N. Scott Reading

Clinical utility of next‐generation sequencing in the diagnosis of hereditary haemolytic anaemias

Archana M. Agarwal, Roberto Nussenzveig, N. Scott Reading et al. · British Journal of Haematology · 2016 · 97 citations

Medicine, Genetics, Molecular Genetics +16

Gain-of-function EGLN1 prolyl hydroxylase (PHD2 D4E:C127S) in combination with EPAS1 (HIF-2α) polymorphism lowers hemoglobin concentration in Tibetan highlanders

Tsewang Tashi, N. Scott Reading, Tanna Wuren et al. · Journal of Molecular Medicine · 2017 · 80 citations

Life Sciences, Genetics, Molecular Genetics +9

Concordance of assays designed for the quantification of JAK2V617F: a multicenter study

Éric Lippert, François Girodon, E. Hammond et al. · Haematologica · 2008 · 77 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Angiogenic and Inflammatory Markers of Cardiopulmonary Changes in Children and Adolescents with Sickle Cell Disease

Xiaomei Niu, Mehdi Nouraie, Andrew Campbell et al. · PLoS ONE · 2009 · 70 citations · Full text

Medicine, Cardiology, Pediatrics +16

Unexplained extreme hyperbilirubinemia among neonates in a multihospital healthcare system

Robert D. Christensen, Diane K. Lambert, Erick Henry et al. · Blood Cells Molecules and Diseases · 2012 · 61 citations

Medicine, Child Health, Pediatrics +11