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Update on noninvasive prenatal testing: A review based on current worldwide research

The journal of obstetrics and gynaecology research, 2020-08, Vol.46 (8), p.1246-1254

Samura, Osamu

2020

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A commentary on comparison of the performance of Ion Torrent chips in noninvasive prenatal trisomy detection

Journal of human genetics, 2014-08, Vol.59 (8), p.421-422

Samura, Osamu

2014

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Autonomous trisomic rescue of Down syndrome cells

Laboratory investigation, 2019-06, Vol.99 (6), p.885-897

2019

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Utilizing Repetitive Serial Placental Ultrasounds for Diagnosing a Massive Subchorionic Thrombohematoma: Insights Into Soluble FMS-Like Tyrosine Kinase-1/Placental Growth Factor (sFlt-1/PlGF) Trends

Curēus (Palo Alto, CA), 2024-07

2024

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Pure preeclampsia at 16 weeks of gestation with an increasing trend of sFlt-1/PlGF ratio: A case report and literature review

Hypertension research in pregnancy, 2023-11, Vol.11 (4), p.63-67, Article HRP2023-004

2023

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Socioeconomic inequity in survival for deliveries at 22-24 weeks of gestation

Archives of disease in childhood. Fetal and neonatal edition, 2018-05, Vol.103 (3), p.F202-F207

2018

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Maternal age-specific risk for trisomy 21 based on the clinical performance of NIPT and empirically derived NIPT age-specific positive and negative predictive values in Japan

Journal of human genetics, 2018-10, Vol.63 (10), p.1035-1040

2018

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Spontaneously conceived heterotopic pregnancy with abdominal pregnancy implanted on the vesicouterine pouch: A case report and literature review

The journal of obstetrics and gynaecology research, 2021-10, Vol.47 (10), p.3720-3726

2021

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Novel gross deletion mutation c.‐105_4042+498del in the TNXB gene in a Japanese woman with classical‐like Ehlers–Danlos syndrome: A case of uneventful pregnancy and delivery

Journal of dermatology, 2021-05, Vol.48 (5), p.e227-e228

2021

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Retrospective details of false-positive and false-negative results in non-invasive prenatal testing for fetal trisomies 21, 18 and 13

European journal of obstetrics & gynecology and reproductive biology, 2021-01, Vol.256, p.75-81

2021

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Direct Assessment of Single-Cell DNA Using Crudely Purified Live Cells: A Proof of Concept for Noninvasive Prenatal Definitive Diagnosis

The Journal of molecular diagnostics : JMD, 2020-02, Vol.22 (2), p.132-140

2020

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Novel missense COL2A1 variant in a fetus with achondrogenesis type II

Human genome variation, 2022-11, Vol.9 (1), p.40-40, Article 40

2022

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Missense BICD2 variants in fetuses with congenital arthrogryposis and pterygia

Human genome variation, 2024-08, Vol.11 (1), p.32-4

2024

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Alteration of circulating cell‐free DNA level by external cephalic version: A potential biomarker for direct evaluation of placental damage

The journal of obstetrics and gynaecology research, 2021-09, Vol.47 (9), p.3144-3150

2021

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Study on pregnancy after radical trachelectomy in our hospital

Journal of Japan Society of Perinatal and Neonatal Medicine, 2020, Vol.56(1), pp.90-95

2020

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Restoration of keratinocytic phenotypes in autonomous trisomy-rescued cells

Stem cell research & therapy, 2021-08, Vol.12 (1), p.1-476, Article 476

2021

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A Case of Uterine Necrosis after Uterine Artery Embolization for Postpartum Hemorrhage

Journal of Japan Society of Perinatal and Neonatal Medicine, 2023, Vol.59(2), pp.277-281

2023

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Spontaneous Remission of Sick Sinus Syndrome in a Fetus with Pulmonary Stenosis Regurgitation

American journal of perinatology reports, 2019-10, Vol.9 (4), p.e372-e375

2019

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Microchimerism of presumed fetal origin in thyroid specimens from women: a case-control study

