Concepedia

Author

Michaela Hýblová

Comenius University BratislavaORCID

Also Known As

M. Hyblova, M. Hýblová, Michaela Hyblova, Michaela Hyblová, Michaela Hýblová

38

Publications

319

Citations

9

H-Index

36

Concepts

All Affiliations

Comenius University BratislavaGeneton (Slovakia)Medirex Group AcademySlovak Centre of Scientific and Technical InformationBiomedical Research Center of the Slovak Academy of Sciences
MH

About

Michaela Hýblová is an author at Comenius University Bratislava specializing in genetics, medicine, and genomics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

5

5

158

2

Public Health

3

3

96

3

Biostatistics

2

2

64

4

Natural Sciences

1

1

51

5

Biology

1

1

51

Michaela Hýblová

×

9

Publications

235

Citations

9

H-Index

YearCitations

Ionome and expression level of Si transporter genes (Lsi1, Lsi2, and Lsi6) affected by Zn and Si interaction in maize

Boris Bokor, Silvia Bokorová, Slavomír Ondoš,

Environmental Science and Pollution Research

2014

51

Non-invasive prenatal testing (NIPT) by low coverage genomic sequencing: Detection limits of screened chromosomal microdeletions

Marcel Kucharík, Andrej Gnip, Michaela Hýblová,

PLoS ONE

2020

47

Utilization of Benchtop Next Generation Sequencing Platforms Ion Torrent PGM and MiSeq in Noninvasive Prenatal Testing for Chromosome 21 Trisomy and Testing of Impact of In Silico and Physical Size Selection on Its Analytical Performance

Gabriel Minárik, Gabriela Repiská, Michaela Hýblová,

PLoS ONE

2015

43

Complex phenotypes blur conventional borders between Say–Barber–Biesecker–Young–Simpson syndrome and genitopatellar syndrome

Ján Radvánszky, Michaela Hýblová, Darina Ďurovčíková,

Clinical Genetics

2016

32

Validation of Copy Number Variants Detection from Pregnant Plasma Using Low-Pass Whole-Genome Sequencing in Noninvasive Prenatal Testing-Like Settings

Michaela Hýblová, Mária Haršányová, Diana Nikulenkov-Grochova,

Diagnostics

2020

17

Copy Number Variant Detection with Low-Coverage Whole-Genome Sequencing Represents a Viable Alternative to the Conventional Array-CGH

Marcel Kucharík, Jaroslav Budiš, Michaela Hýblová,

Diagnostics

2021

13

On the critical evaluation and confirmation of germline sequence variants identified using massively parallel sequencing

Zuzana Kubiritova, Marianna Gyurászová, E. Nagyova,

Journal of Biotechnology

2019

11

Spinal muscular atrophy caused by a novel <i>Alu</i>‐mediated deletion of exons 2a‐5 in <i>SMN1</i> undetectable with routine genetic testing

Ivana Jedličková, Anna Přistoupilová, Lenka Nosková,

Molecular Genetics & Genomic Medicine

2020

11

Comparison of the ABC and ACMG systems for variant classification

Gunnar Houge, Eirik Bratland, Ingvild Aukrust,

European Journal of Human Genetics

2024

10

Page 1