174 related articles for article (PubMed ID: 36508432)
1. Prenatal exome sequencing and impact on perinatal outcome: cohort study.
Poljak B; Agarwal U; Alfirevic Z; Allen S; Canham N; Higgs J; Kaelin Agten A; Khalil A; Roberts D; Mone F; Navaratnam K
Ultrasound Obstet Gynecol; 2023 Mar; 61(3):339-345. PubMed ID: 36508432
[TBL] [Abstract][Full Text] [Related]
2. Evolving fetal phenotypes and clinical impact of progressive prenatal exome sequencing pathways: cohort study.
Mone F; Abu Subieh H; Doyle S; Hamilton S; Mcmullan DJ; Allen S; Marton T; Williams D; Kilby MD
Ultrasound Obstet Gynecol; 2022 Jun; 59(6):723-730. PubMed ID: 34940998
[TBL] [Abstract][Full Text] [Related]
3. Utility of trio-based prenatal exome sequencing incorporating splice-site and mitochondrial genome assessment in pregnancies with fetal ultrasound anomalies: prospective cohort study.
Zhu X; Gao Z; Wang Y; Huang W; Li Q; Jiao Z; Liu N; Kong X
Ultrasound Obstet Gynecol; 2022 Dec; 60(6):780-792. PubMed ID: 35726512
[TBL] [Abstract][Full Text] [Related]
4. Fetal hydrops and the Incremental yield of Next-generation sequencing over standard prenatal Diagnostic testing (FIND) study: prospective cohort study and meta-analysis.
Mone F; Eberhardt RY; Hurles ME; Mcmullan DJ; Maher ER; Lord J; Chitty LS; Dempsey E; Homfray T; Giordano JL; Wapner RJ; Sun L; Sparks TN; Norton ME; Kilby MD
Ultrasound Obstet Gynecol; 2021 Oct; 58(4):509-518. PubMed ID: 33847422
[TBL] [Abstract][Full Text] [Related]
5. Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses.
Fu F; Li R; Yu Q; Wang D; Deng Q; Li L; Lei T; Chen G; Nie Z; Yang X; Han J; Pan M; Zhen L; Zhang Y; Jing X; Li F; Li F; Zhang L; Yi C; Li Y; Lu Y; Zhou H; Cheng K; Li J; Xiang L; Zhang J; Tang S; Fang P; Li D; Liao C
Genome Med; 2022 Oct; 14(1):123. PubMed ID: 36307859
[TBL] [Abstract][Full Text] [Related]
6. Incremental yield of whole-genome sequencing over chromosomal microarray analysis and exome sequencing for congenital anomalies in prenatal period and infancy: systematic review and meta-analysis.
Shreeve N; Sproule C; Choy KW; Dong Z; Gajewska-Knapik K; Kilby MD; Mone F
Ultrasound Obstet Gynecol; 2024 Jan; 63(1):15-23. PubMed ID: 37725747
[TBL] [Abstract][Full Text] [Related]
7. From diagnostic yield to clinical impact: a pilot study on the implementation of prenatal exome sequencing in routine care.
de Koning MA; Haak MC; Adama van Scheltema PN; Peeters-Scholte CMPCD; Koopmann TT; Nibbeling EAR; Aten E; den Hollander NS; Ruivenkamp CAL; Hoffer MJV; Santen GWE
Genet Med; 2019 Oct; 21(10):2303-2310. PubMed ID: 30918357
[TBL] [Abstract][Full Text] [Related]
8. Exome sequencing as first-tier test for fetuses with severe central nervous system structural anomalies.
Yaron Y; Ofen Glassner V; Mory A; Zunz Henig N; Kurolap A; Bar Shira A; Brabbing Goldstein D; Marom D; Ben Sira L; Baris Feldman H; Malinger G; Krajden Haratz K; Reches A
Ultrasound Obstet Gynecol; 2022 Jul; 60(1):59-67. PubMed ID: 35229910
[TBL] [Abstract][Full Text] [Related]
9. Prenatal exome sequencing analysis in fetuses with central nervous system anomalies.
Zhi Y; Liu L; Wang H; Chen X; Lv Y; Cui X; Chang H; Wang Y; Cui S
Ultrasound Obstet Gynecol; 2023 Nov; 62(5):721-726. PubMed ID: 37204857
[TBL] [Abstract][Full Text] [Related]
10. Congenital hypotonia: systematic approach for prenatal detection.
Weissbach T; Hausman-Kedem M; Yanay Z; Meyer R; Bar-Yosef O; Leibovitch L; Berkenstadt M; Chorin O; Shani H; Massarwa A; Achiron R; Weisz B; Sharon R; Mazaki-Tovi S; Kassif E
Ultrasound Obstet Gynecol; 2023 Jul; 62(1):94-105. PubMed ID: 36779229
[TBL] [Abstract][Full Text] [Related]
11. Whole-genome sequencing in prenatally detected congenital malformations: prospective cohort study in clinical setting.