The Lancet (British edition), 2001-12, Vol.358 (9298), p.2034-2038

2001

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Factors affecting parental decisions to terminate pregnancy in the presence of chromosome abnormalities: a Japanese multicenter study

Prenatal diagnosis, 2016-12, Vol.36 (12), p.1121-1126

2016

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Correction: Maternal age-specific risk for trisomy 21 based on the clinical performance of NIPT and empirically derived NIPT age-specific positive and negative predictive values in Japan

Journal of human genetics, 2018-10, Vol.63 (10), p.1097-1098

2018

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Pregnancy Outcome and Postnatal Chromosome Analysis of the Cord Blood and Chorionic Villi in Two Cases after Intrauterine Transfer of Mosaic Aneuploid Blastocysts

Case reports in obstetrics and gynecology, 2022-07, Vol.2022, p.1-6

2022

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Preface

Placenta (Eastbourne), 2019-09, Vol.84, p.2-3

2019

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Investigation of mental care required for pregnant women affected by COVID-19

Journal of Japan Society of Perinatal and Neonatal Medicine, 2022, Vol.58(3), pp.504-509

2022

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Novel TFAP2A mutation in a Japanese family with Branchio-oculo-facial syndrome

Human genome variation, 2018-01, Vol.5 (1), p.5-5, Article 5

2018

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Update on noninvasive prenatal testing: A review based on current worldwide research

A commentary on comparison of the performance of Ion Torrent chips in noninvasive prenatal trisomy detection

Autonomous trisomic rescue of Down syndrome cells

Utilizing Repetitive Serial Placental Ultrasounds for Diagnosing a Massive Subchorionic Thrombohematoma: Insights Into Soluble FMS-Like Tyrosine Kinase-1/Placental Growth Factor (sFlt-1/PlGF) Trends

Pure preeclampsia at 16 weeks of gestation with an increasing trend of sFlt-1/PlGF ratio: A case report and literature review

Socioeconomic inequity in survival for deliveries at 22-24 weeks of gestation

Maternal age-specific risk for trisomy 21 based on the clinical performance of NIPT and empirically derived NIPT age-specific positive and negative predictive values in Japan

Spontaneously conceived heterotopic pregnancy with abdominal pregnancy implanted on the vesicouterine pouch: A case report and literature review

Novel gross deletion mutation c.‐105_4042+498del in the TNXB gene in a Japanese woman with classical‐like Ehlers–Danlos syndrome: A case of uneventful pregnancy and delivery

Retrospective details of false-positive and false-negative results in non-invasive prenatal testing for fetal trisomies 21, 18 and 13

Direct Assessment of Single-Cell DNA Using Crudely Purified Live Cells: A Proof of Concept for Noninvasive Prenatal Definitive Diagnosis

Novel missense COL2A1 variant in a fetus with achondrogenesis type II

Missense BICD2 variants in fetuses with congenital arthrogryposis and pterygia

Alteration of circulating cell‐free DNA level by external cephalic version: A potential biomarker for direct evaluation of placental damage

Study on pregnancy after radical trachelectomy in our hospital

Restoration of keratinocytic phenotypes in autonomous trisomy-rescued cells

A Case of Uterine Necrosis after Uterine Artery Embolization for Postpartum Hemorrhage

Spontaneous Remission of Sick Sinus Syndrome in a Fetus with Pulmonary Stenosis Regurgitation

Microchimerism of presumed fetal origin in thyroid specimens from women: a case-control study

Factors affecting parental decisions to terminate pregnancy in the presence of chromosome abnormalities: a Japanese multicenter study

Correction: Maternal age-specific risk for trisomy 21 based on the clinical performance of NIPT and empirically derived NIPT age-specific positive and negative predictive values in Japan

Pregnancy Outcome and Postnatal Chromosome Analysis of the Cord Blood and Chorionic Villi in Two Cases after Intrauterine Transfer of Mosaic Aneuploid Blastocysts

Preface

Investigation of mental care required for pregnant women affected by COVID-19

Novel TFAP2A mutation in a Japanese family with Branchio-oculo-facial syndrome

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