Zimeng Ye

Heidelberg, VIC 3084, Australia

Last Updated: 09/26/2026

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Found 20 publications

Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia.

Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia.

Journal: medRxiv : the preprint server for health sciences

Published: December 03, 2025

Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia.

Deep tissue sequencing improves genetic diagnostic yield in focal cortical dysplasia.

Journal: Progress in neuro-psychopharmacology & biological psychiatry

Published: November 23, 2025

Correction To: Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema.

Correction To: Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema.

Journal: Orphanet journal of rare diseases

Published: February 06, 2025

Exploring physiological beta-hydroxybutyrate level in children treated with the classical ketogenic diet for drug-resistant epilepsy.

Exploring physiological beta-hydroxybutyrate level in children treated with the classical ketogenic diet for drug-resistant epilepsy.

Journal: Acta epileptologica

Published: October 03, 2024

Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema.

Uncovering a novel SERPING1 pathogenic variant: insights into the aggregation of C1-INH in hereditary angioedema.

Journal: Orphanet journal of rare diseases

Published: December 12, 2023

Leveraging multiple approaches for the detection of pathogenic deep intronic variants in developmental and epileptic encephalopathies: A case report.

Leveraging multiple approaches for the detection of pathogenic deep intronic variants in developmental and epileptic encephalopathies: A case report.

Journal: Epilepsia open

Published: September 29, 2023

Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless.

Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless.

Journal: Orphanet journal of rare diseases

Published: August 09, 2023

Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy.

Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy.

Journal: JAMA neurology

Published: May 01, 2023

Are Germline Mosaic TSC1/2 Variants Present in Controls? Implications for Diagnosis.

Are Germline Mosaic TSC1/2 Variants Present in Controls? Implications for Diagnosis.

Journal: Pediatric neurology

Published: December 15, 2022

Somatic Mosaic Pathogenic Variant Gradient Detected in Trace Brain Tissue From Stereo-EEG Depth Electrodes.

Somatic Mosaic Pathogenic Variant Gradient Detected in Trace Brain Tissue From Stereo-EEG Depth Electrodes.

Journal: Neurology

Published: March 16, 2022

Mosaicism in tuberous sclerosis complex: Lowering the threshold for clinical reporting.

Mosaicism in tuberous sclerosis complex: Lowering the threshold for clinical reporting.

Journal: Human mutation

Published: March 10, 2022

Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions.

Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions.

Journal: Human molecular genetics

Published: November 04, 2021

Showing 1-12 of 20

Last Updated: 09/26/2026