Ida Vogel - Genetic Mutations

Author Information

Ida Vogel is affiliated with the Department of Clinical Genetics and the Center for Fetal Diagnostics at Aarhus University Hospital in Aarhus, Denmark. Her research focuses on various aspects of genetics, particularly related to prenatal diagnostics and chromosomal abnormalities.

Research Contributions

Ida Vogel has made significant contributions to the field of genetics, with a particular focus on prenatal diagnostics and chromosomal abnormalities. Her research in 2022 includes studies on the flow from screening to diagnostics, women's preferences towards prenatal genomic testing, and insights into genomic features associated with developmental disorders. Notably, her work also covers the expression of markers in extravillous trophoblasts, detection of the 47,XXY genotype in twin pregnancies, and the complexities of interpreting mosaicism for copy number variations in the placenta. In 2021, her research addressed uncertain results from chromosomal microarray and exome sequencing, trends in prenatal screening and invasive testing in Denmark and Israel, and a novel homozygous variant causing severe intrauterine growth restriction (IUGR), edema, and cardiomyopathy in fetuses.

Aliases

Ida Vogel is also known by the aliases I Vogel, I. Vogel, and Ida Vogel.

Publication and Citation Metrics

Metric Value
Citation Count 3593
H-Index 33
Paper Count 178

Publications:

DOI: 10.1016/b978-0-12-823329-0.00007-6

Year: 2022

DOI: 10.1016/b978-0-12-823329-0.00020-9

Year: 2022

DOI: 10.3389/fgene.2022.842092

Year: 2022

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