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Patient attitudes and preferences about expanded noninvasive prenatal testing

Frontiers in genetics, 2023-04, Vol.14, p.976051-976051

2023

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Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomes

Frontiers in genetics, 2022-08, Vol.13, p.975987-975987

2022

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Clinical outcomes of screen-positive genome-wide cfDNA cases for trisomy 20: results from the global expanded NIPT Consortium

Molecular cytogenetics, 2024-04, Vol.17 (1), p.9-9, Article 9

2024

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Use of cell-free signals as biomarkers for early and easy prediction of preeclampsia

Frontiers in medicine, 2023-05, Vol.10, p.1191163-1191163

2023

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Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations

American journal of medical genetics. Part A, 2016-04, Vol.170A (4), p.896-907

2016

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Amniotic stem cells for cellular cardiomyoplasty: Promises and premises

Catheterization and cardiovascular interventions, 2009-06, Vol.73 (7), p.917-924

2009

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Cost-effectiveness and accuracy of prenatal Down syndrome screening strategies: should the combined test continue to be widely used?

American journal of obstetrics and gynecology, 2011-02, Vol.204 (2), p.175.e1-175.e8

2011

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Myoblasts Derived From Normal hESCs and Dystrophic hiPSCs Efficiently Fuse With Existing Muscle Fibers Following Transplantation

Molecular therapy, 2012-11, Vol.20 (11), p.2153-2167

2012

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eP473: Patient attitudes and preferences about expanded noninvasive prenatal screening

Genetics in medicine, 2022-03, Vol.24 (3), p.S300-S300

2022

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Current perspectives on the etiology of agnathia-otocephaly

European journal of medical genetics, 2010-11, Vol.53 (6), p.358-366

2010

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Prospective head-to-head comparison of accuracy of two sequencing platforms for screening for fetal aneuploidy by cell-free DNA: the PEGASUS study

European journal of human genetics : EJHG, 2019-11, Vol.27 (11), p.1701-1715

2019

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Cell-Free DNA–Based Non-invasive Prenatal Screening for Common Aneuploidies in a Canadian Province: A Cost-Effectiveness Analysis

Journal of obstetrics and gynaecology Canada, 2018-01, Vol.40 (1), p.48-60

2018

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Juvenile myelomonocytic leukemia-associated variants are associated with neo-natal lethal Noonan syndrome

European journal of human genetics : EJHG, 2017-04, Vol.25 (4), p.509-511

2017

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Comparison of first‐tier cell‐free DNA screening for common aneuploidies with conventional publically funded screening

Prenatal diagnosis, 2017-12, Vol.37 (12), p.1238-1244

2017

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Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues

Application of clinical genetics, 2016-01, Vol.9 (Issue 1), p.15-26

2016

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Rapid testing versus karyotyping in Down's syndrome screening: cost-effectiveness and detection of clinically significant chromosome abnormalities

European journal of human genetics : EJHG, 2011-01, Vol.19 (1), p.3-9

2011

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Recurrent anencephaly: A case report and examination of the VANGL1 and FOXN1 genes

Fetal and pediatric pathology, 2013-07, Vol.32 (4), p.293-297

2013

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Holoprosencephaly-Polydactyly (Pseudotrisomy 13) Syndrome: Case Report and Diagnostic Criteria

Fetal and pediatric pathology, 2012-10, Vol.31 (5), p.315-318

2012

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Cerebro-costo-mandibular syndrome in a father and a female fetus: early prenatal ultrasonographic diagnosis and autosomal dominant transmission

Prenatal diagnosis, 2001-10, Vol.21 (10), p.890-893

2001

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Midtrimester intra-amniotic sludge and the risk of spontaneous preterm birth

American journal of perinatology, 2011-12, Vol.28 (10), p.815

2011

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In vitro and in vivo study of human amniotic fluid-derived stem cell differentiation into myogenic lineage

Clinical and experimental medicine, 2010-03, Vol.10 (1), p.1-6

2010

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Clinical validity of karyotyping for the diagnosis of chromosomal imbalance following array comparative genomic hybridisation

Journal of medical genetics, 2011-12, Vol.48 (12), p.851-855

2011

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PRENATAL DIAGNOSIS AND MOLECULAR GENETIC STUDIES ON A NEW CASE OF AGNATHIA-OTOCEPHALY

Fetal and pediatric pathology, 2010-01, Vol.29 (4), p.207-211

2010

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Molecular prenatal diagnosis of a sporadic alobar holoprosencephalic fetus: genotype-phenotype correlations

Journal of prenatal medicine, 2012-07, Vol.6 (3), p.36-39

2012

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Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma

Application of clinical genetics, 2014-01, Vol.7 (default), p.127-131

2014

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Patient attitudes and preferences about expanded noninvasive prenatal testing

Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomes

Clinical outcomes of screen-positive genome-wide cfDNA cases for trisomy 20: results from the global expanded NIPT Consortium

Use of cell-free signals as biomarkers for early and easy prediction of preeclampsia

Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations

Amniotic stem cells for cellular cardiomyoplasty: Promises and premises

Cost-effectiveness and accuracy of prenatal Down syndrome screening strategies: should the combined test continue to be widely used?

Myoblasts Derived From Normal hESCs and Dystrophic hiPSCs Efficiently Fuse With Existing Muscle Fibers Following Transplantation

eP473: Patient attitudes and preferences about expanded noninvasive prenatal screening

Current perspectives on the etiology of agnathia-otocephaly

Prospective head-to-head comparison of accuracy of two sequencing platforms for screening for fetal aneuploidy by cell-free DNA: the PEGASUS study

Cell-Free DNA–Based Non-invasive Prenatal Screening for Common Aneuploidies in a Canadian Province: A Cost-Effectiveness Analysis

Juvenile myelomonocytic leukemia-associated variants are associated with neo-natal lethal Noonan syndrome

Comparison of first‐tier cell‐free DNA screening for common aneuploidies with conventional publically funded screening

Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues

Rapid testing versus karyotyping in Down's syndrome screening: cost-effectiveness and detection of clinically significant chromosome abnormalities

Recurrent anencephaly: A case report and examination of the VANGL1 and FOXN1 genes

Holoprosencephaly-Polydactyly (Pseudotrisomy 13) Syndrome: Case Report and Diagnostic Criteria

Cerebro-costo-mandibular syndrome in a father and a female fetus: early prenatal ultrasonographic diagnosis and autosomal dominant transmission

Midtrimester intra-amniotic sludge and the risk of spontaneous preterm birth

In vitro and in vivo study of human amniotic fluid-derived stem cell differentiation into myogenic lineage

Clinical validity of karyotyping for the diagnosis of chromosomal imbalance following array comparative genomic hybridisation

PRENATAL DIAGNOSIS AND MOLECULAR GENETIC STUDIES ON A NEW CASE OF AGNATHIA-OTOCEPHALY

Molecular prenatal diagnosis of a sporadic alobar holoprosencephalic fetus: genotype-phenotype correlations

Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma

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