Mads Engel Hauberg
Mads Engel Hauberg
Internal medicine at Horsens Hospital
Verified email at - Homepage
Cited by
Cited by
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
D Demontis, RK Walters, J Martin, M Mattheisen, TD Als, E Agerbo, ...
Nature genetics 51 (1), 63-75, 2019
Identification of common genetic risk variants for autism spectrum disorder
J Grove, S Ripke, TD Als, M Mattheisen, RK Walters, H Won, J Pallesen, ...
Nature genetics 51 (3), 431-444, 2019
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
Brain cell type specific gene expression and co-expression network architectures
AT McKenzie, M Wang, ME Hauberg, JF Fullard, A Kozlenkov, A Keenan, ...
Scientific reports 8 (1), 8868, 2018
The Mount Sinai cohort of large-scale genomic, transcriptomic and proteomic data in Alzheimer's disease
M Wang, ND Beckmann, P Roussos, E Wang, X Zhou, Q Wang, C Ming, ...
Scientific data 5 (1), 1-16, 2018
A Bayesian framework for multiple trait colocalization from summary association statistics
C Giambartolomei, J Zhenli Liu, W Zhang, M Hauberg, H Shi, J Boocock, ...
Bioinformatics 34 (15), 2538-2545, 2018
CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder
GE Hoffman, J Bendl, G Voloudakis, KS Montgomery, L Sloofman, ...
Scientific data 6 (1), 180, 2019
A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder
J Martin, RK Walters, D Demontis, M Mattheisen, SH Lee, E Robinson, ...
Biological psychiatry 83 (12), 1044-1053, 2018
An atlas of chromatin accessibility in the adult human brain
JF Fullard, ME Hauberg, J Bendl, G Egervari, MD Cirnaru, SM Reach, ...
Genome research 28 (8), 1243-1252, 2018
Dysregulation of miRNA-9 in a subset of schizophrenia patient-derived neural progenitor cells
A Topol, S Zhu, BJ Hartley, J English, ME Hauberg, N Tran, ...
Cell reports 15 (5), 1024-1036, 2016
Common genetic variation influencing human white matter microstructure
B Zhao, T Li, Y Yang, X Wang, T Luo, Y Shan, Z Zhu, D Xiong, ...
Science 372 (6548), eabf3736, 2021
Cell-specific histone modification maps in the human frontal lobe link schizophrenia risk to the neuronal epigenome
K Girdhar, GE Hoffman, Y Jiang, L Brown, M Kundakovic, ME Hauberg, ...
Nature neuroscience 21 (8), 1126-1136, 2018
Analyzing the role of microRNAs in schizophrenia in the context of common genetic risk variants
ME Hauberg, P Roussos, J Grove, AD Břrglum, M Mattheisen, ...
JAMA psychiatry 73 (4), 369-377, 2016
Large-scale identification of common trait and disease variants affecting gene expression
ME Hauberg, W Zhang, C Giambartolomei, O Franzén, DL Morris, TJ Vyse, ...
The American Journal of Human Genetics 100 (6), 885-894, 2017
Open chromatin profiling of human postmortem brain infers functional roles for non-coding schizophrenia loci
JF Fullard, C Giambartolomei, ME Hauberg, K Xu, G Voloudakis, Z Shao, ...
Human molecular genetics 26 (10), 1942-1951, 2017
Common schizophrenia risk variants are enriched in open chromatin regions of human glutamatergic neurons
ME Hauberg, J Creus-Muncunill, J Bendl, A Kozlenkov, B Zeng, C Corwin, ...
Nature communications 11 (1), 5581, 2020
Common variants contribute to intrinsic human brain functional networks
B Zhao, T Li, SM Smith, D Xiong, X Wang, Y Yang, T Luo, Z Zhu, Y Shan, ...
Nature Genetics 54 (4), 508-517, 2022
Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls
ME Hauberg, JF Fullard, L Zhu, AT Cohain, C Giambartolomei, R Misir, ...
Molecular psychiatry 24 (11), 1685-1695, 2019
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups
M Mattheisen, J Grove, TD Als, J Martin, G Voloudakis, S Meier, ...
Nature genetics 54 (10), 1470-1478, 2022
Identification of the BRD1 interaction network and its impact on mental disorder risk
T Fryland, JH Christensen, J Pallesen, M Mattheisen, J Palmfeldt, M Bak, ...
Genome medicine 8, 1-20, 2016
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