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P Epstein

Showing results (151-160 of 210) with videos related to

Pageof 21
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Epilepsia|May 13, 2024
Familial aggregation of seizure outcomes in four familial epilepsy cohortsColin A Ellis, Danni Tu, Karen L Oliver, et al.
Plos Genetics|July 17, 2025
Expectations for papers performing Mendelian randomization analysesScott M Williams, Hua Tang, Gregory M Cooper, et al.
Alzheimer'S Research & Therapy|June 18, 2025
Proteome-wide association studies using summary pQTL data of brain, CSF, and plasma identify 30 risk genes of Alzheimer's disease dementiaTingyang Hu, Qiang Liu, Qile Dai, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 11, 2012
Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphismsJessica Ezzell Hunter, Mary Leslie, Gloria Novak, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|July 7, 2025
An Analytic Pipeline to Obtain Reliable Genetic Ancestry Estimates from Tumor-Derived RNA Sequencing DataCourtney E Johnson, Ximing Ran, Julia Wrobel, et al.
American Journal of Human Genetics|June 25, 2019
TIGAR: An Improved Bayesian Tool for Transcriptomic Data Imputation Enhances Gene Mapping of Complex TraitsSini Nagpal, Xiaoran Meng, Michael P Epstein, et al.
American Journal of Human Genetics|March 24, 2015
A statistical approach for rare-variant association testing in affected sibshipsMichael P Epstein, Richard Duncan, Erin B Ware, et al.
Medrxiv : the Preprint Server for Health Sciences|February 17, 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.
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.
Pageof 21

Showing results (151-160 of 210) with videos related to

Sort By:
Pageof 21
Epilepsia|May 13, 2024
Familial aggregation of seizure outcomes in four familial epilepsy cohortsColin A Ellis, Danni Tu, Karen L Oliver, et al.
Plos Genetics|July 17, 2025
Expectations for papers performing Mendelian randomization analysesScott M Williams, Hua Tang, Gregory M Cooper, et al.
Alzheimer'S Research & Therapy|June 18, 2025
Proteome-wide association studies using summary pQTL data of brain, CSF, and plasma identify 30 risk genes of Alzheimer's disease dementiaTingyang Hu, Qiang Liu, Qile Dai, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 11, 2012
Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphismsJessica Ezzell Hunter, Mary Leslie, Gloria Novak, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|July 7, 2025
An Analytic Pipeline to Obtain Reliable Genetic Ancestry Estimates from Tumor-Derived RNA Sequencing DataCourtney E Johnson, Ximing Ran, Julia Wrobel, et al.
American Journal of Human Genetics|June 25, 2019
TIGAR: An Improved Bayesian Tool for Transcriptomic Data Imputation Enhances Gene Mapping of Complex TraitsSini Nagpal, Xiaoran Meng, Michael P Epstein, et al.
American Journal of Human Genetics|March 24, 2015
A statistical approach for rare-variant association testing in affected sibshipsMichael P Epstein, Richard Duncan, Erin B Ware, et al.
Medrxiv : the Preprint Server for Health Sciences|February 17, 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.
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.
Pageof 21