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Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
December 5, 2021
Sex-specific association of RAGE and HMGB1 genotype variations with susceptibility to ischemic stroke in Caucasians
Philipp Hendrix, Andrea Berger, Thomas N Person, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
January 31, 2022
Erratum to "Sex-specific association of RAGE and HMGB1 genotype variations with susceptibility to ischemic stroke in Caucasians" [J. Clin. Neurosci. 94C (2021) 328-331]
Philipp Hendrix, Andrea Berger, Thomas N Person, et al.
Stroke
|
November 9, 2020
Cysteine-Altering <i>NOTCH3</i> Variants Are a Risk Factor for Stroke in the Elderly Population
Remco J Hack, Julie W Rutten, Thomas N Person, et al.
BMC Medical Genomics
|
May 5, 2019
Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population
Jason E Miller, Raghu P Metpally, Thomas N Person, et al.
BMC Medical Genomics
|
May 24, 2019
Correction to: Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population
Jason E Miller, Raghu P Metpally, Thomas N Person, et al.
Stroke
|
April 23, 2019
Risk Factors for Acute Ischemic Stroke Caused by Anterior Large Vessel Occlusion
Philipp Hendrix, Nelson Sofoluke, Matthew D Adams, et al.
BMJ Health & Care Informatics
|
May 8, 2021
User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis
Alanna Kulchak Rahm, Nephi A Walton, Lynn K Feldman, et al.
Plos One
|
June 26, 2020
Matrix Gla protein polymorphism rs1800801 associates with recurrence of ischemic stroke
Philipp Hendrix, Nelson Sofoluke, Matthew Adams, et al.
Journal of Medical Genetics
|
January 15, 2015
SeqHBase: a big data toolset for family based sequencing data analysis
Min He, Thomas N Person, Scott J Hebbring, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 5, 2017
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing
Christopher M Haggerty, Cynthia A James, Hugh Calkins, et al.
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Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
December 5, 2021
Sex-specific association of RAGE and HMGB1 genotype variations with susceptibility to ischemic stroke in Caucasians
Philipp Hendrix, Andrea Berger, Thomas N Person, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
January 31, 2022
Erratum to "Sex-specific association of RAGE and HMGB1 genotype variations with susceptibility to ischemic stroke in Caucasians" [J. Clin. Neurosci. 94C (2021) 328-331]
Philipp Hendrix, Andrea Berger, Thomas N Person, et al.
Stroke
|
November 9, 2020
Cysteine-Altering <i>NOTCH3</i> Variants Are a Risk Factor for Stroke in the Elderly Population
Remco J Hack, Julie W Rutten, Thomas N Person, et al.
BMC Medical Genomics
|
May 5, 2019
Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population
Jason E Miller, Raghu P Metpally, Thomas N Person, et al.
BMC Medical Genomics
|
May 24, 2019
Correction to: Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population
Jason E Miller, Raghu P Metpally, Thomas N Person, et al.
Stroke
|
April 23, 2019
Risk Factors for Acute Ischemic Stroke Caused by Anterior Large Vessel Occlusion
Philipp Hendrix, Nelson Sofoluke, Matthew D Adams, et al.
BMJ Health & Care Informatics
|
May 8, 2021
User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosis
Alanna Kulchak Rahm, Nephi A Walton, Lynn K Feldman, et al.
Plos One
|
June 26, 2020
Matrix Gla protein polymorphism rs1800801 associates with recurrence of ischemic stroke
Philipp Hendrix, Nelson Sofoluke, Matthew Adams, et al.
Journal of Medical Genetics
|
January 15, 2015
SeqHBase: a big data toolset for family based sequencing data analysis
Min He, Thomas N Person, Scott J Hebbring, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 5, 2017
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing
Christopher M Haggerty, Cynthia A James, Hugh Calkins, et al.
Page
of 2