I. Vogel

发表

Reference population for international comparisons and time trend surveillance of preterm delivery proportions in three countries

B. Jacobsson, J. Langhoff‐Roos, N. Morken, 2008, BMC women's health.

Spontaneous preterm delivery in primiparous women at low risk in Denmark: population based study

Bo Jacobsson, B. Jacobsson, J. Langhoff‐Roos, 2006, BMJ : British Medical Journal.

Trends in Non-invasive Prenatal Screening and Invasive Testing in Denmark (2000–2019) and Israel (2011–2019)

I. Vogel, L. Sagi‐Dain, A. Singer, 2021, Frontiers in Medicine.

Cell‐based noninvasive prenatal testing (cbNIPT) detects pathogenic copy number variations

N. Uldbjerg, R. Christensen, I. Vogel, 2020, Clinical case reports.

Population-Based Screening for Trisomies and Atypical Chromosomal Abnormalities: Improving Efficacy using the Combined First Trimester Screening Algorithm as well as Individual Risk Parameters

I. Vogel, A. Tabor, J. Hyett, 2018, Fetal Diagnosis and Therapy.

Fetal cells in maternal blood for prenatal diagnosis: a love story rekindled.

N. Uldbjerg, I. Vogel, O. Petersen, 2017, Biomarkers in medicine.

Screening for Fetal Aneuploidy and Sex Chromosomal Anomalies in a Pregnant Woman With Mosaicism for Turner Syndrome—Applications and Advantages of Cell-Based NIPT

I. Vogel, L. Hatt, Ripudaman Singh, 2021, Frontiers in Genetics.

The Role of Growth Factors in Diabetic Kidney Disease

H. Grønbæk, A. Flyvbjerg, I. Vogel, 1996 .

Potential diagnostic consequences of applying non‐invasive prenatal testing: population‐based study from a country with existing first‐trimester screening

I. Vogel, A. Tabor, J. Hyett, 2014, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

PSCC: Sensitive and Reliable Population-Scale Copy Number Variation Detection Method Based on Low Coverage Sequencing

Xiuqing Zhang, Hui Jiang, R. Christensen, 2014, PloS one.

First trimester biomarkers for prediction of gestational diabetes mellitus.

K. Nicolaides, H. Møller, O. Koren, 2020, Placenta.

A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing

Å. Borg, U. Jensen, L. Sunde, 2011, Breast Cancer Research and Treatment.

Existing data sources for clinical epidemiology: Danish registries for studies of medical genetic diseases

L. Sunde, I. Vogel, E. Svensson, 2013, Clinical epidemiology.

Bacterial vaginosis in early pregnancy is associated with low birth weight and small for gestational age, but not with spontaneous preterm birth: A population-based study on Danish women

B. Jacobsson, J. Olsen, I. Vogel, 2006, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Goblet Cell Carcinoid in a Patient with Neurofibromatosis Type 1: A Rare Combination

T. Gregersen, K. Krogh, H. Grønbaek, 2012, Case reports in gastrointestinal medicine.

Implementation of exome sequencing in fetal diagnostics—Data and experiences from a tertiary center in Denmark

R. Christensen, I. Vogel, O. Petersen, 2020, Acta obstetricia et gynecologica Scandinavica.

Identification of biological/biochemical marker(s) for preterm delivery.

D E Schendel, J. Olsen, A. Deshpande, 2001, Paediatric and perinatal epidemiology.

Mid‐pregnancy maternal plasma levels of interleukin 2, 6, and 12, tumor necrosis factor‐alpha, interferon‐gamma, and granulocyte‐macrophage colony‐stimulating factor and spontaneous preterm delivery

D. Hougaard, W. Flanders, J. Olsen, 2007 .

Chlamydia trachomatis C-complex serovars are a risk factor for preterm birth.

I. Vogel, B. Jeune, P. Thorsen, 2007, In vivo.

Insulin-like growth factor binding protein 1 (IGFBP-1) in vaginal fluid in pregnancy.

H. Grønbaek, A. Flyvbjerg, I. Vogel, 2004, In vivo.

Albumin in vaginal fluid is a marker of infection in early pregnancy

H. Grønbæk, A. Flyvbjerg, I. Vogel, 2003, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Parental response to severe or lethal prenatal diagnosis: a systematic review of qualitative studies

I. Vogel, L. Jensen, O. Petersen, 2017, Prenatal diagnosis.

Effects of blood sample handling procedures on measurable inflammatory markers in plasma, serum and dried blood spot samples.

