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Paternal uniparental disomy of chromosome 2 resulting in a concurrent presentation of Crigler–Najjar syndrome type I and long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency

American journal of medical genetics. Part A, 2022-06, Vol.188 (6), p.1848-1852

2022

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Puzzling outcome of the nationwide genetic survey of severe/moderate female haemophilia B in Poland

Haemophilia : the official journal of the World Federation of Hemophilia, 2019-11, Vol.25 (6), p.e373-e376

2019

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Human Induced Pluripotent Stem Cell‐Derived Microvesicles Transmit RNAs and Proteins to Recipient Mature Heart Cells Modulating Cell Fate and Behavior

Stem cells (Dayton, Ohio), 2015-09, Vol.33 (9), p.2748-2761

2015

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Impact of antenatal glucocorticosteroids on whole-genome expression in preterm babies

Acta Paediatrica, 2013-04, Vol.102 (4), p.349-355

2013

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Short- and long-term impact of hyperoxia on the blood and retinal cells' transcriptome in a mouse model of oxygen-induced retinopathy

Pediatric research, 2020-02, Vol.87 (3), p.485-493

2020

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Transcriptome analysis reveals dysregulation of genes involved in oxidative phosphorylation in a murine model of retinopathy of prematurity

Pediatric research, 2020-09, Vol.88 (3), p.391-397

2020

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Gene expression profiling in preterm infants: new aspects of bronchopulmonary dysplasia development

PloS one, 2013-10, Vol.8 (10), p.e78585-e78585

2013

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The rs113883650 variant of SLC7A5 (LAT1) gene may alter brain phenylalanine content in PKU

Molecular genetics and metabolism reports, 2021-06, Vol.27, p.100751-100751, Article 100751

2021

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Analysis of miRNAs in Osteogenesis imperfecta Caused by Mutations in COL1A1 and COL1A2: Insights into Molecular Mechanisms and Potential Therapeutic Targets

Pharmaceuticals (Basel, Switzerland), 2023-10, Vol.16 (10), p.1414

2023

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Comparative two time-point proteome analysis of the plasma from preterm infants with and without bronchopulmonary dysplasia

Italian journal of pediatrics, 2019-08, Vol.45 (1), p.112-9, Article 112

2019

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Carriership of the rs113883650/rs2287120 haplotype of the SLC7A5 (LAT1) gene increases the risk of obesity in infants with phenylketonuria

Molecular genetics and metabolism reports, 2020-12, Vol.25, p.100640-100640, Article 100640

2020

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Transcriptome profiling of the newborn mouse brain after hypoxia-reoxygenation: hyperoxic reoxygenation induces inflammatory and energy failure responsive genes

Pediatric research, 2014-04, Vol.75 (4), p.517-526

2014

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Additional risk factor for the development of ALL

Pediatric blood & cancer, 2009-09, Vol.53 (3), p.515-515

2009

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Increased nuchal translucency and associated chromosomal aberrations detected by array comparative genomic hybridisation (acgh) among patients referred to national polish prenatal screening program: A multicenter cohort study

European journal of obstetrics & gynecology and reproductive biology, 2024-02, Vol.293, p.128

2024

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Hyperoxia induces epigenetic changes in newborn mice lungs

Free radical biology & medicine, 2018-06, Vol.121, p.51-56

2018

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Cardiovascular Anomalies among 1005 Fetuses Referred to Invasive Prenatal Testing—A Comprehensive Cohort Study of Associated Chromosomal Aberrations

International journal of environmental research and public health, 2022-08, Vol.19 (16), p.10019

2022

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Is Nuchal Translucency of 3.0–3.4 mm an Indication for cfDNA Testing or Microarray? – A Multicenter Retrospective Clinical Cohort Study

Fetal diagnosis and therapy, 2024-05, Vol.51 (5), p.453-462

2024

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Analysis of miRNAs in IOsteogenesis imperfecta/I Caused by Mutations in ICOL1A1/I and ICOL1A2/I: Insights into Molecular Mechanisms and Potential Therapeutic Targets

Pharmaceuticals (Basel, Switzerland), 2023-10, Vol.16 (10)

2023

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An iTRAQ-Based Quantitative Proteomic Analysis of Plasma Proteins in Preterm Newborns With Retinopathy of Prematurity

Investigative ophthalmology & visual science, 2018-11, Vol.59 (13), p.5312-5319

2018

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Immune System Regulation Affected by a Murine Experimental Model of Bronchopulmonary Dysplasia: Genomic and Epigenetic Findings

