Works matching DE "PRENATAL genetic testing"

Results: 480

Genetic Testing, Birth, and the Quest for Health.

Published in:

Science, Technology & Human Values, 2014, v. 39, n. 3, p. 374, doi. 10.1177/0162243913509413

By:

Vailly, Joëlle

Publication type:

Article

Informing policy for the Australian context – Costs, outcomes and cost savings of prenatal carrier screening for cystic fibrosis.

Published in:

Australian & New Zealand Journal of Obstetrics & Gynaecology, 2010, v. 50, n. 1, p. 51, doi. 10.1111/j.1479-828X.2009.01111.x

By:

MAXWELL, Susannah;
BRAMELD, Kate;
YOUNGS, Leanne;
GEELHOED, Elizabeth;
O’LEARY, Peter

Publication type:

Article

Are pregnant Australian women well informed about prenatal genetic screening? A systematic investigation using the Multidimensional Measure of Informed Choice.

Published in:

Australian & New Zealand Journal of Obstetrics & Gynaecology, 2006, v. 46, n. 5, p. 433, doi. 10.1111/j.1479-828X.2006.00630.x

By:

Rowe, Heather J.;
Fisher, Jane R. W.;
Quinlivan, Julie A.

Publication type:

Article

AUTONOMÍA DE LA VOLUNTAD Y SELECCIÓN EMBRIONARIA EN EL MARCO DE LAS TÉCNICAS DE REPRODUCCIÓN ASISTIDA.

Published in:

Revista Jurídica de la Universidad Autonóma de Madrid, 2018, n. 38, p. 317, doi. 10.15366/rjuam2018.38.011

By:

MACÍA MORILLO, ANDREA

Publication type:

Article

Response to Correspondence by Piacentini et al.

Published in:

Pediatric Cardiology, 2024, v. 45, n. 2, p. 455, doi. 10.1007/s00246-023-03369-6

By:

Kohli, Utkarsh

Publication type:

Article

The Evaluation of Fetal Cardiac Remote Screening in the Second Trimester of Pregnancy Using the Spatio-Temporal Image Correlation Method.

Published in:

Pediatric Cardiology, 2020, v. 41, n. 5, p. 979, doi. 10.1007/s00246-020-02346-7

By:

Inamura, Noboru;
Taniguchi, Takeshi;
Yamada, Tatsumi;
Tanaka, Tomohiko;
Watanabe, Ken;
Kumagaya, Ken;
Ishii, Yoichiro;
Ishii, Tsubura;
Hayashi, George;
Shiono, Nobuko;
Ikeda, Tomoaki

Publication type:

Article

The impact of third-trimester genetic counseling.

Published in:

2018

By:

Sharony, Reuven;
Engel, Offra;
Litz-Philipsborn, Shira;
Sukenik-Halevy, Rivka;
Biron-Shental, Tal;
Evans, Mark I.

Publication type:

journal article

Prenatal-screening companies expand scope of DNA tests.

Published in:

Nature, 2014, v. 507, n. 7490, p. 19, doi. 10.1038/507019a

By:

Check Hayden, Erika

Publication type:

Article

Non-invasive prenatal measurement of the fetal genome.

Published in:

Nature, 2012, v. 487, n. 7407, p. 320, doi. 10.1038/nature11251

By:

Fan, H. Christina;
Gu, Wei;
Wang, Jianbin;
Blumenfeld, Yair J.;
El-Sayed, Yasser Y.;
Quake, Stephen R.

Publication type:

Article

Internet-Based Abnormal Chromosomal Diagnosis During Pregnancy Using a Noninvasive Innovative Approach to Detecting Chromosomal Abnormalities in the Fetus: Scoping Review.

Published in:

JMIR Bioinformatics & Biotechnology, 2024, v. 5, n. 1, p. 1, doi. 10.2196/58439

By:

Oyovwi, Mega Obukohwo Sr;
Ohwin, Ejiro Peggy;
Rotu, Rume Arientare;
Olowe, Temitope Gideon

Publication type:

Article

20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey.

