Volkan Karaman

Istanbul, Turkey

Last Updated: 09/26/2026

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Found 27 publications

Corrigendum to "Qualitative assessment of DNA isolation from fresh, frozen, and ancient human bone using a homogenizer-assisted workflow" [Forensic Sci. Int. 380 (2026) 112807].

Corrigendum to "Qualitative assessment of DNA isolation from fresh, frozen, and ancient human bone using a homogenizer-assisted workflow" [Forensic Sci. Int. 380 (2026) 112807].

Journal: Forensic science international

Published: August 04, 2026

Expanded clinical and genetic characterization of autosomal recessive HMGCR-related muscular dystrophy.

Expanded clinical and genetic characterization of autosomal recessive HMGCR-related muscular dystrophy.

Journal: Journal of neuromuscular diseases

Published: March 29, 2026

Evaluation of the Impact of a PUS7 Gene Variant on Dental Development: A Rare Case Report.

Evaluation of the Impact of a PUS7 Gene Variant on Dental Development: A Rare Case Report.

Journal: Molecular syndromology

Published: February 11, 2026

Hemodynamic and microvascular abnormalities in P450 oxidoreductase deficiency: evidence for COX-dependent dysfunction.

Hemodynamic and microvascular abnormalities in P450 oxidoreductase deficiency: evidence for COX-dependent dysfunction.

Journal: European journal of endocrinology

Published: December 19, 2025

Genotype-phenotype correlations in phenylketonuria: PAH variants and BH4 responsiveness for treatment design.

Genotype-phenotype correlations in phenylketonuria: PAH variants and BH4 responsiveness for treatment design.

Journal: Human genomics

Published: December 11, 2025

Prenatal and Postmortem Characterization of FGFR2-Related Fetal Craniosynostosis: Emphasizing Rare and Atypical Anomalies.

Prenatal and Postmortem Characterization of FGFR2-Related Fetal Craniosynostosis: Emphasizing Rare and Atypical Anomalies.

Journal: Prenatal diagnosis

Published: December 09, 2025

Assessment of cardiometabolic risk using single point insulin sensitivity estimator (SPISE) in pediatric Bardet-Biedl Syndrome: a pilot study.

Assessment of cardiometabolic risk using single point insulin sensitivity estimator (SPISE) in pediatric Bardet-Biedl Syndrome: a pilot study.

Journal: Orphanet journal of rare diseases

Published: November 19, 2025

Qualitative assessment of DNA isolation from fresh, frozen, and ancient human bone using a homogenizer-assisted workflow.

Qualitative assessment of DNA isolation from fresh, frozen, and ancient human bone using a homogenizer-assisted workflow.

Journal: Forensic science international

Published: October 20, 2025

Use of serum MKRN3 and DLK1 levels in precocious puberty: association with an MKRN3 pathogenic variant.

Use of serum MKRN3 and DLK1 levels in precocious puberty: association with an MKRN3 pathogenic variant.

Journal: Therapeutic advances in endocrinology and metabolism

Published: September 01, 2025

Molecular Diagnosis of 46,XY Disorders of Sex Development: An Efficient Initial Molecular Analysis Using a Custom-Designed Targeted Gene Panel in a Single-Center Study.

Molecular Diagnosis of 46,XY Disorders of Sex Development: An Efficient Initial Molecular Analysis Using a Custom-Designed Targeted Gene Panel in a Single-Center Study.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation

Published: August 29, 2025

Evaluation of Serum FGF21 Levels in Patients with Mitochondrial Aminoacyl-tRNA Synthetase Deficiency.

Evaluation of Serum FGF21 Levels in Patients with Mitochondrial Aminoacyl-tRNA Synthetase Deficiency.

Journal: International journal of molecular sciences

Published: July 28, 2025

Long-term follow-up of growth and puberty in 3-M syndrome: effects of growth hormone therapy and response variability.

Long-term follow-up of growth and puberty in 3-M syndrome: effects of growth hormone therapy and response variability.

Journal: Endocrine

Published: May 04, 2025

Showing 1-12 of 27

Last Updated: 09/26/2026