User profiles for G. Roshchupkin
Gennady V RoshchupkinErasmus MC Verified email at erasmusmc.nl Cited by 4273 |
Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
…, MP Frosch, H Thonberg, W Maier, G Roshchupkin… - Nature …, 2019 - nature.com
Risk for late-onset Alzheimer’s disease (LOAD), the most prevalent dementia, is partially
driven by genetics. To identify LOAD risk loci, we performed a large genome-wide association …
driven by genetics. To identify LOAD risk loci, we performed a large genome-wide association …
[HTML][HTML] Stroke genetics informs drug discovery and risk prediction across ancestries
Previous genome-wide association studies (GWASs) of stroke — the second leading cause
of death worldwide — were conducted predominantly in populations of European ancestry 1 …
of death worldwide — were conducted predominantly in populations of European ancestry 1 …
Genetic variants associated with longitudinal changes in brain structure across the lifespan
…, J Repple, G Roberts, GV Roshchupkin… - Nature …, 2022 - nature.com
Human brain structure changes throughout the lifespan. Altered brain growth or rates of
decline are implicated in a vast range of psychiatric, developmental and neurodegenerative …
decline are implicated in a vast range of psychiatric, developmental and neurodegenerative …
Genetic architecture of subcortical brain structures in 38,851 individuals
Subcortical brain structures are integral to motion, consciousness, emotions and learning.
We identified common genetic variation related to the volumes of the nucleus accumbens, …
We identified common genetic variation related to the volumes of the nucleus accumbens, …
Gray matter age prediction as a biomarker for risk of dementia
…, WJ Niessen, GV Roshchupkin - Proceedings of the …, 2019 - National Acad Sciences
The gap between predicted brain age using magnetic resonance imaging (MRI) and chronological
age may serve as a biomarker for early-stage neurodegeneration. However, owing to …
age may serve as a biomarker for early-stage neurodegeneration. However, owing to …
[HTML][HTML] Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
Perivascular space (PVS) burden is an emerging, poorly understood, magnetic resonance
imaging marker of cerebral small vessel disease, a leading cause of stroke and dementia. …
imaging marker of cerebral small vessel disease, a leading cause of stroke and dementia. …
[HTML][HTML] Statistical and machine learning techniques in human microbiome studies: contemporary challenges and solutions
…, M Nedyalkova, I Elbere, G Roshchupkin… - Frontiers in …, 2021 - frontiersin.org
The human microbiome has emerged as a central research topic in human biology and
biomedicine. Current microbiome studies generate high-throughput omics data across different …
biomedicine. Current microbiome studies generate high-throughput omics data across different …
Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensities
Background and Purpose: Periventricular white matter hyperintensities (WMH; PVWMH) and
deep WMH (DWMH) are regional classifications of WMH and reflect proposed differences …
deep WMH (DWMH) are regional classifications of WMH and reflect proposed differences …
[HTML][HTML] Heritability of the shape of subcortical brain structures in the general population
The volumes of subcortical brain structures are highly heritable, but genetic underpinnings
of their shape remain relatively obscure. Here we determine the relative contribution of …
of their shape remain relatively obscure. Here we determine the relative contribution of …
[HTML][HTML] Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults
Cortical thickness, surface area and volumes vary with age and cognitive function, and in
neurological and psychiatric diseases. Here we report heritability, genetic correlations and …
neurological and psychiatric diseases. Here we report heritability, genetic correlations and …