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Variation in the TEK gene is not associated with asthma but with allergic conjunctivitis

International journal of immunogenetics, 2018-06, Vol.45 (3), p.102-108

2018

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Accelerated clearance alone explains ultra‐large multimers in von Willebrand disease Vicenza

Journal of thrombosis and haemostasis, 2010-06, Vol.8 (6), p.1273-1280

2010

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In interaction with gender a common CYP3A4 polymorphism may influence the survival rate of chemotherapy for childhood acute lymphoblastic leukemia

The pharmacogenomics journal, 2015-06, Vol.15 (3), p.241-247

2015

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Effectiveness of a Hungarian peer education handwashing programme in primary and secondary schools

Developments in health sciences (Online), 2020-11

2020

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1158 Candidate Gene Association Study in Childhood Acute Lymphoblastic Leukemia

European journal of cancer (1990), 2012-07, Vol.48, p.S278-S278

2012

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Comparing depression comorbidity networks of different age groups

Neuroscience Applied, 2022, Vol.1, p.100173, Article 100173

2022

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Pharmacogenetics of the Central Nervous System—Toxicity and Relapse Affecting the CNS in Pediatric Acute Lymphoblastic Leukemia

Cancers, 2021-05, Vol.13 (10), p.2333

2021

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Systems biology approaches to investigating the roles of extracellular vesicles in human diseases

Experimental and Molecular Medicine, 2019, 51(0), , pp.1-11

2019

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GNN4DM: a graph neural network-based method to identify overlapping functional disease modules

Bioinformatics (Oxford, England), 2024-10, Vol.40 (10)

2024

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Prevalence and characterization of severe asthma in Hungary

Scientific reports, 2020-06, Vol.10 (1), p.9274, Article 9274

2020

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Shared extracellular vesicle miRNA profiles of matched ductal pancreatic adenocarcinoma organoids and blood plasma samples show the power of organoid technology

Cellular and molecular life sciences : CMLS, 2021-03, Vol.78 (6), p.3005-3020

2021

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Plasma neutrophil extracellular trap level is modified by disease severity and inhaled corticosteroids in chronic inflammatory lung diseases

Scientific reports, 2020-03, Vol.10 (1), p.4320-4320, Article 4320

2020

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Investigation of circulating lncRNAs as potential biomarkers in chronic respiratory diseases

Journal of translational medicine, 2020-11, Vol.18 (1), p.422-15, Article 422

2020

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MicroRNA-181a as novel liquid biopsy marker of central nervous system involvement in pediatric acute lymphoblastic leukemia

Journal of translational medicine, 2020-06, Vol.18 (1), p.250-250, Article 250

2020

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Circulating microRNAs as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia

Journal of translational medicine, 2019-11, Vol.17 (1), p.372-372, Article 372

2019

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Author Correction: Plasma neutrophil extracellular trap level is modified by disease severity and inhaled corticosteroids in chronic inflammatory lung diseases

Scientific reports, 2020-07, Vol.10 (1), p.13182-13182, Article 13182

2020

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MiR-128-3p as blood based liquid biopsy biomarker in childhood acute lymphoblastic leukemia

Molecular and cellular probes, 2023-02, Vol.67, p.101893-101893, Article 101893

2023

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Possible roles of genetic variations in chemotherapy related cardiotoxicity in pediatric acute lymphoblastic leukemia and osteosarcoma

BMC cancer, 2018-07, Vol.18 (1), p.704-704, Article 704

2018

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Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion

Behavioral and brain functions, 2018-02, Vol.14 (1), p.4-4, Article 4

2018

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The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials

Frontiers in genetics, 2019-10, Vol.10, p.1061-1061

2019

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The Impact of Ethical and Legal Decision-Making in Neonatal Intensive Care on Psychosocial Wellbeing of the Health Care Professionals: The Overview of the HUNIC Project Study Design

European journal of mental health, 2019-12, Vol.14 (2), p.311-323

2019

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Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder Patients

Frontiers in genetics, 2019-05, Vol.10, p.434-434

2019

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Corrigendum: Investigation of the Possible Role of Tie2 Pathway and TEK Gene in Asthma and Allergic Conjunctivitis

Frontiers in genetics, 2020-07, Vol.11, p.702-702

2020

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NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement

Frontiers in genetics, 2018-08, Vol.9, p.335

2018

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Roles of genetic polymorphisms in the folate pathway in childhood acute lymphoblastic leukemia evaluated by Bayesian relevance and effect size analysis

PloS one, 2013-08, Vol.8 (8), p.e69843-e69843

2013

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Variation in the TEK gene is not associated with asthma but with allergic conjunctivitis

Accelerated clearance alone explains ultra‐large multimers in von Willebrand disease Vicenza

In interaction with gender a common CYP3A4 polymorphism may influence the survival rate of chemotherapy for childhood acute lymphoblastic leukemia

Effectiveness of a Hungarian peer education handwashing programme in primary and secondary schools

1158 Candidate Gene Association Study in Childhood Acute Lymphoblastic Leukemia

Comparing depression comorbidity networks of different age groups

Pharmacogenetics of the Central Nervous System—Toxicity and Relapse Affecting the CNS in Pediatric Acute Lymphoblastic Leukemia

Systems biology approaches to investigating the roles of extracellular vesicles in human diseases

GNN4DM: a graph neural network-based method to identify overlapping functional disease modules

Prevalence and characterization of severe asthma in Hungary

Shared extracellular vesicle miRNA profiles of matched ductal pancreatic adenocarcinoma organoids and blood plasma samples show the power of organoid technology

Plasma neutrophil extracellular trap level is modified by disease severity and inhaled corticosteroids in chronic inflammatory lung diseases

Investigation of circulating lncRNAs as potential biomarkers in chronic respiratory diseases

MicroRNA-181a as novel liquid biopsy marker of central nervous system involvement in pediatric acute lymphoblastic leukemia

Circulating microRNAs as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia

Author Correction: Plasma neutrophil extracellular trap level is modified by disease severity and inhaled corticosteroids in chronic inflammatory lung diseases

MiR-128-3p as blood based liquid biopsy biomarker in childhood acute lymphoblastic leukemia

Possible roles of genetic variations in chemotherapy related cardiotoxicity in pediatric acute lymphoblastic leukemia and osteosarcoma

Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion

The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials

The Impact of Ethical and Legal Decision-Making in Neonatal Intensive Care on Psychosocial Wellbeing of the Health Care Professionals: The Overview of the HUNIC Project Study Design

Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder Patients

Corrigendum: Investigation of the Possible Role of Tie2 Pathway and TEK Gene in Asthma and Allergic Conjunctivitis

NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement

Roles of genetic polymorphisms in the folate pathway in childhood acute lymphoblastic leukemia evaluated by Bayesian relevance and effect size analysis

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