| Establishing optimal quantitative-polymerase chain reaction assays for routine diagnosis and tracking of minimal residual disease in JAK2-V617F-associated myeloproliferative … JV Jovanovic, A Ivey, AM Vannucchi, E Lippert, E Oppliger Leibundgut, ... Leukemia 27 (10), 2032-2039, 2013 | 129 | 2013 |
| Clinical utility of next‐generation sequencing in the diagnosis of hereditary haemolytic anaemias AM Agarwal, RH Nussenzveig, NS Reading, JL Patel, N Sangle, ... British journal of haematology 174 (5), 806-814, 2016 | 93 | 2016 |
| Concordance of assays designed for the quantification of JAK2V617F: a multicenter study E Lippert, F Girodon, E Hammond, J Jelinek, NS Reading, B Fehse, ... haematologica 94 (1), 38-45 PMID: 19001280, 2009 | 92 | 2009 |
| The'GGCC'haplotype of JAK2 confers susceptibility to JAK2 exon 12 mutation-positive polycythemia vera. D Olcaydu, RC Skoda, R Looser, S Li, M Cazzola, D Pietra, F Passamonti, ... Leukemia 23 (10), 1924 PMID: 19440215, 2009 | 85 | 2009 |
| Angiogenic and inflammatory markers of cardiopulmonary changes in children and adolescents with sickle cell disease X Niu, M Nouraie, A Campbell, S Rana, CP Minniti, C Sable, D Darbari, ... PLoS one 4 (11), e7956, 2009 | 73 | 2009 |
| Gain-of-function EGLN1 prolyl hydroxylase (PHD2 D4E:C127S) in combination with EPAS1 (HIF-2α) polymorphism lowers hemoglobin concentration in Tibetan … T Tashi, N Scott Reading, T Wuren, X Zhang, LG Moore, H Hu, F Tang, ... Journal of Molecular Medicine 95, 665-670, 2017 | 71 | 2017 |
| Relative Stability of Recombinant Versus Native Peroxidases from Phanerochaete chrysosporium G Nie, NS Reading, SD Aust Archives of biochemistry and biophysics 365 (2), 328-334, 1999 | 70 | 1999 |
| Unexplained extreme hyperbilirubinemia among neonates in a multihospital healthcare system RD Christensen, DK Lambert, E Henry, LD Eggert, HM Yaish, ... Blood Cells, Molecules, and Diseases 50 (2), 105-109, 2013 | 68 | 2013 |
| Engineering a disulfide bond in recombinant manganese peroxidase results in increased thermostability NS Reading, SD Aust Biotechnology progress 16 (3), 326-333, 2000 | 68 | 2000 |
| Expression of the lignin peroxidase h2 gene from Phanerochaete chrysosporium in escherichia coli G Nie, NS Reading, SD Aust Biochemical and biophysical research communications 249 (1), 146-150, 1998 | 68 | 1998 |
| Mechanisms for protection against inactivation of manganese peroxidase by hydrogen peroxide SL Timofeevski, NS Reading, SD Aust Archives of Biochemistry and Biophysics 356 (2), 287-295, 1998 | 57 | 1998 |
| Genetic predisposition in type 2 diabetes: a promising approach toward a personalized management of diabetes MM Sirdah, NS Reading Clinical Genetics 98 (6), 525-547, 2020 | 55 | 2020 |
| Addition of veratryl alcohol oxidase activity to manganese peroxidase by site-directed mutagenesis SL Timofeevski, G Nie, NS Reading, SD Aust Biochemical and biophysical research communications 256 (3), 500-504, 1999 | 55 | 1999 |
| Substrate specificity of lignin peroxidase and a S168W variant of manganese peroxidase SL Timofeevski, G Nie, NS Reading, SD Aust Archives of Biochemistry and Biophysics 373 (1), 147-153, 2000 | 54 | 2000 |
| Expression of the Rho‐family GTPase gene RHOF in lymphocyte subsets and malignant lymphomas LG Gouw, N Scott Reading, SD Jenson, MS Lim, KSJ Elenitoba‐Johnson British journal of haematology 129 (4), 531-533, 2005 | 50 | 2005 |
| Association of G6PD202A,376G with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia M Nouraie, NS Reading, A Campbell, CP Minniti, SR Rana, ... British journal of haematology 150 (2), 218-225, 2010 | 44 | 2010 |
| Hemolysis and Mediterranean G6PD mutation (c. 563 C> T) and c. 1311 C> T polymorphism among Palestinians at Gaza Strip M Sirdah, NS Reading, SL Perkins, M Shubair, L Aboud, JT Prchal Blood Cells, Molecules, and Diseases 48 (4), 203-208, 2012 | 32 | 2012 |
| Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Gaza Strip Palestinians M Sirdah, NS Reading, H Vankayalapati, SL Perkins, ME Shubair, ... Blood Cells, Molecules, and Diseases 49 (3-4), 152-158, 2012 | 31 | 2012 |
| A quantitative allele-specific PCR test for the BRAF V600E mutation using a single heterozygous control plasmid for quantitation: a model for qPCR testing without standard curves P Szankasi, NS Reading, CP Vaughn, JT Prchal, DW Bahler, TW Kelley The Journal of Molecular Diagnostics 15 (2), 248-254, 2013 | 30 | 2013 |
| Neonatal death suspected to be from sepsis was found to be kernicterus with G6PD deficiency RD Christensen, HM Yaish, SE Wiedmeier, NS Reading, TJ Pysher, ... Pediatrics 132 (6), e1694-e1698, 2013 | 29 | 2013 |
Josef Prchaluniversity of utah在 hsc.utah.edu 的电子邮件经过验证
