Martin Hynek - Gynecology

Author Information

Martin Hynek is affiliated with Gennet, Centre for Fetal Medicine and Reproductive Genetics, Prague, Czech Republic, and the Department of Gynecology and Obstetrics, Thomayer Hospital, Prague, Czech Republic. His work primarily revolves around fetal medicine and reproductive genetics.

Research Contributions

Martin Hynek has made significant contributions to the field of fetal medicine, particularly in the areas of prenatal diagnosis and chromosomal aneuploidies. His research includes the real-time quality control of nuchal translucency measurements, cell-free DNA testing for chromosomal abnormalities in non-viable pregnancies, and the use of whole-genome array as a first-line cytogenetic test in invasive prenatal diagnosis. His work has been published in reputable journals such as the Taiwanese Journal of Obstetrics & Gynecology and various conferences under the International Society of Ultrasound in Obstetrics and Gynecology (ISUOG).

Aliases

Martin Hynek is also known by the aliases M Hynek and M. Hynek.

Publication and Citation Metrics

Metric	Value
Citation Count	54
H-Index	4
Paper Count	79

Publications:

Corrigendum to <'Real-time quality control of nuchal translucency measurements using the exponentially weighted moving average chart' [Taiwanese Journal of Obstetrics & Gynecology 60 (2021) 84-89].

DOI: 10.1016/j.tjog.2021.11.036

Year: 2022

Real-time quality control of nuchal translucency measurements using the exponentially weighted moving average chart.

DOI: 10.1016/j.tjog.2020.11.012

Year: 2021

VP29.12: Cell‐free DNA testing in the detection of chromosomal aneuploidies in non‐viable pregnancies

DOI: 10.1002/uog.22790

Year: 2020

P01.09: The levels of cell‐free fetal DNA in cases of early fetal demise and miscarriage

DOI: 10.1002/uog.20882

Year: 2019

Physical methods for increasing press accuracy

DOI: 10.1051/matecconf/201929304002

Year: 2019

OC06.06: Cell‐free DNA in the detection of chromosomal aneuploidies in early fetal demise and miscarriage

DOI: 10.1002/uog.20461

Year: 2019

EP11.08: Neural tube defects: prenatal diagnosis in GENNET centre 2007–2017, Czech Republic

DOI: 10.1002/uog.19968

Year: 2018

OC02.04: Non‐commercial cell‐free DNA testing in routine clinical aneuploidy screening: a three‐year experience

DOI: 10.1002/uog.19214

Year: 2018

Statistical methods for constructing gestational age-related charts for fetal size and pregnancy dating using longitudinal data

DOI: 10.1016/J.BBE.2018.09.001

Year: 2018

P20.06: The experience with whole‐genome array as a first‐line cytogenetic test in invasive prenatal diagnosis

DOI: 10.1002/uog.19782

Year: 2018

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