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 59 Citations 11,019 108 World Ranking 8431 National Ranking 3812

Research.com Recognitions

Awards & Achievements

2016 - Fellow of the American Association for the Advancement of Science (AAAS)

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Enzyme
  • Amino acid

The scientist’s investigation covers issues in Biochemistry, Lysosome, Mannose 6-phosphate receptor, Mutation and CLN8. His study in Lysosome is interdisciplinary in nature, drawing from both Glycoprotein, Lipid metabolism, Lipid Transport, Transmembrane protein and Cell biology. His work in Mannose 6-phosphate receptor is not limited to one particular discipline; it also encompasses Receptor.

His studies in Mutation integrate themes in fields like Genotype and NPC1. His studies deal with areas such as Binding protein and Pathogenesis as well as NPC1. His work carried out in the field of Mannose brings together such families of science as Molecular biology and Signal peptide.

His most cited work include:

  • Identification of HE1 as the Second Gene of Niemann-Pick C Disease (699 citations)
  • Identification of HE1 as the Second Gene of Niemann-Pick C Disease (699 citations)
  • Association of Mutations in a Lysosomal Protein with Classical Late-Infantile Neuronal Ceroid Lipofuscinosis (498 citations)

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

His primary areas of study are Biochemistry, Lysosome, Mannose, Neuronal ceroid lipofuscinosis and Mannose 6-phosphate receptor. The various areas that he examines in his Biochemistry study include Molecular biology and Cell biology. His Lysosome study incorporates themes from Proteome, Proteomics, Cell fractionation, Subcellular localization and Organelle.

His research in Mannose intersects with topics in Golgi apparatus, Receptor, Peptide sequence, Phosphorylation and Gel electrophoresis. His Neuronal ceroid lipofuscinosis study integrates concerns from other disciplines, such as Lysosomal storage disease and Pharmacology. His NPC1 study combines topics in areas such as Mutation and Niemann–Pick disease.

He most often published in these fields:

  • Biochemistry (79.29%)
  • Lysosome (46.43%)
  • Mannose (34.29%)

What were the highlights of his more recent work (between 2011-2020)?

  • Neuronal ceroid lipofuscinosis (37.86%)
  • Biochemistry (79.29%)
  • Tripeptidyl peptidase (25.00%)

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

His primary scientific interests are in Neuronal ceroid lipofuscinosis, Biochemistry, Tripeptidyl peptidase, Lysosome and Cell biology. His Neuronal ceroid lipofuscinosis research is multidisciplinary, incorporating perspectives in Cerebrospinal fluid, Pharmacology and Enzyme replacement therapy. His work in the fields of Biochemistry, such as Tripeptidyl peptidase I and Recombinant DNA, intersects with other areas such as Isobaric labeling.

He works in the field of Lysosome, namely Mannose 6-phosphate receptor. His Mannose 6-phosphate receptor research is multidisciplinary, incorporating elements of Mannose 6-phosphate, Niemann–Pick disease, Fusion protein and Prosaposin. Peter Lobel interconnects Mutation and Phenotype in the investigation of issues within Enzyme.

Between 2011 and 2020, his most popular works were:

  • Accounting for protein subcellular localization: A compartmental map of the rat liver proteome (40 citations)
  • Effective intravenous therapy for neurodegenerative disease with a therapeutic enzyme and a peptide that mediates delivery to the brain. (36 citations)
  • Effective intravenous therapy for neurodegenerative disease with a therapeutic enzyme and a peptide that mediates delivery to the brain. (36 citations)

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

  • Gene
  • Enzyme
  • Amino acid

Peter Lobel focuses on Biochemistry, Tripeptidyl peptidase I, Lysosome, Fusion protein and Mannose 6-phosphate receptor. His Tripeptidyl peptidase I research is classified as research in Neuronal ceroid lipofuscinosis. Peter Lobel has researched Neuronal ceroid lipofuscinosis in several fields, including Spleen, Pharmacokinetics, Nanoparticles for drug delivery to the brain and Recombinant DNA.

Peter Lobel combines subjects such as Golgi apparatus, Endoplasmic reticulum, Proteome and Protein subcellular localization prediction with his study of Lysosome. His Proteome research is multidisciplinary, incorporating perspectives in Lysosomal storage disease, Glycoprotein, Mannose 6-phosphate, Acid phosphatase and Mannose. His studies in Fusion protein integrate themes in fields like mCherry, Green fluorescent protein, Cell biology, Protein folding and Cell fusion.

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

Identification of HE1 as the Second Gene of Niemann-Pick C Disease

Saule Naureckiene;David. E. Sleat;David. E. Sleat;Henry Lackland;Anthony Fensom.
Science (2000)

939 Citations

Mannose 6-Phosphate Receptors and Lysosomal Enzyme Targeting

N. M. Dahms;P. Lobel;Stuart Kornfeld.
Journal of Biological Chemistry (1989)

625 Citations

Association of Mutations in a Lysosomal Protein with Classical Late-Infantile Neuronal Ceroid Lipofuscinosis

David E. Sleat;David E. Sleat;Robert J. Donnelly;Henry Lackland;Henry Lackland;Chang Gong Liu.
Science (1997)

601 Citations

Genetic evidence for nonredundant functional cooperativity between NPC1 and NPC2 in lipid transport

David E. Sleat;Jennifer A. Wiseman;Mukarram El-Banna;Sandy M. Price.
Proceedings of the National Academy of Sciences of the United States of America (2004)

393 Citations

STRUCTURE OF A CHOLESTEROL-BINDING PROTEIN DEFICIENT IN NIEMANN-PICK TYPE C2 DISEASE

Natalia Friedland;Heng-Ling Liou;Peter Lobel;Ann M. Stock.
Proceedings of the National Academy of Sciences of the United States of America (2003)

336 Citations

Mutations in the cytoplasmic domain of the 275 kd mannose 6-phosphate receptor differentially alter lysosomal enzyme sorting and endocytosis.

Peter Lobel;Karen Fujimoto;Richard D. Ye;Gareth Griffiths.
Cell (1989)

324 Citations

Proteomics of the Lysosome

Torben Lübke;Peter Lobel;Peter Lobel;David E. Sleat;David E. Sleat.
Biochimica et Biophysica Acta (2009)

265 Citations

A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration

Jaana Tyynelä;Istvan Sohar;David E. Sleat;Rosalie M. Gin.
The EMBO Journal (2000)

256 Citations

Cloning and sequence analysis of the cation-independent mannose 6-phosphate receptor.

P. Lobel;N. M. Dahms;Stuart Kornfeld.
Journal of Biological Chemistry (1988)

247 Citations

Activation of microglia acidifies lysosomes and leads to degradation of Alzheimer amyloid fibrils.

Amitabha Majumdar;Dana Cruz;Nikiya Asamoah;Adina Buxbaum.
Molecular Biology of the Cell (2007)

242 Citations

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