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

Denis Baird

Showing results (11-20 of 20) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 20 results.
Bioinformatics (Oxford, England)|September 4, 2016
HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statisticsJie Zheng, Santiago Rodriguez, Charles Laurin, et al.
Elife|May 31, 2018
The MR-Base platform supports systematic causal inference across the human phenomeGibran Hemani, Jie Zheng, Benjamin Elsworth, et al.
Nature Genetics|February 24, 2023
Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseasesNiek de Klein, Ellen A Tsai, Martijn Vochteloo, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 7, 2019
Mendelian Randomization Analysis Reveals a Causal Influence of Circulating Sclerostin Levels on Bone Mineral Density and FracturesJie Zheng, Winfried Maerz, Ingrid Gergei, et al.
Nature Genetics|September 8, 2020
Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseasesJie Zheng, Valeriia Haberland, Denis Baird, et al.
Genome Biology|January 5, 2021
Genome-wide association study implicates novel loci and reveals candidate effector genes for longitudinal pediatric bone accrualDiana L Cousminer, Yadav Wagley, James A Pippin, et al.
Nature|October 4, 2023
Plasma proteomic associations with genetics and health in the UK BiobankBenjamin B Sun, Joshua Chiou, Matthew Traylor, et al.
Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.
Nature Genetics|December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
Nature Genetics|February 1, 2022
Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Bioinformatics (Oxford, England)|September 4, 2016
HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statisticsJie Zheng, Santiago Rodriguez, Charles Laurin, et al.
Elife|May 31, 2018
The MR-Base platform supports systematic causal inference across the human phenomeGibran Hemani, Jie Zheng, Benjamin Elsworth, et al.
Nature Genetics|February 24, 2023
Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseasesNiek de Klein, Ellen A Tsai, Martijn Vochteloo, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 7, 2019
Mendelian Randomization Analysis Reveals a Causal Influence of Circulating Sclerostin Levels on Bone Mineral Density and FracturesJie Zheng, Winfried Maerz, Ingrid Gergei, et al.
Nature Genetics|September 8, 2020
Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseasesJie Zheng, Valeriia Haberland, Denis Baird, et al.
Genome Biology|January 5, 2021
Genome-wide association study implicates novel loci and reveals candidate effector genes for longitudinal pediatric bone accrualDiana L Cousminer, Yadav Wagley, James A Pippin, et al.
Nature|October 4, 2023
Plasma proteomic associations with genetics and health in the UK BiobankBenjamin B Sun, Joshua Chiou, Matthew Traylor, et al.
Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.
Nature Genetics|December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
Nature Genetics|February 1, 2022
Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
Pageof 2