Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Eric Boerwinkle

Showing results (621-630 of 1,215) with videos related to

Pageof 122
Sort By:
Scientific Reports|January 31, 2019
Associations between SLC16A11 variants and diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)Bertha A Hidalgo, Tamar Sofer, Qibin Qi, et al.
BMC Medical Genomics|June 22, 2018
Blood pressure signature genes and blood pressure response to thiazide diuretics: results from the PEAR and PEAR-2 studiesAna Caroline C Sá, Amy Webb, Yan Gong, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 21, 2024
Key variants via the Alzheimer's Disease Sequencing Project whole genome sequence dataYanbing Wang, Chloé Sarnowski, Honghuang Lin, et al.
Diabetes Care|June 25, 2026
Proteomic Signatures of 3-Year Progression From Impaired Fasting Glucose to Diabetes: The Atherosclerosis Risk in Communities (ARIC) StudyMary R Rooney, Justin B Echouffo Tcheugui, Jingsha Chen, et al.
American Journal of Human Genetics|July 24, 2018
Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function AllelesZeynep Coban-Akdemir, Janson J White, Xiaofei Song, et al.
Journal of Personalized Medicine|December 15, 2018
The 9th Santorini Conference: Systems Medicine, Personalised Health and Therapy. "The Odyssey from Hope to Practice", Santorini, Greece, 30 September⁻3 October 2018Sophie Visvikis-Siest, Vesna Gorenjak, Maria G Stathopoulou, et al.
American Journal of Human Genetics|May 18, 2005
Polymorphisms within the C-reactive protein (CRP) promoter region are associated with plasma CRP levelsChristopher S Carlson, Shelley Force Aldred, Philip K Lee, et al.
Blood|May 22, 2013
Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing ProjectJill M Johnsen, Paul L Auer, Alanna C Morrison, et al.
Thrombosis and Haemostasis|March 17, 2017
Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregationJohn D Eicher, Ming-Huei Chen, Achilleas N Pitsillides, et al.
Lancet Regional Health. Americas|December 11, 2023
Wastewater analysis of Mpox virus in a city with low prevalence of Mpox disease: an environmental surveillance studyJeremiah Oghuan, Carlos Chavarria, Scout R Vanderwal, et al.
Pageof 122

Showing results (621-630 of 1,215) with videos related to

Sort By:
Pageof 122
Scientific Reports|January 31, 2019
Associations between SLC16A11 variants and diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)Bertha A Hidalgo, Tamar Sofer, Qibin Qi, et al.
BMC Medical Genomics|June 22, 2018
Blood pressure signature genes and blood pressure response to thiazide diuretics: results from the PEAR and PEAR-2 studiesAna Caroline C Sá, Amy Webb, Yan Gong, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 21, 2024
Key variants via the Alzheimer's Disease Sequencing Project whole genome sequence dataYanbing Wang, Chloé Sarnowski, Honghuang Lin, et al.
Diabetes Care|June 25, 2026
Proteomic Signatures of 3-Year Progression From Impaired Fasting Glucose to Diabetes: The Atherosclerosis Risk in Communities (ARIC) StudyMary R Rooney, Justin B Echouffo Tcheugui, Jingsha Chen, et al.
American Journal of Human Genetics|July 24, 2018
Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function AllelesZeynep Coban-Akdemir, Janson J White, Xiaofei Song, et al.
Journal of Personalized Medicine|December 15, 2018
The 9th Santorini Conference: Systems Medicine, Personalised Health and Therapy. "The Odyssey from Hope to Practice", Santorini, Greece, 30 September⁻3 October 2018Sophie Visvikis-Siest, Vesna Gorenjak, Maria G Stathopoulou, et al.
American Journal of Human Genetics|May 18, 2005
Polymorphisms within the C-reactive protein (CRP) promoter region are associated with plasma CRP levelsChristopher S Carlson, Shelley Force Aldred, Philip K Lee, et al.
Blood|May 22, 2013
Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing ProjectJill M Johnsen, Paul L Auer, Alanna C Morrison, et al.
Thrombosis and Haemostasis|March 17, 2017
Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregationJohn D Eicher, Ming-Huei Chen, Achilleas N Pitsillides, et al.
Lancet Regional Health. Americas|December 11, 2023
Wastewater analysis of Mpox virus in a city with low prevalence of Mpox disease: an environmental surveillance studyJeremiah Oghuan, Carlos Chavarria, Scout R Vanderwal, et al.
Pageof 122