Chui DH - 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: chui dh. Nat Genet. 2011 Mar 20;43(4):295-301. doi: 10.1038/ng.785. Nat Genet. 2011. PMID: 21423179 Free PMC article.

2

HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update.

Giardine B, van Baal S, Kaimakis P, Riemer C, Miller W, Samara M, Kollia P, Anagnou NP, Chui DH, Wajcman H, Hardison RC, Patrinos GP. Giardine B, et al. Among authors: chui dh. Hum Mutat. 2007 Feb;28(2):206. doi: 10.1002/humu.9479. Hum Mutat. 2007. PMID: 17221864

3

HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server.

Hardison RC, Chui DH, Giardine B, Riemer C, Patrinos GP, Anagnou N, Miller W, Wajcman H. Hardison RC, et al. Among authors: chui dh. Hum Mutat. 2002 Mar;19(3):225-33. doi: 10.1002/humu.10044. Hum Mutat. 2002. PMID: 11857738

4

Strategies to improve pharmacogenomic-guided treatment options for patients with β-hemoglobinopathies.

Patrinos GP, Chui DHK, Hardison RC, Steinberg MH. Patrinos GP, et al. Among authors: chui dhk. Expert Rev Hematol. 2021 Oct;14(10):883-885. doi: 10.1080/17474086.2021.1977117. Epub 2021 Sep 8. Expert Rev Hematol. 2021. PMID: 34490838 Free PMC article.

5

Databases of human hemoglobin variants and other resources at the globin gene server.

Hardison RC, Chui DH, Riemer C, Giardine B, Lehväslaiho H, Wajcman H, Miller W. Hardison RC, et al. Among authors: chui dh. Hemoglobin. 2001 May;25(2):183-93. doi: 10.1081/hem-100104027. Hemoglobin. 2001. PMID: 11480780 Review.

6

PhenCode: connecting ENCODE data with mutations and phenotype.

Giardine B, Riemer C, Hefferon T, Thomas D, Hsu F, Zielenski J, Sang Y, Elnitski L, Cutting G, Trumbower H, Kern A, Kuhn R, Patrinos GP, Hughes J, Higgs D, Chui D, Scriver C, Phommarinh M, Patnaik SK, Blumenfeld O, Gottlieb B, Vihinen M, Väliaho J, Kent J, Miller W, Hardison RC. Giardine B, et al. Hum Mutat. 2007 Jun;28(6):554-62. doi: 10.1002/humu.20484. Hum Mutat. 2007. PMID: 17326095

7

Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies.

Patrinos GP, Giardine B, Riemer C, Miller W, Chui DH, Anagnou NP, Wajcman H, Hardison RC. Patrinos GP, et al. Among authors: chui dh. Nucleic Acids Res. 2004 Jan 1;32(Database issue):D537-41. doi: 10.1093/nar/gkh006. Nucleic Acids Res. 2004. PMID: 14681476 Free PMC article.

8

Access to a syllabus of human hemoglobin variants (1996) via the World Wide Web.

Hardison RC, Chui DH, Riemer CR, Miller W, Carver MF, Molchanova TP, Efremov GD, Huisman TH. Hardison RC, et al. Among authors: chui dh. Hemoglobin. 1998 Mar;22(2):113-27. doi: 10.3109/03630269809092136. Hemoglobin. 1998. PMID: 9576329

9

Electronic access to sequence alignments, experimental results, and human mutations as an aid to studying globin gene regulation.

Hardison R, Riemer C, Chui DH, Huisman TH, Miller W. Hardison R, et al. Among authors: chui dh. Genomics. 1998 Feb 1;47(3):429-37. doi: 10.1006/geno.1997.5147. Genomics. 1998. PMID: 9480762 No abstract available.

10

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. Among authors: chui dh. Haematologica. 2007 May;92(5):e68. doi: 10.3324/haematol.11572. Haematologica. 2007. PMID: 17562600 Free article. No abstract available.

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