Hilmi Bolat

Balikesir, 10145, Turkey

Last Updated: 09/26/2026

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Found 43 publications

Circulating miR-221/222 and Serum IL-23 in Treatment-Naïve Multiple Sclerosis: A Case-Control Study.

Circulating miR-221/222 and Serum IL-23 in Treatment-Naïve Multiple Sclerosis: A Case-Control Study.

Journal: Medicina (Kaunas, Lithuania)

Published: June 23, 2026

Relationship between BDNF rs6265 (VAL66MET) polymorphism and serum BDNF LEVELS in anxiety disorders.

Relationship between BDNF rs6265 (VAL66MET) polymorphism and serum BDNF LEVELS in anxiety disorders.

Journal: Molecular biology reports

Published: June 05, 2026

TRMT10A-Related Neurodevelopmental Disorder Without Metabolic Findings.

TRMT10A-Related Neurodevelopmental Disorder Without Metabolic Findings.

Journal: Human mutation

Published: March 30, 2026

Rare Variants in Purinergic P2X Receptor Genes (P2RX4, P2RX5, P2RX7) in Individuals With Autism Spectrum Disorder: An Exploratory Study.

Rare Variants in Purinergic P2X Receptor Genes (P2RX4, P2RX5, P2RX7) in Individuals With Autism Spectrum Disorder: An Exploratory Study.

Journal: Human mutation

Published: March 08, 2026

Epigenetic regulators and inflammation antagonists in familial Mediterranean fever: the role of hsa-miR-335-5p, hsa-miR-26b-5p, hsa-miR-16-5p miRNAs and IL-36Ra levels in pathogenesis.

Epigenetic regulators and inflammation antagonists in familial Mediterranean fever: the role of hsa-miR-335-5p, hsa-miR-26b-5p, hsa-miR-16-5p miRNAs and IL-36Ra levels in pathogenesis.

Journal: Immunologic research

Published: December 02, 2025

Revisiting Wiedemann-Steiner Syndrome: Novel KMT2A Variants and Broadened Clinical Spectrum.

Revisiting Wiedemann-Steiner Syndrome: Novel KMT2A Variants and Broadened Clinical Spectrum.

Journal: Balkan medical journal

Published: December 01, 2025

Keipert syndrome beyond classical features: novel GPC4 variant associated with epilepsy but preserved cognition.

Keipert syndrome beyond classical features: novel GPC4 variant associated with epilepsy but preserved cognition.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: November 17, 2025

Clinical Insights Into a Rare SETD2 Disorder: Report of a Novel Variant.

Clinical Insights Into a Rare SETD2 Disorder: Report of a Novel Variant.

Journal: Developmental neurobiology

Published: November 07, 2025

A novel compound heterozygous YY1AP1 variant in Grange syndrome: importance of early signs in preventing life-threatening vascular complications.

A novel compound heterozygous YY1AP1 variant in Grange syndrome: importance of early signs in preventing life-threatening vascular complications.

Journal: Journal of human genetics

Published: November 06, 2025

Novel RORA Variants Reveal Genotype-Phenotype Diversity and Variable Expressivity in Neurodevelopmental Disorders.

Novel RORA Variants Reveal Genotype-Phenotype Diversity and Variable Expressivity in Neurodevelopmental Disorders.

Journal: Clinical genetics

Published: November 01, 2025

Testing DAT1 and DRD4 Genes in Attention Deficit Hyperactivity Disorder Using a Wide Spectrum of Neurocognitive Batteries.

Testing DAT1 and DRD4 Genes in Attention Deficit Hyperactivity Disorder Using a Wide Spectrum of Neurocognitive Batteries.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Published: October 31, 2025

ATP6V0A2-Related Cutis Laxa: Identification of a Recurrent Exon 16 Deletion With Founder Effect in Southeastern Türkiye and a Novel Frameshift Variant.

ATP6V0A2-Related Cutis Laxa: Identification of a Recurrent Exon 16 Deletion With Founder Effect in Southeastern Türkiye and a Novel Frameshift Variant.

Journal: American journal of medical genetics. Part A

Published: October 22, 2025

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Last Updated: 09/26/2026