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

Nancy William

2PUBLICATIONS

10CO-AUTHORS

Neurogenetics

Featured researcher

Get your video featured.

Publish with JoVE

Featured researcher

Get your video featured.

Publish with JoVE

Publications (2)

Sort by Publication Date:

|Apr 02, 2024

De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsy.

Samin A Sajan, Ralph Gradisch, Florian D Vogel

|Jun 25, 2021

Neurexin 1 variants as risk factors for suicide death.

Nancy William, Carsten Reissner, Robert Sargent

Pageof 1

Frequent Collaborators

1 joint publications

Qingqin S Li

1 joint publications

Ken R Smith

1 joint publications

Erik D Christensen

1 joint publications

Markus Missler

1 joint publications

Ralph Gradisch

1 joint publications

Alison J Coffey

1 joint publications

Dominik S Westphal

1 joint publications

Matias Wagner

1 joint publications

Amy Clarke

1 joint publications

Martin Krenn

Frequent Collaborators

1 joint publications

Qingqin S Li

1 joint publications

Ken R Smith

1 joint publications

Erik D Christensen

1 joint publications

Markus Missler

Top Related Videos

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

Osmotic Avoidance in <em>Caenorhabditis elegans</em>: Synaptic Function of Two Genes, Orthologues of Human <em>NRXN1</em> and <em>NLGN1</em>, as Candidates for Autism

Osmotic Avoidance in <em>Caenorhabditis elegans</em>: Synaptic Function of Two Genes, Orthologues of Human <em>NRXN1</em> and <em>NLGN1</em>, as Candidates for Autism

Published on : Dec 11, 2009

See more related videos

Top Related Videos

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

Osmotic Avoidance in <em>Caenorhabditis elegans</em>: Synaptic Function of Two Genes, Orthologues of Human <em>NRXN1</em> and <em>NLGN1</em>, as Candidates for Autism

Osmotic Avoidance in <em>Caenorhabditis elegans</em>: Synaptic Function of Two Genes, Orthologues of Human <em>NRXN1</em> and <em>NLGN1</em>, as Candidates for Autism

Published on : Dec 11, 2009

See more related videos