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Authors
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Year

Prenatal array comparative genomic hybridization in a well-defined cohort of high-risk pregnancies. A 3-year implementation results in a public tertiary academic referral hospital

Peer-reviewed
DOI
10.1002/pd.5877
Tanner, Laura M.; Alitalo, Tiina; Stefanovic, Vedran
Prenatal diagnosis2021

Genetic spectrum of prenatally diagnosed skeletal dysplasias in a Finnish patient cohort

Peer-reviewed
Open access
DOI
10.1002/pd.6186
Rajala, Katri; Kasanen, Ellamaija; Toiviainen-Salo, Sanna; Valta, Helena; Mäkitie, Outi; Stefanovic,...
Prenatal diagnosis2022

Convicting a wrong molecule?

Open access
DOI
10.1515/dx-2023-0129
Janket, Sok-Ja; Meurman, Jukka H.; Diamandis, Eleftherios P.
Diagnosis2023

The Role of Prenatal Ultrasound and Added Value of Post-Mortem Radiographic Imaging With X-Ray and CT in Suspected Fetal Skeletal Dysplasia

Peer-reviewed
Open access
DOI
10.1002/pd.6732
Rajala, Katri; Toiviainen-Salo, Sanna; Mäkitie, Outi; Stefanovic, Vedran; Tanner, Laura
Prenatal diagnosis2025

BinDel:Detecting Clinically Relevant Fetal Genomic Microdeletions Using Low-Coverage Whole-Genome Sequencing-Based NIPT

Peer-reviewed
Open access
DOI
10.1002/pd.6758
Paluoja, Priit; Jatsenko, Tatjana; Teder, Hindrek; Krjutskov, Kaarel; Vermeesch, Joris Robert; Salum...
Prenatal Diagnosis2025

X-linked pyruvate dehydrogenase complex deficiency due to a novel PDHA1 variant associated with structural brain abnormalities in a fetus

Peer-reviewed
Open access
DOI
10.1002/pd.6349
Tanner, Laura M.; Tynninen, Olli; Piippo, Kirsi; Puhakka, Antti M.
Prenatal diagnosis2023

Inclusion of sex chromosomes in noninvasive prenatal testing in Asia, Australia, Europe and the USA:A survey study

Peer-reviewed
Open access
DOI
10.1002/pd.6322
The NIPT-SCA-map Study Group; Steffensen, Ellen Hollands; Skakkebæk, Anne; Gadsbøll, Kasper; Peterse...
Prenatal diagnosis2023

Fetal alcohol spectrum disorders: genetic and epigenetic mechanisms

Peer-reviewed
Open access
DOI
10.1002/pd.5731
Kaminen-Ahola, Nina
Prenatal Diagnosis2020

Creating basis for introducing non-invasive prenatal testing in the Estonian public health setting

Peer-reviewed
DOI
10.1002/pd.5578
Zilina, Olga; Rekker, Kadri; Kaplinski, Lauris; Sauk, Martin; Paluoja, Priit; Teder, Hindrek; Ustav,...
Prenatal diagnosis2019

Placental and fetal hemodynamics in prolonged pregnancies

Peer-reviewed
DOI
10.1002/pd.4828
Kauppinen, Tuomas; Kantomaa, Tiina; Tekay, Aydin; Makikallio, Kaarin
Prenatal diagnosis2016

Prenatal array comparative genomic hybridization in a well-defined cohort of high-risk pregnancies. A 3-year implementation results in a public tertiary academic referral hospital

Peer-reviewed
DOI
10.1002/pd.5877
2021

Genetic spectrum of prenatally diagnosed skeletal dysplasias in a Finnish patient cohort

Peer-reviewed
Open access
DOI
10.1002/pd.6186
2022

Convicting a wrong molecule?

Open access
DOI
10.1515/dx-2023-0129
2023

The Role of Prenatal Ultrasound and Added Value of Post-Mortem Radiographic Imaging With X-Ray and CT in Suspected Fetal Skeletal Dysplasia

Peer-reviewed
Open access
DOI
10.1002/pd.6732
2025

BinDel:Detecting Clinically Relevant Fetal Genomic Microdeletions Using Low-Coverage Whole-Genome Sequencing-Based NIPT

Peer-reviewed
Open access
DOI
10.1002/pd.6758
2025

X-linked pyruvate dehydrogenase complex deficiency due to a novel PDHA1 variant associated with structural brain abnormalities in a fetus

Peer-reviewed
Open access
DOI
10.1002/pd.6349
2023

Inclusion of sex chromosomes in noninvasive prenatal testing in Asia, Australia, Europe and the USA:A survey study

Peer-reviewed
Open access
DOI
10.1002/pd.6322
2023

Fetal alcohol spectrum disorders: genetic and epigenetic mechanisms

Peer-reviewed
Open access
DOI
10.1002/pd.5731
2020

Creating basis for introducing non-invasive prenatal testing in the Estonian public health setting

Peer-reviewed
DOI
10.1002/pd.5578
2019

Placental and fetal hemodynamics in prolonged pregnancies

Peer-reviewed
DOI
10.1002/pd.4828
2016