D. Hougaard, B. No̸rgaard-Pedersen, B. Jacobsson, 2008, Journal of immunological methods.

Factors that impact on women's decision‐making around prenatal genomic tests: An international discrete choice survey

K. Ormond, M. Choolani, L. Chitty, 2022, Prenatal diagnosis.

Biomarkers for the prediction of preterm delivery

N. Uldbjerg, I. Vogel, P. Thorsen, 2005, Acta obstetricia et gynecologica Scandinavica.

First reported case of Simpson–Golabi–Behmel syndrome in a female fetus diagnosed prenatally with chromosomal microarray

I. Vogel, E. Vestergaard, M. Ramsing, 2017, Clinical case reports.

Epilepsy and cataplexy in Angelman syndrome. Genotype-phenotype correlations.

R. Christensen, J. Østergaard, I. Vogel, 2016, Research in developmental disabilities.

Phenotype in 18 Danish subjects with genetically verified CHARGE syndrome

S. Kreiborg, I. Vogel, H. Hove, 2013, Clinical genetics.

Low serum interleukin‐17 is associated with preterm delivery

N. Uldbjerg, D. Hougaard, I. Vogel, 2011, Acta obstetricia et gynecologica Scandinavica.

Interleukin-18 and interleukin-12 in maternal serum and spontaneous preterm delivery.

D. Hougaard, B. Jacobsson, J. Langhoff‐Roos, 2008, Journal of reproductive immunology.

Maternal plasma cytokines in early- and mid-gestation of normal human pregnancy and their association with maternal factors.

D. Hougaard, W. Flanders, D. Schendel, 2008, Journal of reproductive immunology.

Mid-pregnancy maternal plasma levels of interleukin 2, 6, and 12, tumor necrosis factor-alpha, interferon-gamma, and granulocyte-macrophage colony-stimulating factor and spontaneous preterm delivery.

D. Hougaard, W. Flanders, J. Olsen, 2008, Acta obstetricia et gynecologica Scandinavica.

Racial disparity in amniotic fluid concentrations of tumor necrosis factor (TNF)-alpha and soluble TNF receptors in spontaneous preterm birth.

Scott M. Williams, Chun Xing Li, B. Jacobsson, 2008, American journal of obstetrics and gynecology.

Novel TRPV4 variant causes a severe form of metatropic dysplasia

I. Vogel, A. Haagerup, P. A. Gregersen, 2018, Clinical case reports.

Mechanism of pancreatic and liver malformations in human fetuses with short-rib polydactyly syndrome.

I. Vogel, G. Ramm, T. Pereira, 2016, Birth defects research. Part A, Clinical and molecular teratology.

Increased prenatal detection of 22q11.2 deletion and 22q11.2 duplication after introduction of nationwide prenatal screening for trisomy 21, trisomy 13, and trisomy 18

C. Fagerberg, I. Bache, I. Vogel, 2020, Prenatal diagnosis.

Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross‐sectional study with healthcare professionals

K. Ormond, M. Choolani, I. Vogel, 2021, Prenatal diagnosis.

Parenting a child with Down syndrome: A qualitative study of everyday practices in Danish families

S. Santoro, I. Vogel, S. Lou, 2021, Journal of genetic counseling.

How are uncertain prenatal genetic results perceived and managed two years after they were received? A qualitative interview study

I. Vogel, S. Lou, Amalie Hahn Jensen, 2021, Journal of genetic counseling.

Do extravillous trophoblasts isolated from maternal blood and cervical canal express the same markers?

N. Uldbjerg, I. Vogel, L. Hatt, 2022 .

On the road to replacing invasive testing with cell‐based NIPT: Five clinical cases with aneuploidies, microduplication, unbalanced structural rearrangement, or mosaicism

N. Uldbjerg, R. Christensen, I. Vogel, 2017, Prenatal diagnosis.

Eating behavior, prenatal and postnatal growth in Angelman syndrome.

