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Author Title [ Type(Desc)] Year
Filters: Author is Armstrong, Nicola J  [Clear All Filters]
Journal Article
van der Meer D, Sønderby IE, Kaufmann T, G Walters B, Abdellaoui A, Ames D, Amunts K, Andersson M, Armstrong NJ, Bernard M et al..  2020.  Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.. JAMA Psychiatry. 77(4):420-430.
Armstrong NJ, Mather KA, Sargurupremraj M, Knol MJ, Malik R, Satizabal CL, Yanek LR, Wen W, Gudnason VG, Dueker ND et al..  2020.  Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.. Stroke. 51(7):2111-2121.
de Rojas I, Moreno-Grau S, Tesi N, Grenier-Boley B, Andrade V, Jansen IE, Pedersen NL, Stringa N, Zettergren A, Hernández I et al..  2021.  Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.. Nat Commun. 12(1):3417.
Chauhan G, Adams HHH, Satizabal CL, Bis JC, Teumer A, Sargurupremraj M, Hofer E, Trompet S, Hilal S, Smith AVernon et al..  2019.  Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting.. Neurology.
Satizabal CL, Adams HHH, Hibar DP, White CC, Knol MJ, Stein JL, Scholz M, Sargurupremraj M, Jahanshad N, Roshchupkin GV et al..  2019.  Genetic architecture of subcortical brain structures in 38,851 individuals.. Nat Genet. 51(11):1624-1636.
Grasby KL, Jahanshad N, Painter JN, Colodro-Conde L, Bralten J, Hibar DP, Lind PA, Pizzagalli F, Ching CRK, McMahon MAgnes B et al..  2020.  The genetic architecture of the human cerebral cortex.. Science. 367(6484)
Hofer E, Roshchupkin GV, Adams HHH, Knol MJ, Lin H, Li S, Zare H, Ahmad S, Armstrong NJ, Satizabal CL et al..  2020.  Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.. Nat Commun. 11(1):4796.
Zhang Q, Sidorenko J, Couvy-Duchesne B, Marioni RE, Wright MJ, Goate AM, Marcora E, Huang K-L, Porter T, Laws SM et al..  2020.  Risk prediction of late-onset Alzheimer's disease implies an oligogenic architecture.. Nat Commun. 11(1):4799.

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