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Donald Latner

Senior Scientist

HudsonAlpha Institute for Biotechnology

United States

Research Interests

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Articles (9)

Year:

2026

Year:

2026

Year:

2026

Year:

2025

Year:

2025

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2024

Year:

2024

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2023

Year:

2023

Collaborators (5)

Laura Hendon

Associate Professor, Certified Genetic Counselor

University of Mississippi Medical Center

UNITED STATES

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Gregory Cooper

HudsonAlpha Institute for Biotechnology

UNITED STATES

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Aubin Moutal

Assitant Professor (Tenure Track)

Saint Louis University

UNITED STATES

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Frederic Laumonnier

Team Leader, Research Director

INSERM

FRANCE

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Anna CE Hurst

Associate Professor

The University of Alabama

UNITED STATES

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Donald Latner

Research Interests

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Articles (9)

Monoallelic variants in BRSK1 are associated with a neurodevelopmental disorder with or without epilepsy

Heterozygous RNF13 Truncating Variants Are Associated With Developmental and Epileptic Encephalopathy.

Pathological disruption of CELF2 shuttling causes neuronal hyperactivity, learning deficits, and seizures.

Biallelic FGF4 Variants Linked to Thoracic Dystrophy and Respiratory Insufficiency

Missense variants in <i>DPYSL5</i> associated with neurodevelopmental disorders and brain malformations cause impaired neuronal maturation in vitro

Long-read genome sequencing and variant reanalysis increase diagnostic yield in neurodevelopmental disorders.

Structure-based design of glycoprotein subunit vaccines for mumps

Parents’ Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit

Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testing.

Collaborators (5)

Laura Hendon

Gregory Cooper

Aubin Moutal

Frederic Laumonnier

Anna CE Hurst

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