182 related articles for article (PubMed ID: 32267001)
1. Nonimmune hydrops fetalis: Genetic analysis and clinical outcome.
Deng Q; Fu F; Yu Q; Li R; Li F; Wang D; Lei T; Yang X; Liao C
Prenat Diagn; 2020 Jun; 40(7):803-812. PubMed ID: 32267001
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Cost-Effectiveness of Exome Sequencing versus Targeted Gene Panels for Prenatal Diagnosis of Fetal Effusions and Non-Immune Hydrops Fetalis.
Avram CM; Caughey AB; Norton ME; Sparks TN
Am J Obstet Gynecol MFM; 2022 Nov; 4(6):100724. PubMed ID: 35995366
[TBL] [Abstract][Full Text] [Related]
4. The many etiologies of nonimmune hydrops fetalis diagnosed by exome sequencing.
Wagner T; Fahham D; Frumkin A; Shaag A; Yagel S; Yanai N; Porat S; Mor-Shaked H; Meiner V; Daum H
Prenat Diagn; 2022 Jun; 42(7):881-889. PubMed ID: 34132406
[TBL] [Abstract][Full Text] [Related]
5. Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalis.
Correa ARE; Naini K; Mishra P; Dadhwal V; Agarwal R; Shukla R; Kabra M; Gupta N
Prenat Diagn; 2021 Oct; 41(11):1414-1424. PubMed ID: 34302381
[TBL] [Abstract][Full Text] [Related]
6. Genetic disorders and pregnancy outcomes of non-immune hydrops fetalis in a tertiary referral center.
Guo D; He S; Lin N; Dai Y; Li Y; Xu L; Wu X
BMC Med Genomics; 2023 Apr; 16(1):83. PubMed ID: 37081464
[TBL] [Abstract][Full Text] [Related]
7. Exome sequencing vs targeted gene panels for the evaluation of nonimmune hydrops fetalis.
Norton ME; Ziffle JV; Lianoglou BR; Hodoglugil U; Devine WP; Sparks TN
Am J Obstet Gynecol; 2022 Jan; 226(1):128.e1-128.e11. PubMed ID: 34331894
[TBL] [Abstract][Full Text] [Related]
8. The Value of Exome Sequencing in Thoracoamniotic Shunt for Severe Pleural Effusion with Fetal Hydrops: A Retrospective Clinical Study.
Wei X; Zhou X; Zhou J; Zou G; Yang Y; Zhou F; Xiong S; Chen J; Sun L
Fetal Diagn Ther; 2022; 49(3):138-144. PubMed ID: 35139508
[TBL] [Abstract][Full Text] [Related]
9. An Investigation of the Etiologies of Non-Immune Hydrops Fetalis in the Era of Next-Generation Sequence-A Single Center Experience.
Wei X; Yang Y; Zhou J; Zhou X; Xiong S; Chen J; Zhou F; Zou G; Sun L
Genes (Basel); 2022 Nov; 13(12):. PubMed ID: 36553497
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Utility of chromosomal microarray for diagnosis in cases of nonimmune hydrops fetalis.
Mardy AH; Rangwala N; Hernandez-Cruz Y; Gosnell KA; Gonzalez JM; Norton ME; Sparks TN
Prenat Diagn; 2020 Mar; 40(4):492-496. PubMed ID: 31981373
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.
Sparks TN; Lianoglou BR; Adami RR; Pluym ID; Holliman K; Duffy J; Downum SL; Patel S; Faubel A; Boe NM; Field NT; Murphy A; Laurent LC; Jolley J; Uy C; Slavotinek AM; Devine P; Hodoglugil U; Van Ziffle J; Sanders SJ; MacKenzie TC; Norton ME; ;
N Engl J Med; 2020 Oct; 383(18):1746-1756. PubMed ID: 33027564
[TBL] [Abstract][Full Text] [Related]
14. RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis.
Makhamreh MM; Shivashankar K; Araji S; Critchlow E; O'Brien BM; Wodoslawsky S; Berger SI; Al-Kouatly HB
Am J Med Genet A; 2024 May; 194(5):e63494. PubMed ID: 38156365
[TBL] [Abstract][Full Text] [Related]
15. High diagnosis rate for nonimmune hydrops fetalis with prenatal clinical exome from the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study.
Al-Kouatly HB; Makhamreh MM; Rice SM; Smith K; Harman C; Quinn A; Valcarcel BN; Firman B; Liu R; Hegde M; Critchlow E; Berger SI
Genet Med; 2021 Jul; 23(7):1325-1333. PubMed ID: 33686258
[TBL] [Abstract][Full Text] [Related]
16. Non-Immune Hydrops Fetalis: Do Placentomegaly and Polyhydramnios Matter?
Berger VK; Sparks TN; Jelin AC; Derderian C; Jeanty C; Gosnell K; Mackenzie T; Gonzalez JM
J Ultrasound Med; 2018 May; 37(5):1185-1191. PubMed ID: 29076544
[TBL] [Abstract][Full Text] [Related]
17. A systematic review of monogenic etiologies of nonimmune hydrops fetalis.
Quinn AM; Valcarcel BN; Makhamreh MM; Al-Kouatly HB; Berger SI
Genet Med; 2021 Jan; 23(1):3-12. PubMed ID: 33082562
[TBL] [Abstract][Full Text] [Related]
18. Nonimmune hydrops fetalis in a children's hospital: a six-year series.
Ng ZM; Seet MJ; Erng MN; Buendia F; Chang AS; Sriram B
Singapore Med J; 2013 Sep; 54(9):487-90. PubMed ID: 24068055
[TBL] [Abstract][Full Text] [Related]
19. A system-based approach to the genetic etiologies of non-immune hydrops fetalis.
Mardy AH; Chetty SP; Norton ME; Sparks TN
Prenat Diagn; 2019 Aug; 39(9):732-750. PubMed ID: 31087399
[TBL] [Abstract][Full Text] [Related]
20. Identification of novel PIEZO1 variants using prenatal exome sequencing and correlation to ultrasound and autopsy findings of recurrent hydrops fetalis.
Datkhaeva I; Arboleda VA; Senaratne TN; Nikpour G; Meyerson C; Geng Y; Afshar Y; Scibetta E; Goldstein J; Quintero-Rivera F; Crandall BF; Grody WW; Deignan J; Janzen C
Am J Med Genet A; 2018 Dec; 176(12):2829-2834. PubMed ID: 30244526
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]