James Taylor to Polymorphism, Single Nucleotide
This is a "connection" page, showing publications James Taylor has written about Polymorphism, Single Nucleotide.
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Diaw L, Youngblood V, Taylor JG. Introduction to next-generation nucleic acid sequencing in cardiovascular disease research. Methods Mol Biol. 2013; 1027:157-79.
Score: 0.342
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Idelman G, Taylor JG, Tongbai R, Chen RA, Haggerty CM, Bilke S, Chanock SJ, Gardner K. Functional profiling of uncommon VCAM1 promoter polymorphisms prevalent in African American populations. Hum Mutat. 2007 Aug; 28(8):824-9.
Score: 0.059
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Chanock S, Taylor JG. Using genetic variation to study immunomodulation. Curr Opin Pharmacol. 2002 Aug; 2(4):463-9.
Score: 0.042
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Milton JN, Gordeuk VR, Taylor JG, Gladwin MT, Steinberg MH, Sebastiani P. Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models. Circ Cardiovasc Genet. 2014 Apr; 7(2):110-5.
Score: 0.023
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Nekhai S, Xu M, Foster A, Kasvosve I, Diaz S, Machado RF, Castro OL, Kato GJ, Taylor JG, Gordeuk VR. Reduced sensitivity of the ferroportin Q248H mutant to physiological concentrations of hepcidin. Haematologica. 2013 Mar; 98(3):455-63.
Score: 0.021
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Solovieff N, Hartley SW, Baldwin CT, Klings ES, Gladwin MT, Taylor JG, Kato GJ, Farrer LA, Steinberg MH, Sebastiani P. Ancestry of African Americans with sickle cell disease. Blood Cells Mol Dis. 2011 Jun 15; 47(1):41-5.
Score: 0.019
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Kumkhaek C, Taylor JG, Zhu J, Hoppe C, Kato GJ, Rodgers GP. Fetal haemoglobin response to hydroxycarbamide treatment and sar1a promoter polymorphisms in sickle cell anaemia. Br J Haematol. 2008 Apr; 141(2):254-9.
Score: 0.015
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Eck P, Erichsen HC, Taylor JG, Yeager M, Hughes AL, Levine M, Chanock S. Comparison of the genomic structure and variation in the two human sodium-dependent vitamin C transporters, SLC23A1 and SLC23A2. Hum Genet. 2004 Sep; 115(4):285-94.
Score: 0.012