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
Biology and Biochemistry D-index 64 Citations 12,941 217 World Ranking 6327 National Ranking 455

Overview

What is he best known for?

The fields of study he is best known for:

  • Enzyme
  • Gene
  • Biochemistry

Biochemistry, Potassium channel, Biophysics, Methionine sulfoxide reductase and Methionine are his primary areas of study. His Biochemistry research includes themes of Gating and Cell biology. His Potassium channel research incorporates themes from Protein subunit and Pharmacology.

The Biophysics study combines topics in areas such as Patch clamp, Electrophysiology, Xenopus, Inward-rectifier potassium ion channel and Divalent. In his work, Methionine synthase, Oxidative stress, Mitochondrion and Molecular biology is strongly intertwined with MSRA, which is a subfield of Methionine sulfoxide reductase. Stefan H. Heinemann has researched Methionine sulfoxide in several fields, including Cysteine and Enzyme.

His most cited work include:

  • Drosophila odorant receptors are both ligand-gated and cyclic-nucleotide-activated cation channels (655 citations)
  • High-quality life extension by the enzyme peptide methionine sulfoxide reductase (389 citations)
  • Regulation of cell function by methionine oxidation and reduction (281 citations)

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

Stefan H. Heinemann mainly focuses on Biochemistry, Biophysics, Potassium channel, BK channel and Sodium channel. His works in Methionine, Methionine sulfoxide reductase, Enzyme, MSRA and Reactive oxygen species are all subjects of inquiry into Biochemistry. His studies in Biophysics integrate themes in fields like Patch clamp, Electrophysiology, HEK 293 cells, Intracellular and Inward-rectifier potassium ion channel.

His work investigates the relationship between Potassium channel and topics such as Xenopus that intersect with problems in Calmodulin and Cell biology. His research on BK channel also deals with topics like

  • Stereochemistry and Membrane potential most often made with reference to Gating,
  • Heme that connect with fields like Plasma protein binding. The various areas that he examines in his Sodium channel study include Receptor, Conotoxin, Molecular biology and Binding site.

He most often published in these fields:

  • Biochemistry (33.05%)
  • Biophysics (32.62%)
  • Potassium channel (23.61%)

What were the highlights of his more recent work (between 2014-2021)?

  • Biophysics (32.62%)
  • Crystallography (4.72%)
  • Stereochemistry (10.73%)

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

His primary scientific interests are in Biophysics, Crystallography, Stereochemistry, BK channel and Gating. Stefan H. Heinemann works on Biophysics which deals in particular with Potassium channel. His work on Calcium-activated potassium channel as part of general Potassium channel study is frequently connected to Modulation, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.

His Stereochemistry research is multidisciplinary, incorporating elements of Residue, Conotoxin, Disulfide bond and Binding site. The concepts of his BK channel study are interwoven with issues in Docosahexaenoic acid and Heme. His Gating research incorporates elements of Patch clamp, Allosteric regulation, Transmembrane domain and Cell biology.

Between 2014 and 2021, his most popular works were:

  • Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutant (47 citations)
  • Structure Elucidation and Activity of Kolossin A, the D-/L-Pentadecapeptide Product of a Giant Nonribosomal Peptide Synthetase† (35 citations)
  • CORM-EDE1: A Highly Water-Soluble and Nontoxic Manganese-Based photoCORM with a Biogenic Ligand Sphere. (27 citations)

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

  • Enzyme
  • Gene
  • Amino acid

Stefan H. Heinemann focuses on Stereochemistry, Gating, Cell biology, Potassium channel and Peptide. Stefan H. Heinemann interconnects Residue, Plasma protein binding, BK channel and Double bond in the investigation of issues within Stereochemistry. His biological study spans a wide range of topics, including Cell signaling, Mode of action, Endogeny, Patch clamp and Pharmacology.

His Cell biology research is multidisciplinary, incorporating perspectives in Immune system, Rheumatoid arthritis, Proinflammatory cytokine, Interleukin and Heme binding. Potassium channel is a subfield of Biophysics that Stefan H. Heinemann tackles. His Peptide study combines topics in areas such as Nonribosomal peptide, Biosynthesis and Photorhabdus luminescens.

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

Drosophila odorant receptors are both ligand-gated and cyclic-nucleotide-activated cation channels

Dieter Wicher;Ronny Schäfer;René Bauernfeind;Marcus C. Stensmyr.
Nature (2008)

907 Citations

High-quality life extension by the enzyme peptide methionine sulfoxide reductase

Hongyu Ruan;Xiang Dong Tang;Mai-Lei Chen;Mei-Ling A. Joiner.
Proceedings of the National Academy of Sciences of the United States of America (2002)

508 Citations

Regulation of cell function by methionine oxidation and reduction

Toshinori Hoshi;Stefan H. Heinemann.
The Journal of Physiology (2001)

428 Citations

Molecular determinants for activation and inactivation of HERG, a human inward rectifier potassium channel.

R Schönherr;S H Heinemann.
The Journal of Physiology (1996)

428 Citations

Carbon monoxide – physiology, detection and controlled release

Stefan H. Heinemann;Toshinori Hoshi;Matthias Westerhausen;Alexander Schiller.
Chemical Communications (2014)

412 Citations

Haem can bind to and inhibit mammalian calcium-dependent Slo1 BK channels

Xiang Dong Tang;Rong Xu;Mark F. Reynolds;Maria L. Garcia.
Nature (2003)

365 Citations

Peptide methionine sulfoxide reductase: structure, mechanism of action, and biological function

Herbert Weissbach;Frantzy Etienne;Toshinori Hoshi;Stefan H. Heinemann.
Archives of Biochemistry and Biophysics (2002)

333 Citations

The inhibitory effect of the antipsychotic drug haloperidol on HERG potassium channels expressed in Xenopus oocytes

H Suessbrich;R Schönherr;S H Heinemann;B Attali.
British Journal of Pharmacology (1997)

300 Citations

A de novo gain-of-function mutation in SCN11A causes loss of pain perception

Enrico Leipold;Lutz Liebmann;G Christoph Korenke;Theresa Heinrich.
Nature Genetics (2013)

279 Citations

Functional characterization of Kv channel beta-subunits from rat brain

S H Heinemann;J Rettig;H R Graack;O Pongs.
The Journal of Physiology (1996)

254 Citations

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