Paul Marcogliese

Assistant Professor

University of Manitoba

Canada

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Articles (10)

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2022

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2022

Year:

2022

Year:

2021

Year:

2021

Year:

2020

Collaborators (11)

Stefan Barakat

Associate professor

Erasmus MC

NETHERLANDS

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Danita Velasco

University of Arkansas for Medical Sciences Department of Pediatrics

UNITED STATES

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Hugo Bellen

Professor

UNITED STATES

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Jacob McCauley

Professor

University of Miami Miller School of Medicine

UNITED STATES

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Venkata Hemanjani Bhavana

Baylor College of Medicine

UNITED STATES

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Oguz Kanca

Assistant Professor

Baylor College of Medicine

UNITED STATES

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Matthew Moulton

Assistant Professor

Texas A&M University

UNITED STATES

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Ryan German

Baylor College of Medicine

UNITED STATES

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Shinya Yamamoto

Assistant Professor (tenure-track)

Baylor College of Medicine

UNITED STATES

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Peter McCaffery

University of Aberdeen

UNITED KINGDOM

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Jamie Kramer

Associate Professor

Dalhousie University

CANADA

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Paul Marcogliese

Research Interests

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Articles (10)

A defect in mitochondrial fatty acid synthesis impairs iron metabolism and causes elevated ceramide levels

Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases.

A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder.

De novo variants in EMC1 lead to neurodevelopmental delay and cerebellar degeneration and affect glial function in drosophila.

Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development.

Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures.

Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling

TM2D genes regulate Notch signaling and neuronal function in Drosophila

Neuronal ROS-induced glial lipid droplet formation is altered by loss of Alzheimer's disease-associated genes.

Missense variants in CTNNB1 can be associated with vitreoretinopathy-Seven new cases of CTNNB1-associated neurodevelopmental disorder including a previously unreported retinal phenotype.

Collaborators (11)

Stefan Barakat

Danita Velasco

Hugo Bellen

Jacob McCauley

Venkata Hemanjani Bhavana

Oguz Kanca

Matthew Moulton

Ryan German

Shinya Yamamoto

Peter McCaffery

Jamie Kramer

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