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Eleanor Feingold

Showing results (121-130 of 175) with videos related to

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Community Dentistry and Oral Epidemiology|April 18, 2019
Predictors of dental care utilization in north-central Appalachia in the USAMengxia Chen, Casey D Wright, Oluwabunmi Tokede, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 22, 2012
Connexin 47 mutations increase risk for secondary lymphedema following breast cancer treatmentDavid N Finegold, Catherine J Baty, Kelly Z Knickelbein, et al.
Frontiers in Genetics|August 26, 2021
<i>PRICKLE1</i> × <i>FOCAD</i> Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial TraitsDongjing Liu, Hyo-Jeong Ban, Ahmed M El Sergani, et al.
Scientific Reports|June 2, 2018
GWAS reveals loci associated with velopharyngeal dysfunctionJonathan Chernus, Jasmien Roosenboom, Matthew Ford, et al.
Critical Care Explorations|October 30, 2025
Genetic Variation in the Alternative Complement Pathway Contributes to Individual Susceptibility to Bacteremia and SepsisKyle Inman, Jonathan Chernus, Myoungkeun Lee, et al.
Scientific Reports|January 13, 2021
Impact of low-frequency coding variants on human facial shapeDongjing Liu, Nora Alhazmi, Harold Matthews, et al.
HGG Advances|April 5, 2021
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lipSarah W Curtis, Daniel Chang, Myoung Keun Lee, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|August 29, 2015
Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European AncestryF Yesim Demirci, Xingbin Wang, Jennifer A Kelly, et al.
Genes|January 21, 2023
Association of Early Childhood Caries with Bitter Taste Receptors: A Meta-Analysis of Genome-Wide Association Studies and Transcriptome-Wide Association StudyEkaterina Orlova, Tom Dudding, Jonathan M Chernus, et al.
Genetic Epidemiology|August 19, 2010
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndromeAdam E Locke, Kenneth J Dooley, Stuart W Tinker, et al.
Pageof 18

Showing results (121-130 of 175) with videos related to

Sort By:
Pageof 18
Community Dentistry and Oral Epidemiology|April 18, 2019
Predictors of dental care utilization in north-central Appalachia in the USAMengxia Chen, Casey D Wright, Oluwabunmi Tokede, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 22, 2012
Connexin 47 mutations increase risk for secondary lymphedema following breast cancer treatmentDavid N Finegold, Catherine J Baty, Kelly Z Knickelbein, et al.
Frontiers in Genetics|August 26, 2021
<i>PRICKLE1</i> × <i>FOCAD</i> Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial TraitsDongjing Liu, Hyo-Jeong Ban, Ahmed M El Sergani, et al.
Scientific Reports|June 2, 2018
GWAS reveals loci associated with velopharyngeal dysfunctionJonathan Chernus, Jasmien Roosenboom, Matthew Ford, et al.
Critical Care Explorations|October 30, 2025
Genetic Variation in the Alternative Complement Pathway Contributes to Individual Susceptibility to Bacteremia and SepsisKyle Inman, Jonathan Chernus, Myoungkeun Lee, et al.
Scientific Reports|January 13, 2021
Impact of low-frequency coding variants on human facial shapeDongjing Liu, Nora Alhazmi, Harold Matthews, et al.
HGG Advances|April 5, 2021
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lipSarah W Curtis, Daniel Chang, Myoung Keun Lee, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|August 29, 2015
Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European AncestryF Yesim Demirci, Xingbin Wang, Jennifer A Kelly, et al.
Genes|January 21, 2023
Association of Early Childhood Caries with Bitter Taste Receptors: A Meta-Analysis of Genome-Wide Association Studies and Transcriptome-Wide Association StudyEkaterina Orlova, Tom Dudding, Jonathan M Chernus, et al.
Genetic Epidemiology|August 19, 2010
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndromeAdam E Locke, Kenneth J Dooley, Stuart W Tinker, et al.
Pageof 18