Published in:

Turkish Journal of Medical Sciences, 2021, v. 51, n. 4, p. 1775, doi. 10.3906/sag-2006-103

By:

DURMAZ, Burak;
BOLAT, Hilmi;
CENGİSİZ, Zehra;
AKERCAN, Fuat;
TÜRK, Tuba SÖZEN;
PARILTAY, Erhan;
SOLMAZ, Aslı Ece;
KAZANDI, Mert;
KARACA, Emin;
DURMAZ, Asude;
AYKUT, Ayça;
SAĞOL, Sermet;
AKIN, Haluk;
ÖZKINAY, Ferda;
ÇOĞULU, Özgür

Publication type:

Article

Is the management of Rh-Rh incompatibility with noninvasive fetal Rh genotyping for targeted prophylaxis cost-effective in the Turkish population?

Published in:

Turkish Journal of Medical Sciences, 2018, v. 48, n. 1, p. 1, doi. 10.3906/sag-1511-87

By:

DEMİREL, Emine;
KELEKÇİ, Sefa;
EKMEKCİ, Emre;
ŞENGÜL, Mustafa;
İRİ, Raziye;
ATASEVER, Melahat

Publication type:

Article

Genetic carrier screening in pregnancy Informing patients.

Published in:

Medicine Today, 2023, v. 24, n. 3, p. 39

By:

PARSONS, SALLY;
HAYSOM, GEORGIE

Publication type:

Article

Non-Invasive Testing, Non-Invasive Counseling.

Published in:

Journal of Law, Medicine & Ethics, 2015, v. 43, n. 2, p. 228, doi. 10.1111/jlme.12237

By:

Rebouché, Rachel

Publication type:

Article

Reproductive Information and Reproductive Decision-Making.

Published in:

Journal of Law, Medicine & Ethics, 2015, v. 43, n. 2, p. 241, doi. 10.1111/jlme.12238

By:

Mehlman, Maxwell J.

Publication type:

Article

Another Strike Against Eugenic Abortion.

Published in:

Human Life Review, 2021, v. 47, n. 4, p. 49

By:

Somarriba, Mary Rose

Publication type:

Article

An Evening with Sarah.

Published in:

Human Life Review, 2019, v. 45, n. 1, p. 85

By:

Grondelski, John

Publication type:

Article

Eugenics Triumphant in Prenatal Testing.

Published in:

Human Life Review, 2009, v. 35, n. 4, p. 87

By:

Meehan, Mary

Publication type:

Article

孕中期超声联合无创产前基因筛查在检出染色体异常胎儿中的应用价值.

Published in:

Progress in Modern Biomedicine, 2023, v. 23, n. 17, p. 3382, doi. 10.13241/j.cnki.pmb.2023.17.035

By:

孙美云;
李扬;
文晓燕;
崔照领;
焦红燕;
封露露;
李强

Publication type:

Article

Current practice and future perspective of the Prenatal Genetic Service in Slovenia.

Published in:

Paediatria Croatica, 2015, v. 59, n. 2, p. 106, doi. 10.13112/PC.2015.17

By:

Volk, Marija;
Teran, Nataša;
Maver, Aleš;
Lovrečić, Luca;
Peterlin, Borut

Publication type:

Article

Mortality in Neonatal Intensive Care Units in Iran: A Systematic Review and Meta-Analysis.

Published in:

Iranian Journal of Neonatology, 2019, v. 10, n. 3, p. 70, doi. 10.22038/ijn.2019.36647.1566

By:

Karimi, Parviz;
Mahmudi, Leily;
Azami, Milad;
Badfar, Gholamreza

Publication type:

Article

Advancing prenatal diagnosis through comprehensive fetal cell‐free DNA screening.

Published in:

Clinical & Translational Medicine, 2024, v. 14, n. 12, p. 1, doi. 10.1002/ctm2.70129

By:

Luo, Qiong;
Wu, Yanting;
Chen, Songchang;
Xu, Chenming;
Zhang, Dan;
Huang, Hefeng;
Zhang, Jinglan

Publication type:

Article

A new strategy for prenatal genetic screening of copy number variations in the DMD gene: A large cohort study based on NIPT analysis.

