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
Medicine D-index 92 Citations 32,277 235 World Ranking 6994 National Ranking 238

Overview

What is he best known for?

The fields of study he is best known for:

  • Enzyme
  • Gene
  • Internal medicine

His primary scientific interests are in Pharmacology, P-glycoprotein, Abcg2, ATP-binding cassette transporter and Internal medicine. His biological study spans a wide range of topics, including CYP3A and In vivo. His studies deal with areas such as Biochemistry, Blood–brain barrier and Transfection as well as P-glycoprotein.

Alfred H. Schinkel has included themes like Carcinogen, Secretion, Lactation, Vitamin and Drug resistance in his Abcg2 study. His ATP-binding cassette transporter study incorporates themes from Multiple drug resistance, Topotecan and Doxorubicin. His research in Internal medicine intersects with topics in Endocrinology and Hepatocyte.

His most cited work include:

  • Disruption of the mouse mdr1a P-glycoprotein gene leads to a deficiency in the blood-brain barrier and to increased sensitivity to drugs (1972 citations)
  • Mammalian drug efflux transporters of the ATP binding cassette (ABC) family: an overview. (1230 citations)
  • Normal viability and altered pharmacokinetics in mice lacking mdr1-type (drug-transporting) P-glycoproteins (834 citations)

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

His primary areas of investigation include Pharmacology, P-glycoprotein, Pharmacokinetics, Abcg2 and In vivo. The study incorporates disciplines such as Toxicity, CYP3A and Multidrug resistance-associated protein 2, ATP-binding cassette transporter in addition to Pharmacology. His study in P-glycoprotein is interdisciplinary in nature, drawing from both Transgene, Molecular biology, Blood–brain barrier and Transfection.

His Pharmacokinetics study combines topics in areas such as Selected reaction monitoring, Bioavailability, Endocrinology and Chromatography. His Abcg2 study integrates concerns from other disciplines, such as Efflux, Knockout mouse, Tyrosine-kinase inhibitor and Carcinogen. Alfred H. Schinkel interconnects Metabolite, Genetically modified mouse, In vitro and Methotrexate in the investigation of issues within In vivo.

He most often published in these fields:

  • Pharmacology (52.61%)
  • P-glycoprotein (32.53%)
  • Pharmacokinetics (32.13%)

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

  • Pharmacokinetics (32.13%)
  • Pharmacology (52.61%)
  • Chromatography (13.25%)

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

His main research concerns Pharmacokinetics, Pharmacology, Chromatography, Bioanalysis and Protein precipitation. As a part of the same scientific family, Alfred H. Schinkel mostly works in the field of Pharmacokinetics, focusing on Oral administration and, on occasion, Bioavailability and Distribution. His Pharmacology research includes elements of P-glycoprotein, Abcg2, CYP3A4, CYP3A and Genetically modified mouse.

Alfred H. Schinkel works mostly in the field of P-glycoprotein, limiting it down to concerns involving In vivo and, occasionally, FLT3 Inhibitor. In Bioanalysis, Alfred H. Schinkel works on issues like Analyte, which are connected to Extraction. As a member of one scientific family, he mostly works in the field of Organic anion-transporting polypeptide, focusing on Endocrinology and, on occasion, Internal medicine.

Between 2017 and 2021, his most popular works were:

  • Cytochrome P450 3A4, 3A5, and 2C8 expression in breast, prostate, lung, endometrial, and ovarian tumors : relevance for resistance to taxanes (15 citations)
  • Development and validation of a bioanalytical method for the quantification of the CDK4/6 inhibitors abemaciclib, palbociclib, and ribociclib in human and mouse matrices using liquid chromatography-tandem mass spectrometry. (15 citations)
  • P-glycoprotein (MDR1/ABCB1) restricts brain accumulation and cytochrome P450-3A (CYP3A) limits oral availability of the novel ALK/ROS1 inhibitor lorlatinib (11 citations)

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

  • Gene
  • Enzyme
  • Cancer

Alfred H. Schinkel focuses on Pharmacokinetics, Bioanalysis, Chromatography, Abcg2 and Transgene. His studies deal with areas such as Selected reaction monitoring, Liquid chromatography–mass spectrometry and Protein precipitation as well as Bioanalysis. Alfred H. Schinkel has included themes like P-glycoprotein, Blood–brain barrier, Gene knockout, CYP3A and Genetically modified mouse in his Abcg2 study.

His P-glycoprotein research is multidisciplinary, incorporating perspectives in Toxicity and Oral administration, Bioavailability, Pharmacology. His Pharmacology study frequently draws connections between adjacent fields such as CYP3A4. His Transgene research is multidisciplinary, relying on both Cancer research, Knockout mouse and Tyrosine-kinase inhibitor.

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

Disruption of the mouse mdr1a P-glycoprotein gene leads to a deficiency in the blood-brain barrier and to increased sensitivity to drugs

A.H. Schinkel;J.J.M. Smit;O. van Tellingen;J.H. Beijnen.
Cell (1994)

2580 Citations

Mammalian drug efflux transporters of the ATP binding cassette (ABC) family: an overview.

Alfred H Schinkel;Johan W Jonker.
Advanced Drug Delivery Reviews (2003)

1867 Citations

P-Glycoprotein, a gatekeeper in the blood-brain barrier.

Alfred H Schinkel.
Advanced Drug Delivery Reviews (1999)

1208 Citations

Normal viability and altered pharmacokinetics in mice lacking mdr1-type (drug-transporting) P-glycoproteins

A. H. Schinkel;U. Mayer;E. Wagenaar;C. A. A. M. Mol.
Proceedings of the National Academy of Sciences of the United States of America (1997)

1150 Citations

MDR1 P-Glycoprotein Is a Lipid Translocase of Broad Specificity, While MDR3 P-Glycoprotein Specifically Translocates Phosphatidylcholine

Ardy van Helvoort;Alexander J Smith;Hein Sprong;Ingo Fritzsche.
Cell (1996)

1080 Citations

The breast cancer resistance protein protects against a major chlorophyll-derived dietary phototoxin and protoporphyria

Johan W. Jonker;Marije Buitelaar;Els Wagenaar;Martin A. van der Valk.
Proceedings of the National Academy of Sciences of the United States of America (2002)

956 Citations

Potent and specific inhibition of the breast cancer resistance protein multidrug transporter in vitro and in mouse intestine by a novel analogue of fumitremorgin C.

John D Allen;Arnold van Loevezijn;Jeany M Lakhai;Martin van der Valk.
Molecular Cancer Therapeutics (2002)

944 Citations

Response to antiretroviral treatment in HIV-1-infected individuals with allelic variants of the multidrug resistance transporter 1: a pharmacogenetics study.

Jacques Fellay;Catia Marzolini;Emma R. Meaden;David J. Back.
The Lancet (2002)

818 Citations

Role of Breast Cancer Resistance Protein in the Bioavailability and Fetal Penetration of Topotecan

Johan W. Jonker;Johan W. Smit;Remco F. Brinkhuis;Marc Maliepaard.
Journal of the National Cancer Institute (2000)

814 Citations

The physiological function of drug-transporting P-glycoproteins

Alfred H. Schinkel.
Seminars in Cancer Biology (1997)

640 Citations

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