What is he best known for?
The fields of study he is best known for:
- Gene
- Mutation
- Internal medicine
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.
His most cited work include:
- Subgroup-specific structural variation across 1,000 medulloblastoma genomes (565 citations)
- Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. (342 citations)
- The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload. (251 citations)
What are the main themes of his work throughout his whole career to date?
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
- Endocrinology that intertwine with fields like Hemolytic anemia and Ineffective erythropoiesis,
- Bioinformatics most often made with reference to Oncology.
His Molecular biology study which covers Spectrin that intersects with Band 3.
His study looks at the relationship between Gene and topics such as Cancer research, which overlap with Tumor suppressor gene and Cell cycle.
He most often published in these fields:
- Genetics (24.49%)
- Internal medicine (23.91%)
- Molecular biology (17.20%)
What were the highlights of his more recent work (between 2017-2021)?
- Internal medicine (23.91%)
- Anemia (11.95%)
- Gene (15.45%)
In recent papers he was focusing on the following fields of study:
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.
Between 2017 and 2021, his most popular works were:
- Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias. (53 citations)
- Resolution of sickle cell disease-associated inflammation and tissue damage with 17R-resolvin D1. (29 citations)
- Fine mapping of 2q35 high‐risk neuroblastoma locus reveals independent functional risk variants and suggests full‐length BARD1 as tumor‐suppressor (24 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Mutation
- Internal medicine
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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