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Edith Hofer

Showing results (61-70 of 119) with videos related to

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Translational Psychiatry|March 2, 2022
Correction: Association of low-frequency and rare coding variants with information processing speedJan Bressler, Gail Davies, Albert V Smith, et al.
Translational Psychiatry|December 5, 2021
Association of low-frequency and rare coding variants with information processing speedJan Bressler, Gail Davies, Albert V Smith, et al.
Stroke|October 10, 2015
White Matter Lesion Progression: Genome-Wide Search for Genetic InfluencesEdith Hofer, Margherita Cavalieri, Joshua C Bis, 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|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.
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.
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.
Pageof 12

Showing results (61-70 of 119) with videos related to

Sort By:
Pageof 12
Translational Psychiatry|March 2, 2022
Correction: Association of low-frequency and rare coding variants with information processing speedJan Bressler, Gail Davies, Albert V Smith, et al.
Translational Psychiatry|December 5, 2021
Association of low-frequency and rare coding variants with information processing speedJan Bressler, Gail Davies, Albert V Smith, et al.
Stroke|October 10, 2015
White Matter Lesion Progression: Genome-Wide Search for Genetic InfluencesEdith Hofer, Margherita Cavalieri, Joshua C Bis, 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|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.
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.
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.
Pageof 12