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

J Bohlender

Showing results (41-50 of 52) with videos related to

Pageof 6
Sort By:
The Journal of Biological Chemistry|May 12, 1995
A mutation of angiotensinogen in a patient with preeclampsia leads to altered kinetics of the renin-angiotensin systemI Inoue, A Rohrwasser, C Helin, et al.
The American Journal of Cardiology|April 4, 1998
Angiotensin-converting enzyme and angiotensinogen gene polymorphisms and heart rate variability in twinsA Busjahn, A Voss, H Knoblauch, et al.
Genetic Epidemiology|June 27, 2026
DRIVE v3: Command Line Application for Identity-by-Descent Haplotype Clustering in Large Biobank Scale DataJames T Baker, Hung-Hsin Chen, Grahame F Evans, et al.
Nucleic Acids Research|January 3, 2018
XPAT: a toolkit to conduct cross-platform association studies with heterogeneous sequencing datasetsYao Yu, Hao Hu, Ryan J Bohlender, et al.
Elife|July 18, 2018
Introgression of regulatory alleles and a missense coding mutation drive plumage pattern diversity in the rock pigeonAnna I Vickrey, Rebecca Bruders, Zev Kronenberg, et al.
Human Molecular Genetics|February 11, 2022
Polygenic risk impacts PDGFRA mutation penetrance in non-syndromic cleft lip and palateYao Yu, Rolando Alvarado, Lauren E Petty, et al.
HGG Advances|January 20, 2022
A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic cancer riskYao Yu, Kyle Chang, Jiun-Sheng Chen, et al.
American Journal of Human Genetics|December 28, 2020
Host genetic effects in pneumoniaHung-Hsin Chen, Douglas M Shaw, Lauren E Petty, et al.
American Journal of Human Genetics|October 10, 2025
COMPADRE: Combined pedigree-aware distant relatedness estimation for improved pedigree reconstructionGrahame F Evans, James T Baker, Lauren E Petty, et al.
American Journal of Human Genetics|November 4, 2023
RAB1A haploinsufficiency phenocopies the 2p14-p15 microdeletion and is associated with impaired neuronal differentiationJonathan J Rios, Yang Li, Nandina Paria, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
The Journal of Biological Chemistry|May 12, 1995
A mutation of angiotensinogen in a patient with preeclampsia leads to altered kinetics of the renin-angiotensin systemI Inoue, A Rohrwasser, C Helin, et al.
The American Journal of Cardiology|April 4, 1998
Angiotensin-converting enzyme and angiotensinogen gene polymorphisms and heart rate variability in twinsA Busjahn, A Voss, H Knoblauch, et al.
Genetic Epidemiology|June 27, 2026
DRIVE v3: Command Line Application for Identity-by-Descent Haplotype Clustering in Large Biobank Scale DataJames T Baker, Hung-Hsin Chen, Grahame F Evans, et al.
Nucleic Acids Research|January 3, 2018
XPAT: a toolkit to conduct cross-platform association studies with heterogeneous sequencing datasetsYao Yu, Hao Hu, Ryan J Bohlender, et al.
Elife|July 18, 2018
Introgression of regulatory alleles and a missense coding mutation drive plumage pattern diversity in the rock pigeonAnna I Vickrey, Rebecca Bruders, Zev Kronenberg, et al.
Human Molecular Genetics|February 11, 2022
Polygenic risk impacts PDGFRA mutation penetrance in non-syndromic cleft lip and palateYao Yu, Rolando Alvarado, Lauren E Petty, et al.
HGG Advances|January 20, 2022
A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic cancer riskYao Yu, Kyle Chang, Jiun-Sheng Chen, et al.
American Journal of Human Genetics|December 28, 2020
Host genetic effects in pneumoniaHung-Hsin Chen, Douglas M Shaw, Lauren E Petty, et al.
American Journal of Human Genetics|October 10, 2025
COMPADRE: Combined pedigree-aware distant relatedness estimation for improved pedigree reconstructionGrahame F Evans, James T Baker, Lauren E Petty, et al.
American Journal of Human Genetics|November 4, 2023
RAB1A haploinsufficiency phenocopies the 2p14-p15 microdeletion and is associated with impaired neuronal differentiationJonathan J Rios, Yang Li, Nandina Paria, et al.
Pageof 6