Works matching IS 01973851 AND DT 2022 AND VI 42 AND IP 6

Results: 16

Implementing a rapid fetal exome sequencing service: What do parents and health professionals think?

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 6, p. 783, doi. 10.1002/pd.6140

By:

Mellis, Rhiannon;
Tapon, Dagmar;
Shannon, Nora;
Dempsey, Esther;
Pandya, Pranav;
Chitty, Lyn S.;
Hill, Melissa

Publication type:

Article

Cover Image.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 6, p. i, doi. 10.1002/pd.6198

By:

Liu, Pengfei;
Vossaert, Liesbeth

Publication type:

Article

International Society for Prenatal Diagnosis Updated Position Statement on the use of genome-wide sequencing for prenatal diagnosis.

Published in:

2022

By:

Van den Veyver, Ignatia B.;
Chandler, Natalie;
Wilkins‐Haug, Louise E.;
Wapner, Ronald J.;
Chitty, Lyn S.;
Wilkins-Haug, Louise E;
ISPD Board of Directors

Publication type:

journal article

Prenatal exomes and genomes - so much new and so much more to learn.

Published in:

2022

By:

Van den Veyver, Ignatia B

Publication type:

Editorial

Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: A systematic review and meta‐analysis.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 6, p. 662, doi. 10.1002/pd.6115

By:

Mellis, Rhiannon;
Oprych, Kathryn;
Scotchman, Elizabeth;
Hill, Melissa;
Chitty, Lyn S

Publication type:

Article

Parental motivations for and adaptation to trio‐exome sequencing in a prospective prenatal testing cohort: Beyond the diagnosis.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 6, p. 775, doi. 10.1002/pd.6112

By:

Talati, Asha N.;
Gilmore, Kelly L.;
Hardisty, Emily E.;
Lyerly, Anne D.;
Rini, Christine;
Vora, Neeta L.

Publication type:

Article

Emerging technologies for prenatal diagnosis: The application of whole genome and RNA sequencing.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 6, p. 686, doi. 10.1002/pd.6146

By:

Liu, Pengfei;
Vossaert, Liesbeth

Publication type:

Article

Fetal central nervous system anomalies: When should we offer exome sequencing?

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 6, p. 736, doi. 10.1002/pd.6145

By:

Baptiste, Caitlin;
Mellis, Rhiannon;
Aggarwal, Vimla;
Lord, Jenny;
Eberhardt, Ruth;
Kilby, Mark D.;
Maher, Eamonn R.;
Wapner, Ronald;
Giordano, Jessica;
Chitty, Lyn

Publication type:

Article

Prenatal exome sequencing in fetuses with callosal anomalies.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 6, p. 744, doi. 10.1002/pd.6107

By:

Lei, Ting‐ying;
She, Qin;
Fu, Fang;
Zhen, Li;
Li, Ru;
Yu, Qiu‐xia;
Wang, Dan;
Li, Ying‐si;
Cheng, Ken;
Zhou, Hang;
Yang, Xin;
Pan, Min;
Li, Dong‐zhi;
Liao, Can

Publication type:

Article

Retrospective identification of prenatal fetal anomalies associated with diagnostic neonatal genomic sequencing results.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 6, p. 705, doi. 10.1002/pd.6111

By:

Zhang‐Rutledge, Kathy;
Owen, Mallory;
Sweeney, Nathaly M.;
Dimmock, David;
Kingsmore, Stephen F.;
Laurent, Louise C.

Publication type:

Article

The prevalence of prenatal sonographic findings in postnatal diagnostic exome sequencing performed for neurocognitive phenotypes: A cohort study.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 6, p. 717, doi. 10.1002/pd.6095

By:

Sukenik‐Halevy, Rivka;
Perlman, Sharon;
Ruhrman‐Shahar, Noa;
Engel, Offra;
Orenstein, Naama;
Gonzaga‐Jauregui, Claudia;
Shuldiner, Alan R.;
Magal, Nurit;
Hagari, Ofir;
Azulay, Noy;
Lidzbarsky, Gabriel Arie;
Bazak, Lily;
Basel‐Salmon, Lina

Publication type:

Article

A framework for reporting secondary and incidental findings in prenatal sequencing: When and for whom?

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 6, p. 697, doi. 10.1002/pd.6097

By:

Vears, Danya;
Amor, David J.

Publication type:

Article

Parental experiences of rapid exome sequencing in cases with major ultrasound anomalies during pregnancy.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 6, p. 762, doi. 10.1002/pd.6056

By:

Plantinga, Mirjam;
Zwienenberg, Lauren;
van Dijk, Eva;
Breet, Hanna;
Diphoorn, Janouk;
El Mecky, Julia;
Bouman, Katelijne;
Verheij, Joke;
Birnie, Erwin;
Ranchor, Adelita V.;
Corsten‐Janssen, Nicole;
van Langen, Irene M.

Publication type:

Article

High rate of abnormal findings in Prenatal Exome Trio in low risk pregnancies and apparently normal fetuses.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 6, p. 725, doi. 10.1002/pd.6077

By:

Vaknin, Noam;
Azoulay, Noy;
Tsur, Erez;
Tripolszki, Kornelia;
Urzi, Alice;
Rolfs, Arndt;
Bauer, Peter;
Achiron, Reuven;
Lipitz, Shlomo;
Goldberg, Yael;
Berger, Rachel;
Shohat, Mordechai

Publication type:

Article

Preference for secondary findings in prenatal and pediatric exome sequencing.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 6, p. 753, doi. 10.1002/pd.5973

By:

Swanson, Kate;
Sparks, Teresa N.;
Lianoglou, Billie R.;
Chen, Flavia;
Downum, Sarah;
Patel, Sachi;
Rego, Shannon;
Yip, Tiffany;
Van Ziffle, Jessica;
Koenig, Barbara A.;
Slavotinek, Anne M.;
Norton, Mary E.

Publication type:

Article

Issue Information.

Published in:: Prenatal Diagnosis, 2022, v. 42, n. 6, p. 657, doi. 10.1002/pd.5963
Publication type:: Article