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 76 Citations 22,023 282 World Ranking 3139 National Ranking 1623

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Enzyme
  • Biochemistry

His primary areas of study are Biochemistry, Phospholipase D, Cell biology, PLD2 and Phosphatidylinositol. His study in Signal transduction, Lysophosphatidic acid, Protein kinase C, Binding site and Phospholipase D activity falls within the category of Biochemistry. Andrew J. Morris combines subjects such as Phosphatidic acid, Golgi apparatus, ADP ribosylation factor and Second messenger system with his study of Phospholipase D.

His studies deal with areas such as Secretion, Exocytosis and Bone marrow as well as Cell biology. The PLD2 study combines topics in areas such as Membrane biogenesis, Phospholipase, Complementary DNA, Kinase and RHOA. As part of one scientific family, Andrew J. Morris deals mainly with the area of Phosphatidylinositol, narrowing it down to issues related to the Phospholipase C, and often Myristoylation, MARCKS, Biophysics, Phosphatidylserine and Phospholipid.

His most cited work include:

  • Phosphatidylinositol 4-Phosphate 5-Kinase α Is a Downstream Effector of the Small G Protein ARF6 in Membrane Ruffle Formation (727 citations)
  • Phospholipase D2, a distinct phospholipase D isoform with novel regulatory properties that provokes cytoskeletal reorganization (633 citations)
  • Human ADP-ribosylation Factor-activated Phosphatidylcholine-specific Phospholipase D Defines a New and Highly Conserved Gene Family (593 citations)

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

His scientific interests lie mostly in Biochemistry, Cell biology, Internal medicine, Endocrinology and Lysophosphatidic acid. Many of his studies on Biochemistry involve topics that are commonly interrelated, such as Cell culture. His research brings together the fields of Cell migration and Cell biology.

His studies link Cardiology with Internal medicine. His Lysophosphatidic acid research is multidisciplinary, relying on both Sphingosine and Lipid signaling. His Phospholipase D research integrates issues from PLD2, Phosphatidic acid, Protein kinase C and ADP ribosylation factor.

He most often published in these fields:

  • Biochemistry (38.34%)
  • Cell biology (27.80%)
  • Internal medicine (29.71%)

What were the highlights of his more recent work (between 2018-2021)?

  • Internal medicine (29.71%)
  • Endocrinology (27.48%)
  • Lysophosphatidic acid (24.60%)

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

Andrew J. Morris mainly focuses on Internal medicine, Endocrinology, Lysophosphatidic acid, Autotaxin and Cancer research. His Lysophosphatidic acid research is multidisciplinary, incorporating perspectives in Cytotoxic T cell and Pharmacology. His study on Autotaxin also encompasses disciplines like

  • Inflammation which intersects with area such as Myocardial infarction, Cell, Angiogenesis, Heart failure and Sympathetic nervous system,
  • Phosphatidylcholine which is related to area like Breast cancer, Choline and Phospholipase D.

His Choline study improves the overall literature in Biochemistry. Many of his studies on Biochemistry apply to Streptococcus pyogenes as well. His Gene expression study combines topics in areas such as Transcription factor and Cell biology.

Between 2018 and 2021, his most popular works were:

  • Trimethylamine N-Oxide Binds and Activates PERK to Promote Metabolic Dysfunction (54 citations)
  • Trimethylamine N-Oxide Binds and Activates PERK to Promote Metabolic Dysfunction (54 citations)
  • The β3-adrenergic receptor agonist mirabegron improves glucose homeostasis in obese humans (39 citations)

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

  • Gene
  • Enzyme
  • Internal medicine

The scientist’s investigation covers issues in Endocrinology, Internal medicine, Lysophosphatidic acid, Adipose tissue and Cancer research. He has researched Endocrinology in several fields, including Inflammation, Autotaxin and Fatty liver. His Internal medicine study combines topics from a wide range of disciplines, such as Downregulation and upregulation and Gene expression.

His study on LPAR4 is often connected to CD68 as part of broader study in Lysophosphatidic acid. His work on White adipose tissue as part of general Adipose tissue study is frequently linked to Mirabegron, therefore connecting diverse disciplines of science. His Cancer research research also works with subjects such as

  • Apoptosis, which have a strong connection to Spermidine, Polyamine, Signal transduction, Psychological repression and Acetylation,
  • Fatty acid synthase, which have a strong connection to Kinase.

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

Phosphatidylinositol 4-Phosphate 5-Kinase α Is a Downstream Effector of the Small G Protein ARF6 in Membrane Ruffle Formation

Akira Honda;Masahiro Nogami;Takeaki Yokozeki;Masakazu Yamazaki.
Cell (1999)

968 Citations

Phospholipase D2, a distinct phospholipase D isoform with novel regulatory properties that provokes cytoskeletal reorganization

William C. Colley;Tsung-Chang Sung;Richard Roll;John Jenco.
Current Biology (1997)

822 Citations

Characterization of Two Alternately Spliced Forms of Phospholipase D1 ACTIVATION OF THE PURIFIED ENZYMES BY PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE, ADP-RIBOSYLATION FACTOR, AND RHO FAMILY MONOMERIC GTP-BINDING PROTEINS AND PROTEIN KINASE C-α

Scott M. Hammond;John M. Jenco;Shigeru Nakashima;Karen Cadwallader.
Journal of Biological Chemistry (1997)

765 Citations

Human ADP-ribosylation Factor-activated Phosphatidylcholine-specific Phospholipase D Defines a New and Highly Conserved Gene Family

Scott M. Hammond;Yelena M. Altshuller;Tsung Chang Sung;Simon A. Rudge.
Journal of Biological Chemistry (1995)

732 Citations

Physiological regulation of G protein-linked signaling.

Andrew J. Morris;Craig C. Malbon.
Physiological Reviews (1999)

584 Citations

Regulation of phospholipase D2: selective inhibition of mammalian phospholipase D isoenzymes by alpha- and beta-synucleins.

John M. Jenco;Andrew Rawlingson;Brenda Daniels;Andrew J. Morris.
Biochemistry (1998)

557 Citations

Synucleins are a novel class of substrates for G protein-coupled receptor kinases.

Alexey N. Pronin;Andrew J. Morris;Andrei Surguchov;Jeffrey L. Benovic.
Journal of Biological Chemistry (2000)

437 Citations

Bayesian refinement of association signals for 14 loci in 3 common diseases.

Julian B. Maller;Gilean McVean;Gilean McVean;Jake Byrnes;Damjan Vukcevic.
Nature Genetics (2012)

427 Citations

ATR-X Syndrome Protein Targets Tandem Repeats and Influences Allele-Specific Expression in a Size-Dependent Manner

Martin J. Law;Karen M. Lower;Hsiao P.J. Voon;Jim R. Hughes.
Cell (2010)

400 Citations

Mutagenesis of phospholipase D defines a superfamily including a trans-Golgi viral protein required for poxvirus pathogenicity.

Tsung Chang Sung;Rachel L. Roper;Yue Zhang;Simon A. Rudge.
The EMBO Journal (1997)

394 Citations

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