D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Microbiology D-index 43 Citations 6,484 128 World Ranking 4153 National Ranking 17

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Antibody
  • DNA

Inger Sandlie mostly deals with Neonatal Fc receptor, Receptor, Molecular biology, Antibody and Immunoglobulin G. Her Neonatal Fc receptor research includes themes of Human serum albumin, Albumin, Biochemistry and Histidine. Her research investigates the connection between Biochemistry and topics such as Complement system that intersect with issues in Peptide sequence.

Her work in Receptor addresses issues such as MHC class I, which are connected to fields such as Residue, Recombinant DNA and Receptor recycling. Inger Sandlie combines subjects such as Mutation, Mutant, Expression vector, Fusion protein and Epitope with her study of Molecular biology. Her research combines Cell biology and Antibody.

Her most cited work include:

  • Therapeutic antibodies for human diseases at the dawn of the twenty-first century (568 citations)
  • Versatile vectors for transient and stable expression of recombinant antibody molecules in mammalian cells (201 citations)
  • The structural requirements for complement activation by IgG: does it hinge on the hinge? (157 citations)

What are the main themes of her work throughout her whole career to date?

Her primary areas of investigation include Molecular biology, Antibody, Cell biology, Antigen and Neonatal Fc receptor. The study incorporates disciplines such as Recombinant DNA, Mutation, Mutant, Peptide sequence and Peptide in addition to Molecular biology. The Antibody study combines topics in areas such as Immune system and Virology.

Her Cell biology course of study focuses on Complement system and Hapten. Her Neonatal Fc receptor study combines topics in areas such as Receptor, Biochemistry, Albumin and Histidine. Her study looks at the relationship between Albumin and fields such as Intracellular, as well as how they intersect with chemical problems.

She most often published in these fields:

  • Molecular biology (44.85%)
  • Antibody (48.97%)
  • Cell biology (36.60%)

What were the highlights of her more recent work (between 2017-2021)?

  • Cell biology (36.60%)
  • Antigen (29.90%)
  • Albumin (23.71%)

In recent papers she was focusing on the following fields of study:

Her primary areas of study are Cell biology, Antigen, Albumin, Major histocompatibility complex and Epitope. Inger Sandlie interconnects Immunoglobulin G, Complement system, Classical complement pathway, Receptor and Transduction in the investigation of issues within Cell biology. Her Antigen research incorporates themes from Antibody and Immune system.

Inger Sandlie mostly deals with Monoclonal antibody in her studies of Antibody. Her Albumin research integrates issues from Pharmacokinetics and Intracellular. She studied Major histocompatibility complex and T-cell receptor that intersect with Computational biology, Periplasmic space, Protein structure, Chaperone and Biochemistry.

Between 2017 and 2021, her most popular works were:

  • The Neonatal Fc Receptor (FcRn): A Misnomer? (78 citations)
  • Binding to Nanopatterned Antigens is Dominated by the Spatial Tolerance of Antibodies (44 citations)
  • Binding to Nanopatterned Antigens is Dominated by the Spatial Tolerance of Antibodies (44 citations)

In her most recent research, the most cited papers focused on:

  • Gene
  • Antibody
  • DNA

The scientist’s investigation covers issues in Cell biology, Immune system, Complement system, Intracellular and Plasma protein binding. Her Cell biology study combines topics from a wide range of disciplines, such as Immunoglobulin G, Virus, Fc receptor, Transduction and Classical complement pathway. Her studies deal with areas such as Endothelial stem cell, Cellular Assay, Albumin, Genetically modified mouse and Serum albumin as well as Immunoglobulin G.

Inger Sandlie has included themes like Epitope and Antibody in her Immune system study. She has researched Antibody in several fields, including Biophysics, Bivalent, Immune tolerance, Antigen and DNA origami. Her studies in Complement system integrate themes in fields like Transgene, Cell membrane, Viral replication, Antibody receptor and Effector.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Therapeutic antibodies for human diseases at the dawn of the twenty-first century

Ole Henrik Brekke;Inger Sandlie.
Nature Reviews Drug Discovery (2003)

888 Citations

Competition for FcRn-mediated transport gives rise to short half-life of human IgG3 and offers therapeutic potential

Nigel M. Stapleton;Jan Terje Andersen;Jan Terje Andersen;Annette M. Stemerding;Stefania P. Bjarnarson.
Nature Communications (2011)

236 Citations

Versatile vectors for transient and stable expression of recombinant antibody molecules in mammalian cells

Lars Norderhaug;Tove Olafsen;Terje E Michaelsen;Inger Sandlie.
Journal of Immunological Methods (1997)

216 Citations

Unraveling the Interaction between FcRn and Albumin: Opportunities for Design of Albumin-Based Therapeutics

Kine Marita Knudsen Sand;Kine Marita Knudsen Sand;Malin C. Bern;Malin C. Bern;Jeannette Nilsen;Jeannette Nilsen;Hanna Theodora Noordzij;Hanna Theodora Noordzij.
Frontiers in Immunology (2015)

205 Citations

The structural requirements for complement activation by IgG: does it hinge on the hinge?

Ole Henrik Brekke;Terje E. Michaelsen;Inger Sandlie.
Immunology Today (1995)

204 Citations

Neonatal Fc receptor for IgG (FcRn) regulates cross-presentation of IgG immune complexes by CD8-CD11b+ dendritic cells.

Kristi Baker;Shuo-Wang Qiao;Timothy T. Kuo;Victoria G. Aveson.
Proceedings of the National Academy of Sciences of the United States of America (2011)

196 Citations

Cross-species Binding Analyses of Mouse and Human Neonatal Fc Receptor Show Dramatic Differences in Immunoglobulin G and Albumin Binding

Jan Terje Andersen;Muluneh Bekele Daba;Gøril Berntzen;Terje Einar Michaelsen;Terje Einar Michaelsen.
Journal of Biological Chemistry (2010)

179 Citations

Structure-based mutagenesis reveals the albumin-binding site of the neonatal Fc receptor.

Jan Terje Andersen;Bjørn Dalhus;Jason Cameron;Muluneh Bekele Daba;Muluneh Bekele Daba.
Nature Communications (2012)

176 Citations

Lysine 322 in the human IgG3 C(H)2 domain is crucial for antibody dependent complement activation.

John E Thommesen;Terje E Michaelsen;Geir Åge Løset;Inger Sandlie.
Molecular Immunology (2000)

163 Citations

Aglycosylated IgG variants expressed in bacteria that selectively bind FcγRI potentiate tumor cell killing by monocyte-dendritic cells

Sang Taek Jung;Sai T. Reddy;Tae Hyun Kang;M. Jack Borrok.
Proceedings of the National Academy of Sciences of the United States of America (2010)

152 Citations

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