Zaid Afawi

Rotterdam, ZH, Netherlands

Last Updated: 09/26/2026

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Found 47 publications

Phenotypic Spectrum in Individuals With Pathogenic GABRG2 Loss- and Gain-of-Function Variants.

Phenotypic Spectrum in Individuals With Pathogenic GABRG2 Loss- and Gain-of-Function Variants.

Journal: Neurology

Published: June 26, 2025

Ethnic Disparities in Chronic Diseases: Comparison Between Arabs and Jews in Israel.

Ethnic Disparities in Chronic Diseases: Comparison Between Arabs and Jews in Israel.

Journal: The Israel Medical Association journal : IMAJ

Published: December 18, 2024

A machine learning approach to differentiate stage IV from stage I colorectal cancer.

A machine learning approach to differentiate stage IV from stage I colorectal cancer.

Journal: Computers in biology and medicine

Published: March 19, 2024

Adherence to liraglutide among individuals with overweight and obesity: Patient characteristics and clinical measures.

Adherence to liraglutide among individuals with overweight and obesity: Patient characteristics and clinical measures.

Journal: Diabetes, obesity & metabolism

Published: October 04, 2023

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

Journal: medRxiv : the preprint server for health sciences

Published: March 03, 2023

Chronic hepatitis C: Diagnosis and treatment made easy.

Chronic hepatitis C: Diagnosis and treatment made easy.

Journal: The European journal of general practice

Published: May 17, 2022

Gene and Cell Therapy for Epilepsy: A Mini Review.

Gene and Cell Therapy for Epilepsy: A Mini Review.

Journal: Frontiers in molecular neuroscience

Published: February 02, 2022

Whole exome sequencing and co-expression analysis identify an SCN1A variant that modifies pathogenicity in a family with genetic epilepsy and febrile seizures plus.

Whole exome sequencing and co-expression analysis identify an SCN1A variant that modifies pathogenicity in a family with genetic epilepsy and febrile seizures plus.

Journal: Epilepsia

Published: December 29, 2021

Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes.

Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes.

Journal: American journal of human genetics

Published: June 29, 2020

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns.

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns.

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

Published: June 08, 2020

Whole-exome and HLA sequencing in Febrile infection-related epilepsy syndrome.

Whole-exome and HLA sequencing in Febrile infection-related epilepsy syndrome.

Journal: Annals of clinical and translational neurology

Published: April 03, 2020

The 5th International Lafora Epilepsy Workshop: Basic science elucidating therapeutic options and preparing for therapies in the clinic.

The 5th International Lafora Epilepsy Workshop: Basic science elucidating therapeutic options and preparing for therapies in the clinic.

Journal: Epilepsy & behavior : E&B

Published: November 23, 2019

Showing 1-12 of 47

Last Updated: 09/26/2026