BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

716 related articles for article (PubMed ID: 35726512)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohort.
    Su J; Qin Z; Fu H; Luo J; Huang Y; Huang P; Zhang S; Liu T; Lu W; Li W; Jiang T; Wei S; Yang S; Shen Y
    Ultrasound Obstet Gynecol; 2022 Feb; 59(2):226-233. PubMed ID: 34090309
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes.
    Qi Q; Jiang Y; Zhou X; Meng H; Hao N; Chang J; Bai J; Wang C; Wang M; Guo J; Ouyang Y; Xu Z; Xiao M; Zhang VW; Liu J
    Genes (Basel); 2020 Nov; 11(12):. PubMed ID: 33255631
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A single center experience of prenatal parent-fetus trio exome sequencing for pregnancies with congenital anomalies.
    Dufke A; Hoopmann M; Waldmüller S; Prodan NC; Beck-Wödl S; Grasshoff U; Heinrich T; Riess A; Kehrer M; Falb RJ; Liebmann A; Roggia C; Stampfer M; Schadeck M; Müller AJ; Grimmel M; Stöbe P; Gauck D; Buchert-Lo R; Baumann S; Schäferhoff K; Bertrand M; Menden B; Sturm M; Schütz L; Riess O; Ossowski S; Haack TB; Kagan KO
    Prenat Diagn; 2022 Jun; 42(7):901-910. PubMed ID: 35574990
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Rapid prenatal diagnosis of skeletal dysplasia using medical trio exome sequencing: Benefit for prenatal counseling and pregnancy management.
    Han J; Yang YD; He Y; Liu WJ; Zhen L; Pan M; Yang X; Zhang VW; Liao C; Li DZ
    Prenat Diagn; 2020 Apr; 40(5):577-584. PubMed ID: 31994750
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 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. Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies.
    Quinlan-Jones E; Lord J; Williams D; Hamilton S; Marton T; Eberhardt RY; Rinck G; Prigmore E; Keelagher R; McMullan DJ; Maher ER; Hurles ME; Kilby MD
    Genet Med; 2019 May; 21(5):1065-1073. PubMed ID: 30293990
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 36.