Timur Tuncalı

Ankara, 06620, Turkey

Last Updated: 09/26/2026

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Found 19 publications

Post-Treatment Persistent Erythrocytosis in Patients with Hodgkin Lymphoma: Molecular Mechanisms Underlying the Pathogenesis of Erythrocytosis.

Post-Treatment Persistent Erythrocytosis in Patients with Hodgkin Lymphoma: Molecular Mechanisms Underlying the Pathogenesis of Erythrocytosis.

Journal: Cancers

Published: June 27, 2026

Diagnostic Yield and Clinical Utility of Genetic Testing in Turkish Adults with Suspected Inherited Kidney Disease: Insights from a Population with High Parental Consanguinity.

Diagnostic Yield and Clinical Utility of Genetic Testing in Turkish Adults with Suspected Inherited Kidney Disease: Insights from a Population with High Parental Consanguinity.

Journal: Journal of clinical practice and research

Published: January 21, 2026

Innate immunogenetic synergy between KIR and Neanderthal-derived OAS variants predicts COVID-19 outcomes.

Innate immunogenetic synergy between KIR and Neanderthal-derived OAS variants predicts COVID-19 outcomes.

Journal: PloS one

Published: October 14, 2025

Somatic variants and frequencies of familial myeloma germline predisposition genes among patients within the CoMMpass dataset.

Somatic variants and frequencies of familial myeloma germline predisposition genes among patients within the CoMMpass dataset.

Journal: Expert review of hematology

Published: September 25, 2025

Familial Multiple Myeloma: Insights From Epidemiology and Underlying Germline Genetic Predisposition to the Clinic.

Familial Multiple Myeloma: Insights From Epidemiology and Underlying Germline Genetic Predisposition to the Clinic.

Journal: Clinical lymphoma, myeloma & leukemia

Published: November 07, 2024

X-linked Dyskeratosis Congenita Case with Mutation 1058C>T(p.Ala353Val) in Dyskerine Gene.

X-linked Dyskeratosis Congenita Case with Mutation 1058C>T(p.Ala353Val) in Dyskerine Gene.

Journal: Indian journal of dermatology

Published: April 04, 2024

Germline genetic variants in Turkish familial multiple myeloma/monoclonal gammopathy of undetermined significance cases.

Germline genetic variants in Turkish familial multiple myeloma/monoclonal gammopathy of undetermined significance cases.

Journal: British journal of haematology

Published: October 06, 2023

Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia.

Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia.

Journal: Journal of medical virology

Published: December 09, 2022

Phenotypic and molecular characterization of five patients with PIK3CA-related overgrowth spectrum (PROS).

Phenotypic and molecular characterization of five patients with PIK3CA-related overgrowth spectrum (PROS).

Journal: American journal of medical genetics. Part A

Published: September 17, 2021

ROHMM-A flexible hidden Markov model framework to detect runs of homozygosity from genotyping data.

ROHMM-A flexible hidden Markov model framework to detect runs of homozygosity from genotyping data.

Journal: Human mutation

Published: September 09, 2021

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.

Journal: Functional & integrative genomics

Published: July 09, 2021

Right Anterior Theta Hypersynchrony as a Quantitative Measure Associated with Autistic Traits and K-Cl Cotransporter KCC2 Polymorphism.

Right Anterior Theta Hypersynchrony as a Quantitative Measure Associated with Autistic Traits and K-Cl Cotransporter KCC2 Polymorphism.

Journal: Journal of autism and developmental disorders

Published: February 10, 2021

Showing 1-12 of 19

Last Updated: 09/26/2026