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 43 Citations 11,336 124 World Ranking 14190 National Ranking 1049

Overview

What is he best known for?

The fields of study he is best known for:

  • Enzyme
  • Gene
  • Biochemistry

Dieter Schrenk mostly deals with Biochemistry, Pharmacology, Multidrug resistance-associated protein 2, Aryl hydrocarbon receptor and World health. His Metabolite, Organic anion transport and Mutation study in the realm of Biochemistry connects with subjects such as Conjugated system. His Pharmacology study combines topics from a wide range of disciplines, such as Cell culture and P-glycoprotein.

His Aryl hydrocarbon receptor research incorporates elements of Cancer research, Stereochemistry, Cytochrome P450 and Enzyme inducer. Throughout his World health studies, Dieter Schrenk incorporates elements of other sciences such as Polychlorinated dibenzodioxins, Environmental health, Polybrominated Biphenyls and Environmental chemistry. His Polybrominated Biphenyls research incorporates themes from Dioxins and dioxin-like compounds and Polychlorinated naphthalene.

His most cited work include:

  • The 2005 World Health Organization reevaluation of human and Mammalian toxic equivalency factors for dioxins and dioxin-like compounds. (2674 citations)
  • An endogenous tumour-promoting ligand of the human aryl hydrocarbon receptor (1047 citations)
  • Inhibition of histone-deacetylase activity by short-chain fatty acids and some polyphenol metabolites formed in the colon. (320 citations)

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

Dieter Schrenk focuses on Biochemistry, Toxicity, Pharmacology, Carcinogen and Internal medicine. His research in Toxicity intersects with topics in Environmental chemistry and In vitro. His study in Environmental chemistry focuses on Polychlorinated dibenzofurans in particular.

His Carcinogen research is multidisciplinary, relying on both Mode of action and Genotoxicity. Dieter Schrenk works mostly in the field of Internal medicine, limiting it down to topics relating to Endocrinology and, in certain cases, Tumor promotion and Hepatocyte. His study looks at the relationship between Cytochrome P450 and fields such as Aryl hydrocarbon receptor, as well as how they intersect with chemical problems.

He most often published in these fields:

  • Biochemistry (25.66%)
  • Toxicity (14.60%)
  • Pharmacology (13.72%)

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

  • Toxicity (14.60%)
  • Pyrrolizidine (5.31%)
  • Carcinogen (13.27%)

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

Dieter Schrenk mainly focuses on Toxicity, Pyrrolizidine, Carcinogen, Toxicology and Biochemistry. The various areas that Dieter Schrenk examines in his Toxicity study include Incidence, Environmental health, Adult age, European population and Physiology. His studies deal with areas such as Young age, Tolerable daily intake and Honey Bees as well as Environmental health.

His Pyrrolizidine research includes themes of Glutathione, Genotoxicity, Cytotoxicity, Traditional medicine and Pharmacology. In his works, Dieter Schrenk conducts interdisciplinary research on Toxicology and Quinolizidine. His Microsome, Metabolism and Cytochrome P450 study are his primary interests in Biochemistry.

Between 2017 and 2021, his most popular works were:

  • Guidance on harmonised methodologies for human health, animal health and ecological risk assessment of combined exposure to multiple chemicals (111 citations)
  • Risk to human health related to the presence of perfluoroalkyl substances in food. (43 citations)
  • Risk assessment of aflatoxins in food (39 citations)

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

  • Enzyme
  • Gene
  • Biochemistry

His main research concerns Toxicology, Genotoxicity, Body weight, Toxicokinetics and Toxicity. His study deals with a combination of Toxicology and Quinolizidine. Dieter Schrenk has researched Genotoxicity in several fields, including Chromatography, Fraction and Toxicity aspects.

His study in Body weight is interdisciplinary in nature, drawing from both Adult age, European population, Animal science and Human study. His Toxicokinetics study is focused on Pharmacology in general. His research integrates issues of Glyphosate, Adverse effect, Physiology and Genetically modified organism in his study of Toxicity.

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

The 2005 World Health Organization reevaluation of human and Mammalian toxic equivalency factors for dioxins and dioxin-like compounds.

Martin Van den Berg;Linda S. Birnbaum;Michael Denison;Mike De Vito.
Toxicological Sciences (2006)

3417 Citations

An endogenous tumour-promoting ligand of the human aryl hydrocarbon receptor

Christiane A. Opitz;Ulrike M. Litzenburger;Ulrike M. Litzenburger;Felix Sahm;Martina Ott.
Nature (2011)

1305 Citations

Inhibition of histone-deacetylase activity by short-chain fatty acids and some polyphenol metabolites formed in the colon.

Markus Waldecker;Tanja Kautenburger;Heike Daumann;Cordula Busch.
Journal of Nutritional Biochemistry (2008)

532 Citations

Opinion of the Scientific Panel on Contaminants in the Food chain on perfluorooctane sulfonate (PFOS), perfluorooctanoic acid (PFOA) and their salts

D. Benford;J. de Boer;A. Carere;A. di Domenico.
EFSA Journal (2008)

405 Citations

Dioxins: WHO’s tolerable daily intake (TDI) revisited

F.X.Rolaf van Leeuwen;Mark Feeley;Dieter Schrenk;John Christian Larsen.
Chemosphere (2000)

403 Citations

Induction of P‐glycoprotein by rifampin increases intestinal secretion of talinolol in human beings: A new type of drug/drug interaction

Kristin Westphal;Anita Weinbrenner;Michael Zschiesche;Gerd Franke.
Clinical Pharmacology & Therapeutics (2000)

368 Citations

The effect of rifampin treatment on intestinal expression of human MRP transporters

Martin F. Fromm;Hans-Martin Kauffmann;Peter Fritz;Oliver Burk.
American Journal of Pathology (2000)

307 Citations

Bioactive compounds: definition and assessment of activity

Hans-Konrad Biesalski;Lars Ove Dragsted;Ibrahim Elmadfa;Rolf Grossklaus.
Nutrition (2009)

285 Citations

The influence of environmental and genetic factors on CYP2D6, CYP1A2 and UDP-glucuronosyltransferases in man using sparteine, caffeine, and paracetamol as probes.

Karl Bock;Dieter Schrenk;Adelheid Forster;Ernst-Ulrich Griese.
Pharmacogenetics (1994)

274 Citations

Gene and Protein Expression of P-Glycoprotein, MRP1, MRP2, and CYP3A4 in the Small and Large Human Intestine

Sofia Berggren;Christine Gall;Nadine Wollnitz;Mats Ekelund.
Molecular Pharmaceutics (2007)

234 Citations

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