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Marie Balslev-Harder

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Prenatal Diagnosis|June 7, 2017
The length of Y-chromosomal sequence reads in noninvasive prenatal testing reflect allogeneic bone marrow transplantMarie Balslev-Harder, Finn Stener Jørgensen, Susanne Kjaergaard, et al.
Prenatal Diagnosis|July 21, 2017
Correlation between Z score, fetal fraction, and sequencing reads in non-invasive prenatal testingMarie Balslev-Harder, Stine R Richter, Susanne Kjaergaard, et al.
Prenatal Diagnosis|March 31, 2016
Open source non-invasive prenatal testing platform and its performance in a public health laboratoryPeter Johansen, Stine R Richter, Marie Balslev-Harder, et al.
American Journal of Medical Genetics. Part A|January 22, 2026
Novel MYL1 Intron Variant With Expanded PhenotypeMaria Barington, Marie Balslev-Harder, Thomas Krag, et al.
Journal of Medical Genetics|September 16, 2016
Carriers of a <i>VEGFA</i> enhancer polymorphism selectively binding CHOP/DDIT3 are predisposed to increased circulating levels of thyroid-stimulating hormoneTarunveer Singh Ahluwalia, Jesper Thorvald Troelsen, Marie Balslev-Harder, et al.
Clinical Genetics|February 23, 2020
upd(20)mat is a rare cause of the Silver-Russell-syndrome-like phenotype: Two unrelated cases and screening of large cohortsTina D Hjortshøj, Anna R Sørensen, Melodi Yusibova, et al.
Plos One|May 28, 2021
Genetic markers of abdominal obesity and weight loss after gastric bypass surgeryMartin Aasbrenn, Mathilde Svendstrup, Theresia M Schnurr, et al.
Obesity Surgery|April 20, 2019
Genetic Determinants of Weight Loss After Bariatric SurgeryMartin Aasbrenn, Theresia Maria Schnurr, Christian Theil Have, et al.
Ugeskrift for Laeger|May 13, 2025
[Genetics in fetal medicine]Simon Horsholt Thomsen, Tina Duelund Hjortshøj, Malou Barbosa, et al.
European Heart Journal|July 11, 2015
Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT intervalJonas Ghouse, Christian Theil Have, Peter Weeke, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Prenatal Diagnosis|June 7, 2017
The length of Y-chromosomal sequence reads in noninvasive prenatal testing reflect allogeneic bone marrow transplantMarie Balslev-Harder, Finn Stener Jørgensen, Susanne Kjaergaard, et al.
Prenatal Diagnosis|July 21, 2017
Correlation between Z score, fetal fraction, and sequencing reads in non-invasive prenatal testingMarie Balslev-Harder, Stine R Richter, Susanne Kjaergaard, et al.
Prenatal Diagnosis|March 31, 2016
Open source non-invasive prenatal testing platform and its performance in a public health laboratoryPeter Johansen, Stine R Richter, Marie Balslev-Harder, et al.
American Journal of Medical Genetics. Part A|January 22, 2026
Novel MYL1 Intron Variant With Expanded PhenotypeMaria Barington, Marie Balslev-Harder, Thomas Krag, et al.
Journal of Medical Genetics|September 16, 2016
Carriers of a <i>VEGFA</i> enhancer polymorphism selectively binding CHOP/DDIT3 are predisposed to increased circulating levels of thyroid-stimulating hormoneTarunveer Singh Ahluwalia, Jesper Thorvald Troelsen, Marie Balslev-Harder, et al.
Clinical Genetics|February 23, 2020
upd(20)mat is a rare cause of the Silver-Russell-syndrome-like phenotype: Two unrelated cases and screening of large cohortsTina D Hjortshøj, Anna R Sørensen, Melodi Yusibova, et al.
Plos One|May 28, 2021
Genetic markers of abdominal obesity and weight loss after gastric bypass surgeryMartin Aasbrenn, Mathilde Svendstrup, Theresia M Schnurr, et al.
Obesity Surgery|April 20, 2019
Genetic Determinants of Weight Loss After Bariatric SurgeryMartin Aasbrenn, Theresia Maria Schnurr, Christian Theil Have, et al.
Ugeskrift for Laeger|May 13, 2025
[Genetics in fetal medicine]Simon Horsholt Thomsen, Tina Duelund Hjortshøj, Malou Barbosa, et al.
European Heart Journal|July 11, 2015
Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT intervalJonas Ghouse, Christian Theil Have, Peter Weeke, et al.
Pageof 2