These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 32915977)

  • 1. A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data.
    Chang TC; Haupfear KM; Yu J; Rampersaud E; Sheehan VA; Flanagan JM; Hankins JS; Weiss MJ; Wu G; Vege S; Westhoff CM; Chou ST; Zheng Y
    Blood Adv; 2020 Sep; 4(18):4347-4357. PubMed ID: 32915977
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Machine learning to optimize automated RH genotyping using whole-exome sequencing data.
    Chang TC; Yu J; Wang Z; Hankins JS; Weiss MJ; Wu G; Westhoff CM; Chou ST; Zheng Y
    Blood Adv; 2024 Jun; 8(11):2651-2659. PubMed ID: 38522094
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinically relevant RHD-CE genotypes in patients with sickle cell disease and in African Brazilian donors.
    Gaspardi AC; Sippert EA; De Macedo MD; Pellegrino J; Costa FF; Castilho L
    Blood Transfus; 2016 Sep; 14(5):449-54. PubMed ID: 27177398
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Overcoming the challenges of interpreting complex and uncommon RH alleles from whole genomes.
    Halls JBL; Vege S; Simmons DP; Aeschlimann J; Bujiriri B; Mah HH; Lebo MS; Vijay Kumar PK; Westhoff CM; Lane WJ
    Vox Sang; 2020 Nov; 115(8):790-801. PubMed ID: 32567058
    [TBL] [Abstract][Full Text] [Related]  

  • 5. RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients.
    Dezan MR; Ribeiro IH; Oliveira VB; Vieira JB; Gomes FC; Franco LAM; Varuzza L; Ribeiro R; Chinoca KZ; Levi JE; Krieger JE; Pereira AC; Gualandro SFM; Rocha VG; Mendrone-Junior A; Sabino EC; Dinardo CL
    Blood Cells Mol Dis; 2017 Jun; 65():8-15. PubMed ID: 28388467
    [TBL] [Abstract][Full Text] [Related]  

  • 6. From the investigation of RHD-CE hybrid genes to the recognition of RHCE variants and RHD zygosity. Expanding the analysis by QMPSF in Brazilian donors and in patients with sickle cell disease.
    de Paula Vendrame TA; Arnoni CP; Latini FRM; Pereira Cortez AJ; Bénech C; Fichou Y; Castilho L
    Blood Transfus; 2023 May; 21(3):202-208. PubMed ID: 35848626
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular matching for patients with haematological diseases expressing altered RHD-RHCE genotypes.
    Cruz BR; de Souza Silva TC; de Souza Castro B; Chiba AK; Moritz E; Braga JP; Figueiredo MS; Bordin JO
    Vox Sang; 2019 Aug; 114(6):605-615. PubMed ID: 31087345
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodies.
    Dinardo CL; Kelly S; Dezan MR; Ribeiro IH; Castilho SL; Schimidt LC; Valgueiro MDC; Preiss LR; Custer B; Sabino EC; Westhoff CM;
    Transfusion; 2019 Oct; 59(10):3228-3235. PubMed ID: 31408202
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genomic analyses of RH alleles to improve transfusion therapy in patients with sickle cell disease.
    Reid ME; Halter Hipsky C; Hue-Roye K; Hoppe C
    Blood Cells Mol Dis; 2014 Apr; 52(4):195-202. PubMed ID: 24309423
    [TBL] [Abstract][Full Text] [Related]  

  • 10. RH genotypes and red cell alloimmunization rates in chronically transfused patients with sickle cell disease: A multisite study in the USA.
    Israelyan N; Vege S; Friedman DF; Zhang Z; Uter S; Fasano RM; Yee M; Piccone C; Kelly S; Hankins JS; Zheng Y; Westhoff CM; Chou ST
    Transfusion; 2024 Mar; 64(3):526-535. PubMed ID: 38289184
    [TBL] [Abstract][Full Text] [Related]  

  • 11. RHCE variants inherited with altered RHD alleles in Brazilian blood donors.
    Prisco Arnoni C; Guilhem Muniz J; de Paula Vendrame TA; de Medeiros Person R; Roche Moreira Latini F; Castilho L
    Transfus Med; 2016 Aug; 26(4):285-90. PubMed ID: 27111588
    [TBL] [Abstract][Full Text] [Related]  

  • 12. RHD and RHCE variant and zygosity genotyping via multiplex ligation-dependent probe amplification.
    Haer-Wigman L; Veldhuisen B; Jonkers R; Lodén M; Madgett TE; Avent ND; de Haas M; van der Schoot CE
    Transfusion; 2013 Jul; 53(7):1559-74. PubMed ID: 23043317
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Accurate long-read sequencing allows assembly of the duplicated RHD and RHCE genes harboring variants relevant to blood transfusion.
    Zhang Z; An HH; Vege S; Hu T; Zhang S; Mosbruger T; Jayaraman P; Monos D; Westhoff CM; Chou ST
    Am J Hum Genet; 2022 Jan; 109(1):180-191. PubMed ID: 34968422
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Challenges in providing compatible blood with Rh genotype-matching in Brazilian patients with sickle cell disease.
    Santos TD; Macedo MD; Menegati SFP; Gilli S; Castilho L
    Transfus Med; 2019 Dec; 29(6):423-429. PubMed ID: 31631427
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A variant RhAG protein encoded by the RHAG*572A allele causes serological weak D expression while maintaining normal RhCE phenotypes.
    Wen J; Verhagen OJHM; Jia S; Liang Q; Wang Z; Wei L; Luo H; Luo G; Vidarsson G; van den Akker E; Ji Y; van der Schoot CE
    Transfusion; 2019 Jan; 59(1):405-411. PubMed ID: 30284303
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evaluation of targeted exome sequencing for 28 protein-based blood group systems, including the homologous gene systems, for blood group genotyping.
    Schoeman EM; Lopez GH; McGowan EC; Millard GM; O'Brien H; Roulis EV; Liew YW; Martin JR; McGrath KA; Powley T; Flower RL; Hyland CA
    Transfusion; 2017 Apr; 57(4):1078-1088. PubMed ID: 28338218
    [TBL] [Abstract][Full Text] [Related]  

  • 17. RH genotyping by nonspecific quantitative next-generation sequencing.
    Stef M; Fennell K; Apraiz I; Arteta D; González C; Nogués N; Ochoa-Garay G
    Transfusion; 2020 Nov; 60(11):2691-2701. PubMed ID: 32871036
    [TBL] [Abstract][Full Text] [Related]  

  • 18. RHD/CE typing by polymerase chain reaction using sequence-specific primers.
    Gassner C; Schmarda A; Kilga-Nogler S; Jenny-Feldkircher B; Rainer E; Müller TH; Wagner FF; Flegel WA; Schönitzer D
    Transfusion; 1997 Oct; 37(10):1020-6. PubMed ID: 9354819
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Novel RHCE*cE (c.827C>A) Allele, Containing the Single-Nucleotide Change, Encodes Altered c/E Antigens.
    Wu CL; Yi P; Tang BD; Zhang QL; Du X; Hong WX; Ou ZY; Shao CP
    Clin Lab; 2023 Oct; 69(10):. PubMed ID: 37844047
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole-exome sequencing for
    Chou ST; Flanagan JM; Vege S; Luban NLC; Brown RC; Ware RE; Westhoff CM
    Blood Adv; 2017 Aug; 1(18):1414-1422. PubMed ID: 29296782
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.