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Angela Morgan

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

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European Urology|December 12, 2018
Homeobox B13 G84E Mutation and Prostate Cancer RiskTommy Nyberg, Koveela Govindasami, Goska Leslie, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|December 5, 2023
Self-Reported Stuttering Severity Is Accurate: Informing Methods for Large-Scale Data Collection in StutteringSarah Horton, Victoria Jackson, Jessica Boyce, et al.
Expert Review of Neurotherapeutics|May 4, 2026
Rationale and study design for the first precision medicine randomized placebo-controlled trial in the 16p11.2 deletion syndromeHannah M Rea, Julia T Mattson, Vardan Arutiunian, et al.
American Journal of Medical Genetics. Part A|February 29, 2024
De novo variants predicting haploinsufficiency for DIP2C are associated with expressive speech delayThoa Ha, Angela Morgan, Meghan N Bartos, et al.
JAMA Pediatrics|May 17, 2021
Early Intervention for Children Aged 0 to 2 Years With or at High Risk of Cerebral Palsy: International Clinical Practice Guideline Based on Systematic ReviewsCatherine Morgan, Linda Fetters, Lars Adde, et al.
European Journal of Human Genetics : EJHG|May 23, 2025
Biallelic loss-of-function variants in ZNF142 are associated with a robust DNA methylation signature affecting a limited number of genomic lociMathis Hildonen, Andrea Ciolfi, Marco Ferilli, et al.
Plos Genetics|February 20, 2014
Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancerEdward J Saunders, Tokhir Dadaev, Daniel A Leongamornlert, et al.
Human Molecular Genetics|March 29, 2013
Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expressionZsofia Kote-Jarai, Edward J Saunders, Daniel A Leongamornlert, et al.
The Journal of Clinical Investigation|September 18, 2025
PTBP1 variants displaying altered nucleocytoplasmic distribution are responsible for a neurodevelopmental disorder with skeletal dysplasiaAymeric Masson, Julien Paccaud, Martina Orefice, et al.
Nature Genetics|March 29, 2013
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping arrayRosalind A Eeles, Ali Amin Al Olama, Sara Benlloch, et al.
Pageof 8

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

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 80 results.
European Urology|December 12, 2018
Homeobox B13 G84E Mutation and Prostate Cancer RiskTommy Nyberg, Koveela Govindasami, Goska Leslie, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|December 5, 2023
Self-Reported Stuttering Severity Is Accurate: Informing Methods for Large-Scale Data Collection in StutteringSarah Horton, Victoria Jackson, Jessica Boyce, et al.
Expert Review of Neurotherapeutics|May 4, 2026
Rationale and study design for the first precision medicine randomized placebo-controlled trial in the 16p11.2 deletion syndromeHannah M Rea, Julia T Mattson, Vardan Arutiunian, et al.
American Journal of Medical Genetics. Part A|February 29, 2024
De novo variants predicting haploinsufficiency for DIP2C are associated with expressive speech delayThoa Ha, Angela Morgan, Meghan N Bartos, et al.
JAMA Pediatrics|May 17, 2021
Early Intervention for Children Aged 0 to 2 Years With or at High Risk of Cerebral Palsy: International Clinical Practice Guideline Based on Systematic ReviewsCatherine Morgan, Linda Fetters, Lars Adde, et al.
European Journal of Human Genetics : EJHG|May 23, 2025
Biallelic loss-of-function variants in ZNF142 are associated with a robust DNA methylation signature affecting a limited number of genomic lociMathis Hildonen, Andrea Ciolfi, Marco Ferilli, et al.
Plos Genetics|February 20, 2014
Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancerEdward J Saunders, Tokhir Dadaev, Daniel A Leongamornlert, et al.
Human Molecular Genetics|March 29, 2013
Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expressionZsofia Kote-Jarai, Edward J Saunders, Daniel A Leongamornlert, et al.
The Journal of Clinical Investigation|September 18, 2025
PTBP1 variants displaying altered nucleocytoplasmic distribution are responsible for a neurodevelopmental disorder with skeletal dysplasiaAymeric Masson, Julien Paccaud, Martina Orefice, et al.
Nature Genetics|March 29, 2013
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping arrayRosalind A Eeles, Ali Amin Al Olama, Sara Benlloch, et al.
Pageof 8