469 related articles for article (PubMed ID: 32304219)
1. 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]
2. 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]
3. 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]
4. Prenatal whole-exome sequencing for fetal structural anomalies: a retrospective analysis of 145 Chinese cases.
Qin Y; Yao Y; Liu N; Wang B; Liu L; Li H; Gao T; Xu R; Wang X; Zhang F; Song J
BMC Med Genomics; 2023 Oct; 16(1):262. PubMed ID: 37880672
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Whole exome sequencing of fetal structural anomalies detected by ultrasonography.
Aoi H; Mizuguchi T; Suzuki T; Makino S; Yamamoto Y; Takeda J; Maruyama Y; Seyama R; Takeuchi S; Uchiyama Y; Azuma Y; Hamanaka K; Fujita A; Koshimizu E; Miyatake S; Mitsuhashi S; Takata A; Miyake N; Takeda S; Itakura A; Matsumoto N
J Hum Genet; 2021 May; 66(5):499-507. PubMed ID: 33144663
[TBL] [Abstract][Full Text] [Related]
8. Whole-exome sequencing increases the diagnostic rate for prenatal fetal structural anomalies.
Lei L; Zhou L; Xiong JJ
Eur J Med Genet; 2021 Sep; 64(9):104288. PubMed ID: 34246755
[TBL] [Abstract][Full Text] [Related]
9. Whole exome sequencing for prenatal diagnosis in cases with fetal anomalies: Criteria to improve diagnostic yield.
Yadava SM; Ashkinadze E
J Genet Couns; 2019 Apr; 28(2):251-255. PubMed ID: 30629328
[TBL] [Abstract][Full Text] [Related]
10. Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes.
Al-Hamed MH; Kurdi W; Khan R; Tulbah M; AlNemer M; AlSahan N; AlMugbel M; Rafiullah R; Assoum M; Monies D; Shah Z; Rahbeeni Z; Derar N; Hakami F; Almutairi G; AlOtaibi A; Ali W; AlShammasi A; AlMubarak W; AlDawoud S; AlAmri S; Saeed B; Bukhari H; Ali M; Akili R; Alquayt L; Hagos S; Elbardisy H; Akilan A; Almuhana N; AlKhalifah A; Abouelhoda M; Ramzan K; Sayer JA; Imtiaz F
Hum Genet; 2022 Jan; 141(1):101-126. PubMed ID: 34853893
[TBL] [Abstract][Full Text] [Related]
11. Importance of complete phenotyping in prenatal whole exome sequencing.
Aarabi M; Sniezek O; Jiang H; Saller DN; Bellissimo D; Yatsenko SA; Rajkovic A
Hum Genet; 2018 Feb; 137(2):175-181. PubMed ID: 29392406
[TBL] [Abstract][Full Text] [Related]
12. Trio exome sequencing is highly relevant in prenatal diagnostics.
Gabriel H; Korinth D; Ritthaler M; Schulte B; Battke F; von Kaisenberg C; Wüstemann M; Schulze B; Friedrich-Freksa A; Pfeiffer L; Entezami M; Schröer A; Bürger J; Schwaibold EMC; Lebek H; Biskup S
Prenat Diagn; 2022 Jun; 42(7):845-851. PubMed ID: 34958143
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Trio-whole-exome sequencing and preimplantation genetic diagnosis for unexplained recurrent fetal malformations.
Guo W; Lai Y; Yan Z; Wang Y; Nie Y; Guan S; Kuo Y; Zhang W; Zhu X; Peng M; Zhi X; Wei Y; Yan L; Qiao J
Hum Mutat; 2020 Feb; 41(2):432-448. PubMed ID: 31680349
[TBL] [Abstract][Full Text] [Related]
15. Comprehensive prenatal diagnostics: Exome versus genome sequencing.
Miceikaite I; Fagerberg C; Brasch-Andersen C; Torring PM; Kristiansen BS; Hao Q; Sperling L; Ibsen MH; Löser K; Bendsen EA; Ousager LB; Larsen MJ
Prenat Diagn; 2023 Aug; 43(9):1132-1141. PubMed ID: 37355983
[TBL] [Abstract][Full Text] [Related]
16. Prenatal trio-based whole exome sequencing in fetuses with abnormalities of the skeletal system.
Yang Y; Wang M; Wang H
Mol Genet Genomics; 2022 Jul; 297(4):1017-1026. PubMed ID: 35583673
[TBL] [Abstract][Full Text] [Related]
17. Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities.
Fu F; Li R; Li Y; Nie ZQ; Lei T; Wang D; Yang X; Han J; Pan M; Zhen L; Ou Y; Li J; Li FT; Jing X; Li D; Liao C
Ultrasound Obstet Gynecol; 2018 Apr; 51(4):493-502. PubMed ID: 28976722
[TBL] [Abstract][Full Text] [Related]
18. Whole-exome sequencing in deceased fetuses with ultrasound anomalies: a retrospective analysis.
Huang W; Zhu X; Sun G; Gao Z; Kong X
BMC Med Genomics; 2023 Feb; 16(1):25. PubMed ID: 36797717
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]