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Narelle K Hansell
Narelle K Hansell
Research Fellow, Queensland Brain Institute, The University of Queensland
Verified email at uq.edu.au
Title
Cited by
Cited by
Year
Common genetic variants influence human subcortical brain structures
DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivičres, ...
Nature 520 (7546), 224-229, 2015
7102015
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
JE Savage, PR Jansen, S Stringer, K Watanabe, J Bryois, CA De Leeuw, ...
Nature genetics 50 (7), 912-919, 2018
6912018
Identification of common variants associated with human hippocampal and intracranial volumes
JL Stein, SE Medland, AA Vasquez, DP Hibar, RE Senstad, AM Winkler, ...
Nature genetics 44 (5), 552-561, 2012
6402012
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
G Davies, M Lam, SE Harris, JW Trampush, M Luciano, WD Hill, ...
Nature communications 9 (1), 1-16, 2018
3912018
Meta-analysis of genome-wide association studies for personality
MHM De Moor, PT Costa, A Terracciano, RF Krueger, EJC De Geus, ...
Molecular psychiatry 17 (3), 337-349, 2012
3792012
The genetic architecture of the human cerebral cortex
KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ...
Science 367 (6484), eaay6690, 2020
2802020
Common variants in the trichohyalin gene are associated with straight hair in Europeans
SE Medland, DR Nyholt, JN Painter, BP McEvoy, AF McRae, G Zhu, ...
The American Journal of Human Genetics 85 (5), 750-755, 2009
2792009
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L
B Benyamin, BS Pourcain, OS Davis, G Davies, NK Hansell, MJA Brion, ...
Molecular psychiatry 19 (2), 253-258, 2014
2752014
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
CA Rietveld, T Esko, G Davies, TH Pers, P Turley, B Benyamin, ...
Proceedings of the National Academy of Sciences 111 (38), 13790-13794, 2014
2692014
Meta-analysis of genome-wide association studies for neuroticism, and the polygenic association with major depressive disorder
MHM De Moor, SM Van Den Berg, KJH Verweij, RF Krueger, M Luciano, ...
JAMA psychiatry 72 (7), 642-650, 2015
2642015
Novel genetic loci associated with hippocampal volume
DP Hibar, HHH Adams, N Jahanshad, G Chauhan, JL Stein, E Hofer, ...
Nature communications 8 (1), 1-12, 2017
2302017
Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium
XZ Kong, SR Mathias, T Guadalupe, ENIGMA Laterality Working Group, ...
Proceedings of the National Academy of Sciences 115 (22), E5154-E5163, 2018
2232018
Genetics of cognition: outline of a collaborative twin study
M Wright, E De Geus, J Ando, M Luciano, D Posthuma, Y Ono, N Hansell, ...
Twin Research and Human Genetics 4 (1), 48-56, 2001
2192001
Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis
S Macgregor, PA Lind, KK Bucholz, NK Hansell, PAF Madden, ...
Human molecular genetics 18 (3), 580-593, 2009
2142009
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept
B Franke, JL Stein, S Ripke, V Anttila, DP Hibar, KJE Van Hulzen, ...
Nature neuroscience 19 (3), 420-431, 2016
1972016
Novel genetic loci underlying human intracranial volume identified through genome-wide association
HHH Adams, DP Hibar, V Chouraki, JL Stein, PA Nyquist, ME Renterķa, ...
Nature neuroscience 19 (12), 1569-1582, 2016
1852016
Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population
TK Clarke, MK Lupton, AM Fernandez-Pujals, J Starr, G Davies, S Cox, ...
Molecular psychiatry 21 (3), 419-425, 2016
1852016
Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity
N Jahanshad, P Rajagopalan, X Hua, DP Hibar, TM Nir, AW Toga, ...
Proceedings of the National Academy of Sciences 110 (12), 4768-4773, 2013
1552013
Meta-analysis of genome-wide association studies for extraversion: findings from the genetics of personality consortium
SM Van den Berg, MHM de Moor, KJH Verweij, RF Krueger, M Luciano, ...
Behavior genetics 46 (2), 170-182, 2016
1522016
Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness
Y Lu, DP Dimasi, PG Hysi, AW Hewitt, KP Burdon, TY Toh, JB Ruddle, ...
PLoS genetics 6 (5), e1000947, 2010
1502010
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