R. Christensen, J. Østergaard, I. Vogel, 2014, Research in developmental disabilities.

Angelman syndrome in Denmark. Birth incidence, genetic findings, and age at diagnosis

R. Christensen, J. Østergaard, I. Vogel, 2013, American journal of medical genetics. Part A.

First‐trimester maternal plasma cytokine levels, pre‐pregnancy body mass index, and spontaneous preterm delivery

D. Hougaard, W. Flanders, J. Olsen, 2009, Acta obstetricia et gynecologica Scandinavica.

Ultrasound in Prenatal Diagnostics and Its Impact on the Epidemiology of Spina Bifida in a National Cohort from Denmark with a Comparison to Sweden

I. Vogel, A. Tabor, O. Petersen, 2018, BioMed research international.

Preterm delivery predicted by soluble CD163 and CRP in women with symptoms of preterm delivery

N. Uldbjerg, S. Moestrup, H. Møller, 2005, BJOG : an international journal of obstetrics and gynaecology.

A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variability

L. Sunde, I. Vogel, O. Petersen, 2013, American journal of medical genetics. Part A.

The joint effect of vaginal Ureaplasma urealyticum and bacterial vaginosis on adverse pregnancy outcomes

B. Jacobsson, L. Schieve, V. Hogan, 2006, Acta obstetricia et gynecologica Scandinavica.

Incidental finding of maternal malignancy in an unusual non‐invasive prenatal test and a review of similar cases

I. Vogel, A. Skytte, M. Srebniak, 2022, Clinical case reports.

Polymorphisms in the promoter region of relaxin-2 and preterm birth: involvement of relaxin in the etiology of preterm birth.

D. Hougaard, J. Grove, M. Hollegaard, 2009, In vivo.

A novel homozygous variant in C1QBP causes severe IUGR, edema, and cardiomyopathy in two fetuses

I. Vogel, P. Sandager, Morten Alstrup, 2021, JIMD reports.

Prediction of preterm delivery using changes in serum relaxin in low risk pregnancies.

N. Uldbjerg, I. Vogel, P. Thorsen, 2006, European journal of obstetrics, gynecology, and reproductive biology.

Prenatal diagnosis: array comparative genomic hybridization in fetuses with abnormal sonographic findings

R. Christensen, I. Vogel, O. Petersen, 2013, Acta obstetricia et gynecologica Scandinavica.

Cell-Based NIPT Detects 47,XXY Genotype in a Twin Pregnancy

R. Christensen, I. Vogel, O. Petersen, 2022, Frontiers in Genetics.

[22q11 deletion syndrome].

M. Lauritsen, J. Østergaard, M. Boers, 2010, Ugeskrift for laeger.

Metatarsal bony syndactyly in 2 fetuses with Smith‐Lemli‐Opitz syndrome: An under‐recognized part of the clinical spectrum

G. Mortier, P. Nürnberg, Shahida Moosa, 2017, Clinical Genetics.

Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders

Erez Lieberman Aiden, Ryan L. Collins, S. G. Temel, 2022, medRxiv.

Experiences and expectations in the first trimester of pregnancy: a qualitative study

I. Vogel, O. Petersen, S. Lou, 2017, Health expectations : an international journal of public participation in health care and health policy.

A prospective double-blinded non-selection trial of reproductive outcomes and chromosomal normalcy of newborns derived from putative low/moderate-degree mosaic IVF embryos

A. Farcomeni, C. Simón, C. Rubio, 2021, medRxiv.

Assessing women’s preferences towards tests that may reveal uncertain results from prenatal genomic testing: Development of attributes for a discrete choice experiment, using a mixed-methods design

K. Ormond, I. Vogel, L. Hui, 2022, PloS one.

Preferences for prenatal tests for Down syndrome: an international comparison of the views of pregnant women and health professionals

A. Barrett, S. Morris, S. Langlois, 2015, European Journal of Human Genetics.

Serum 17 &bgr;-Estradiol in Newborn and Neonatal Hip Instability

N. Uldbjerg, I. Vogel, J. Andersson, 2002, Journal of pediatric orthopedics.

Case of successful IVF treatment of an oligospermic male with 46,XX/46,XY chimerism

C. Gravholt, P. Humaidan, I. Vogel, 2018, Journal of Assisted Reproduction and Genetics.

The influence of amphotericin B and neomycin on the effect of human relaxin-2 on foetal membranes and isolated myometrium.

N. Uldbjerg, H. Grønbaek, I. Vogel, 2004, Basic & clinical pharmacology & toxicology.

Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders.

Bradley P. Coe, B. Coe, J. Schuurs-Hoeijmakers, 2016, American journal of human genetics.

Heterozygous variants in KMT2E cause a spectrum of neurodevelopmental disorders and epilepsy

Carol J. Saunders, C. Saunders, I. Thiffault, 2019, bioRxiv.

Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.

Reinhard Ullmann, Zeynep Tümer, Niels Tommerup, 2008, American journal of human genetics.

Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype

W. Chong, K. Choy, T. Leung, 2011, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Chromosomal microarray as primary diagnostic genomic tool for pregnancies at increased risk within a population‐based combined first‐trimester screening program

R. Christensen, I. Vogel, J. Hyett, 2018, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

M. Larsen, C. Fagerberg, L. Krogh, 2019, European journal of medical genetics.

Cell-free DNA in pregnancy with choriocarcinoma and coexistent live fetus

L. Sunde, I. Vogel, M. Christiansen, 2016, Medicine.

Trisomy 8 mosaicism in the placenta: A Danish cohort study of 37 cases and a literature review

C. Fagerberg, I. Bache, I. Vogel, 2020, Prenatal diagnosis.

First trimester screening for other trisomies than trisomy 21, 18, and 13

N. Uldbjerg, N. Tørring, I. Vogel, 2015, Prenatal diagnosis.

Cell-based non-invasive prenatal testing for monogenic disorders: confirmation of unaffected fetuses following preimplantation genetic testing

N. Uldbjerg, H. Okkels, I. Vogel, 2021, Journal of Assisted Reproduction and Genetics.

Receiving a prenatal diagnosis of Down syndrome by phone: a qualitative study of the experiences of pregnant couples

I. Vogel, O. Petersen, S. Lou, 2019, BMJ Open.

Increased prenatal detection of 22q11.2 deletion and 22q11.2 duplication 1 after introduction of nationwide prenatal screening for 2 trisomy 21, and

I. Vogel, J. Hyett, O. Petersen, 2021 .

Biphasic effect of relaxin, inhibitable by a collagenase inhibitor, on the strength of human fetal membranes.

N. Uldbjerg, A. Petersen, I. Vogel, 2004, In vivo.

Current use of noninvasive prenatal testing in Europe, Australia and the USA: A graphical presentation

B. Jacobsson, R. Wapner, I. Vogel, 2020, Acta obstetricia et gynecologica Scandinavica.

Unexplained cholestasis in adults and adolescents: diagnostic benefit of genetic examination

P. Ott, H. Grønbaek, H. Vilstrup, 2018, Scandinavian journal of gastroenterology.

The development of hepatic stellate cells in normal and abnormal human fetuses – an immunohistochemical study

I. Vogel, G. Ramm, T. Pereira, 2015, Physiological reports.

PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans

F. Béna, R. Christensen, P. Jouk, 2017, Journal of Medical Genetics.

How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies

K. Ormond, I. Vogel, M. Srebniak, 2021, Clinical genetics.

How do geneticists and prospective parents interpret and negotiate an uncertain prenatal genetic result? An analysis of clinical interactions

K. Lomborg, I. Vogel, O. Petersen, 2020, Journal of genetic counseling.

The Number of Circulating Fetal Extravillous Trophoblasts Varies from Gestational Week 6 to 20

N. Uldbjerg, I. Vogel, L. Hatt, 2020, Reproductive Sciences.

Pallister–Killian syndrome in a girl with mild developmental delay and mosaicism for hexasomy 12p

I. Vogel, J. Hertz, T. Lyngbye, 2009, American journal of medical genetics. Part A.

National data on the early clinical use of non‐invasive prenatal testing in public and private healthcare in Denmark 2013–2017

C. Fagerberg, I. Vogel, A. Tabor, 2020, Acta obstetricia et gynecologica Scandinavica.

Prenatal screening for atypical chromosomal abnormalities: past or future?

I. Vogel, O. Petersen, 2018, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Potential Diagnostic Consequences of Applying Noninvasive Prenatal Testing: Population-Based Study From a Country With Existing First-Trimester Screening

I. Vogel, A. Tabor, J. Hyett, 2014 .

First‐trimester screening for trisomy 21 in Denmark: implications for detection and birth rates of trisomy 18 and trisomy 13

S. Kjaergaard, I. Vogel, A. Tabor, 2011, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Early second-trimester inflammatory markers and short cervical length and the risk of recurrent preterm birth.

D. Hougaard, I. Vogel, W. Andrews, 2007, Journal of reproductive immunology.

Relaxin (hRLX-2)-induced weakening of human fetal membranes in vitro.

