United States R00 LM011384 / LM / NLM NIH HHS / United States R01 AG019771 / AG / NIA NIH HHS / United States R01 AG041232 / AG / NIA NIH HHS / United States R01 LM011360 / LM / NLM NIH HHS / United States R01 NS059873 / NS / NINDS NIH HHS / United States RC2 AG036535 / AG / NIA NIH HHS / United States U01 AG024904 / AG / NIA NIH HHS / United States U24 AG021886 / AG / NIA NIH HHS / United States |
