Onur E. Onat

A homozygous missense variant, p.Ser166Leu in the PRPF40B gene, in a 7.7 Mb region of homozygosity in a consanguineous Turkish family with essential tremor.

Journal: Frontiers in neurology

Published: January 26, 2026

Escape From X-Chromosome Inactivation Enables Survival in a Male With an Unbalanced X;19 Translocation.

Journal: Annals of the New York Academy of Sciences

Published: January 21, 2026

Effects of essential tremor on longevity and mortality rates in families.

Journal: PloS one

Published: June 14, 2024

Prevalence estimate of sphingosine phosphate lyase insufficiency syndrome in worldwide and select populations.

Journal: Genetics in medicine open

Published: May 25, 2023

Meta-analysis of commonly mutated genes in leptomeningeal carcinomatosis.

Journal: PeerJ

Published: January 26, 2023

The genetic structure of the Turkish population reveals high levels of variation and admixture.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: August 24, 2021

Multiscale analysis of SRY-positive 46,XX testicular disorder of sex development: Presentation of nine cases.

Journal: Andrologia

Published: March 06, 2020

Human CRY1 variants associate with attention deficit/hyperactivity disorder.

Journal: The Journal of clinical investigation

Published: December 05, 2019

Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation.

Journal: Diagnostic and interventional radiology (Ankara, Turkey)

Published: November 09, 2018

Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder.

Journal: Cell

Published: January 14, 2017

Genomic landscape of the Greater Middle East.

Journal: Nature genetics

Published: August 31, 2016

Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis.

Journal: PloS one

Published: March 18, 2016

A homozygous missense variant, p.Ser166Leu in the PRPF40B gene, in a 7.7 Mb region of homozygosity in a consanguineous Turkish family with essential tremor.

A homozygous missense variant, p.Ser166Leu in the PRPF40B gene, in a 7.7 Mb region of homozygosity in a consanguineous Turkish family with essential tremor.

Escape From X-Chromosome Inactivation Enables Survival in a Male With an Unbalanced X;19 Translocation.

Escape From X-Chromosome Inactivation Enables Survival in a Male With an Unbalanced X;19 Translocation.

Effects of essential tremor on longevity and mortality rates in families.

Effects of essential tremor on longevity and mortality rates in families.

Prevalence estimate of sphingosine phosphate lyase insufficiency syndrome in worldwide and select populations.

Prevalence estimate of sphingosine phosphate lyase insufficiency syndrome in worldwide and select populations.

Meta-analysis of commonly mutated genes in leptomeningeal carcinomatosis.

Meta-analysis of commonly mutated genes in leptomeningeal carcinomatosis.

The genetic structure of the Turkish population reveals high levels of variation and admixture.

The genetic structure of the Turkish population reveals high levels of variation and admixture.

Multiscale analysis of SRY-positive 46,XX testicular disorder of sex development: Presentation of nine cases.

Multiscale analysis of SRY-positive 46,XX testicular disorder of sex development: Presentation of nine cases.

Human CRY1 variants associate with attention deficit/hyperactivity disorder.

Human CRY1 variants associate with attention deficit/hyperactivity disorder.

Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation.

Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation.

Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder.

Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder.

Genomic landscape of the Greater Middle East.

Genomic landscape of the Greater Middle East.

Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis.

Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis.

A homozygous missense variant, p.Ser166Leu in the PRPF40B gene, in a 7.7 Mb region of homozygosity in a consanguineous Turkish family with essential tremor.

A homozygous missense variant, p.Ser166Leu in the PRPF40B gene, in a 7.7 Mb region of homozygosity in a consanguineous Turkish family with essential tremor.