N. Uldbjerg, I. Vogel, H. Oxlund, 1994, European journal of obstetrics, gynecology, and reproductive biology.

New tight junction protein 2 variant causing progressive familial intrahepatic cholestasis type 4 in adults: A case report

P. Ott, H. Grønbæk, I. Vogel, 2020, World journal of gastroenterology.

Increased bioavailability of TNF-alpha in African Americans during in vitro infection: predisposing evidence for immune imbalance.

B. Jacobsson, S. Fortunato, R. Menon, 2007, Placenta.

Acquisition and Elimination of Bacterial Vaginosis During Pregnancy: A Danish Population-Based Study

B. Jacobsson, I. Vogel, B. Jeune, 2006, Infectious diseases in obstetrics and gynecology.

Neurodevelopmental outcome in Angelman syndrome: genotype-phenotype correlations.

R. Christensen, I. Vogel, J. Hertz, 2014, Research in developmental disabilities.

Risk factors for bacterial vaginosis in pregnancy: a population‐based study on Danish women

B. Jacobsson, I. Vogel, B. Jeune, 2006, Acta obstetricia et gynecologica Scandinavica.

Atypicality index: avoiding false reassurance in prenatal screening

K. Nicolaides, I. Vogel, A. Wright, 2022, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Nuchal translucency distributions for different chromosomal anomalies in a large unselected population cohort

I. Vogel, A. Tabor, J. Hyett, 2016, Prenatal diagnosis.

Serum relaxin in the newborn is not a marker of neonatal hip instability.

N. Uldbjerg, I. Vogel, J. Andersson, 1998, Journal of pediatric orthopedics.

Variations in serum relaxin (hRLX‐2) concentrations during human pregnancy

N. Uldbjerg, I. Vogel, L. K. Petersen, 1995, Acta obstetricia et gynecologica Scandinavica.

Phenotypic presentations of Hajdu-Cheney syndrome according to age - 5 distinct clinical presentations.

M. Irving, I. Vogel, M. Davidsen, 2020, European journal of medical genetics.

Circulating relaxin and cervical length in midpregnancy are independently associated with spontaneous preterm birth.

N. Uldbjerg, I. Vogel, T. Henriksen, 2009, American journal of obstetrics and gynecology.

Early mid-trimester serum relaxin, soluble CD163, and cervical length in women at high risk for preterm delivery.

H. Møller, I. Vogel, W. Andrews, 2006, American journal of obstetrics and gynecology.

S‐relaxin as a predictor of preterm delivery in women with symptoms of preterm labour

N. Uldbjerg, I. Vogel, F. Armbruster, 2002, BJOG : an international journal of obstetrics and gynaecology.

Is carriership of a balanced translocation or inversion an indication for non-invasive prenatal testing?

I. Vogel, M. Srebniak, D. Van Opstal, 2018, Expert review of molecular diagnostics.

Cytokines and the Risk of Preterm Delivery in Twin Pregnancies

N. Uldbjerg, D. Hougaard, I. Vogel, 2012, Obstetrics and gynecology.

Association between raised serum relaxin levels during the eighteenth gestational week and very preterm delivery.

N. Uldbjerg, I. Vogel, J. D. Salvig, 2001, American journal of obstetrics and gynecology.

Preterm delivery predicted by serum relaxin

N. Uldbjerg, I. Vogel, P. Thorsen, 2001 .

OC06.01: Vaginal progesterone and the risk of preterm delivery in high‐risk twin gestations ‐ secondary analysis of a placebo‐controlled randomized trial

N. Uldbjerg, K. Nicolaides, B. M. Hansen, 2011 .

OC01.01: Prevention of preterm delivery in twin gestations (PREDICT): a multicentre randomised placebo‐controlled trial on the effect of vaginal micronised progesterone

N. Uldbjerg, K. Nicolaides, B. M. Hansen, 2011 .

Non‐invasive prenatal testing offered as part of a combined first‐trimester screening program identifies tetrasomy 18p in a high‐risk pregnancy

I. Vogel, E. Vestergaard, D. Lildballe, 2016, Prenatal diagnosis.

Testing for 22q11 microdeletion in 146 fetuses with nuchal translucency above the 99th percentile and a normal karyotype

S. Kjaergaard, C. Fagerberg, C. Lautrup, 2008, Acta obstetricia et gynecologica Scandinavica.

Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function

M. Brown, E. Duncan, A. Zankl, 2016, Scientific Reports.

Does Maternal Body Mass Index Affect the Quantity of Circulating Fetal Cells Available to Use for Cell-Based Noninvasive Prenatal Test in High-Risk Pregnancies?