Neonatology (Basel, Switzerland), 2019-10, Vol.116 (3), p.269-277

2019

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Genetic analysis of the paired box transcription factor (PAX8) gene in a cohort of Polish patients with primary congenital hypothyroidism and dysgenetic thyroid glands

Journal of Pediatric Endocrinology and Metabolism, 2015-07, Vol.28 (7-8), p.735

2015

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Pulmonary vascular disease is evident in gene regulation of experimental bronchopulmonary dysplasia

The journal of maternal-fetal & neonatal medicine, 2020-06, Vol.33 (12), p.2122-2130

2020

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Identification of deletions in children with congenital hypothyroidism and thyroid dysgenesis with the use of multiplex ligation-dependent probe amplification

Journal of Pediatric Endocrinology and Metabolism, 2015-01, Vol.28 (1-2), p.171

2015

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Development and Maturation of the Immune System in Preterm Neonates: Results from a Whole Genome Expression Study

BioMed research international, 2014-01, Vol.2014, p.498318-8

2014

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Paternal uniparental disomy of chromosome 2 resulting in a concurrent presentation of Crigler–Najjar syndrome type I and long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency

Puzzling outcome of the nationwide genetic survey of severe/moderate female haemophilia B in Poland

Human Induced Pluripotent Stem Cell‐Derived Microvesicles Transmit RNAs and Proteins to Recipient Mature Heart Cells Modulating Cell Fate and Behavior

Impact of antenatal glucocorticosteroids on whole-genome expression in preterm babies

Short- and long-term impact of hyperoxia on the blood and retinal cells' transcriptome in a mouse model of oxygen-induced retinopathy

Transcriptome analysis reveals dysregulation of genes involved in oxidative phosphorylation in a murine model of retinopathy of prematurity

Gene expression profiling in preterm infants: new aspects of bronchopulmonary dysplasia development

The rs113883650 variant of SLC7A5 (LAT1) gene may alter brain phenylalanine content in PKU

Analysis of miRNAs in Osteogenesis imperfecta Caused by Mutations in COL1A1 and COL1A2: Insights into Molecular Mechanisms and Potential Therapeutic Targets

Polymorphisms of SLC19A1 80 G>A, MTHFR 677 C>T, and Tandem TS Repeats Influence Pharmacokinetics, Acute Liver Toxicity, and Vomiting in Children With Acute Lymphoblastic Leukemia Treated With High Doses of Methotrexate

Comparative two time-point proteome analysis of the plasma from preterm infants with and without bronchopulmonary dysplasia

Carriership of the rs113883650/rs2287120 haplotype of the SLC7A5 (LAT1) gene increases the risk of obesity in infants with phenylketonuria

Transcriptome profiling of the newborn mouse brain after hypoxia-reoxygenation: hyperoxic reoxygenation induces inflammatory and energy failure responsive genes

Additional risk factor for the development of ALL

Increased nuchal translucency and associated chromosomal aberrations detected by array comparative genomic hybridisation (acgh) among patients referred to national polish prenatal screening program: A multicenter cohort study

Hyperoxia induces epigenetic changes in newborn mice lungs

Cardiovascular Anomalies among 1005 Fetuses Referred to Invasive Prenatal Testing—A Comprehensive Cohort Study of Associated Chromosomal Aberrations

Is Nuchal Translucency of 3.0–3.4 mm an Indication for cfDNA Testing or Microarray? – A Multicenter Retrospective Clinical Cohort Study

Analysis of miRNAs in IOsteogenesis imperfecta/I Caused by Mutations in ICOL1A1/I and ICOL1A2/I: Insights into Molecular Mechanisms and Potential Therapeutic Targets

An iTRAQ-Based Quantitative Proteomic Analysis of Plasma Proteins in Preterm Newborns With Retinopathy of Prematurity

Immune System Regulation Affected by a Murine Experimental Model of Bronchopulmonary Dysplasia: Genomic and Epigenetic Findings

Genetic analysis of the paired box transcription factor (PAX8) gene in a cohort of Polish patients with primary congenital hypothyroidism and dysgenetic thyroid glands

Pulmonary vascular disease is evident in gene regulation of experimental bronchopulmonary dysplasia

Identification of deletions in children with congenital hypothyroidism and thyroid dysgenesis with the use of multiplex ligation-dependent probe amplification

Development and Maturation of the Immune System in Preterm Neonates: Results from a Whole Genome Expression Study

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