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Communications Biology|August 10, 2019
A genome-wide association study identifies genetic loci associated with specific lobar brain volumesSven J van der Lee, Maria J Knol, Ganesh Chauhan, et al.
Cerebral Cortex (New York, N.Y. : 1991)|March 22, 2020
Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational AptitudesJean Shin, Shaojie Ma, Edith Hofer, et al.
Communications Biology|July 4, 2023
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosisCarolina Medina-Gomez, Benjamin H Mullin, Alessandra Chesi, et al.
Neurology|September 11, 2020
Association of common genetic variants with brain microbleeds: A genome-wide association studyMaria J Knol, Dongwei Lu, Matthew Traylor, et al.
Brain : a Journal of Neurology|May 5, 2022
Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidateAniket Mishra, Cécile Duplaà, Dina Vojinovic, et al.
Aging|January 13, 2017
The complex genetics of gait speed: genome-wide meta-analysis approachDan Ben-Avraham, David Karasik, Joe Verghese, et al.
Space Science Reviews|February 14, 2022
A Review of the EUSO-Balloon Pathfinder for the JEM-EUSO ProgramJ H Adams, S Ahmad, D Allard, et al.
Stroke|July 14, 2018
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance ImagingXueqiu Jian, Claudia L Satizabal, Albert V Smith, et al.
Nature Medicine|April 17, 2023
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel diseaseMarie-Gabrielle Duperron, Maria J Knol, Quentin Le Grand, et al.
Stroke|June 11, 2020
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter HyperintensitiesNicola J Armstrong, Karen A Mather, Muralidharan Sargurupremraj, et al.
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