Publications by authors named "Michael Ricos"

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Identification of New KCNT1-Epilepsy Drugs by In Silico, Cell, and Drosophila Modeling.
Michael G Ricos, Bethan A Cole, Rashid Hussain, Grigori Y Rychkov, Zeeshan Shaukat

Ann Neurol· December 2025

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A Novel Pathogenic Variant in a Croatian Infant Is Linked to a Severe Tubulinopathy with Walker-Warburg-like Features.
Akzam Saidin, Anet Papazovska Cherepnalkovski, Zeeshan Shaukat, Todor Arsov, Rashid Hussain, Michael G Ricos

Genes (Basel)· August 2024

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Aneuploidy is Linked to Neurological Phenotypes Through Oxidative Stress.
Anowarul Islam, Zeeshan Shaukat, Rashid Hussain, Michael G Ricos, Leanne M Dibbens

J Mol Neurosci· May 2024

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Drosophila expressing mutant human KCNT1 transgenes make an effective tool for targeted drug screening in a whole animal model of KCNT1-epilepsy.
Rashid Hussain, Chiao Xin Lim, Zeeshan Shaukat, Anowarul Islam, Emily A Caseley, Michael G Ricos

Sci Rep· February 2024

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Chromosomal Instability Causes Sensitivity to Polyamines and One-Carbon Metabolism.
Anowarul Islam, Zeeshan Shaukat, David L Newman, Rashid Hussain, Michael G Ricos

Metabolites· May 2023

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Investigating genetic variants in microRNA regulators of Neurokinin-1 receptor in sudden infant death syndrome.
Zeeshan Shaukat, Roger W Byard, Robert Vink, Rashid Hussain, Michael G Ricos

Acta Paediatr· February 2023

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Functional Effects of Epilepsy Associated Mutations Suggest Pathogenesis via Aberrant Inhibitory Neuronal Activity.
Grigori Y Rychkov, Zeeshan Shaukat, Chiao Xin Lim, Rashid Hussain, Ben J Roberts, Michael G Ricos

Int J Mol Sci· December 2022

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Knockout of the epilepsy gene Depdc5 in mice causes severe embryonic dysmorphology with hyperactivity of mTORC1 signalling.
James Hughes, Ruby Dawson, Melinda Tea, Dale McAninch, Sandra Piltz, Michael G Ricos

Sci Rep· October 2017

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KCNT1 mutations in seizure disorders: the phenotypic spectrum and functional effects.
Chiao Xin Lim, Michael G Ricos, Leanne M Dibbens, Sarah E Heron

J Med Genet· April 2016

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Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy.
Michael G Ricos, Bree L Hodgson, Tommaso Pippucci, Akzam Saidin, Yeh Sze Ong

Ann Neurol· January 2016

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Mutations in KCNT1 cause a spectrum of focal epilepsies.
Rikke S Møller, Sarah E Heron, Line H G Larsen, Chiao Xin Lim, Michael G Ricos

Epilepsia· September 2015

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Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations.
Ingrid E Scheffer, Sarah E Heron, Brigid M Regan, Simone Mandelstam, Douglas E Crompton, Michael G Ricos

Ann Neurol· May 2014

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dPak is required for integrity of the leading edge cytoskeleton during Drosophila dorsal closure but does not signal through the JNK cascade.
Ryan Conder, Hong Yu, Michael Ricos, Huey Hing, William Chia

Dev Biol· December 2004

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Drac1 and Crumbs participate in amnioserosa morphogenesis during dorsal closure in Drosophila.
Nicholas Harden, Michael Ricos, Kelly Yee, Justina Sanny, Caillin Langmann

J Cell Sci· May 2002

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