Published in:

Clinical & Translational Medicine, 2024, v. 14, n. 5, p. 1, doi. 10.1002/ctm2.1706

By:

Wang, Yan;
Sun, Yan;
Meng, Lulu;
He, Quanze;
Zhao, Jingyu;
Zhou, Ran;
Wang, Zhonghua;
Tan, Jianxin;
Ma, Dingyuan;
Fan, Linlin;
Chen, Yunmei;
Wang, Yuguo;
Jiang, Zhu;
Qiao, Zhihong;
Wu, Xiaojuan;
Shao, Binbin;
Xue, Ying;
Song, Lijie;
Wang, Ting;
Hu, Ping

Publication type:

Article

Targeted Sequencing and RNA Assay Reveal a Noncanonical JAG1 Splicing Variant Causing Alagille Syndrome.

Published in:

Frontiers in Genetics, 2020, v. 10, p. 1, doi. 10.3389/fgene.2019.01363

By:

Chen, Yiyao;
Liu, Xueli;
Chen, Songchang;
Zhang, Junyu;
Xu, Chenming

Publication type:

Article

Using Comparison Scenarios to Improve Prenatal Risk Communication.

Published in:

2013

By:

Pighin, Stefania;
Savadori, Lucia;
Barilli, Elisa;
Rumiati, Rino;
Bonalumi, Sara;
Ferrari, Maurizio;
Cremonesi, Laura

Publication type:

Journal Article

Testing Times Ahead: Non‐Invasive Prenatal Testing and the Kind of Community We Want to Be.

Published in:

Modern Law Review, 2018, v. 81, n. 4, p. 646, doi. 10.1111/1468-2230.12355

By:

Brownsword, Roger;
Wale, Jeff

Publication type:

Article

Expert Knowledge Influences Decision-Making for Couples Receiving Positive Prenatal Chromosomal Microarray Testing Results.

Published in:

2017

By:

Rubel, M.;
Werner-Lin, A.;
Barg, F.;
Bernhardt, B.;
Rubel, M A;
Barg, F K;
Bernhardt, B A

Publication type:

journal article

Implication of Genetic Testing and Pregnancy Outcome in a Woman with Unbalanced Translocation t(1;6).

Published in:

American Journal of Case Reports, 2022, v. 23, p. 2, doi. 10.12659/AJCR.935370

By:

Jurčenko, Marija;
Auzenbaha, Madara;
Mičule, Ieva;
Grīnfelde, Ieva;
Dzalbs, Aigars;
Mālniece, Ieva

Publication type:

Article

Hereditary Neuromuscular Disorders in Reproductive Medicine.

Published in:

Genes, 2024, v. 15, n. 11, p. 1409, doi. 10.3390/genes15111409

By:

Luglio, Agnese;
Maggi, Elena;
Riviello, Francesco Nicola;
Conforti, Alessandro;
Sorrentino, Ugo;
Zuccarello, Daniela

Publication type:

Article

Non-Invasive Prenatal Screening from a Genetic Counseling Prospective: Pre and Post-Genetic Counseling Regarding Rare Chromosomal Abnormalities and Incidental Finding.

Published in:

Genes, 2024, v. 15, n. 10, p. 1349, doi. 10.3390/genes15101349

By:

Matteo, Della Monica;
Lorenzo, Cipriano;
Raffaele, Piscopo;
Carmelo, Piscopo

Publication type:

Article

Early Non-Invasive Prenatal Testing at 6–9 Weeks of Gestation.

Published in:

Genes, 2024, v. 15, n. 7, p. 895, doi. 10.3390/genes15070895

By:

Katrachouras, Alexandros;
Kontos, Harry;
Konis, Kyriacos;
Skentou, Chara;
Makrydimas, George

Publication type:

Article

A Case Report of a Feto-Placental Mosaicism Involving a Segmental Aneuploidy: A Challenge for Genome Wide Screening by Non-Invasive Prenatal Testing of Cell-Free DNA in Maternal Plasma.

