Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Dimitri James Stavropoulos

3PUBLICATIONS

19CO-AUTHORS

Cellular nervous systemGene expression (incl. microarray and other genome-wide approaches)Psychological methodology, design and analysis

Featured researcher

Get your video featured.

Publish with JoVE

Featured researcher

Get your video featured.

Publish with JoVE

Publications (3)

Sort by Publication Date:

|May 04, 2021

New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency Disorder.

Justin O Szot, Anne Slavotinek, Karen Chong

|Aug 11, 2018

Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar.

Erin R Riggs, Tristan Nelson, Andrew Merz

|May 26, 2017

Disruption of YWHAE gene at 17p13.3 causes learning disabilities and brain abnormalities.

A Noor, S Bogatan, N Watkins

Pageof 1

Frequent Collaborators

1 joint publications

Erin R Riggs

1 joint publications

Justin O Szot

1 joint publications

Anne Slavotinek

1 joint publications

Marjan Nezarati

1 joint publications

Anna M Cueto-González

1 joint publications

Millan S Patel

1 joint publications

Walter P Devine

1 joint publications

Shannon Rego

1 joint publications

Susan Blaser

1 joint publications

Tim V Mieghem

Frequent Collaborators

1 joint publications

Erin R Riggs

1 joint publications

Justin O Szot

1 joint publications

Anne Slavotinek

1 joint publications

Marjan Nezarati

Top Related Videos

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

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

Published on : Jun 15, 2011

Genetic Variant Detection in the <em>CALR</em> gene using High Resolution Melting Analysis

Genetic Variant Detection in the <em>CALR</em> gene using High Resolution Melting Analysis

Published on : Aug 26, 2020

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

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

Published on : Dec 01, 2017

See more related videos

Top Related Videos

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

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

Published on : Jun 15, 2011

Genetic Variant Detection in the <em>CALR</em> gene using High Resolution Melting Analysis

Genetic Variant Detection in the <em>CALR</em> gene using High Resolution Melting Analysis

Published on : Aug 26, 2020

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

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

Published on : Dec 01, 2017

See more related videos