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Author Details
Full Name
Peter E Newburger
Affiliation
ORCID
Career Start Year
1974
Papers
185
H Index
56
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36939030
Reply to: Stand with Ukraine.
2023
38034420
Clinical Remission of Severe Crohn's Disease with Empagliflozin Monotherapy in a Pediatric Patient with Glycogen Storage Disease Type 1b.
2023
37008163
The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action.
2023
33513358
Dissecting ELANE neutropenia pathogenicity by human HSC gene editing.
Cell Stem Cell
2021
32043619
Genotype-phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency.
Am J Hematol
2020
31255364
Benign ethnic neutropenia.
Blood Reviews
2019
30260027
Gene expression in chronic granulomatous disease and interferon-γ receptor-deficient cells treated in vitro with interferon-γ.
Journal of Cellular Biochemistry
2019
30213831
Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate Kinase Deficiency Natural History Study.
Haematologica
2019
30536760
Neutropenia in the age of genetic testing: Advances and challenges.
American Journal of Hematology
2019
30294941
How we approach: Severe congenital neutropenia and myelofibrosis due to mutations in VPS45.
Pediatric Blood and Cancer
2019
30735661
The Genetic Landscape of Diamond-Blackfan Anemia.
Am J Hum Genet
2019
29549173
Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study.
Blood
2018
30503522
The Genetic Landscape of Diamond-Blackfan Anemia.
Am J Hum Genet
2018
30518921
Trisomy silencing by XIST normalizes Down syndrome cell pathogenesis demonstrated for hematopoietic defects in vitro.
Nature Communications
2018
29380530
How I approach⿦-A new series in Pediatric Blood & Cancer.
Pediatric Blood and Cancer
2018
29119580
Comment on: Phenotypic Prenatal Diagnosis of Chronic Granulomatous Disease: A Useful Tool in the Absence of Molecular Diagnosis.
Scandinavian Journal of Immunology
2018
27888688
An oral Hemokine, α-methylhydrocinnamate, enhances myeloid and neutrophil recovery following irradiation in vivo.
Blood Cells, Molecules, and Diseases
2017
28453180
A novel homozygous VPS45 p.P468L mutation leading to severe congenital neutropenia with myelofibrosis.
Pediatr Blood Cancer
2017
29211670
Long-Term Effects of G-CSF Therapy in Cyclic Neutropenia.
N Engl J Med
2017
28266767
Laurence A. Boxer, MD, 1940-2017.
Pediatric Blood and Cancer
2017
27913460
Autoimmune and other acquired neutropenias.
Hematology. American Society of Hematology. Education Program
2016
26965635
Frontline Science: Splenic progenitors aid in maintaining high neutrophil numbers at sites of sterile chronic inflammation.
Journal of Leukocyte Biology
2016
27117572
Mild Microcytic Anemia in an Infant with a Compound Heterozygosity for Hb C (HBB: c.19Gâ¿¿>â¿¿A) and Hb Osu Christiansborg (HBB: c.157Gâ¿¿>â¿¿A).
Hemoglobin
2016
26104864
In memoriam: Robert J. Arceci.
Pediatric Blood and Cancer
2015
25752509
Regulation of CYBB Gene Expression in Human Phagocytes by a Distant Upstream NF-κB Binding Site.
Journal of Cellular Biochemistry
2015
25542884
Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency.
Journal of Allergy and Clinical Immunology
2015
25560125
Use of granulocyte colony-stimulating factor during pregnancy in women with chronic neutropenia.
Obstetrics and Gynecology
2015
25427142
The diversity of mutations and clinical outcomes for ELANE-associated neutropenia.
Curr Opin Hematol
2015
26355958
Neutrophil Responses to Sterile Implant Materials.
PLoS ONE
2015
26491070
Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9.
Blood
2015
24824789
Long intergenic non-coding RNA HOTAIRM1 regulates cell cycle progression during myeloid maturation in NB4 human promyelocytic leukemia cells.
RNA Biology
2014
23649634
HOX antisense lincRNA HOXA-AS2 is an apoptosis repressor in all trans retinoic acid treated NB4 promyelocytic leukemia cells.
Journal of Cellular Biochemistry
2013
23953336
Evaluation and management of patients with isolated neutropenia.
Seminars in Hematology
2013
23812780
Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond-Blackfan anemia.
Hum Genet
2013
23577835
Advances in understanding the pathogenesis of HLH.
British Journal of Haematology
2013
22431104
Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia.
Hum Mutat
2012
21278736
Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease.
Nature Immunology
2011
21204900
The human NADPH oxidase: primary and secondary defects impairing the respiratory burst function and the microbicidal ability of phagocytes.
Scandinavian Journal of Immunology
2011
21370424
Hemophagocytic lymphohistiocytosis with MUNC13-4 gene mutation or reduced natural killer cell function prior to onset of childhood leukemia.
Pediatric Blood and Cancer
2011
20582973
Cyclic neutropenia and severe congenital neutropenia in patients with a shared ELANE mutation and paternal haplotype: evidence for phenotype determination by modifying genes.
Pediatric Blood and Cancer
2010
20485380
Local arterial nanoparticle delivery of siRNA for NOX2 knockdown to prevent restenosis in an atherosclerotic rat model.
Gene Therapy
2010
20133578
X chromosome-wide analyses of genomic DNA methylation states and gene expression in male and female neutrophils.
Proc Natl Acad Sci U S A
2010
20116044
Ribosomal protein genes RPS10 and RPS26 are commonly mutated in Diamond-Blackfan anemia.
American Journal of Human Genetics
2010
20456363
Stable long-term risk of leukaemia in patients with severe congenital neutropenia maintained on G-CSF therapy.
Br J Haematol
2010
19144990
A myelopoiesis-associated regulatory intergenic noncoding RNA transcript within the human HOXA cluster.
Blood
2009
19214977
Use of rituximab for refractory cytopenias associated with autoimmune lymphoproliferative syndrome (ALPS).
Pediatr Blood Cancer
2009
19208418
Cyclic neutropenia in animals.
American Journal of Hematology
2009
19726766
Comment on "Impaired priming and activation of the neutrophil NADPH oxidase in patients with IRAK4 or NEMO deficiency".
Journal of Immunology
2009
19607874
Dynamics of alpha-globin locus chromatin structure and gene expression during erythroid differentiation of human CD34(+) cells in culture.
Experimental Hematology
2009
18544685
Toll-like receptor-mediated activation of neutrophils by influenza A virus.
Blood
2008
1 - 50 of 185
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