Munis S. Dundar

Erciyes, Turkey

Last Updated: 09/26/2026

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Found 154 publications

Investigation of testicular METRNL and RARRES2 expression in non-obstructive azoospermia.

Investigation of testicular METRNL and RARRES2 expression in non-obstructive azoospermia.

Journal: Journal of applied genetics

Published: June 05, 2026

Blended Hereditary Neuropathy Phenotype Caused by Biallelic PRX and SCN9A Variants: A Case Report.

Blended Hereditary Neuropathy Phenotype Caused by Biallelic PRX and SCN9A Variants: A Case Report.

Journal: Molecular syndromology

Published: March 20, 2026

Association of Vitamin D Receptor (VDR) Gene Polymorphisms with Osteoporotic Vertebral Fracture Risk: A Case-Control Study.

Association of Vitamin D Receptor (VDR) Gene Polymorphisms with Osteoporotic Vertebral Fracture Risk: A Case-Control Study.

Journal: Genes

Published: March 17, 2026

A novel de novo frameshift variant in ZMYM2 expands the neuropsychiatric spectrum of NECRC syndrome: a case report.

A novel de novo frameshift variant in ZMYM2 expands the neuropsychiatric spectrum of NECRC syndrome: a case report.

Journal: Molecular biology reports

Published: March 16, 2026

Differential and Combined Therapeutic Effects of Mesenchymal Stem Cells and Glutathione on Methotrexate-Induced Mucositis.

Differential and Combined Therapeutic Effects of Mesenchymal Stem Cells and Glutathione on Methotrexate-Induced Mucositis.

Journal: Journal of biochemical and molecular toxicology

Published: February 23, 2026

The Development of a Fuzzy Logic System Using MATLAB for Early Detection of Hereditary Cancer in BRCA1/2 Negative Cases.

The Development of a Fuzzy Logic System Using MATLAB for Early Detection of Hereditary Cancer in BRCA1/2 Negative Cases.

Journal: Balkan journal of medical genetics : BJMG

Published: November 07, 2025

Multicenter experience of Kabuki syndrome: a case series of eight patients including three novel KMT2D variants and a brief review.

Multicenter experience of Kabuki syndrome: a case series of eight patients including three novel KMT2D variants and a brief review.

Journal: Neurogenetics

Published: October 27, 2025

Genotype-Phenotype Correlations in Phenylketonuria and Hyperphenylalaninemia: A Single-Center Study.

Genotype-Phenotype Correlations in Phenylketonuria and Hyperphenylalaninemia: A Single-Center Study.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: October 21, 2025

Bietti crystalline dystrophy in Türkiye: A genetic crossroads between Asia and Europe.

Bietti crystalline dystrophy in Türkiye: A genetic crossroads between Asia and Europe.

Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Published: October 21, 2025

Assessment of biotinidase activity changes over time in biotinidase deficient patients.

Assessment of biotinidase activity changes over time in biotinidase deficient patients.

Journal: Frontiers in pediatrics

Published: August 27, 2025

Rare X;13 translocation with NR0B1 duplication in partial gonadal dysgenesis: A novel karyotype in DSD cases.

Rare X;13 translocation with NR0B1 duplication in partial gonadal dysgenesis: A novel karyotype in DSD cases.

Journal: Molecular biology reports

Published: August 06, 2025

Co-occurrence of homozygous ALMS1 variant, 17q11.2 mosaic and germline deletions, and VSX2 nonsense variant in a single family.

Co-occurrence of homozygous ALMS1 variant, 17q11.2 mosaic and germline deletions, and VSX2 nonsense variant in a single family.

Journal: Molecular biology reports

Published: August 06, 2025

Showing 1-12 of 154

Last Updated: 09/26/2026