Ahmed N. Sahly

Jeddah, Saudi Arabia

Last Updated: 09/26/2026

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Found 17 publications

Genotype-phenotype correlation in CLCN4-related developmental and epileptic encephalopathy.

Genotype-phenotype correlation in CLCN4-related developmental and epileptic encephalopathy.

Journal: Human genetics

Published: February 17, 2024

Shifting spatial, temporal and demographic patterns of dengue incidence and associated meteorological factors in Jazan Region of Saudi Arabia from 2015-2020.

Shifting spatial, temporal and demographic patterns of dengue incidence and associated meteorological factors in Jazan Region of Saudi Arabia from 2015-2020.

Journal: Journal of vector borne diseases

Published: January 28, 2024

Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals.

Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: June 05, 2023

Potential Biomarkers for Parkinson Disease from Functional Enrichment and Bioinformatic Analysis of Global Gene Expression Patterns of Blood and Substantia Nigra Tissues.

Potential Biomarkers for Parkinson Disease from Functional Enrichment and Bioinformatic Analysis of Global Gene Expression Patterns of Blood and Substantia Nigra Tissues.

Journal: Bioinformatics and biology insights

Published: January 30, 2023

Epilepsy surgery outcomes in patients with GATOR1 gene complex variants: Report of new cases and review of literature.

Epilepsy surgery outcomes in patients with GATOR1 gene complex variants: Report of new cases and review of literature.

Journal: Seizure

Published: November 15, 2022

The epileptology of Wiedemann-Steiner syndrome: Electroclinical findings in five patients with KMT2A pathogenic variants.

The epileptology of Wiedemann-Steiner syndrome: Electroclinical findings in five patients with KMT2A pathogenic variants.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: June 28, 2022

MT-TA pathogenic variants may cause developmental and epileptic encephalopathy without myopathy.

MT-TA pathogenic variants may cause developmental and epileptic encephalopathy without myopathy.

Journal: American journal of medical genetics. Part A

Published: May 07, 2022

Molecular differential analysis of uterine leiomyomas and leiomyosarcomas through weighted gene network and pathway tracing approaches.

Molecular differential analysis of uterine leiomyomas and leiomyosarcomas through weighted gene network and pathway tracing approaches.

Journal: Systems biology in reproductive medicine

Published: March 09, 2021

SUDEP risk and autonomic dysfunction in genetic epilepsies.

SUDEP risk and autonomic dysfunction in genetic epilepsies.

Journal: Autonomic neuroscience : basic & clinical

Published: February 28, 2021

Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families.

Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families.

Journal: Frontiers in pediatrics

Published: January 11, 2021

Severe DNM1 encephalopathy with dysmyelination due to recurrent splice site pathogenic variant.

Severe DNM1 encephalopathy with dysmyelination due to recurrent splice site pathogenic variant.

Journal: Human genetics

Published: May 10, 2020

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.

Journal: American journal of human genetics

Published: October 05, 2019

Showing 1-12 of 17

Last Updated: 09/26/2026