What is he best known for?
The fields of study he is best known for:
His primary areas of study are Genetics, DiGeorge syndrome, TBX1, Molecular biology and Gene.
Antonio Baldini has included themes like Endocrinology, Mutant, Haploinsufficiency, Internal medicine and Neuroscience in his DiGeorge syndrome study.
His TBX1 research is multidisciplinary, incorporating elements of Progenitor cell, Multipotent Stem Cell, Anatomy, Pharyngeal apparatus and Cell biology.
His studies in Cell biology integrate themes in fields like Cellular differentiation and FGF10.
His Molecular biology study combines topics from a wide range of disciplines, such as Hybridization probe, Molecular probe, Complementary DNA, Northern blot and Polymerase chain reaction.
His study in Gene is interdisciplinary in nature, drawing from both Senescence, Cell aging and Cell division.
His most cited work include:
- p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene. (864 citations)
- Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice (845 citations)
- Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia. (481 citations)
What are the main themes of his work throughout his whole career to date?
Antonio Baldini mainly focuses on Genetics, TBX1, Molecular biology, Gene and DiGeorge syndrome.
His work in Gene mapping, Phenotype, Chromosome, Fluorescence in situ hybridization and Locus is related to Genetics.
His studies deal with areas such as Cellular differentiation, Transcription factor, Pharyngeal apparatus, Haploinsufficiency and Cell biology as well as TBX1.
Within one scientific family, he focuses on topics pertaining to Mesoderm under Cell biology, and may sometimes address concerns connected to Anatomy.
He works mostly in the field of Molecular biology, limiting it down to topics relating to Chromosome 17 and, in certain cases, Smith–Magenis syndrome, as a part of the same area of interest.
His DiGeorge syndrome research incorporates elements of Mutation, Pharyngeal arch, Neural crest, Internal medicine and Chromosome 22.
He most often published in these fields:
- Genetics (53.16%)
- TBX1 (40.93%)
- Molecular biology (33.33%)
What were the highlights of his more recent work (between 2013-2021)?
- TBX1 (40.93%)
- Cell biology (24.89%)
- Transcription factor (9.70%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are TBX1, Cell biology, Transcription factor, Haploinsufficiency and Chromatin.
Antonio Baldini interconnects Phenotype, Chromatin remodeling, Transgene and Pathology in the investigation of issues within TBX1.
His Phenotype course of study focuses on Mutation and Mutant and DiGeorge syndrome.
His research integrates issues of Molecular biology and Histone in his study of Transcription factor.
His Haploinsufficiency research is multidisciplinary, incorporating perspectives in Pharyngeal apparatus, Endoderm and Regulation of gene expression.
His research in Genetics intersects with topics in Heart disease and Etiology.
Between 2013 and 2021, his most popular works were:
- Rebalancing gene haploinsufficiency in vivo by targeting chromatin (40 citations)
- Tbx1: Transcriptional and Developmental Functions. (30 citations)
- TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome (29 citations)
In his most recent research, the most cited papers focused on:
TBX1, Genetics, DiGeorge syndrome, Regulation of gene expression and Heart development are his primary areas of study.
Antonio Baldini combines subjects such as Mutation, Penetrance, Craniofacial, Physiology and Embryo with his study of TBX1.
His Mutation study incorporates themes from Phenotype and Transcription factor.
His studies in Genetics integrate themes in fields like Heart disease and Cell biology.
His biological study spans a wide range of topics, including Noonan syndrome, Etiology and 22q11 2ds.
His Regulation of gene expression research incorporates themes from Conditional gene knockout, Progenitor cell, Haploinsufficiency, PITX2 and Epigenetics.
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