Ida Vogel

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Aarhus University

Denmark

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Professors in Medical Science

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Recent Grants

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Prenatal testing in Denmark – detection, counselling and outcome

Open Date: 2016-12-01

Close Date: 2021-11-01

Grant: Close

Prenatal testing in Denmark – detection, counselling and outcome

Open Date: 2016-01-01

Close Date: 2016-12-31

Articles (28)

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Collaborators (28)

Morten Krogh Herlin

Aarhus University

DENMARK

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Niels Uldbjerg

Aarhus University

DENMARK

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Lone Sunde

Aarhus University

DENMARK

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Stina Lou

Aarhus University

DENMARK

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Martin Jakob Larsen

Associate Professor

University of Southern Denmark

DENMARK

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Felix Boschann

GERMANY

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Lars Henning Pedersen

Aarhus University

DENMARK

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Phillip Grote

Goethe University Frankfurt

GERMANY

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Puk Sandager

Aarhus University

DENMARK

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Else Marie Vestergaard

Aarhus University

DENMARK

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Manuela Morleo

Assistant Professor

University of Campania “Luigi Vanvitelli”

ITALY

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Ellen Steffensen

Aarhus University

DENMARK

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Dorte Lildballe

Aarhus University

DENMARK

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Inger Dorf

Aarhus University

DENMARK

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Jonathan Hyett

Professor

University of Western Sydney

AUSTRALIA

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Simon Horsholt Thomsen

Aarhus University

DENMARK

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Anne Skakkebæk

Aarhus University

DENMARK

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D. Wright

UNITED KINGDOM

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Hanne Kristine Hegaard

Københavns Universitet

DENMARK

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C. Vedel

DENMARK

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Lone Krebs

DENMARK

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Stine Willum Adrian

Aalborg University

DENMARK

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Morten Deleuran Terkildsen

Aarhus University

DENMARK

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Claus Gravholt

Professor

Aarhus Universitetshospital

DENMARK

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Allan Pacey

The University of Manchester

UNITED KINGDOM

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Marianne Munk Sinding

Aalborg University

DENMARK

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Adrian Woolf

The University of Manchester

UNITED KINGDOM

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O. B. Petersen

DENMARK

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Ida Vogel

Research Interests

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Recent Grants

Articles (28)

Whole Genome Sequencing in Prenatal Diagnostics

Mosaic STS gene deletions in chorionic villus samples are often confined to the placenta, and they differ in size from STS gene deletions in patients with X-linked Ichthyosis

Genetik i føtalmedicin

Non‐Invasive Prenatal Testing by Cell‐Free DNA (cfNIPT) for Detecting Turner Syndrome With Mosaicism and Structural Variants—Prenatal Findings and Postnatal Outcomes

Reply

Parental experience of the diagnostic process and its role in the decision to terminate pregnancy due to fetal abnormality; A qualitative interview study

Prenatal Testing for Cystic Fibrosis in the Central Denmark Region (2012-2023)

Making Sense of a Prenatal Detection of Trisomy 16 Mosaicism in the Placenta: A Qualitative Study of Pregnant Women's Decision Making

Increased nuchal translucency thickness and normal chromosomal microarray

A time/space bubble

Combined first‐trimester screening and invasive diagnostics for atypical chromosomal aberrations: Danish nationwide study of prenatal profiles and detection compared with NIPT

Atypicality index as an add‐on to combined first‐trimester screening for chromosomal aberrations

Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies.

Inflammatory markers in relation to maternal lifestyle and adverse pregnancy outcomes in twin pregnancies

Understanding the diagnostic odyssey of women with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome in Denmark

Experiences of vaginal lengthening treatment and sexual well‐being in women with Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome: An interview study

Use of cell-free non-invasive prenatal testing in pregnancies affected by placental mosaicism

Has the introduction of increased genetic prenatal testing affected rates of termination of pregnancy due to fetal abnormality?

A decade of change – lessons learned from prenatal diagnostics in Central Denmark region in 2008–2018

How does cell-based non-invasive prenatal test (NIPT) perform against chorionic villus sampling and cell-free NIPT in detecting trisomies and copy number variations?

Experiences and attitudes of Danish men who were sperm donors more than 10 years ago; a qualitative interview study

Inclusion of sex chromosomes in noninvasive prenatal testing in Asia, Australia, Europe and the USA

Prenatal detection of orofacial clefts in Denmark from 2009 to 2018

Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return

Decoding 22q11.2: prenatal profiling and first‐trimester risk assessment from a Danish nationwide cohort

Diagnosis of hydatidiform moles using circulating gestational trophoblasts isolated from maternal blood

A life course perspective on Mayer-Rokitansky-Küster-Hauser syndrome: women’s experiences and negotiations of living with an underdeveloped uterus and vagina

Atypicality index: avoiding false reassurance in prenatal screening

Collaborators (28)

Morten Krogh Herlin

Niels Uldbjerg

Lone Sunde

Stina Lou

Martin Jakob Larsen

Felix Boschann

Lars Henning Pedersen

Phillip Grote

Puk Sandager

Else Marie Vestergaard

Manuela Morleo

Ellen Steffensen

Dorte Lildballe

Inger Dorf

Jonathan Hyett

Simon Horsholt Thomsen

Anne Skakkebæk

D. Wright

Hanne Kristine Hegaard

C. Vedel

Lone Krebs

Stine Willum Adrian

Morten Deleuran Terkildsen

Claus Gravholt

Allan Pacey

Marianne Munk Sinding

Adrian Woolf

O. B. Petersen

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