Published in:

2023

By:

De Falco, Luigia;
Vitiello, Giuseppina;
Savarese, Giovanni;
Suero, Teresa;
Ruggiero, Raffaella;
Savarese, Pasquale;
Ianniello, Monica;
Petrillo, Nadia;
Bruno, Mariasole;
Legnante, Antonietta;
Passaretti, Francesco Fioravanti;
Ardisia, Carmela;
Di Spiezio Sardo, Attilio;
Fico, Antonio

Publication type:

Case Study

Prenatal Detection of a FOXF1 Deletion in a Fetus with ACDMPV and Hydronephrosis.

Published in:

Genes, 2023, v. 14, n. 3, p. 563, doi. 10.3390/genes14030563

By:

Bzdęga, Katarzyna;
Kutkowska-Kaźmierczak, Anna;
Deutsch, Gail H.;
Plaskota, Izabela;
Smyk, Marta;
Niemiec, Magdalena;
Barczyk, Artur;
Obersztyn, Ewa;
Modzelewski, Jan;
Lipska, Iwona;
Stankiewicz, Paweł;
Gajecka, Marzena;
Rydzanicz, Małgorzata;
Płoski, Rafał;
Szczapa, Tomasz;
Karolak, Justyna A.

Publication type:

Article

Next Generation Sequencing after Invasive Prenatal Testing in Fetuses with Congenital Malformations: Prenatal or Neonatal Investigation.

Published in:

Genes, 2022, v. 13, n. 9, p. 1517, doi. 10.3390/genes13091517

By:

Emms, Alexandra;
Castleman, James;
Allen, Stephanie;
Williams, Denise;
Kinning, Esther;
Kilby, Mark

Publication type:

Article

Optical Genome Mapping as a Next-Generation Cytogenomic Tool for Detection of Structural and Copy Number Variations for Prenatal Genomic Analyses.

Published in:

Genes, 2021, v. 12, n. 3, p. 398, doi. 10.3390/genes12030398

By:

Sahajpal, Nikhil Shri;
Barseghyan, Hayk;
Kolhe, Ravindra;
Hastie, Alex;
Chaubey, Alka;
Choy, Richard

Publication type:

Article

The Pregnancy Outcome of Mosaic Embryo Transfer: A Prospective Multicenter Study and Meta-Analysis.

Published in:

Genes, 2020, v. 11, n. 9, p. 973, doi. 10.3390/genes11090973

By:

Zhang, Ying Xin;
Chen, Jang Jih;
Nabu, Sunanta;
Yeung, Queenie Sum Yee;
Li, Ying;
Tan, Jia Hui;
Suksalak, Wanwisa;
Chanchamroen, Sujin;
Quangkananurug, Wiwat;
Wong, Pak Seng;
Chung, Jacqueline Pui Wah;
Choy, Kwong Wai

Publication type:

Article

Non-invasive prenatal testing: a review of international implementation and challenges.

Published in:

International Journal of Women's Health, 2015, v. 7, p. 113, doi. 10.2147/IJWH.S67124

By:

Allyse, Megan;
Minear, Mollie A.;
Berson, Elisa;
Sridhar, Shilpa;
Rote, Margaret;
Hung, Anthony;
Chandrasekharan, Subhashini

Publication type:

Article

She Has Her Mother's Laugh: The Powers, Perversions, and Potential of Heredity.

Published in:: Journal of the Association of Genetic Technologists, 2019, v. 45, n. 2, p. 81
Publication type:: Article

Novel Application of HDlive Silhouette and HDliveFlow: Clinical Significance of the 'See-through Fashion' in Prenatal Diagnosis.

Published in:

Donald School Journal of Ultrasound in Obstetrics & Gynecology, 2016, v. 10, n. 1, p. 90, doi. 10.5005/jp-journals-10009-1447

By:

Pooh, Ritsuko K.

