Works matching DE "PRENATAL genetic testing"

Results: 513

Prenatal diagnosis following preimplantation genetic testing for monogenic conditions: a single centre record linkage study.

Published in:

Journal of Assisted Reproduction & Genetics, 2025, v. 42, n. 1, p. 275, doi. 10.1007/s10815-024-03346-9

By:

Poulton, Alice;
Menezes, Melody;
Hardy, Tristan;
Lewis, Sharon;
Hui, Lisa

Publication type:

Article

What to advise to patients with only one good quality blastocyst, PGT-A or not? Outcomes of 2064 cycles.

Published in:

Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 3, p. 691, doi. 10.1007/s10815-023-02731-0

By:

Orvieto, Raoul;
Gleicher, Norbert;
Patrizio, Pasquale

Publication type:

Article

Down syndrome live births following assisted reproductive technology in Japan: a nationwide survey between 2007 and 2016.

Published in:

Journal of Assisted Reproduction & Genetics, 2022, v. 39, n. 7, p. 1625, doi. 10.1007/s10815-022-02501-4

By:

Jwa, Seung Chik;
Namba, Akira;
Tamaru, Shunsuke;
Kuwahara, Akira;
Sago, Haruhiko;
Ishihara, Osamu;
Kamei, Yoshimasa

Publication type:

Article

Genetic counseling decisions in gestational carrier pregnancies.

Published in:

Journal of Assisted Reproduction & Genetics, 2022, v. 39, n. 6, p. 1249, doi. 10.1007/s10815-022-02483-3

By:

Rasouli, Melody A.;
Roberts, Hailey E.;
Jackson, David N.

Publication type:

Article

Reproductive outcomes after preimplantation genetic testing in mosaic Turner syndrome: a retrospective cohort study of 100 cycles.

Published in:

Journal of Assisted Reproduction & Genetics, 2021, v. 38, n. 5, p. 1247, doi. 10.1007/s10815-021-02127-y

By:

Liao, Jingnan;
Luo, Keli;
Cheng, Dehua;
Xie, Pingyuan;
Tan, Yueqiu;
Hu, Liang;
Lu, Guangxiu;
Gong, Fei;
Lin, Ge

Publication type:

Article

Association between growth dynamics, morphological parameters, the chromosomal status of the blastocysts, and clinical outcomes in IVF PGS cycles with single embryo transfer.

Published in:

Journal of Assisted Reproduction & Genetics, 2017, v. 34, n. 8, p. 1007, doi. 10.1007/s10815-017-0944-0

By:

Barash, Oleksii;
Ivani, Kristen;
Willman, Susan;
Rosenbluth, Evan;
Wachs, Deborah;
Hinckley, Mary;
Pittenger Reid, Sara;
Weckstein, Louis

Publication type:

Article

Complex chromosomal rearrangement-a lesson learned from PGS.

Published in:

Journal of Assisted Reproduction & Genetics, 2017, v. 34, n. 8, p. 1095, doi. 10.1007/s10815-017-0954-y

By:

Frumkin, Tsvia;
Peleg, Sagit;
Gold, Veronica;
Reches, Adi;
Asaf, Shiri;
Azem, Foad;
Ben-Yosef, Dalit;
Malcov, Mira

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

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

Patients' preimplantation genetic testing decision-making experience: an opinion on related psychological frameworks.

Published in:

Human Reproduction Open, 2019, v. 2019, n. 4, p. N.PAG, doi. 10.1093/hropen/hoz019

By:

Pastore, L M;
Mitchell, C N Cordeiro;
Rubin, L R;
Nicoloro-SantaBarbara, J;
Garzon, M C Genoff;
Lobel, M

Publication type:

Article

Comparison of next-generation sequencing and Oxford nanopore technology for noninvasive prenatal testing in thalassemia screening: a comprehensive review.

Published in:

Egyptian Journal of Haematology, 2025, v. 50, n. 1, p. 1, doi. 10.4103/ejh.ejh_36_24

By:

Ali, Abdirasak Sharif;
Mirghani, Leena B.

Publication type:

Article

Analysis of Attitude of Public Towards Prenatal Screening for Diagnosis of Genetic Disorders.

Published in:

Egyptian Academic Journal of Biological Sciences. B, Zoology, 2023, v. 15, n. 1, p. 287, doi. 10.21608/EAJBSZ.2023.306575

By:

Shoba, S. Prakash;
Anusha, V. Princy;
Varshaa, T. B.;
Anitha, C.

