Gaia Gestri

Queen Square Institute Of Neurology
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 26 publications

Recessive loss of DIAPH1 function causes a progressive neurodevelopmental syndrome with variable immunological involvement.

Recessive loss of DIAPH1 function causes a progressive neurodevelopmental syndrome with variable immunological involvement.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 05, 2025

Recessive Loss of DIAPH1 Function Causes a Progressive Neurodevelopmental Syndrome with Variable Immunological Involvement.

Recessive Loss of DIAPH1 Function Causes a Progressive Neurodevelopmental Syndrome with Variable Immunological Involvement.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 05, 2025

Neuropilin 1 (NRP1) conveys SEMA3A signals to restrict physiological angiogenesis.

Neuropilin 1 (NRP1) conveys SEMA3A signals to restrict physiological angiogenesis.

Journal: Angiogenesis

Published: May 03, 2025

frizzled 5 mutant zebrafish are genetically sensitised to developing microphthalmia and coloboma.

frizzled 5 mutant zebrafish are genetically sensitised to developing microphthalmia and coloboma.

Journal: Disease models & mechanisms

Published: January 06, 2025

Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder.

Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder.

Journal: medRxiv : the preprint server for health sciences

Published: August 16, 2024

Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder.

Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder.

Journal: American journal of human genetics

Published: August 09, 2024

Cachd1 interacts with Wnt receptors and regulates neuronal asymmetry in the zebrafish brain.

Cachd1 interacts with Wnt receptors and regulates neuronal asymmetry in the zebrafish brain.

Journal: Science (New York, N.Y.)

Published: May 02, 2024

Foxd1-dependent induction of a temporal retinal character is required for visual function.

Foxd1-dependent induction of a temporal retinal character is required for visual function.

Journal: Development (Cambridge, England)

Published: May 12, 2022

A versatile, automated and high-throughput drug screening platform for zebrafish embryos.

A versatile, automated and high-throughput drug screening platform for zebrafish embryos.

Journal: Biology open

Published: December 17, 2020

Developmental delay during eye morphogenesis underlies optic cup and neurogenesis defects in mab21l2u517 zebrafish mutants.

Developmental delay during eye morphogenesis underlies optic cup and neurogenesis defects in mab21l2u517 zebrafish mutants.

Journal: The International journal of developmental biology

Published: September 15, 2020

A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypes.

A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypes.

Journal: eLife

Published: June 04, 2020

Abrogation of Stem Loop Binding Protein (Slbp) function leads to a failure of cells to transition from proliferation to differentiation, retinal coloboma and midline axon guidance deficits.

Abrogation of Stem Loop Binding Protein (Slbp) function leads to a failure of cells to transition from proliferation to differentiation, retinal coloboma and midline axon guidance deficits.

Journal: PloS one

Published: November 01, 2018

Showing 1-12 of 26

Last Updated: 09/26/2026