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
Chemistry D-index 40 Citations 6,792 112 World Ranking 12736 National Ranking 3442
Biology and Biochemistry D-index 42 Citations 6,014 92 World Ranking 14986 National Ranking 6257

Overview

What is she best known for?

The fields of study she is best known for:

  • Enzyme
  • Organic chemistry
  • Biochemistry

The scientist’s investigation covers issues in Estrogen receptor, Stereochemistry, Estrogen receptor alpha, Ligand and Biochemistry. Her Estrogen receptor research incorporates themes from Receptor, Tamoxifen, Nuclear receptor, Estrogen and Binding site. The various areas that she examines in her Stereochemistry study include Molecule, Binding selectivity, Chemical synthesis, Double bond and Isostructural.

Her work is dedicated to discovering how Estrogen receptor alpha, Estrogen receptor beta are connected with Nuclear receptor coactivator 3 and Endocrinology and other disciplines. In her study, Estradiol binding, Ligand binding assay, Amino acid, Pharmacophore and Ligand efficiency is strongly linked to Cooperative binding, which falls under the umbrella field of Ligand. Her Biochemistry study incorporates themes from Promoter and Pyrazine.

Her most cited work include:

  • Estrogen receptor-β potency-selective ligands: Structure-activity relationship studies of diarylpropionitriles and their acetylene and polar analogues (605 citations)
  • The estradiol pharmacophore: Ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site (518 citations)
  • Synthesis and biological evaluation of a novel series of furans: Ligands selective for estrogen receptor α (179 citations)

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

Her primary scientific interests are in Estrogen receptor, Stereochemistry, Receptor, Ligand and Estrogen receptor alpha. She has researched Estrogen receptor in several fields, including Biochemistry, Estrogen and Cell biology. Her research integrates issues of Ligand, Structure–activity relationship, Chemical synthesis and Binding site in her study of Stereochemistry.

Her research investigates the link between Chemical synthesis and topics such as Molecular model that cross with problems in Docking. Kathryn E. Carlson combines subjects such as Endocrinology, Uterus, Estrogen receptor binding, Steric effects and Progesterone receptor with her study of Receptor. Her Estrogen receptor alpha study combines topics from a wide range of disciplines, such as Antiestrogen, Tamoxifen, Bazedoxifene and Cancer research.

She most often published in these fields:

  • Estrogen receptor (68.18%)
  • Stereochemistry (40.91%)
  • Receptor (26.52%)

What were the highlights of her more recent work (between 2015-2021)?

  • Estrogen receptor (68.18%)
  • Estrogen receptor alpha (24.24%)
  • Cancer research (13.64%)

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

Her scientific interests lie mostly in Estrogen receptor, Estrogen receptor alpha, Cancer research, Antiestrogen and Breast cancer. Her studies deal with areas such as Tamoxifen, Receptor, Ligand and Cell biology as well as Estrogen receptor. Her study focuses on the intersection of Receptor and fields such as Coactivator with connections in the field of Biochemistry.

Her Estrogen receptor alpha study incorporates themes from Fulvestrant, Stereochemistry, Pharmacology, Binding site and Bazedoxifene. Her studies in Stereochemistry integrate themes in fields like Protein structure, Reporter gene and Structure–activity relationship. Her Antiestrogen research focuses on Selective estrogen receptor modulator and how it relates to Potency and Isoliquiritigenin.

Between 2015 and 2021, her most popular works were:

  • Activating ESR1 Mutations Differentially Affect the Efficacy of ER Antagonists (153 citations)
  • Estrogen receptor alpha somatic mutations Y537S and D538G confer breast cancer endocrine resistance by stabilizing the activating function-2 binding conformation (137 citations)
  • Structural and Molecular Mechanisms of Cytokine-Mediated Endocrine Resistance in Human Breast Cancer Cells. (63 citations)

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

  • Enzyme
  • Organic chemistry
  • Biochemistry

Her primary areas of study are Estrogen receptor alpha, Estrogen receptor, Tamoxifen, Pharmacology and Antiestrogen. Her Estrogen receptor alpha research integrates issues from Nuclear receptor and Signal transduction, Cell biology. Her Nuclear receptor study combines topics in areas such as Cell growth and Ligand.

As part of her studies on Estrogen receptor, Kathryn E. Carlson frequently links adjacent subjects like Endocrinology. Kathryn E. Carlson has included themes like Cancer, Receptor, Fulvestrant, Estrogen Receptor Antagonists and Estrogen in her Pharmacology study. The concepts of her Antiestrogen study are interwoven with issues in Agonist and Isoliquiritigenin.

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

Estrogen receptor-β potency-selective ligands: Structure-activity relationship studies of diarylpropionitriles and their acetylene and polar analogues

Marvin J. Meyers;Jun Sun;Kathryn E. Carlson;Gwendolyn A. Marriner.
Journal of Medicinal Chemistry (2001)

764 Citations

The estradiol pharmacophore: Ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site

Gregory M. Anstead;Kathryn E. Carlson;John A. Katzenellenbogen.
Steroids (1997)

741 Citations

Studies on the uterine, cytoplasmic estrogen binding protein. Thermal stability and ligand dissociation rate. An assay of empty and filled sites by exchange.

John A. Katzenellenbogen;Howard J. Johnson;Kathryn E. Carlson.
Biochemistry (1973)

400 Citations

Synthesis and biological evaluation of a novel series of furans: Ligands selective for estrogen receptor α

Deborah S. Mortensen;Alice L. Rodriguez;Kathryn E. Carlson;Jun Sun.
Journal of Medicinal Chemistry (2001)

300 Citations

Altered Ligand Binding Properties and Enhanced Stability of a Constitutively Active Estrogen Receptor: Evidence That an Open Pocket Conformation Is Required for Ligand Interaction†

Kathryn E. Carlson;Inho Choi;Arvin Gee;Benita S. Katzenellenbogen.
Biochemistry (1997)

245 Citations

Pyrazolo[1,5-a]pyrimidines: Estrogen Receptor Ligands Possessing Estrogen Receptor β Antagonist Activity

Dennis R. Compton;Shubin Sheng;Kathryn E. Carlson;Natalie A. Rebacz.
Journal of Medicinal Chemistry (2004)

223 Citations

Efficient and highly selective covalent labeling of the estrogen receptor with [3H]tamoxifen aziridine

J A Katzenellenbogen;K E Carlson;D F Heiman;D W Robertson.
Journal of Biological Chemistry (1983)

216 Citations

Activating ESR1 Mutations Differentially Affect the Efficacy of ER Antagonists

Weiyi Toy;Hazel Weir;Pedram Razavi;Mandy Lawson.
Cancer Discovery (2017)

210 Citations

Coactivator peptides have a differential stabilizing effect on the binding of estrogens and antiestrogens with the estrogen receptor.

Arvin C. Gee;Kathryn E. Carlson;Paolo G. V. Martini;Benita S. Katzenellenbogen.
Molecular Endocrinology (1999)

182 Citations

11 beta-methoxy-, 11 beta-ethyl- and 17 alpha-ethynyl-substituted 16 alpha-fluoroestradiols: receptor-based imaging agents with enhanced uptake efficiency and selectivity.

Martin G. Pomper;Henry VanBrocklin;Andrea M. Thieme;Ralph D. Thomas.
Journal of Medicinal Chemistry (1990)

179 Citations

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