N. Uldbjerg, I. Vogel, O. Petersen, 2018, Fetal Diagnosis and Therapy.

Nuchal translucency of 3.0‐3.4 mm an indication for NIPT or microarray? Cohort analysis and literature review

L. Arends, M. Knapen, I. Vogel, 2020, Acta obstetricia et gynecologica Scandinavica.

Noninvasive prenatal screening for cystic fibrosis using circulating trophoblasts: Detection of the 50 most common disease‐causing variants

I. Vogel, L. Hatt, Ripudaman Singh, 2022, Prenatal diagnosis.

Do fetal extravillous trophoblasts circulate in maternal blood postpartum?

N. Uldbjerg, I. Vogel, L. Hatt, 2020, Acta obstetricia et gynecologica Scandinavica.

Placental mosaicism in the era of chromosomal microarrays.

A. Sørensen, R. Christensen, A. Petersen, 2020, European journal of medical genetics.

Prevalence of mosaicism in uncultured chorionic villus samples after chromosomal microarray and clinical outcome in pregnancies affected by confined placental mosaicism

R. Christensen, I. Vogel, O. Petersen, 2019, Prenatal diagnosis.

Mosaicism for copy number variations in the placenta is even more difficult to interpret than mosaicism for whole chromosome aneuploidy

N. Uldbjerg, A. Petersen, I. Vogel, 2021, Prenatal diagnosis.

Cell‐based non‐invasive prenatal diagnosis in a pregnancy at risk of cystic fibrosis

N. Uldbjerg, I. Vogel, L. Hatt, 2020, Prenatal diagnosis.

Preferences for prenatal testing among pregnant women, partners and health professionals.

L. Chitty, I. Vogel, O. Petersen, 2018, Danish Medical Journal.

A flow from screening to diagnostics

I. Vogel, S. Lou, Olav Bjørn Petersen, 2022, Prenatal Genetic Counseling.

Isochromosome 21q is overrepresented among false-negative cell-free DNA prenatal screening results involving Down syndrome

E. Sistermans, M. Pertile, I. Vogel, 2018, European Journal of Human Genetics.

OC21.04: Chromosomal microarray as a primary diagnostic genomic tool for pregnancies defined as being at increased risk within a population‐based combined first trimester screening program

R. Christensen, I. Vogel, J. Hyett, 2017 .

Chromosomal microarray in fetuses with increased nuchal translucency

R. Christensen, I. Vogel, O. Petersen, 2015, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

National screening guidelines and developments in prenatal diagnoses and live births of Down syndrome in 1973–2016 in Denmark

S. Kjaergaard, I. Vogel, O. Petersen, 2018, Acta obstetricia et gynecologica Scandinavica.

"This is the child we were given": A qualitative study of Danish parents' experiences of a prenatal Down syndrome diagnosis and their decision to continue the pregnancy.

I. Vogel, S. Lou, Olav Bjørn Petersen, 2019, Sexual & reproductive healthcare : official journal of the Swedish Association of Midwives.

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

A. Pacey, G. Pennings, I. Vogel, 2023, PloS one.

Termination of pregnancy following a prenatal diagnosis of Down syndrome: A qualitative study of the decision‐making process of pregnant couples

I. Vogel, O. Petersen, S. Lou, 2018, Acta obstetricia et gynecologica Scandinavica.

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

N. Uldbjerg, L. Sunde, I. Vogel, 2023, Placenta.

No effects of human relaxin on the active and passive biomechanical properties of isolated cervical specimens from nonpregnant women.

N. Uldbjerg, I. Vogel, H. Oxlund, 1997, European journal of obstetrics, gynecology, and reproductive biology.

Isolated congenital hepatic fibrosis associated with TMEM67 mutations: report of a new genotype–phenotype relationship

S. Hamilton-Dutoit, P. Ott, H. Grønbæk, 2017, Clinical case reports.

Novel compound heterozygous mutations in TELO2 in a patient with severe expression of You‐Hoover‐Fong syndrome

R. Christensen, P. Nürnberg, Shahida Moosa, 2017, Molecular genetics & genomic medicine.

Impact of a prenatal screening program on the Down syndrome phenotype: An interrupted time series analysis

