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Michael P Epstein

Showing results (91-100 of 140) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Rare genetic variants in <i>SEC24D</i> modify orofacial cleft phenotypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
Human Genetics|September 7, 2023
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
American Journal of Medical Genetics. Part A|June 23, 2023
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?Kimberly K Diaz Perez, Sydney Chung, S Taylor Head, et al.
Genetic Epidemiology|March 31, 2018
Testing cross-phenotype effects of rare variants in longitudinal studies of complex traitsPratyaydipta Rudra, K Alaine Broadaway, Erin B Ware, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Proteome-wide association studies using summary pQTL data of three tissues identified 30 risk genes of Alzheimer's disease dementiaTingyang Hu, Qiang Liu, Qile Dai, et al.
Genetic Epidemiology|January 31, 2014
Accounting for population stratification in DNA methylation studiesRichard T Barfield, Lynn M Almli, Varun Kilaru, et al.
Nature Communications|January 8, 2026
Integrative transcriptome-wide association analyses reveal PRKCG-linked GABAergic dysfunction in Fragile X-associated tremor/ataxia syndromeYulin Jin, Yiqu Cao, Wenjing Ma, et al.
The Journal of Rheumatology|February 17, 2016
Phenotypic Characterization of Juvenile Idiopathic Arthritis in African American ChildrenLauren Fitzpatrick, K Alaine Broadaway, Lori Ponder, et al.
Genetic Epidemiology|June 15, 2021
FAT4 identified as a potential modifier of orofacial cleft lateralitySarah W Curtis, Daniel Chang, Miranda R Sun, et al.
Pediatrics|December 30, 2018
Developmental Outcomes in Duarte GalactosemiaGrace Carlock, S Taylor Fischer, Mary Ellen Lynch, et al.
Pageof 14

Showing results (91-100 of 140) with videos related to

Sort By:
Pageof 14
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Rare genetic variants in <i>SEC24D</i> modify orofacial cleft phenotypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
Human Genetics|September 7, 2023
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
American Journal of Medical Genetics. Part A|June 23, 2023
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?Kimberly K Diaz Perez, Sydney Chung, S Taylor Head, et al.
Genetic Epidemiology|March 31, 2018
Testing cross-phenotype effects of rare variants in longitudinal studies of complex traitsPratyaydipta Rudra, K Alaine Broadaway, Erin B Ware, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Proteome-wide association studies using summary pQTL data of three tissues identified 30 risk genes of Alzheimer's disease dementiaTingyang Hu, Qiang Liu, Qile Dai, et al.
Genetic Epidemiology|January 31, 2014
Accounting for population stratification in DNA methylation studiesRichard T Barfield, Lynn M Almli, Varun Kilaru, et al.
Nature Communications|January 8, 2026
Integrative transcriptome-wide association analyses reveal PRKCG-linked GABAergic dysfunction in Fragile X-associated tremor/ataxia syndromeYulin Jin, Yiqu Cao, Wenjing Ma, et al.
The Journal of Rheumatology|February 17, 2016
Phenotypic Characterization of Juvenile Idiopathic Arthritis in African American ChildrenLauren Fitzpatrick, K Alaine Broadaway, Lori Ponder, et al.
Genetic Epidemiology|June 15, 2021
FAT4 identified as a potential modifier of orofacial cleft lateralitySarah W Curtis, Daniel Chang, Miranda R Sun, et al.
Pediatrics|December 30, 2018
Developmental Outcomes in Duarte GalactosemiaGrace Carlock, S Taylor Fischer, Mary Ellen Lynch, et al.
Pageof 14