NEIL HANCHARD to Anemia, Sickle Cell
This is a "connection" page, showing publications NEIL HANCHARD has written about Anemia, Sickle Cell.
Connection Strength
1.585
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A locus on chromosome 5 shows African ancestry-limited association with alloimmunization in sickle cell disease. Blood Adv. 2018 12 26; 2(24):3637-3647.
Score: 0.514
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Whole-exome sequencing of sickle cell disease patients with hyperhemolysis syndrome suggests a role for rare variation in disease predisposition. Transfusion. 2018 03; 58(3):726-735.
Score: 0.478
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Classical sickle beta-globin haplotypes exhibit a high degree of long-range haplotype similarity in African and Afro-Caribbean populations. BMC Genet. 2007 Aug 10; 8:52.
Score: 0.234
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The additional genetic diagnosis of homozygous sickle cell disease in a patient with Waardenburg-Shah syndrome: a case report. J Med Case Rep. 2019 Jan 13; 13(1):10.
Score: 0.129
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Beta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa? OMICS. 2015 Mar; 19(3):171-9.
Score: 0.099
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Rate of change of sickle allele frequency may be influenced by total fertility rate: a sesquicentenary reflection on human micro-evolution. Br J Haematol. 2009 Nov; 147(4):582-3.
Score: 0.067
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Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patients. PLoS One. 2009; 4(1):e4218.
Score: 0.065