Related Experiment Video

Updated: Jul 1, 2025

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

8.6K

Bridging the Genetic Divide: Ensuring Equitable Access to Neurologic Genetic Testing

Amélie Pinard1, Aleksandar Rajkovic1

  • 1From the Department of Pathology (A.P., A.R.) and Institute of Human Genetics (A.R.), University of California, San Francisco.

Neurology
|March 6, 2024
PubMed
Summary

No abstract available in PubMed .

More Related Videos

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
09:34

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Published on: April 4, 2018

33.8K
A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
05:51

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia

Published on: June 15, 2011

25.8K

Related Experiment Videos

Last Updated: Jul 1, 2025

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

8.6K
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
09:34

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Published on: April 4, 2018

33.8K
A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
05:51

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia

Published on: June 15, 2011

25.8K

Related Concept Videos

Human Genetics01:28

Human Genetics

566
Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
566
Genetic Screens02:46

Genetic Screens

4.9K
Genetic screens are tools used to identify genes and mutations responsible for phenotypes of interest. Genetic screens help identify individuals or a group of people at risk of developing  genetic diseases and help them with early intervention, targeted therapy, and reproductive options.
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which...
4.9K
Genetic Lingo01:11

Genetic Lingo

102.7K
Overview
102.7K

Articles linked to this work by shared authors, journal, and citation graph.

Burden of heterozygote carriers for autosomal recessive conditions in the Middle East: A study of 14,392 genomes.

HGG advances·2026

HMMER web server: 2026 update.

Nucleic acids research·2026

Maternal Med12 safeguards trophoblast pluripotency and placental development.

Biology of reproduction·2026

The Human Intolerome: A curated database to prioritize genomic variants in stillbirth, pregnancy loss, and neonatal death.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Genetics of Primary Ovarian Insufficiency.

Seminars in reproductive medicine·2026

Leveraging health records to identify diagnoses associated with recurrent pregnancy loss across two medical centers.

iScience·2026

Trends of Mortality and Years of Life Lost Due to Stroke Among Older Adults in China and Its Provinces, 2005-2020.

Neurology·2026

A Novel Homozygous Frameshift GTPBP2 Variant in Jaberi-Elahi Syndrome: First Case Report from Türkiye.

Molecular syndromology·2026

Hippocampal Subfield Volumetry and Navigation in Congenital Blindness.

Hippocampus·2026

A Phenotype-Based Score to Prioritize RNF213 p.R4810K Genotyping in Isolated Intracranial Steno-Occlusive Disease.

Translational stroke research·2026

Genetically inferred effects of brain structure and gene expression on neurodegenerative diseases: a Mendelian randomization study.

Archives of medical science : AMS·2026

Genomic findings in non-cryptogenic cerebral palsy: a systematic review and meta-analysis.

Frontiers in neurology·2026

DNAJC13 Variants Show No Robust Association With Parkinson's Disease in a Multiancestry Cohort.

Movement disorders : official journal of the Movement Disorder Society·2026
See all related articles
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies
Jove
Visualize
Contact Us