Gokhan Yigit

Goettingen, NI, Germany

Last Updated: 09/26/2026

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Found 75 publications

Stem-Cell-Derived Biologic Ventricular Assist Tissue in Heart Failure.

Stem-Cell-Derived Biologic Ventricular Assist Tissue in Heart Failure.

Journal: The New England journal of medicine

Published: May 27, 2026

Evaluation of Surgical and Conservative Approaches in the Treatment of Anal Fissure: A Systematic Review.

Evaluation of Surgical and Conservative Approaches in the Treatment of Anal Fissure: A Systematic Review.

Journal: Acta gastro-enterologica Belgica

Published: January 06, 2026

Generation of pluripotent stem cell line (IPWi001-A) and a corresponding CRISPR/Cas9 modified isogenic rescue control (IPWi001-A-1) from a patient with arrhythmia-induced cardiomyopathy harboring a KCNQ1 truncating mutation.

Generation of pluripotent stem cell line (IPWi001-A) and a corresponding CRISPR/Cas9 modified isogenic rescue control (IPWi001-A-1) from a patient with arrhythmia-induced cardiomyopathy harboring a KCNQ1 truncating mutation.

Journal: Stem cell research

Published: May 30, 2025

Understanding inherited cardiomyopathies: clinical aspects and genetic determinants.

Understanding inherited cardiomyopathies: clinical aspects and genetic determinants.

Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V

Published: April 10, 2025

Mutations in the Key Autophagy Tethering Factor EPG5 Link Neurodevelopmental and Neurodegenerative Disorders Including Early-Onset Parkinsonism.

Mutations in the Key Autophagy Tethering Factor EPG5 Link Neurodevelopmental and Neurodegenerative Disorders Including Early-Onset Parkinsonism.

Journal: Annals of neurology

Published: March 04, 2025

XRCC4-related microcephalic primordial dwarfism: description of a clinical series of 7 cases, phenotype expansion and new diagnostic approaches.

XRCC4-related microcephalic primordial dwarfism: description of a clinical series of 7 cases, phenotype expansion and new diagnostic approaches.

Journal: European journal of human genetics : EJHG

Published: June 24, 2024

Functional characterization of PI3K C2 domain mutations detected in breast cancer circulating tumor cells and metastatic cells.

Functional characterization of PI3K C2 domain mutations detected in breast cancer circulating tumor cells and metastatic cells.

Journal: Cellular signalling

Published: May 05, 2024

Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.

Mutations in TOP3A Cause a Bloom Syndrome-like Disorder.

Journal: American journal of human genetics

Published: May 03, 2024

Phenotypes Linked to Duplication Upstream of SOX9: New Insights Into Presentation and Diagnosis.

Phenotypes Linked to Duplication Upstream of SOX9: New Insights Into Presentation and Diagnosis.

Journal: The Journal of clinical endocrinology and metabolism

Published: February 06, 2024

Lysinuric protein intolerance caused by a homozygous SLC7A7 deletion and presented with hyperferritinemia and osteoporosis in two siblings.

Lysinuric protein intolerance caused by a homozygous SLC7A7 deletion and presented with hyperferritinemia and osteoporosis in two siblings.

Journal: Molecular genetics and metabolism reports

Published: September 06, 2023

Association of Antenatal Evaluations with Postmortem and Genetic Findings in the Series of Fetal Osteogenesis Imperfecta.

Association of Antenatal Evaluations with Postmortem and Genetic Findings in the Series of Fetal Osteogenesis Imperfecta.

Journal: Fetal diagnosis and therapy

Published: August 02, 2023

SEC24C deficiency causes trafficking and glycosylation abnormalities in an epileptic encephalopathy with cataracts and dyserythropoeisis.

SEC24C deficiency causes trafficking and glycosylation abnormalities in an epileptic encephalopathy with cataracts and dyserythropoeisis.

Journal: JCI insight

Published: June 29, 2023

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Last Updated: 09/26/2026