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1.
Maternal carrier screening with single-gene NIPS provides accurate fetal risk assessments for recessive conditions.
Genet Med
; 25(2): 100334, 2023 02.
Article
in English
| MEDLINE | ID: mdl-36454238
2.
Understanding the experiences and perspectives of prenatal screening among a diverse cohort.
Prenat Diagn
; 43(5): 605-612, 2023 05.
Article
in English
| MEDLINE | ID: mdl-36588184
3.
Diagnostic yield and psychological outcomes among women pursuing trio-exome sequencing: Do women with recurrent anomalous fetal phenotypes experience more negative psychological outcomes?
Prenat Diagn
; 43(5): 569-578, 2023 05.
Article
in English
| MEDLINE | ID: mdl-36690925
4.
Parental motivations for and adaptation to trio-exome sequencing in a prospective prenatal testing cohort: Beyond the diagnosis.
Prenat Diagn
; 42(6): 775-782, 2022 05.
Article
in English
| MEDLINE | ID: mdl-35132674
5.
Impact of prenatal exome sequencing for fetal genetic diagnosis on maternal psychological outcomes and decisional conflict in a prospective cohort.
Genet Med
; 23(4): 713-719, 2021 04.
Article
in English
| MEDLINE | ID: mdl-33214710
6.
Correction: An approach to integrating exome sequencing for fetal structural anomalies into clinical practice.
Genet Med
; 22(8): 1426, 2020 Aug.
Article
in English
| MEDLINE | ID: mdl-32555414
7.
An approach to integrating exome sequencing for fetal structural anomalies into clinical practice.
Genet Med
; 22(5): 954-961, 2020 05.
Article
in English
| MEDLINE | ID: mdl-31974414
8.
Use of a novel computerized decision aid for aneuploidy screening: a randomized controlled trial.
Genet Med
; 21(4): 923-929, 2019 04.
Article
in English
| MEDLINE | ID: mdl-30214066
9.
Ethical and counseling challenges in prenatal exome sequencing.
Prenat Diagn
; 38(12): 897-903, 2018 11.
Article
in English
| MEDLINE | ID: mdl-30171820
10.
Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges.
Genet Med
; 19(11): 1207-1216, 2017 11.
Article
in English
| MEDLINE | ID: mdl-28518170
11.
How can prenatal exome sequencing inform future pregnancies?
Am J Obstet Gynecol
; 227(1): 98-99, 2022 07.
Article
in English
| MEDLINE | ID: mdl-35167813
12.
Navigating Noninvasive Prenatal Screening for Subchromosomal Abnormalities.
Am Fam Physician
; 106(6): 612-613, 2022 12.
Article
in English
| MEDLINE | ID: mdl-36521455
13.
Attitudes and Knowledge of Maternal-Fetal Medicine Fellows Regarding Noninvasive Prenatal Testing.
J Genet Couns
; 25(1): 73-8, 2016 Feb.
Article
in English
| MEDLINE | ID: mdl-25925607
14.
Cell free DNA testing-interpretation of results using an online calculator.
Am J Obstet Gynecol
; 213(1): 30.e1-30.e4, 2015 Jul.
Article
in English
| MEDLINE | ID: mdl-25957020
15.
Telehealth to provide prenatal genetics services: Feasibility and importance revealed during global pandemic.
Prenat Diagn
; 40(8): 1040-1041, 2020 07.
Article
in English
| MEDLINE | ID: mdl-32314399
16.
A single center's experience with noninvasive prenatal testing.
Genet Med
; 16(9): 681-7, 2014 Sep.
Article
in English
| MEDLINE | ID: mdl-24675675
17.
Advances in genetic prenatal diagnosis and screening.
Curr Opin Pediatr
; 26(6): 634-8, 2014 Dec.
Article
in English
| MEDLINE | ID: mdl-25211161
18.
Unveiling Fetal Development by Use of "Omics".
Clin Chem
; 63(9): 1549, 2017 Sep 01.
Article
in English
| MEDLINE | ID: mdl-32100829
19.
Trisomy 13-confined placental mosaicism: is there an increased risk of gestational hypertensive disorders?
Prenat Diagn
; 37(9): 938-939, 2017 09.
Article
in English
| MEDLINE | ID: mdl-28671725
20.
Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.
J Med Genet
; 47(8): 513-24, 2010 Aug.
Article
in English
| MEDLINE | ID: mdl-19955556