What is she best known for?
The fields of study she is best known for:
- Organic chemistry
- Enzyme
- Biochemistry
Her primary scientific interests are in Stereochemistry, Glycomimetic, DC-SIGN, Receptor and Organic chemistry.
Her Stereochemistry study combines topics in areas such as Combinatorial chemistry, Integrin, Ligand and Stereoselectivity.
In her study, Molecular mimicry is inextricably linked to Cholera toxin, which falls within the broad field of Glycomimetic.
Her DC-SIGN research incorporates elements of Lectin, Biochemistry, C-type lectin and Virology.
Her Biochemistry research focuses on subjects like Immune system, which are linked to Cell.
Her study on Enantioselective synthesis, Stereocenter and Allylic rearrangement is often connected to Conjugate as part of broader study in Organic chemistry.
Her most cited work include:
- Multivalent glycoconjugates as anti-pathogenic agents (340 citations)
- A comparison and chemometric analysis of several molecular mechanics force fields and parameter sets applied to carbohydrates (125 citations)
- Inhibition of DC-SIGN-Mediated HIV Infection by a Linear Trimannoside Mimic in a Tetravalent Presentation (99 citations)
What are the main themes of her work throughout her whole career to date?
Her main research concerns Stereochemistry, Biochemistry, Organic chemistry, Stereoselectivity and Glycomimetic.
As part of one scientific family, Anna Bernardi deals mainly with the area of Stereochemistry, narrowing it down to issues related to the Cholera toxin, and often Toxin and Ganglioside.
Her study in the fields of Lectin under the domain of Biochemistry overlaps with other disciplines such as Hsp90.
Her Stereoselectivity research integrates issues from Selectivity, Computational chemistry, Aldol reaction and Addition reaction.
Her study focuses on the intersection of Glycomimetic and fields such as DC-SIGN with connections in the field of Mannose.
Her Enantioselective synthesis research includes elements of Oxazolidine, Medicinal chemistry and Aldehyde.
She most often published in these fields:
- Stereochemistry (39.76%)
- Biochemistry (16.93%)
- Organic chemistry (16.54%)
What were the highlights of her more recent work (between 2012-2021)?
- Stereochemistry (39.76%)
- Glycomimetic (12.99%)
- Biochemistry (16.93%)
In recent papers she was focusing on the following fields of study:
Stereochemistry, Glycomimetic, Biochemistry, DC-SIGN and Lectin are her primary areas of study.
The Stereochemistry study which covers Ligand that intersects with Binding site.
Her Glycomimetic research is multidisciplinary, incorporating perspectives in Surface plasmon resonance, Langerin, Receptor, C-type lectin and Mannose.
Her Mannan-binding lectin and In vitro study in the realm of Biochemistry interacts with subjects such as Hsp90 and Scaffold.
The various areas that she examines in her DC-SIGN study include Combinatorial chemistry and Internalization.
Her Lectin research includes themes of Fucose binding, Fucose, Glycoconjugate and Virtual screening.
Between 2012 and 2021, her most popular works were:
- Multivalent glycoconjugates as anti-pathogenic agents (340 citations)
- A multivalent inhibitor of the DC-SIGN dependent uptake of HIV-1 and Dengue virus (73 citations)
- Designing nanomolar antagonists of DC-SIGN-mediated HIV infection: ligand presentation using molecular rods. (52 citations)
In her most recent research, the most cited papers focused on:
- Organic chemistry
- Enzyme
- Biochemistry
Anna Bernardi mainly investigates Glycomimetic, DC-SIGN, Stereochemistry, Biophysics and Biochemistry.
Her Glycomimetic research is multidisciplinary, relying on both Innate immune system, Langerin, Surface plasmon resonance and Cell biology.
Her work carried out in the field of DC-SIGN brings together such families of science as Receptor, Internalization and Binding site.
Her Stereochemistry study incorporates themes from Combinatorial chemistry, Dendrimer and Ligand.
Anna Bernardi has researched Biophysics in several fields, including Protein structure and C-type lectin.
She specializes in Biochemistry, namely Glycoconjugate.
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