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Tim Spector

Showing results (71-80 of 107) with videos related to

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Human Molecular Genetics|January 12, 2018
Deep molecular phenotypes link complex disorders and physiological insult to CpG methylationShaza B Zaghlool, Dennis O Mook-Kanamori, Sara Kader, et al.
Nature Communications|July 2, 2025
A genome-wide association study in 10,000 individuals links plasma N-glycome to liver disease and anti-inflammatory proteinsSodbo Sharapov, Anna Timoshchuk, Olga Zaytseva, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 19, 2007
Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone massJohn Pa Ioannidis, Mandy Y Ng, Pak C Sham, et al.
Human Molecular Genetics|June 5, 2019
Defining the genetic control of human blood plasma N-glycome using genome-wide association studySodbo Zh Sharapov, Yakov A Tsepilov, Lucija Klaric, et al.
Nature Genetics|February 9, 2010
Common variants near TERC are associated with mean telomere lengthVeryan Codd, Massimo Mangino, Pim van der Harst, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|October 4, 2012
A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterolIda Surakka, John B Whitfield, Markus Perola, et al.
The Journal of Urology|April 27, 2021
Genome-Wide Association Study Identifies Two Novel Loci Associated with Female Stress and Urgency Urinary IncontinenceRufus Cartwright, Larissa Franklin, Kari A O Tikkinen, et al.
The Journal of Infection|October 17, 2020
Estimates of the rate of infection and asymptomatic COVID-19 disease in a population sample from SE EnglandPhilippa M Wells, Katie J Doores, Simon Couvreur, et al.
Nature Medicine|March 11, 2021
Attributes and predictors of long COVIDCarole H Sudre, Benjamin Murray, Thomas Varsavsky, et al.
Nature Genetics|April 15, 2014
Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31Unnur Styrkarsdottir, Gudmar Thorleifsson, Hafdis T Helgadottir, et al.
Pageof 11

Showing results (71-80 of 107) with videos related to

Sort By:
Pageof 11
Human Molecular Genetics|January 12, 2018
Deep molecular phenotypes link complex disorders and physiological insult to CpG methylationShaza B Zaghlool, Dennis O Mook-Kanamori, Sara Kader, et al.
Nature Communications|July 2, 2025
A genome-wide association study in 10,000 individuals links plasma N-glycome to liver disease and anti-inflammatory proteinsSodbo Sharapov, Anna Timoshchuk, Olga Zaytseva, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 19, 2007
Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone massJohn Pa Ioannidis, Mandy Y Ng, Pak C Sham, et al.
Human Molecular Genetics|June 5, 2019
Defining the genetic control of human blood plasma N-glycome using genome-wide association studySodbo Zh Sharapov, Yakov A Tsepilov, Lucija Klaric, et al.
Nature Genetics|February 9, 2010
Common variants near TERC are associated with mean telomere lengthVeryan Codd, Massimo Mangino, Pim van der Harst, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|October 4, 2012
A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterolIda Surakka, John B Whitfield, Markus Perola, et al.
The Journal of Urology|April 27, 2021
Genome-Wide Association Study Identifies Two Novel Loci Associated with Female Stress and Urgency Urinary IncontinenceRufus Cartwright, Larissa Franklin, Kari A O Tikkinen, et al.
The Journal of Infection|October 17, 2020
Estimates of the rate of infection and asymptomatic COVID-19 disease in a population sample from SE EnglandPhilippa M Wells, Katie J Doores, Simon Couvreur, et al.
Nature Medicine|March 11, 2021
Attributes and predictors of long COVIDCarole H Sudre, Benjamin Murray, Thomas Varsavsky, et al.
Nature Genetics|April 15, 2014
Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31Unnur Styrkarsdottir, Gudmar Thorleifsson, Hafdis T Helgadottir, et al.
Pageof 11