Reka Nagy-Kovacs
Neuherberg, BY 85764, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 30 publications
A dataset of paired blood mRNA and microRNA sequencing across acute septic shock and recovery.
Journal: Scientific data
Published: July 10, 2025
MicroRNA-Mediated Suppression of Glial Cell Line-Derived Neurotrophic Factor Expression Is Modulated by a Schizophrenia-Associated Non-Coding Polymorphism.
Journal: International journal of molecular sciences
Published: February 29, 2024
Missense Variants of von Willebrand Factor in the Background of COVID-19 Associated Coagulopathy.
Journal: Genes
Published: January 10, 2023
Impaired complex I repair causes recessive Leber's hereditary optic neuropathy.
Journal: The Journal of clinical investigation
Published: March 19, 2020
RINT1 Bi-allelic Variations Cause Infantile-Onset Recurrent Acute Liver Failure and Skeletal Abnormalities.
Journal: American journal of human genetics
Published: December 28, 2018
A De Novo Missense Variant in POU3F2 Identified in a Child with Global Developmental Delay.
Journal: Neuropediatrics
Published: September 11, 2018
HTRA2 Defect: A Recognizable Inborn Error of Metabolism with 3-Methylglutaconic Aciduria as Discriminating Feature Characterized by Neonatal Movement Disorder and Epilepsy-Report of 11 Patients.
Journal: Neuropediatrics
Published: August 17, 2018
A rare P2RX7 variant in a Hungarian family with multiple sclerosis.
Journal: Multiple sclerosis and related disorders
Published: July 05, 2018
Last Updated: 09/26/2026