Waye JS - Search Results

1

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach.

Giardine B, Borg J, Higgs DR, Peterson KR, Philipsen S, Maglott D, Singleton BK, Anstee DJ, Basak AN, Clark B, Costa FC, Faustino P, Fedosyuk H, Felice AE, Francina A, Galanello R, Gallivan MV, Georgitsi M, Gibbons RJ, Giordano PC, Harteveld CL, Hoyer JD, Jarvis M, Joly P, Kanavakis E, Kollia P, Menzel S, Miller W, Moradkhani K, Old J, Papachatzopoulou A, Papadakis MN, Papadopoulos P, Pavlovic S, Perseu L, Radmilovic M, Riemer C, Satta S, Schrijver I, Stojiljkovic M, Thein SL, Traeger-Synodinos J, Tully R, Wada T, Waye JS, Wiemann C, Zukic B, Chui DH, Wajcman H, Hardison RC, Patrinos GP. Giardine B, et al. Among authors: waye js. Nat Genet. 2011 Mar 20;43(4):295-301. doi: 10.1038/ng.785. Nat Genet. 2011. PMID: 21423179 Free PMC article.

2

Hb Evora [alpha 2-35, Ser-->Pro], a novel hemoglobin variant associated with an alpha-thalassemia phenotype.

Waye JS, Chui DH. Waye JS, et al. Haematologica. 2007 May;92(5):e68. doi: 10.3324/haematol.11572. Haematologica. 2007. PMID: 17562600 Free article. No abstract available.

3

β+-Thalassemia trait due to a novel mutation in the β-globin gene promoter: -26 (A>C) [HBB c.-76A>C].

Waye JS, Nakamura-Garrett LM, Eng B, Kanavakis E, Traeger-Synodinos J. Waye JS, et al. Hemoglobin. 2011;35(1):84-6. doi: 10.3109/03630269.2010.529744. Hemoglobin. 2011. PMID: 21250885

4

Good practice guidelines for laboratory investigation of hemoglobinopathies.

Lafferty JD, Waye JS, Chui DH, Crawford L, Raby A, Richardson H; Quality Management Program-Laboratory Services Hematology Committee. Lafferty JD, et al. Among authors: waye js. Lab Hematol. 2003;9(4):237-45. Lab Hematol. 2003. PMID: 14649467

5

Prenatal diagnosis of hemoglobinopathies in Ontario, Canada.

Basran RK, Patterson M, Walker L, Nakamura LM, Eng B, Chui DH, Waye JS. Basran RK, et al. Among authors: waye js. Ann N Y Acad Sci. 2005;1054:507-10. doi: 10.1196/annals.1345.052. Ann N Y Acad Sci. 2005. PMID: 16339708

6

Beta-thalassaemia due to a seventeen basepair deletion.

Waye JS, Chui DH. Waye JS, et al. Br J Haematol. 1997 May;97(2):504. Br J Haematol. 1997. PMID: 9163624 Free article. No abstract available.

7

The alpha-globin gene cluster: genetics and disorders.

Waye JS, Chui DH. Waye JS, et al. Clin Invest Med. 2001 Apr;24(2):103-9. Clin Invest Med. 2001. PMID: 11368147 Review. No abstract available.

8

Identification of a new hemoglobin variant: Hb St. Joseph's [beta77(EF1)His-->Leu].

Patterson M, Walker L, Chui DH, Lafferty JD, McFarlane A, Waye JS. Patterson M, et al. Among authors: waye js. Hemoglobin. 2003 Aug;27(3):181-3. doi: 10.1081/hem-120023382. Hemoglobin. 2003. PMID: 12908803 No abstract available.

9

Carrier detection and prenatal diagnosis of hemoglobinopathies in Ontario.

Waye JS, Eng B, Cai SP, Patterson M, Smith J, Tang W, Chui DH. Waye JS, et al. Clin Invest Med. 1993 Oct;16(5):358-71. Clin Invest Med. 1993. PMID: 8261689 Review.

10

Identification of two new beta-thalassemia splice mutations: IVS-I-1 (G-->C) and IVS-I (-2) (A-->C).

Waye JS, Walker L, Patterson M, Chui DH. Waye JS, et al. Hemoglobin. 2002 Feb;26(1):87-9. doi: 10.1081/hem-120002946. Hemoglobin. 2002. PMID: 11939519 No abstract available.

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