Westenius E; Conner P; Pettersson M; Sahlin E; Papadogiannakis N; Lindstrand A; Iwarsson E
Ultrasound Obstet Gynecol; 2024 May; 63(5):658-663. PubMed ID: 38268232
[TBL] [Abstract][Full Text] [Related]
12. Fetal exome sequencing: yield and limitations in a tertiary referral center.
Daum H; Meiner V; Elpeleg O; Harel T;
Ultrasound Obstet Gynecol; 2019 Jan; 53(1):80-86. PubMed ID: 29947050
[TBL] [Abstract][Full Text] [Related]
13. Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Petrovski S; Aggarwal V; Giordano JL; Stosic M; Wou K; Bier L; Spiegel E; Brennan K; Stong N; Jobanputra V; Ren Z; Zhu X; Mebane C; Nahum O; Wang Q; Kamalakaran S; Malone C; Anyane-Yeboa K; Miller R; Levy B; Goldstein DB; Wapner RJ
Lancet; 2019 Feb; 393(10173):758-767. PubMed ID: 30712878
[TBL] [Abstract][Full Text] [Related]
14. Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Lord J; McMullan DJ; Eberhardt RY; Rinck G; Hamilton SJ; Quinlan-Jones E; Prigmore E; Keelagher R; Best SK; Carey GK; Mellis R; Robart S; Berry IR; Chandler KE; Cilliers D; Cresswell L; Edwards SL; Gardiner C; Henderson A; Holden ST; Homfray T; Lester T; Lewis RA; Newbury-Ecob R; Prescott K; Quarrell OW; Ramsden SC; Roberts E; Tapon D; Tooley MJ; Vasudevan PC; Weber AP; Wellesley DG; Westwood P; White H; Parker M; Williams D; Jenkins L; Scott RH; Kilby MD; Chitty LS; Hurles ME; Maher ER;
Lancet; 2019 Feb; 393(10173):747-757. PubMed ID: 30712880
[TBL] [Abstract][Full Text] [Related]
15. The potential diagnostic yield of whole exome sequencing in pregnancies complicated by fetal ultrasound anomalies.
Diderich KEM; Romijn K; Joosten M; Govaerts LCP; Polak M; Bruggenwirth HT; Wilke M; van Slegtenhorst MA; van Bever Y; Brooks AS; Mancini GMS; van de Laar IMBH; Kromosoeto JNR; Knapen MFCM; Go ATJI; Van Opstal D; Hoefsloot LH; Galjaard RH; Srebniak MI
Acta Obstet Gynecol Scand; 2021 Jun; 100(6):1106-1115. PubMed ID: 33249554
[TBL] [Abstract][Full Text] [Related]
16. Prenatal exome sequencing: A useful tool for the fetal neurologist.
de Koning MA; Hoffer MJV; Nibbeling EAR; Bijlsma EK; Toirkens MJP; Adama-Scheltema PN; Verweij EJ; Veenhof MB; Santen GWE; Peeters-Scholte CMPCD
Clin Genet; 2022 Jan; 101(1):65-77. PubMed ID: 34611884
[TBL] [Abstract][Full Text] [Related]
17. Diagnostic yield of exome sequencing in fetuses with multisystem malformations: systematic review and meta-analysis.
Pauta M; Martinez-Portilla RJ; Borrell A
Ultrasound Obstet Gynecol; 2022 Jun; 59(6):715-722. PubMed ID: 35041238
[TBL] [Abstract][Full Text] [Related]
18. Incidence, clinical features and perinatal outcome in anomalous fetuses with late-onset growth restriction: cohort study.
Dall'Asta A; Stampalija T; Mecacci F; Ramirez Zegarra R; Sorrentino S; Minopoli M; Ottaviani C; Fantasia I; Barbieri M; Lisi F; Simeone S; Castellani R; Fichera A; Rizzo G; Prefumo F; Frusca T; Ghi T
Ultrasound Obstet Gynecol; 2022 Nov; 60(5):632-639. PubMed ID: 35638182
[TBL] [Abstract][Full Text] [Related]
19. Role of magnetic resonance imaging in fetuses with mild or moderate ventriculomegaly in the era of fetal neurosonography: systematic review and meta-analysis.
Di Mascio D; Sileo FG; Khalil A; Rizzo G; Persico N; Brunelli R; Giancotti A; Panici PB; Acharya G; D'Antonio F
Ultrasound Obstet Gynecol; 2019 Aug; 54(2):164-171. PubMed ID: 30549340
[TBL] [Abstract][Full Text] [Related]
20. Implementation of exome sequencing in fetal diagnostics-Data and experiences from a tertiary center in Denmark.
Becher N; Andreasen L; Sandager P; Lou S; Petersen OB; Christensen R; Vogel I
Acta Obstet Gynecol Scand; 2020 Jun; 99(6):783-790. PubMed ID: 32304219
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]