BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 36221164)

  • 1. International Society for Prenatal Diagnosis 2022 debate 3-Fetal genome sequencing should be offered to all pregnant patients.
    Van den Veyver IB; Yaron Y; Deans ZC
    Prenat Diagn; 2023 Apr; 43(4):428-434. PubMed ID: 36221164
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal exome and genome sequencing for fetal structural abnormalities.
    Vora NL; Norton ME
    Am J Obstet Gynecol; 2023 Feb; 228(2):140-149. PubMed ID: 36027950
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Prenatal screening for fetal aneuploidy in singleton pregnancies.
    Chitayat D; Langlois S; Douglas Wilson R; ;
    J Obstet Gynaecol Can; 2011 Jul; 33(7):736-750. PubMed ID: 21749752
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Diagnostic yield of genome sequencing for prenatal diagnosis of fetal structural anomalies.
    Wang Y; Greenfeld E; Watkins N; Belesiotis P; Zaidi SH; Marshall C; Thiruvahindrapuram B; Shannon P; Roifman M; Chong K; Chitayat D; Stavropoulos DJ; Noor A
    Prenat Diagn; 2022 Jun; 42(7):822-830. PubMed ID: 35089622
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Update on the use of exome sequencing in the diagnosis of fetal abnormalities.
    Ferretti L; Mellis R; Chitty LS
    Eur J Med Genet; 2019 Aug; 62(8):103663. PubMed ID: 31085342
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [Expert consensus on the application of prenatal exome sequencing for fetal structural anomalies].
    Application Collaboration Group Of Whole Exome Sequencing In Prenatal Diagnosis ; Lou G; Hou Q; Yang K; Guo L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 May; 39(5):457-463. PubMed ID: 35598257
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management.
    Chandler N; Best S; Hayward J; Faravelli F; Mansour S; Kivuva E; Tapon D; Male A; DeVile C; Chitty LS
    Genet Med; 2018 Nov; 20(11):1430-1437. PubMed ID: 29595812
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Clinical application of medical exome sequencing for prenatal diagnosis of fetal structural anomalies.
    Chen M; Chen J; Wang C; Chen F; Xie Y; Li Y; Li N; Wang J; Zhang VW; Chen D
    Eur J Obstet Gynecol Reprod Biol; 2020 Aug; 251():119-124. PubMed ID: 32502767
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.
    Lowther C; Valkanas E; Giordano JL; Wang HZ; Currall BB; O'Keefe K; Pierce-Hoffman E; Kurtas NE; Whelan CW; Hao SP; Weisburd B; Jalili V; Fu J; Wong I; Collins RL; Zhao X; Austin-Tse CA; Evangelista E; Lemire G; Aggarwal VS; Lucente D; Gauthier LD; Tolonen C; Sahakian N; Stevens C; An JY; Dong S; Norton ME; MacKenzie TC; Devlin B; Gilmore K; Powell BC; Brandt A; Vetrini F; DiVito M; Sanders SJ; MacArthur DG; Hodge JC; O'Donnell-Luria A; Rehm HL; Vora NL; Levy B; Brand H; Wapner RJ; Talkowski ME
    Am J Hum Genet; 2023 Sep; 110(9):1454-1469. PubMed ID: 37595579
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An approach to integrating exome sequencing for fetal structural anomalies into clinical practice.
    Vora NL; Gilmore K; Brandt A; Gustafson C; Strande N; Ramkissoon L; Hardisty E; Foreman AKM; Wilhelmsen K; Owen P; Weck KE; Berg JS; Powell CM; Powell BC
    Genet Med; 2020 May; 22(5):954-961. PubMed ID: 31974414
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US.
    Sahin-Hodoglugil NN; Lianoglou BR; Ackerman S; Sparks TN; Norton ME
    Prenat Diagn; 2023 Oct; 43(11):1394-1405. PubMed ID: 37752660
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The prenatal exome - a door to prenatal diagnostics?
    Castleman JS; Wall E; Allen S; Williams D; Doyle S; Kilby MD
    Expert Rev Mol Diagn; 2021 May; 21(5):465-474. PubMed ID: 33877000
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. Lessons learnt from prenatal exome sequencing.
    Chandler NJ; Scotchman E; Mellis R; Ramachandran V; Roberts R; Chitty LS
    Prenat Diagn; 2022 Jun; 42(7):831-844. PubMed ID: 35506549
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.