BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 36068917)

  • 21. The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change.
    Rehm HL; Alaimo JT; Aradhya S; Bayrak-Toydemir P; Best H; Brandon R; Buchan JG; Chao EC; Chen E; Clifford J; Cohen ASA; Conlin LK; Das S; Davis KW; Del Gaudio D; Del Viso F; DiVincenzo C; Eisenberg M; Guidugli L; Hammer MB; Harrison SM; Hatchell KE; Dyer LH; Hoang LU; Holt JM; Jobanputra V; Karbassi ID; Kearney HM; Kelly MA; Kelly JM; Kluge ML; Komala T; Kruszka P; Lau L; Lebo MS; Marshall CR; McKnight D; McWalter K; Meng Y; Nagan N; Neckelmann CS; Neerman N; Niu Z; Paolillo VK; Paolucci SA; Perry D; Pesaran T; Radtke K; Rasmussen KJ; Retterer K; Saunders CJ; Spiteri E; Stanley C; Szuto A; Taft RJ; Thiffault I; Thomas BC; Thomas-Wilson A; Thorpe E; Tidwell TJ; Towne MC; Zouk H;
    Genet Med; 2023 Dec; 25(12):100947. PubMed ID: 37534744
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Contribution of single-gene defects to congenital cardiac left-sided lesions in the prenatal setting.
    Sun H; Yi T; Hao X; Yan H; Wang J; Li Q; Gu X; Zhou X; Wang S; Wang X; Wan P; Han L; Chen J; Zhu H; Zhang H; He Y
    Ultrasound Obstet Gynecol; 2020 Aug; 56(2):225-232. PubMed ID: 31633846
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Incidentally identified genetic variants in arrhythmogenic right ventricular cardiomyopathy-associated genes among children undergoing exome sequencing reflect healthy population variation.
    Headrick AT; Rosenfeld JA; Yang Y; Tunuguntla H; Allen HD; Penny DJ; Kim JJ; Landstrom AP
    Mol Genet Genomic Med; 2019 Jun; 7(6):e593. PubMed ID: 30985088
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Amino acid-level signal-to-noise analysis of incidentally identified variants in genes associated with long QT syndrome during pediatric whole exome sequencing reflects background genetic noise.
    Landstrom AP; Fernandez E; Rosenfeld JA; Yang Y; Dailey-Schwartz AL; Miyake CY; Allen HD; Penny DJ; Kim JJ
    Heart Rhythm; 2018 Jul; 15(7):1042-1050. PubMed ID: 29501670
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Efficacy and economics of targeted panel versus whole-exome sequencing in 878 patients with suspected primary immunodeficiency.
    Platt CD; Zaman F; Bainter W; Stafstrom K; Almutairi A; Reigle M; Weeks S; Geha RS; Chou J;
    J Allergy Clin Immunol; 2021 Feb; 147(2):723-726. PubMed ID: 32888943
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Fetal central nervous system anomalies: When should we offer exome sequencing?
    Baptiste C; Mellis R; Aggarwal V; Lord J; Eberhardt R; Kilby MD; Maher ER; Wapner R; Giordano J; Chitty L
    Prenat Diagn; 2022 May; 42(6):736-743. PubMed ID: 35411553
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Prospective Evaluation of the Utility of Whole Exome Sequencing in Dilated Cardiomyopathy.
    Ramchand J; Wallis M; Macciocca I; Lynch E; Farouque O; Martyn M; Phelan D; Chong B; Lockwood S; Weintraub R; Thompson T; Trainer A; Zentner D; Vohra J; Chetrit M; Hare DL; James P
    J Am Heart Assoc; 2020 Jan; 9(2):e013346. PubMed ID: 31931689
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Analysis of laboratory reporting practices using a quality assessment of a virtual patient.
    Vears DF; Elferink M; Kriek M; Borry P; van Gassen KL
    Genet Med; 2021 Mar; 23(3):562-570. PubMed ID: 33122805
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions.
    Li X; Nusbaum R; Smith-Hicks C; Jamal L; Dixon S; Mahida S
    J Genet Couns; 2019 Apr; 28(2):304-312. PubMed ID: 30680845
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A report on the impact of rapid prenatal exome sequencing on the clinical management of 52 ongoing pregnancies: a retrospective review.
    Dempsey E; Haworth A; Ive L; Dubis R; Savage H; Serra E; Kenny J; Elmslie F; Greco E; Thilaganathan B; Mansour S; Homfray T; Drury S
    BJOG; 2021 May; 128(6):1012-1019. PubMed ID: 32981126
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prenatal diagnosis of fetuses with ultrasound anomalies by whole-exome sequencing in Luoyang city, China.
    Wang Y; Yin F; Chai Y; Jin J; Zhang P; Tan Q; Chen Z
    Front Genet; 2023; 14():1301439. PubMed ID: 38318287
    [No Abstract]   [Full Text] [Related]  

  • 34. 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]  

  • 35. Whole Exome Sequencing: Applications in Prenatal Genetics.
    Jelin AC; Vora N
    Obstet Gynecol Clin North Am; 2018 Mar; 45(1):69-81. PubMed ID: 29428287
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The diagnostic efficacy of exome data analysis using fixed neurodevelopmental gene lists: Implications for prenatal setting.
    Sukenik-Halevy R; Ruhrman-Shahar N; Orenstein N; Gonzaga-Jauregui C; Shuldiner AR; Magal N; Hagari O; Azulay N; Lidzbarsky GA; Bazak L; Basel-Salmon L
    Prenat Diagn; 2021 May; 41(6):701-707. PubMed ID: 33686681
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Whole Exome Sequencing Identifies Novel Genetic Alterations in Patients with Pheochromocytoma/Paraganglioma.
    Seo SH; Kim JH; Kim MJ; Cho SI; Kim SJ; Kang H; Shin CS; Park SS; Lee KE; Seong MW
    Endocrinol Metab (Seoul); 2020 Dec; 35(4):909-917. PubMed ID: 33397043
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole-exome sequencing.
    Zhou X; Wang Y; Shao B; Wang C; Hu P; Qiao F; Xu Z
    J Clin Lab Anal; 2020 Nov; 34(11):e23480. PubMed ID: 32779812
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.