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Helena Schmidt

Showing results (71-80 of 142) with videos related to

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Plos One|April 18, 2013
The molecular genetic architecture of self-employmentMatthijs J H M van der Loos, Cornelius A Rietveld, Niina Eklund, et al.
American Journal of Human Genetics|March 25, 2014
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhageDaniel Woo, Guido J Falcone, William J Devan, 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.
JAMA|May 13, 2010
Genome-wide analysis of genetic loci associated with Alzheimer diseaseSudha Seshadri, Annette L Fitzpatrick, M Arfan Ikram, 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.
JAMA|July 9, 2009
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association dataRamachandran S Vasan, Nicole L Glazer, Janine F Felix, et al.
The Lancet. Neurology|October 9, 2012
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studiesMatthew Traylor, Martin Farrall, Elizabeth G Holliday, 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 15

Showing results (71-80 of 142) with videos related to

Sort By:
Pageof 15
Plos One|April 18, 2013
The molecular genetic architecture of self-employmentMatthijs J H M van der Loos, Cornelius A Rietveld, Niina Eklund, et al.
American Journal of Human Genetics|March 25, 2014
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhageDaniel Woo, Guido J Falcone, William J Devan, 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.
JAMA|May 13, 2010
Genome-wide analysis of genetic loci associated with Alzheimer diseaseSudha Seshadri, Annette L Fitzpatrick, M Arfan Ikram, 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.
JAMA|July 9, 2009
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association dataRamachandran S Vasan, Nicole L Glazer, Janine F Felix, et al.
The Lancet. Neurology|October 9, 2012
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studiesMatthew Traylor, Martin Farrall, Elizabeth G Holliday, 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 15