I. Vogel, S. Lou, L. Pedersen, 2023, Acta obstetricia et gynecologica Scandinavica.

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

I. Vogel, S. Lou, M. Herlin, 2023, Disability and rehabilitation.

Confirmation of CAGSSS syndrome as a distinct entity in a Danish patient with a novel homozygous mutation in IARS2

P. Nürnberg, T. Cho, Shahida Moosa, 2017, American journal of medical genetics. Part A.

Is the first‐trimester combined screening result associated with the phenotype of Down syndrome? A population‐based cohort study

I. Vogel, S. Lou, L. Pedersen, 2022, Prenatal diagnosis.

Multilocus interactions at maternal tumor necrosis factor-alpha, tumor necrosis factor receptors, interleukin-6 and interleukin-6 receptor genes predict spontaneous preterm labor in European-American women.

Scott M. Williams, M. Merialdi, B. Jacobsson, 2006, American journal of obstetrics and gynecology.

Ethnic Differences in Key Candidate Genes for Spontaneous Preterm Birth: TNF-α and Its Receptors

Scott M. Williams, B. Jacobsson, R. Menon, 2006, Human Heredity.

Screening performance for trisomy 21 comparing first trimester combined screening and a first trimester contingent screening protocol including ductus venosus and tricuspid flow

I. Vogel, A. Tabor, K. Sundberg, 2012, Prenatal diagnosis.

Preterm delivery in primiparous women at low risk: Preterm birth or delivery? Study authors suggest new terms

B. Jacobsson, J. Langhoff‐Roos, I. Vogel, 2006, British medical journal.

Second‐trimester fetal head circumference in more than 350 000 pregnancies: Outcome and suggestion for sex‐dependent cutoffs for small heads

I. Vogel, O. Petersen, P. Sandager, 2019, Prenatal Diagnosis.

"It's probably nothing, but…" Couples' experiences of pregnancy following an uncertain prenatal genetic result

K. Lomborg, I. Vogel, O. Petersen, 2020, Acta obstetricia et gynecologica Scandinavica.

A novel nonsense variant in MED12 associated with malformations in a female fetus

I. Vogel, L. Andreasen, N. Becher, 2021, Clinical case reports.

Personalized medicine for the embryo and the fetus – Options in modern genetics influence preconception and prenatal choices

B. Jacobsson, I. Vogel, U. Kesmodel, 2020, Acta obstetricia et gynecologica Scandinavica.

M. Larsen, C. Fagerberg, L. Krogh, 2019, European journal of medical genetics.

Induction of puberty with human chorionic gonadotropin (hCG) followed by reversal of hypogonadotropic hypogonadism in Kallmann syndrome.

I. Vogel, M. Robaczyk, Malgorzata M Pierzchlewska, 2015, Endokrynologia Polska.

The importance of information and support following a suspected second‐trimester anomaly that is later discarded: A qualitative study of women's experiences

I. Vogel, S. Lou, P. Sandager, 2021, Acta obstetricia et gynecologica Scandinavica.

Danish Sonographers' Experiences of the Introduction of “Moderate Risk” in Prenatal Screening for Down Syndrome

I. Vogel, O. Petersen, S. Lou, 2018, Journal of pregnancy.

Diagnostic performance of quantitative fluorescence PCR analysis in high-risk pregnancies after combined first-trimester screening.

I. Vogel, O. Petersen, E. Vestergaard, 2014, Danish medical journal.

First‐trimester maternal plasma cytokine levels, pre‐pregnancy body mass index, and spontaneous preterm delivery

D. Hougaard, W. Flanders, J. Olsen, 2009, Acta obstetricia et gynecologica Scandinavica.

Ethnic differences in key candidate genes for spontaneous preterm birth: TNF-alpha and its receptors.

Scott M. Williams, B. Jacobsson, R. Menon, 2006, Human heredity.

Metatarsal bony syndactyly in 2 fetuses with Smith‐Lemli‐Opitz syndrome: An under‐recognized part of the clinical spectrum

G. Mortier, P. Nürnberg, Shahida Moosa, 2017, Clinical genetics.

"I had to think: This is not a child." A qualitative exploration of how women/couples articulate their relation to the fetus/child following termination of a wanted pregnancy due to Down syndrome.

I. Vogel, D. Hvidtjørn, M. L. Jørgensen, 2021, Sexual & reproductive healthcare : official journal of the Swedish Association of Midwives.