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John F Pearson

Showing results (81-90 of 97) with videos related to

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Acta Anaesthesiologica Scandinavica|April 26, 2026
Bayesian Analysis of Postoperative Complication Risk Associated With Preoperative Exposure to Fine Particulate Matter: A Single-Center Cohort StudyJohn F Pearson, Cameron K Jacobson, Calvin S Riss, et al.
Scientific Reports|May 17, 2018
Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathyCameron J Lacey, Kit Doudney, Paul G Bridgman, et al.
Plos One|July 7, 2012
The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissuesAnna P Pilbrow, Lasse Folkersen, John F Pearson, et al.
Neurobiology of Aging|May 2, 2025
Presenilin 1 hemizygosity has no overt deleterious phenotypic outcomes in sheep: Potential implications for therapeutic targets in Alzheimer's diseaseNatasha E Mckean, Jun Liu, Skye R Rudiger, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|May 9, 2025
Biomarkers of oxidative and mitochondrial stress are associated with accelerated pace of aging at midlife in a birth cohortTe-Rina J King-Hudson, Andree G Pearson, Caitlin Dunstan-Harrison, et al.
Journal of Huntington'S Disease|August 23, 2021
A Multi-Omic Huntington's Disease Transgenic Sheep-Model Database for Investigating Disease PathogenesisEmily R Mears, Renee R Handley, Matthew J Grant, et al.
Journal of Medical Genetics|March 21, 2019
Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants: an ENIGMA reportIrene Lopez-Perolio, Raphaël Leman, Raquel Behar, et al.
European Journal of Human Genetics : EJHG|February 2, 2017
Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriersLogan C Walker, Louise Marquart, John F Pearson, et al.
European Journal of Human Genetics : EJHG|August 24, 2018
Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriersLogan C Walker, Louise Marquart, John F Pearson, et al.
Contemporary Clinical Trials|October 6, 2018
The Anorexia Nervosa Genetics Initiative (ANGI): Overview and methodsLaura M Thornton, Melissa A Munn-Chernoff, Jessica H Baker, et al.
Pageof 10

Showing results (81-90 of 97) with videos related to

Sort By:
Pageof 10
Acta Anaesthesiologica Scandinavica|April 26, 2026
Bayesian Analysis of Postoperative Complication Risk Associated With Preoperative Exposure to Fine Particulate Matter: A Single-Center Cohort StudyJohn F Pearson, Cameron K Jacobson, Calvin S Riss, et al.
Scientific Reports|May 17, 2018
Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathyCameron J Lacey, Kit Doudney, Paul G Bridgman, et al.
Plos One|July 7, 2012
The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissuesAnna P Pilbrow, Lasse Folkersen, John F Pearson, et al.
Neurobiology of Aging|May 2, 2025
Presenilin 1 hemizygosity has no overt deleterious phenotypic outcomes in sheep: Potential implications for therapeutic targets in Alzheimer's diseaseNatasha E Mckean, Jun Liu, Skye R Rudiger, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|May 9, 2025
Biomarkers of oxidative and mitochondrial stress are associated with accelerated pace of aging at midlife in a birth cohortTe-Rina J King-Hudson, Andree G Pearson, Caitlin Dunstan-Harrison, et al.
Journal of Huntington'S Disease|August 23, 2021
A Multi-Omic Huntington's Disease Transgenic Sheep-Model Database for Investigating Disease PathogenesisEmily R Mears, Renee R Handley, Matthew J Grant, et al.
Journal of Medical Genetics|March 21, 2019
Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants: an ENIGMA reportIrene Lopez-Perolio, Raphaël Leman, Raquel Behar, et al.
European Journal of Human Genetics : EJHG|February 2, 2017
Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriersLogan C Walker, Louise Marquart, John F Pearson, et al.
European Journal of Human Genetics : EJHG|August 24, 2018
Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriersLogan C Walker, Louise Marquart, John F Pearson, et al.
Contemporary Clinical Trials|October 6, 2018
The Anorexia Nervosa Genetics Initiative (ANGI): Overview and methodsLaura M Thornton, Melissa A Munn-Chernoff, Jessica H Baker, et al.
Pageof 10