Found 7 results
Filters: Keyword is Polymorphism, Single Nucleotide  [Clear All Filters]
2018
Cheng-Hathaway PJ, Reed-Geaghan EG, Jay TR, Casali BT, Bemiller SM, Puntambekar SS, von Saucken VE, Williams RY, J Karlo C, Moutinho M et al..  2018.  The Trem2 R47H variant confers loss-of-function-like phenotypes in Alzheimer's disease.. Mol Neurodegener. 13(1):29.
2017
Dincheva I, Yang J, Li A, Marinic T, Freilingsdorf H, Huang C, Casey BJ, Hempstead B, Glatt CE, Lee FS et al..  2017.  Effect of Early-Life Fluoxetine on Anxiety-Like Behaviors in BDNF Val66Met Mice.. Am J Psychiatry. 174(12):1203-1213.
Bonham LW, Sirkis DW, Fan J, Aparicio RE, Tse M, Ramos EMarisa, Wang Q, Coppola G, Rosen HJ, Miller BL et al..  2017.  Identification of a rare coding variant in TREM2 in a Chinese individual with Alzheimer's disease.. Neurocase. 23(1):65-69.
Hosono N, Makishima H, Mahfouz R, Przychodzen B, Yoshida K, Jerez A, LaFramboise T, Polprasert C, Clemente MJ, Shiraishi Y et al..  2017.  Recurrent genetic defects on chromosome 5q in myeloid neoplasms.. Oncotarget. 8(4):6483-6495.
2016
Puckett EE, Park J, Combs M, Blum MJ, Bryant JE, Caccone A, Costa F, Deinum EE, Esther A, Himsworth CG et al..  2016.  Global population divergence and admixture of the brown rat (Rattus norvegicus).. Proc Biol Sci. 283(1841)
Sirkis DW, Bonham LW, Aparicio RE, Geier EG, Ramos EMarisa, Wang Q, Karydas A, Miller ZA, Miller BL, Coppola G et al..  2016.  Rare TREM2 variants associated with Alzheimer's disease display reduced cell surface expression.. Acta Neuropathol Commun. 4(1):98.
2001
Reich DE, Cargill M, Bolk S, Ireland J, Sabeti PC, Richter DJ, Lavery T, Kouyoumjian R, Farhadian SF, Ward R et al..  2001.  Linkage disequilibrium in the human genome.. Nature. 411(6834):199-204.