Publication type:

Article

Reproductive Genetic Testing and Human Genetic Variation in the Era of Genomic Medicine.

Published in:

2015

By:

Lowther, Chelsea;
Costain, Gregory;
Bassett, Anne S.

Publication type:

Opinion

Genetic Testing of Children: The Need for a Family Perspective.

Published in:

American Journal of Bioethics, 2014, v. 14, n. 3, p. 26, doi. 10.1080/15265161.2013.879950

By:

Lucassen, Anneke;
Widdershoven, Guy;
Metselaar, Suzanne;
Fenwick, Angela;
Parker, Michael

Publication type:

Article

Critically Appraising Prenatal Genetic Diagnosis to Prevent Disorders of Sexual Development: An Opportunity Missed.

Published in:

2013

By:

McCullough, LaurenceB.

Publication type:

Editorial

Prenatal genetic screening for intellectual disability.

Published in:

Journal of Intellectual Disability Research, 2003, v. 47, n. 7, p. 526, doi. 10.1046/j.1365-2788.2003.00531.x

By:

Edwards, S. D.

Publication type:

Article

Identity, difference and the ethical politics of prenatal testing.

Published in:

Journal of Intellectual Disability Research, 2003, v. 47, n. 7, p. 533, doi. 10.1046/j.1365-2788.2003.00532.x

By:

Stainton, T.

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

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

Prenatal Genetic Testing in the Era of Next Generation Sequencing: A One-Center Canadian Experience.

Published in:

Genes, 2022, v. 13, n. 11, p. 2019, doi. 10.3390/genes13112019

By:

Almubarak, Asra;
Zhang, Dan;
Kosak, Mackenzie;
Rathwell, Sarah;
Doonanco, Jasmine;
Eaton, Alison J.;
Kannu, Peter;
Lazier, Joanna;
Lui, Monique;
Niederhoffer, Karen Y.;
MacPherson, Melissa J.;
Sorsdahl, Melissa;
Caluseriu, Oana

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

The Turnaway Study: Ten Years, a Thousand Women, and the Consequences of Having—or Being Denied—an Abortion by Diana Green Foster.

Published in:

2021

By:

MacKay, Kathryn

Publication type:

Book Review

Foucault and Feminist Philosophy of Disability.

Published in:

2020

By:

Violet, Tabetha K.

Publication type:

Book Review

Attitudes toward genetic testing in childhood and reproductive decision-making for familial adenomatous polyposis.

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 2, p. 186, doi. 10.1038/ejhg.2009.151

By:

Douma, Kirsten F. L.;
Aaronson, Neil K.;
Vasen, Hans F. A.;
Verhoef, Senno;
Gundy, Chad M.;
Bleiker, Eveline M. A.

Publication type:

Article

When good CF tests go bad.

Published in:

2009

By:

Devitt, Trudi Mc;
Barton, David

Publication type:

Opinion

Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in Israel.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 2, p. 250, doi. 10.1038/sj.ejhg.5201750

By:

Basel-Vanagaite, Lina;
Taub, Ellen;
Halpern, Gabrielle J.;
Drasinover, Valerie;
Magal, Nurit;
Davidov, Bella;
Zlotogora, Joël;
Shohat, Mordechai

Publication type:

Article

Genetic testing in Italy, year 2004.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 8, p. 911, doi. 10.1038/sj.ejhg.5201653

By:

Dallapiccola, Bruno;
Torrente, Isabella;
Morena, Arnaldo;
Dagna-Bricarelli, Franca;
Mingarelli, Rita

Publication type:

Article

Genetic Testing: From chromosomes to DNA, a revolution in prenatal diagnosis.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 5, p. 517, doi. 10.1038/sj.ejhg.5201327

By:

Breuning, Martijn H.

Publication type:

Article

Genetic tool used to diagnose achromatopsia: first case report from India.

Published in:

Egyptian Journal of Medical Human Genetics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s43042-023-00420-2

By:

Pritti, Kumari;
Mishra, Vineet;
Kotecha, Udhaya;
Aggarwal, Somesh

Publication type:

Article

Prenatal diagnosis of 4953 pregnant women with indications for genetic amniocentesis in Northeast China.

