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Utilising red cell antigen genotyping and serological phenotyping in sickle cell disease patients to risk-stratify patients for alloimmunisation risk.
Shih AW, Yan MTS, Elahie AL, Barty RL, Liu Y, Berardi P, Azzam M, Siddiqui R, Parvizian MK, Mcdougall T, Heddle NM, Al-Habsi KS, Goldman M, Cote J, Athale U, Verhovsek MM. Shih AW, et al. Among authors: cote j. Transfus Med. 2020 Aug;30(4):263-274. doi: 10.1111/tme.12685. Epub 2020 May 20. Transfus Med. 2020. PMID: 32432400
Two novel ABCG2 alleles resulting in a Jr(a-) phenotype.
Berardi P, Cote J, Vege S, Aeschlimann J, Cserti-Gazdewich C, Westhoff CM. Berardi P, et al. Among authors: cote j. Transfusion. 2017 Nov;57(11):2811-2812. doi: 10.1111/trf.14302. Epub 2017 Aug 23. Transfusion. 2017. PMID: 28836283 No abstract available.
Identification of six new RHCE variant alleles in individuals of diverse racial origin.
Goldman M, Cemborain A, Cote J, El Hamss R, Flower RL, Garaizar A, Garcia-Sanchez F, Hyland CA, Kalvelage M, Londero D, Lopez GH, Revelli N, Rodriguez-Wilhelmi P, Villa A, Ochoa-Garay G. Goldman M, et al. Among authors: cote j. Transfusion. 2016 Jan;56(1):244-8. doi: 10.1111/trf.13357. Epub 2015 Oct 4. Transfusion. 2016. PMID: 26435076
Weak D type 67 in four related Canadian blood donors.
Berardi P, Bessette E, Ng M, Angus N, Lane D, Gariepy L, Pavenski K, Ochoa-Garay G, Cote J, Goldman M. Berardi P, et al. Among authors: cote j. Immunohematology. 2015;31(4):159-62. Immunohematology. 2015. PMID: 27187196
New RHCE variant alleles encoding the D- - phenotype.
Ochoa-Garay G, Moulds JM, Cote J, Kresie L, Garaizar A, Goldman M, Wynn P. Ochoa-Garay G, et al. Among authors: cote j. Transfusion. 2013 Nov;53(11 Suppl 2):3018-23. doi: 10.1111/trf.12404. Epub 2013 Sep 10. Transfusion. 2013. PMID: 24020803
1,269 results