Publication type:

Article

Patient Decision Aids for Prenatal Genetic Testing: Probability, Embodiment, and Problematic Integration.

Published in:

Health Communication, 2017, v. 32, n. 5, p. 568, doi. 10.1080/10410236.2016.1140500

By:

Kirkscey, Russell

Publication type:

Article

Indications, types, and diagnostic implications of prenatal genetic testing in Sub-Saharan Africa: A descriptive study.

Published in:

PLoS ONE, 2023, v. 18, n. 11, p. 1, doi. 10.1371/journal.pone.0294409

By:

Sium, Abraham Fessehaye;
Shimels, Tariku;
Abdosh, Abdulfetah Abdulkadir;
Diress, Tesfaye;
Tsegaye, Tigist;
Yifrashewa, Tizibt;
Terefework, Zewdu;
Gudu, Wondimu

Publication type:

Article

Biobanks: Challenges for ‘ethics’.

Published in:

2005

By:

Petersen, Alan

Publication type:

Editorial

The SafeBirth Clinic.

Published in:

INFORMS Transactions on Education, 2021, v. 22, n. 1, p. 148, doi. 10.1287/ited.2019.0241cs

By:

Dawande, Milind;
Huh, Woonghee Tim;
Janakiraman, Ganesh;
Nagarajan, Mahesh;
Bo, Yang

Publication type:

Article

Prenatal karyotype results from 2169 invasive tests.

Published in:

Ginekologia Polska, 2023, v. 94, n. 11, p. 1, doi. 10.5603/GP.a2022.0143

By:

Moczulska, Hanna;
Chrzanowska-Steglinska, Marta;
Skoczylas, Beata;
Wojda, Katarzyna;
Borowiec, Maciej;
Sieroszewski, Piotr

Publication type:

Article

Increased risk of low infant birth weight in pregnant women with low PAPP-A values measured in the first trimester.

Published in:

Ginekologia Polska, 2023, v. 94, n. 9, p. 714, doi. 10.5603/GP.a2022.0118

By:

Krawczyk, Jozef;
Ratajczak, Piotr;
Sajdak, Stefan

Publication type:

Article

Strategies to improve early diagnosis of Klinefelter syndrome.

Published in:

2020

By:

Ferlin, Alberto

Publication type:

Editorial

Identification of MicroRNA Profiles in Fetal Spina Bifida: The Role in Pathomechanism and Diagnostic Significance.

Published in:

International Journal of Molecular Sciences, 2024, v. 25, n. 5, p. 2896, doi. 10.3390/ijms25052896

By:

Buczyńska, Angelika;
Sidorkiewicz, Iwona;
Niemira, Magdalena;
Krętowski, Adam Jacek;
Węgrzyn, Piotr;
Kosiński, Przemysław;
Zbucka-Krętowska, Monika

Publication type:

Article

Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing.

Published in:

International Journal of Molecular Sciences, 2017, v. 18, n. 2, p. 453, doi. 10.3390/ijms18020453

By:

Xianlu Laura Peng;
Peiyong Jiang

Publication type:

Article

Experience in prenatal genetic testing and reproductive decision-making for monogenic disorders from a single tertiary care genetics clinic in a low-middle income country.

Published in:

BMC Pregnancy & Childbirth, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12884-023-05698-z

By:

Hanif, Amna;
Akbar, Fizza;
Kirmani, Salman;
Jaffarali, Amyna;
Zainab, Ghulam;
Malik, Ayesha;
Ansar, Zeeshan;
Afroze, Bushra

Publication type:

Article

Fetal genetic findings by chromosomal microarray analysis and karyotyping for fetal growth restriction without structural malformations at a territory referral center: 10-year experience.

Published in:

BMC Pregnancy & Childbirth, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12884-023-05394-y

By:

Wu, Xiaoqing;
He, Shuqiong;
Li, Ying;
Guo, Danhua;
Chen, Xuemei;
Liang, Bin;
Wang, Meiying;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article