Published in:

Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0457-x

By:

Dai, Rulin;
Yu, Yang;
Xi, Qi;
Hu, Xiaonan;
Zhu, Haibo;
Liu, Ruizhi;
Wang, Ruixue

Publication type:

Article

A foetus with 18p11.32-q21.2 duplication and Xp22.33-p11.1 deletion derived from a maternal reciprocal translocation t(X;18)(q13;q21.3).

Published in:

2018

By:

Chen, Jun-Kun;
Liu, Ping;
Hu, Li-Qin;
Xie, Qing;
Huang, Quan-Fei;
Liu, Hai-Liang

Publication type:

Case Study

Expanding preconception carrier screening for the Jewish population using high throughput microfluidics technology and next generation sequencing.

Published in:

BMC Medical Genomics, 2016, v. 9, p. 1, doi. 10.1186/s12920-016-0184-7

By:

Gal, Moran;
Khermesh, Khen;
Michal Barak;
Min Lin;
Lahat, Hadas;
Reznik Wolf, Haike;
Lin, Michael;
Pras, Elon;
Levanon, Erez Y.

Publication type:

Article

NEW EUGENICS IN LIGHT OF INTERNATIONAL HUMAN RIGHTS PROTECTION.

Published in:

Review of International Affairs (04866096), 2019, v. 70, n. 1175, p. 5

By:

ĐUKANOVIĆ, Anđela

Publication type:

Article

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

Competition intensifies over DNA-based tests for prenatal diagnoses.

Published in:

Nature Medicine, 2013, v. 19, n. 4, p. 381, doi. 10.1038/nm0413-381

By:

Jiang, Kevin

Publication type:

Article

Community Corner: Opening the Pandora's box of prenatal genetic testing.

Published in:: Nature Medicine, 2011, v. 17, n. 3, p. 250, doi. 10.1038/nm0311-250
Publication type:: Article

45,X product of conception after preimplantation genetic diagnosis and euploid embryo transfer: evidence of a spontaneous conception confirmed by DNA fingerprinting.

Published in:

Reproductive Biology & Endocrinology, 2016, v. 14, p. 1, doi. 10.1186/s12958-016-0190-9

By:

Bettio, Daniela;
Capalbo, Antonio;
Albani, Elena;
Rienzi, Laura;
Achille, Valentina;
Venci, Anna;
Ubaldi, Filippo Maria;
Levi Setti, Paolo Emanuele

Publication type:

Article

Accuracy of preimplantation genetic screening (PGS) is compromised by degree of mosaicism of human embryos.

Published in:

Reproductive Biology & Endocrinology, 2016, v. 14, p. 1, doi. 10.1186/s12958-016-0193-6

By:

Gleicher, Norbert;
Vidali, Andrea;
Braverman, Jeffrey;
Kushnir, Vitaly A.;
Barad, David H.;
Hudson, Cynthia;
Yang-Guan Wu;
Qi Wang;
Lin Zhang;
Albertini, David F.

Publication type:

Article

Use of a patient decision aid for prenatal screening for Down syndrome: what do pregnant women say?

Published in:

2017

By:

Leiva Portocarrero, Maria Esther;
Giguère, Anik M. C.;
Lépine, Johanie;
Garvelink, Mirjam M.;
Robitaille, Hubert;
Delanoë, Agathe;
Lévesque, Isabelle;
Wilson, Brenda J.;
Rousseau, François;
Légaré, France;
Portocarrero, Maria Esther Leiva

Publication type:

journal article

Prenatally Diagnosed Hemophilia in a Newborn: a Case Report.

Published in:

Fetal & Pediatric Pathology, 2015, v. 34, n. 4, p. 248, doi. 10.3109/15513815.2015.1051250

By:

Jovandaric, Miljana Zivojin;
Jesic, Milos M.

Publication type:

Article

Non‐invasive prenatal testing: clinical utility and ethical concerns about recent advances.

Published in:

Medical Journal of Australia, 2021, v. 215, n. 8, p. 384, doi. 10.5694/mja2.51277

By:

McLean, Alison;
Wu, Kathy

Publication type:

Article

Non‐invasive prenatal testing: clinical utility and ethical concerns about recent advances.

Published in:

Medical Journal of Australia, 2021, v. 215, n. 8, p. 384, doi. 10.5694/mja2.51283

By:

Liley, Helen G;
Peek, Michael J;
Daly, James

Publication type:

Article