Ikuti
Marieke Klein
Marieke Klein
Postdoctoral researcher, Department of Human Genetics, Radboudumc Nijmegen, The Netherlands
Email yang diverifikasi di radboudumc.nl
Judul
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Dikutip oleh
Tahun
Common genetic variants influence human subcortical brain structures
DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivières, ...
Nature 520 (7546), 224-229, 2015
8992015
The genetic architecture of the human cerebral cortex
KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ...
Science 367 (6484), eaay6690, 2020
7152020
ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries
PM Thompson, N Jahanshad, CRK Ching, LE Salminen, SI Thomopoulos, ...
Translational psychiatry 10 (1), 100, 2020
5662020
Novel genetic loci associated with hippocampal volume
DP Hibar, HHH Adams, N Jahanshad, G Chauhan, JL Stein, E Hofer, ...
Nature communications 8 (1), 13624, 2017
3282017
Cortical thickness across the lifespan: Data from 17,075 healthy individuals aged 3–90 years
S Frangou, A Modabbernia, SCR Williams, E Papachristou, GE Doucet, ...
Human brain mapping 43 (1), 431-451, 2022
318*2022
Genetic architecture of subcortical brain structures in 38,851 individuals
CL Satizabal, HHH Adams, DP Hibar, CC White, MJ Knol, JL Stein, ...
Nature genetics 51 (11), 1624-1636, 2019
2652019
Novel genetic loci underlying human intracranial volume identified through genome-wide association
HHH Adams, DP Hibar, V Chouraki, JL Stein, PA Nyquist, ME Rentería, ...
Nature neuroscience 19 (12), 1569-1582, 2016
2632016
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
2402016
Cognitive heterogeneity in adult attention deficit/hyperactivity disorder: A systematic analysis of neuropsychological measurements
JC Mostert, AMH Onnink, M Klein, J Dammers, A Harneit, T Schulten, ...
European Neuropsychopharmacology 25 (11), 2062-2074, 2015
1812015
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex
D Antaki, J Guevara, AX Maihofer, M Klein, M Gujral, J Grove, CE Carey, ...
Nature genetics 54 (9), 1284-1292, 2022
1502022
Genetic variants associated with longitudinal changes in brain structure across the lifespan
RM Brouwer, M Klein, KL Grasby, HG Schnack, N Jahanshad, J Teeuw, ...
Nature neuroscience 25 (4), 421-432, 2022
1492022
Brain imaging genetics in ADHD and beyond–Mapping pathways from gene to disorder at different levels of complexity
M Klein, M Onnink, M van Donkelaar, T Wolfers, B Harich, Y Shi, ...
Neuroscience & Biobehavioral Reviews 80, 115-155, 2017
1442017
Genetic overlap between attention-deficit/hyperactivity disorder and bipolar disorder: evidence from genome-wide association study meta-analysis
KJE van Hulzen, CJ Scholz, B Franke, S Ripke, M Klein, A McQuillin, ...
Biological psychiatry 82 (9), 634-641, 2017
1432017
Genetic influences on hub connectivity of the human connectome
A Arnatkeviciute, BD Fulcher, S Oldham, J Tiego, C Paquola, Z Gerring, ...
Nature Communications 12 (1), 4237, 2021
1342021
Shared genetic background between children and adults with attention deficit/hyperactivity disorder
P Rovira, D Demontis, C Sánchez-Mora, T Zayats, M Klein, NR Mota, ...
Neuropsychopharmacology 45 (10), 1617-1626, 2020
1212020
Consortium neuroscience of attention deficit/hyperactivity disorder and autism spectrum disorder: The ENIGMA adventure
M Hoogman, D Van Rooij, M Klein, P Boedhoe, I Ilioska, T Li, Y Patel, ...
Human brain mapping 43 (1), 37-55, 2022
1172022
Greater male than female variability in regional brain structure across the lifespan
LM Wierenga, GE Doucet, D Dima, I Agartz, M Aghajani, TN Akudjedu, ...
Human brain mapping 43 (1), 470-499, 2022
1102022
Genetic markers of ADHD-related variations in intracranial volume
M Klein, RK Walters, D Demontis, JL Stein, DP Hibar, HH Adams, ...
American Journal of Psychiatry 176 (3), 228-238, 2019
1082019
Case–control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder
C Sánchez-Mora, JA Ramos-Quiroga, R Bosch, M Corrales, ...
Neuropsychopharmacology 40 (4), 915-926, 2015
742015
Variation in a range of mTOR-related genes associates with intracranial volume and intellectual disability
MRF Reijnders, M Kousi, GM Van Woerden, M Klein, J Bralten, ...
Nature communications 8 (1), 1052, 2017
702017
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