Gregers Rom Andersen - Genetic Mutations

Author Information

Gregers Rom Andersen is a distinguished researcher affiliated with the Department of Molecular Biology and Genetics at Aarhus University in Denmark. His work primarily focuses on the structural and functional analysis of proteins involved in the immune system, particularly those related to the complement system. Andersen's research contributes to a deeper understanding of molecular mechanisms that can inform new therapeutic strategies.

Research Contributions

Gregers Rom Andersen has made significant contributions to the field of molecular biology and genetics, with a particular emphasis on the complement system. His recent research includes the exploration of tick-derived complement inhibitors targeting properdin, the structural analysis of properdin oligomers, and the investigation of nanobodies as tools to understand and manipulate the complement cascade. Andersen's work has implications for developing novel therapeutic approaches for diseases involving protein aggregation and immune system dysfunction.

Aliases

Gregers Rom Andersen is known by several aliases in academic publications, including Gregers Andersen, Gregers R. Andersen, G. R. Andersen, Gregers R Andersen, and G R Andersen. These variations often appear in different publications and databases.

Publication and Citation Metrics

Metric	Value
Total Papers	245
Total Citations	5845
H-index	44

Publications:

Structure and function of a family of tick-derived complement inhibitors targeting properdin

DOI: 10.1038/s41467-021-27920-2

Year: 2022

Properdin oligomers adopt rigid extended conformations supporting function

DOI: 10.7554/eLife.63356

Year: 2021

Structure of the integrin receptor αMβ2 headpiece in complex with a function-modulating nanobody

DOI: 10.1101/2021.07.07.451531

Year: 2021

Author response: Properdin oligomers adopt rigid extended conformations supporting function

DOI: 10.7554/ELIFE.63356.SA2

Year: 2021

Complement Receptor 3 Forms a Compact High-Affinity Complex with iC3b

DOI: 10.4049/jimmunol.2001208

Year: 2021

Nanobodies Provide Insight Into the Molecular Mechanisms of the Complement Cascade and Offer New Therapeutic Strategies

DOI: 10.20944/PREPRINTS202101.0151.V1

Year: 2021

Mutation-induced dimerization of transforming growth factor-β–induced protein may drive protein aggregation in granular corneal dystrophy

DOI: 10.1016/j.jbc.2021.100858

Year: 2021

Purification of Human Complement Component C4 and Sample Preparation for Structural Biology Applications.

DOI: 10.1007/978-1-0716-1016-9_22

Year: 2021

Targeting properdin - Structure and function of a novel family of tick-derived complement inhibitors

DOI: 10.1101/2021.04.02.438250

Year: 2021

Nanobodies Provide Insight into the Molecular Mechanisms of the Complement Cascade and Offer New Therapeutic Strategies

DOI: 10.3390/biom11020298

Year: 2021

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