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Nora Franceschini

Showing results (281-290 of 379) with videos related to

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American Journal of Human Genetics|September 3, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Human Genetics|January 24, 2019
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing dataKaren Y He, Xiaoyin Li, Tanika N Kelly, et al.
American Journal of Human Genetics|August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Human Molecular Genetics|April 20, 2013
Genome-wide association study of age at menarche in African-American womenEllen W Demerath, Ching-Ti Liu, Nora Franceschini, et al.
Human Molecular Genetics|February 5, 2014
Meta-analysis of loci associated with age at natural menopause in African-American womenChristina T L Chen, Ching-Ti Liu, Gary K Chen, et al.
Plos One|May 8, 2020
Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucosePeitao Wu, Denis Rybin, Lawrence F Bielak, et al.
Atherosclerosis|February 25, 2012
Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortiumChristina L Wassel, Claudia Lamina, Vijay Nambi, et al.
Nature Methods|December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regionsEric Van Buren, Yi Zhang, Xihao Li, et al.
Human Molecular Genetics|January 12, 2013
A genome-wide association study of early menopause and the combined impact of identified variantsJohn R B Perry, Tanguy Corre, Tõnu Esko, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Pageof 38

Showing results (281-290 of 379) with videos related to

Sort By:
Pageof 38
American Journal of Human Genetics|September 3, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Human Genetics|January 24, 2019
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing dataKaren Y He, Xiaoyin Li, Tanika N Kelly, et al.
American Journal of Human Genetics|August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Human Molecular Genetics|April 20, 2013
Genome-wide association study of age at menarche in African-American womenEllen W Demerath, Ching-Ti Liu, Nora Franceschini, et al.
Human Molecular Genetics|February 5, 2014
Meta-analysis of loci associated with age at natural menopause in African-American womenChristina T L Chen, Ching-Ti Liu, Gary K Chen, et al.
Plos One|May 8, 2020
Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucosePeitao Wu, Denis Rybin, Lawrence F Bielak, et al.
Atherosclerosis|February 25, 2012
Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortiumChristina L Wassel, Claudia Lamina, Vijay Nambi, et al.
Nature Methods|December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regionsEric Van Buren, Yi Zhang, Xihao Li, et al.
Human Molecular Genetics|January 12, 2013
A genome-wide association study of early menopause and the combined impact of identified variantsJohn R B Perry, Tanguy Corre, Tõnu Esko, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Pageof 38