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Eric B Larson

Showing results (391-400 of 458) with videos related to

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Journal of Alzheimer'S Disease : JAD|June 25, 2016
Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer's DiseaseVincent Chouraki, Christiane Reitz, Fleur Maury, et al.
BMC Medicine|July 18, 2019
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE NetworkBahram Namjou, Todd Lingren, Yongbo Huang, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Genome wide association study meta-analysis of neuropathologic lesions of Alzheimer's disease and related dementias in a multi-site autopsy cohortBrenna Cholerton, Dana Godrich, Jeremy Pasteris, et al.
Plos Genetics|June 29, 2026
Genome wide association study meta-analysis of neuropathologic lesions of Alzheimer's disease and related dementias in a multi-site autopsy cohortBrenna Cholerton, Dana Godrich, Jeremy Pasteris, et al.
Circulation|April 29, 2018
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving StatinsWei-Qi Wei, Xiaohui Li, Qiping Feng, et al.
Neurology|February 10, 2015
PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson diseaseGary W Beecham, Dennis W Dickson, William K Scott, et al.
NPJ Genomic Medicine|February 19, 2019
A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>Maya S Safarova, Benjamin A Satterfield, Xiao Fan, et al.
American Journal of Human Genetics|October 11, 2011
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studiesJoshua C Denny, Dana C Crawford, Marylyn D Ritchie, et al.
JAMA Neurology|February 15, 2013
APOE ε4 increases risk for dementia in pure synucleinopathiesDebby Tsuang, James B Leverenz, Oscar L Lopez, et al.
NPJ Digital Medicine|April 14, 2021
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studiesNing Shang, Atlas Khan, Fernanda Polubriaginof, et al.
Pageof 46

Showing results (391-400 of 458) with videos related to

Sort By:
Pageof 46
Journal of Alzheimer'S Disease : JAD|June 25, 2016
Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer's DiseaseVincent Chouraki, Christiane Reitz, Fleur Maury, et al.
BMC Medicine|July 18, 2019
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE NetworkBahram Namjou, Todd Lingren, Yongbo Huang, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Genome wide association study meta-analysis of neuropathologic lesions of Alzheimer's disease and related dementias in a multi-site autopsy cohortBrenna Cholerton, Dana Godrich, Jeremy Pasteris, et al.
Plos Genetics|June 29, 2026
Genome wide association study meta-analysis of neuropathologic lesions of Alzheimer's disease and related dementias in a multi-site autopsy cohortBrenna Cholerton, Dana Godrich, Jeremy Pasteris, et al.
Circulation|April 29, 2018
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving StatinsWei-Qi Wei, Xiaohui Li, Qiping Feng, et al.
Neurology|February 10, 2015
PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson diseaseGary W Beecham, Dennis W Dickson, William K Scott, et al.
NPJ Genomic Medicine|February 19, 2019
A phenome-wide association study to discover pleiotropic effects of <i>PCSK9</i>, <i>APOB</i>, and <i>LDLR</i>Maya S Safarova, Benjamin A Satterfield, Xiao Fan, et al.
American Journal of Human Genetics|October 11, 2011
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studiesJoshua C Denny, Dana C Crawford, Marylyn D Ritchie, et al.
JAMA Neurology|February 15, 2013
APOE ε4 increases risk for dementia in pure synucleinopathiesDebby Tsuang, James B Leverenz, Oscar L Lopez, et al.
NPJ Digital Medicine|April 14, 2021
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studiesNing Shang, Atlas Khan, Fernanda Polubriaginof, et al.
Pageof 46