His scientific interests lie mostly in Genetics, Immunology, Anemia, Internal medicine and Congenital dyserythropoietic anemia. His is involved in several facets of Genetics study, as is seen by his studies on Genome-wide association study, Neuroblastoma, Mutation, Allele and Missense mutation. The concepts of his Mutation study are interwoven with issues in Molecular biology and May–Hegglin anomaly.
The study incorporates disciplines such as Thalassemia, Disease and Hereditary spherocytosis in addition to Anemia. Achille Iolascon combines subjects such as Endocrinology, Gene mutation and Genotype with his study of Internal medicine. His Congenital dyserythropoietic anemia study combines topics in areas such as KLF1, Endoplasmic reticulum, GATA1 and Dyserythropoietic anemia.
Achille Iolascon mainly focuses on Genetics, Internal medicine, Molecular biology, Immunology and Gene. His work on Genetics deals in particular with Mutation, Allele, Locus, Single-nucleotide polymorphism and Missense mutation. His study in Allele is interdisciplinary in nature, drawing from both Neuroblastoma and Genotype.
His research on Internal medicine also deals with topics like
Achille Iolascon focuses on Internal medicine, Anemia, Gene, Disease and Cancer research. His Internal medicine study incorporates themes from Gastroenterology, Endocrinology and Oncology. The various areas that Achille Iolascon examines in his Anemia study include Thalassemia, Phenotype, Pediatrics and Mutation.
His Gene study is related to the wider topic of Genetics. His work on Locus, Single-nucleotide polymorphism and Transcription factor as part of general Genetics study is frequently connected to Treatment resistant schizophrenia, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. Achille Iolascon has researched Cancer research in several fields, including Cancer, Progression-free survival, Neuroblastoma and Lactate dehydrogenase.
His primary scientific interests are in Hepcidin, Anemia, Internal medicine, Cancer research and Pathology. His Hepcidin study integrates concerns from other disciplines, such as Modifier Genes, Ineffective erythropoiesis and Bioinformatics. In most of his Anemia studies, his work intersects topics such as Mutation.
His biological study spans a wide range of topics, including Congenital dyserythropoietic anemia and Pediatrics. His Internal medicine research is multidisciplinary, incorporating perspectives in Gastroenterology, Endocrinology and Downregulation and upregulation. His Pathology research incorporates themes from Phenotype, Compound heterozygosity and Spherocytosis.
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Subgroup-specific structural variation across 1,000 medulloblastoma genomes
Paul A. Northcott;Paul A. Northcott;David J.H. Shih;John Peacock;Livia Garzia.
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.
Seri M;Cusano R;Gangarossa S;Caridi G.
Nature Genetics (2000)
The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload.
Clara Camaschella;Alessandro Campanella;Luigia De Falco;Loredana Boschetto.
Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update.
Paula H. B. Bolton-Maggs;Jacob C. Langer;Achille Iolascon;Paul Tittensor.
British Journal of Haematology (2012)
MicroRNA-199b-5p impairs cancer stem cells through negative regulation of HES1 in medulloblastoma.
Livia Garzia;Immacolata Andolfo;Emilio Cusanelli;Natascia Marino.
PLOS ONE (2009)
Inherited thrombocytopenias: from genes to therapy
Carlo L Balduini;Achille Iolascon;Anna Savoia.
Integrative genomics identifies LMO1 as a neuroblastoma oncogene
Kai Wang;Kai Wang;Sharon J. Diskin;Haitao Zhang;Edward F. Attiyeh.
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.
Klaus Schwarz;Klaus Schwarz;Achille Iolascon;Fatima Verissimo;Nikolaus S Trede;Nikolaus S Trede.
Nature Genetics (2009)
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1
Immacolata Andolfo;Seth L. Alper;Lucia De Franceschi;Carla Auriemma.
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma
Sharon J Diskin;Mario Capasso;Robert W Schnepp;Kristina A Cole;Kristina A Cole.
Nature Genetics (2012)
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