Emese Horváth
University of Szeged(HU)
Publications by Year
Research Areas
Prenatal Screening and Diagnostics, Genetic Syndromes and Imprinting, Parvovirus B19 Infection Studies, Genomic variations and chromosomal abnormalities, Fetal and Pediatric Neurological Disorders
Most-Cited Works
- → Serum serotonin, lactate and pyruvate levels in infantile autistic children(1994)80 cited
- → Four years experience of first‐trimester nuchal translucency screening for fetal aneuploidies with increasing regional availability(2001)28 cited
- → Nasal bone length: prenasal thickness ratio: a strong 2D ultrasound marker for Down syndrome(2014)20 cited
- → Somatic mosaicism of the PIK3CA gene identified in a Hungarian girl with macrodactyly and syndactyly(2016)20 cited
- → Fetomaternal Transfusion and Pregnancy Outcome after Cordocentesis(2001)16 cited
- → Leiden Mutation, Bed Rest and Infection: Simultaneous Triggers for Maternal Deep-Vein Thrombosis and Neonatal Intracranial Hemorrhage?(2004)16 cited
- → Prenatal sonographic diagnosis of Aarskog syndrome.(1999)15 cited
- → Identification of a novel missense GLRA1 gene mutation in hyperekplexia: a case report(2014)12 cited
- → Whole Exome Sequencing in a Series of Patients with a Clinical Diagnosis of Tuberous Sclerosis Not Confirmed by Targeted TSC1/TSC2 Sequencing(2021)11 cited
- → Early detection of Angelman syndrome resulting from de novo paternal isodisomic 15q UPD and review of comparable cases(2013)10 cited