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 103 Citations 35,950 517 World Ranking 4375 National Ranking 2469
Biology and Biochemistry D-index 107 Citations 39,837 586 World Ranking 783 National Ranking 509

Overview

What is he best known for?

The fields of study he is best known for:

  • Enzyme
  • Gene
  • Internal medicine

His scientific interests lie mostly in Protein C, Biochemistry, Internal medicine, Immunology and Thrombin. John H. Griffin mostly deals with Protein S in his studies of Protein C. His Biochemistry research focuses on Factor XII and how it relates to Kinin.

John H. Griffin combines subjects such as Gastroenterology and Endocrinology with his study of Internal medicine. His Immunology research integrates issues from Blood proteins, Cancer research, Protein C deficiency and Antithrombotic. The study incorporates disciplines such as Fibrin, Clotting factor, Factor V and Carboxypeptidase in addition to Thrombin.

His most cited work include:

  • Deficiency of protein C in congenital thrombotic disease. (1075 citations)
  • The cytoprotective protein C pathway. (618 citations)
  • Activated protein C blocks p53-mediated apoptosis in ischemic human brain endothelium and is neuroprotective. (512 citations)

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

The scientist’s investigation covers issues in Protein C, Biochemistry, Internal medicine, Thrombin and Molecular biology. He studies Protein S, a branch of Protein C. The Internal medicine study combines topics in areas such as Gastroenterology, Endocrinology and Cardiology.

His study looks at the relationship between Thrombin and fields such as Cell biology, as well as how they intersect with chemical problems. John H. Griffin focuses mostly in the field of Molecular biology, narrowing it down to matters related to Protein A/G and, in some cases, Protein G. His research in Immunology intersects with topics in Receptor, Cancer research and Antithrombotic.

He most often published in these fields:

  • Protein C (53.50%)
  • Biochemistry (30.33%)
  • Internal medicine (25.82%)

What were the highlights of his more recent work (between 2011-2021)?

  • Protein C (53.50%)
  • Thrombin (24.88%)
  • Pharmacology (14.46%)

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

His main research concerns Protein C, Thrombin, Pharmacology, Immunology and Biochemistry. The various areas that John H. Griffin examines in his Protein C study include Cell signaling, Neuroprotection, Receptor, Molecular biology and In vivo. His Thrombin research is multidisciplinary, incorporating perspectives in Hemostasis, Coagulation, Skeletal muscle and Myosin.

His Pharmacology study incorporates themes from Anticoagulant and Recombinant DNA. His Immunology research includes themes of Venous thrombosis and Downregulation and upregulation. His Internal medicine study combines topics in areas such as Gastroenterology and Cardiology.

Between 2011 and 2021, his most popular works were:

  • Biased agonism of protease-activated receptor 1 by activated protein C caused by noncanonical cleavage at Arg46. (150 citations)
  • Activated protein C: biased for translation (143 citations)
  • Activated protein C: biased for translation (143 citations)

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

  • Enzyme
  • Gene
  • Internal medicine

John H. Griffin mainly focuses on Protein C, Neuroprotection, Receptor, Pharmacology and Immunology. He specializes in Protein C, namely Protein S. His Neuroprotection study integrates concerns from other disciplines, such as Serine protease, Protease, Stroke, Fibrinolytic agent and Neurogenesis.

John H. Griffin has researched Receptor in several fields, including Molecular biology, Cell signaling and Protease-Activated Receptor 1. In his research, Genetic screen is intimately related to Toxicity, which falls under the overarching field of Pharmacology. John H. Griffin interconnects Cancer research and Recombinant DNA in the investigation of issues within Immunology.

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

Deficiency of protein C in congenital thrombotic disease.

John H. Griffin;Bruce Evatt;Theodore S. Zimmerman;Alice J. Kleiss.
Journal of Clinical Investigation (1981)

1809 Citations

The cytoprotective protein C pathway.

Laurent O. Mosnier;Berislav V. Zlokovic;John H. Griffin.
Blood (2007)

892 Citations

Protein synthesis by native chemical ligation: Expanded scope by using straightforward methodology

Tilman M. Hackeng;John H. Griffin;Philip E. Dawson.
Proceedings of the National Academy of Sciences of the United States of America (1999)

778 Citations

Endothelial and Antithrombotic Actions of HDL

Chieko Mineo;Hiroshi Deguchi;John H. Griffin;Philip W. Shaul.
Circulation Research (2006)

763 Citations

Plasma protein S deficiency in familial thrombotic disease.

Hans Peter Schwarz;Hans Peter Schwarz;Michael Fischer;Michael Fischer;Pierre Hopmeier;Pierre Hopmeier;Mary Ann Batard;Mary Ann Batard.
Blood (1984)

726 Citations

Activated protein C blocks p53-mediated apoptosis in ischemic human brain endothelium and is neuroprotective.

Tong Cheng;Dong Liu;John H. Griffin;José A. Fernández.
Nature Medicine (2003)

710 Citations

Anticoagulant protein C pathway defective in majority of thrombophilic patients [see comments]

JH Griffin;B Evatt;C Wideman;JA Fernandez.
Blood (1993)

694 Citations

Anticoagulant protein C pathway defective in majority of thrombophilic patients.

John H. Griffin;Bruce Evatt;Bruce Evatt;Carol Wideman;Carol Wideman;Jose A. Fernandez;Jose A. Fernandez.
Blood (1993)

685 Citations

Normal Flow (TIMI-3) Before Mechanical Reperfusion Therapy Is an Independent Determinant of Survival in Acute Myocardial Infarction Analysis From the Primary Angioplasty in Myocardial Infarction Trials

Gregg W. Stone;David Cox;Eulogio Garcia;Bruce R. Brodie.
Circulation (2001)

655 Citations

Mechanism of action of human activated protein C, a thrombin-dependent anticoagulant enzyme

Richard A. Marlar;Alice J. Kleiss;John H. Griffin.
Blood (1982)

580 Citations

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