Nisha Vasavda

Whole-Genome Scan, in a Complex Disease, Using 11,245 Single-Nucleotide Polymorphisms: Comparison with Microsatellites

Sally John, Neil Shephard, Guoying Liu et al. · The American Journal of Human Genetics · 2004 · 226 citations · Full text

Genetic Analysis, Haplotype Determination, Single-nucleotide Polymorphisms +12

Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia

Julie Makani, Stephan Menzel, Siana Nkya et al. · Blood · 2010 · 105 citations · Full text

The linear effects of <i>α</i>‐thalassaemia, the <i>UGT1A1</i> and <i>HMOX1</i> polymorphisms on cholelithiasis in sickle cell disease

Nisha Vasavda, Stephan Menzel, Emma G. Maytham et al. · British Journal of Haematology · 2007 · 82 citations

Blood transfusion usage among adults with sickle cell disease – a single institution experience over ten years

Emma Drašar, Norris Igbineweka, Nisha Vasavda et al. · British Journal of Haematology · 2011 · 67 citations · Full text

Immunohematology, Blood Transfusion Usage, Blood Cell +16

Quantitation of hepcidin in human urine by liquid chromatography–mass spectrometry

Sukhvinder S. Bansal, John M. Halket, Adrian Bomford et al. · Analytical Biochemistry · 2008 · 42 citations

Human Urine, Urology, Biochemistry +11