Literature DB >> 29315690

Joint Position Statement from the International Society for Prenatal Diagnosis (ISPD), the Society for Maternal Fetal Medicine (SMFM), and the Perinatal Quality Foundation (PQF) on the use of genome-wide sequencing for fetal diagnosis.

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Year:  2018        PMID： 29315690     DOI： 10.1002/pd.5195

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN： 0197-3851            Impact factor:   3.050


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  34 in total

1.  Ethical and counseling challenges in prenatal exome sequencing.

Authors:  Sarah Harris; Kelly Gilmore; Emily Hardisty; Anne Drapkin Lyerly; Neeta L Vora
Journal:  Prenat Diagn       Date:  2018-09-11       Impact factor: 3.050

Review 2.  A system-based approach to the genetic etiologies of non-immune hydrops fetalis.

Authors:  Anne H Mardy; Shilpa P Chetty; Mary E Norton; Teresa N Sparks
Journal:  Prenat Diagn       Date:  2019-06-26       Impact factor: 3.050

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

Authors:  Asha N Talati; Kelly L Gilmore; Emily E Hardisty; Anne D Lyerly; Christine Rini; Neeta L Vora
Journal:  Prenat Diagn       Date:  2022-02-16       Impact factor: 3.242

4.  Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approach.

Authors:  Shannon Rego; Hannah Hoban; Simon Outram; Astrid N Zamora; Flavia Chen; Nuriye Sahin-Hodoglugil; Beatriz Anguiano; Matthew Norstad; Tiffany Yip; Billie Lianoglou; Teresa N Sparks; Mary E Norton; Barbara A Koenig; Anne M Slavotinek; Sara L Ackerman
Journal:  Genet Med       Date:  2022-04-08       Impact factor: 8.864

Review 5.  The current and future impact of genome-wide sequencing on fetal precision medicine.

Authors:  Riwa Sabbagh; Ignatia B Van den Veyver
Journal:  Hum Genet       Date:  2019-11-21       Impact factor: 4.132

6.  Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis.

Authors:  Mary E Norton; Jessica Van Ziffle; Billie R Lianoglou; Ugur Hodoglugil; W Patrick Devine; Teresa N Sparks
Journal:  Am J Obstet Gynecol       Date:  2021-07-28       Impact factor: 8.661

Review 7.  Autosomal Recessive Polycystic Kidney Disease-The Clinical Aspects and Diagnostic Challenges.

Authors:  Dorota Wicher; Łukasz Obrycki; Irena Jankowska
Journal:  J Pediatr Genet       Date:  2020-07-29

8.  Noninvasive Prenatal Whole Genome Sequencing: Pregnant Women's Views and Preferences.

Authors:  Haley K Sullivan; Michelle Bayefsky; Paul G Wakim; Kathi Huddleston; Barbara B Biesecker; Sara Chandros Hull; Benjamin E Berkman
Journal:  Obstet Gynecol       Date:  2019-03       Impact factor: 7.623

9.  Preference for secondary findings in prenatal and pediatric exome sequencing.

Authors:  Kate Swanson; Teresa N Sparks; Billie R Lianoglou; Flavia Chen; Sarah Downum; Sachi Patel; Shannon Rego; Tiffany Yip; Jessica Van Ziffle; Barbara A Koenig; Anne M Slavotinek; Mary E Norton
Journal:  Prenat Diagn       Date:  2021-06-07       Impact factor: 3.242

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

Authors:  Mirjam Plantinga; Lauren Zwienenberg; Eva van Dijk; Hanna Breet; Janouk Diphoorn; Julia El Mecky; Katelijne Bouman; Joke Verheij; Erwin Birnie; Adelita V Ranchor; Nicole Corsten-Janssen; Irene M van Langen
Journal:  Prenat Diagn       Date:  2021-10-22       Impact factor: 3.242
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