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Tulio Guadalupe

Researcher at Max Planck Society

Publications -  37
Citations -  3658

Tulio Guadalupe is an academic researcher from Max Planck Society. The author has contributed to research in topics: Genome-wide association study & Brain asymmetry. The author has an hindex of 22, co-authored 37 publications receiving 3040 citations. Previous affiliations of Tulio Guadalupe include Radboud University Nijmegen & Erasmus University Rotterdam.

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Common genetic variants influence human subcortical brain structures.

Derrek P. Hibar, +344 more
- 09 Apr 2015 - 
TL;DR: In this paper, the authors conduct genome-wide association studies of the volumes of seven subcortical regions and the intracranial volume derived from magnetic resonance images of 30,717 individuals from 50 cohorts.
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The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

Paul M. Thompson, +332 more
TL;DR: The ENIGMA Consortium has detected factors that affect the brain that no individual site could detect on its own, and that require larger numbers of subjects than any individual neuroimaging study has currently collected.
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Novel genetic loci associated with hippocampal volume

Derrek P. Hibar, +432 more
TL;DR: It is shown that genetic variants associated with decreased hippocampal volume are also associated with increased risk for Alzheimer's disease (rg=−0.155), and these findings suggest novel biological pathways through which human genetic variation influences hippocampus volume and risk for neuropsychiatric illness.
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Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA consortium

TL;DR: The structural asymmetries identified and their variabilities and heritability provide a reference resource for future studies on the genetic basis of brain asymmetry and altered laterality in cognitive, neurological, and psychiatric disorders.
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Novel genetic loci underlying human intracranial volume identified through genome-wide association

Hieab H.H. Adams, +435 more
- 01 Dec 2016 - 
TL;DR: Variants for intracranial volume were also related to childhood and adult cognitive function, and Parkinson's disease, and were enriched near genes involved in growth pathways, including PI3K-AKT signaling.