Zeynep Tumer

Copenhagen, Denmark

Last Updated: 09/26/2026

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Found 145 publications

Altered neurodevelopmental trajectories of brain structure in Tourette syndrome and Chronic Tic Disorders.

Altered neurodevelopmental trajectories of brain structure in Tourette syndrome and Chronic Tic Disorders.

Journal: medRxiv : the preprint server for health sciences
Published: June 04, 2026

Transcriptome- and Epigenome-Wide Association Studies of Tic Spectrum Disorder in Discordant Monozygotic Twins.

Transcriptome- and Epigenome-Wide Association Studies of Tic Spectrum Disorder in Discordant Monozygotic Twins.

Journal: Genes
Published: November 13, 2025

Clinical Feasibility of Long-Read WGS for DNA Methylation Signature Analysis.

Clinical Feasibility of Long-Read WGS for DNA Methylation Signature Analysis.

Journal: Clinical genetics
Published: October 20, 2025

DNA methylation signature and clinical delineation of PACS1-related disorder in 24 unreported individuals.

DNA methylation signature and clinical delineation of PACS1-related disorder in 24 unreported individuals.

Journal: European journal of human genetics : EJHG
Published: September 19, 2025

ROGDI-Related Disorder Resulting from Disruption of Complex Interactive Neuro-Dental Developmental Networks: A Review and Description of the First Missense Variant.

ROGDI-Related Disorder Resulting from Disruption of Complex Interactive Neuro-Dental Developmental Networks: A Review and Description of the First Missense Variant.

Journal: Genes
Published: August 20, 2025

Diagnosis of Angelman Syndrome, With 66 Years of Delay, Using Hypothesis-Free DNA Methylation Profiling.

Diagnosis of Angelman Syndrome, With 66 Years of Delay, Using Hypothesis-Free DNA Methylation Profiling.

Journal: Clinical genetics
Published: May 15, 2025

Investigation of multilocus imprinting disturbance (MLID) in 101 Beckwith-Wiedemann spectrum patients.

Investigation of multilocus imprinting disturbance (MLID) in 101 Beckwith-Wiedemann spectrum patients.

Journal: Clinical epigenetics
Published: April 29, 2025

Biallelic loss-of-function variants in ZNF142 are associated with a robust DNA methylation signature affecting a limited number of genomic loci.

Biallelic loss-of-function variants in ZNF142 are associated with a robust DNA methylation signature affecting a limited number of genomic loci.

Journal: European journal of human genetics : EJHG
Published: March 04, 2025

A Novel UPF1 Variant Associated With a Rare UPF1-Related Neurodevelopmental Disorder.

A Novel UPF1 Variant Associated With a Rare UPF1-Related Neurodevelopmental Disorder.

Journal: Clinical genetics
Published: January 24, 2025

Childhood Cancer Predisposition and Evolutionary Constraints: Novel Lessons from Germline Genomes from 1,127 Children with Cancer.

Childhood Cancer Predisposition and Evolutionary Constraints: Novel Lessons from Germline Genomes from 1,127 Children with Cancer.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: January 18, 2025

Concomitant Upd(14)mat and Trisomy 14 Mosaicism in a Newborn Detected by Whole Genome Sequencing.

Concomitant Upd(14)mat and Trisomy 14 Mosaicism in a Newborn Detected by Whole Genome Sequencing.

Journal: Clinical genetics
Published: November 12, 2024

Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon.

Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon.

Journal: Nature genetics
Published: October 21, 2024
Showing 1-12 of 145

Last Updated: 09/26/2026