BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 37725747)

  • 21. 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]  

  • 22. 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]  

  • 23. Diagnostic yield with exome sequencing in prenatal severe bilateral ventriculomegaly: a systematic review and meta-analysis.
    Mustafa HJ; Sambatur EV; Barbera JP; Pagani G; Yaron Y; Baptiste CD; Wapner RJ; Khalil A
    Am J Obstet Gynecol MFM; 2023 Sep; 5(9):101048. PubMed ID: 37311485
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Diagnostic Yield of Exome Sequencing in Fetuses with Sonographic Features of Skeletal Dysplasias but Normal Karyotype or Chromosomal Microarray Analysis: A Systematic Review.
    Tse KY; Surya IU; Irwinda R; Leung KY; Ting YH; Cao Y; Choy KW
    Genes (Basel); 2023 May; 14(6):. PubMed ID: 37372383
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
    Crider K; Williams J; Qi YP; Gutman J; Yeung L; Mai C; Finkelstain J; Mehta S; Pons-Duran C; Menéndez C; Moraleda C; Rogers L; Daniels K; Green P
    Cochrane Database Syst Rev; 2022 Feb; 2(2022):. PubMed ID: 36321557
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The Diagnostic Yield of Prenatal Genetic Technologies in Congenital Heart Disease: A Prospective Cohort Study.
    Mone F; Stott BK; Hamilton S; Seale AN; Quinlan-Jones E; Allen S; Hurles ME; McMullan DJ; Maher ER; Kilby MD
    Fetal Diagn Ther; 2021 Feb; ():1-8. PubMed ID: 33550297
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Outcome of fetuses with congenital cytomegalovirus infection and normal ultrasound at diagnosis: systematic review and meta-analysis.
    Buca D; Di Mascio D; Rizzo G; Giancotti A; D'Amico A; Leombroni M; Makatsarya A; Familiari A; Liberati M; Nappi L; Flacco ME; Manzoli L; Salomon LJ; Scambia G; D'Antonio F
    Ultrasound Obstet Gynecol; 2021 Apr; 57(4):551-559. PubMed ID: 33030767
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Prenatal diagnosis by trio exome sequencing in fetuses with ultrasound anomalies: A powerful diagnostic tool.
    Tran Mau-Them F; Delanne J; Denommé-Pichon AS; Safraou H; Bruel AL; Vitobello A; Garde A; Nambot S; Bourgon N; Racine C; Sorlin A; Moutton S; Marle N; Rousseau T; Sagot P; Simon E; Vincent-Delorme C; Boute O; Colson C; Petit F; Legendre M; Naudion S; Rooryck C; Prouteau C; Colin E; Guichet A; Ziegler A; Bonneau D; Morel G; Fradin M; Lavillaureix A; Quelin C; Pasquier L; Odent S; Vera G; Goldenberg A; Guerrot AM; Brehin AC; Putoux A; Attia J; Abel C; Blanchet P; Wells CF; Deiller C; Nizon M; Mercier S; Vincent M; Isidor B; Amiel J; Dard R; Godin M; Gruchy N; Jeanne M; Schaeffer E; Maillard PY; Payet F; Jacquemont ML; Francannet C; Sigaudy S; Bergot M; Tisserant E; Ascencio ML; Binquet C; Duffourd Y; Philippe C; Faivre L; Thauvin-Robinet C
    Front Genet; 2023; 14():1099995. PubMed ID: 37035737
    [No Abstract]   [Full Text] [Related]  

  • 30. Prenatal and postnatal findings in small-for-gestational-age fetuses without structural ultrasound anomalies at 18-24 weeks.
    de Wit MC; Srebniak MI; Joosten M; Govaerts LC; Kornelisse RF; Papatsonis DN; de Graaff K; Knapen MF; Bruggenwirth HT; de Vries FA; Van Veen S; Van Opstal D; Galjaard RJ; Go AT
    Ultrasound Obstet Gynecol; 2017 Mar; 49(3):342-348. PubMed ID: 27102944
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Diagnostic yield of prenatal exome sequencing in the genetic screening of fetuses with brain anomalies detected by MRI and ultrasonography: A systematic review and meta-analysis.
    Moradi B; Ariaei A; Heidari-Foroozan M; Banihashemian M; Ghorani H; Rashidi-Nezhad A; Kazemi MA; Taheri MS
    BJOG; 2023 Nov; ():. PubMed ID: 37932235
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. 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]  

  • 36. Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing.
    Huang R; Fu F; Zhou H; Zhang L; Lei T; Cheng K; Yan S; Guo F; Wang Y; Ma C; Li R; Yu Q; Deng Q; Li L; Yang X; Han J; Li D; Liao C
    Hum Genet; 2023 Jun; 142(6):835-847. PubMed ID: 37095353
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Next Generation Sequencing after Invasive Prenatal Testing in Fetuses with Congenital Malformations: Prenatal or Neonatal Investigation.
    Emms A; Castleman J; Allen S; Williams D; Kinning E; Kilby M
    Genes (Basel); 2022 Aug; 13(9):. PubMed ID: 36140685
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Exome Sequencing for Prenatal Detection of Genetic Abnormalities in Fetal Ultrasound Anomalies: An Economic Evaluation.
    Kodabuckus SS; Quinlan-Jones E; McMullan DJ; Maher ER; Hurles ME; Barton PM; Kilby MD
    Fetal Diagn Ther; 2020; 47(7):554-564. PubMed ID: 31962312
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Chromosomal microarray analysis in fetuses with congenital anomalies of the kidney and urinary tract: A prospective cohort study and meta-analysis.
    Li S; Han X; Wang Y; Chen S; Niu J; Qian Z; Li P; Jin L; Xu C
    Prenat Diagn; 2019 Feb; 39(3):165-174. PubMed ID: 30650192
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.