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 79 Citations 28,807 363 World Ranking 12218 National Ranking 622
Biology and Biochemistry D-index 75 Citations 27,824 314 World Ranking 3266 National Ranking 242

Overview

What is he best known for?

The fields of study Thomas Klopstock is best known for:

  • Gene
  • Muscular dystrophy
  • Genetics

In his works, Thomas Klopstock undertakes multidisciplinary study on Genetics and Compound heterozygosity. As part of his studies on Compound heterozygosity, he frequently links adjacent subjects like Phenotype. Thomas Klopstock performs multidisciplinary study in the fields of Phenotype and Genotype-phenotype distinction via his papers. Thomas Klopstock integrates Gene with Polymerase in his study. His Internal medicine study frequently draws parallels with other fields, such as Idebenone. His research ties Internal medicine and Idebenone together. He performs integrative Mutation and Stop codon research in his work. In his articles, Thomas Klopstock combines various disciplines, including Stop codon and Mutation. Many of his studies on Ataxia apply to Neuroscience as well.

His most cited work include:

  • Genome-wide, large-scale production of mutant mice by ENU mutagenesis (630 citations)
  • Phenotypic spectrum associated with mutations of the mitochondrial polymerase gene (357 citations)
  • The Spastic Paraplegia Rating Scale (SPRS): A reliable and valid measure of disease severity (194 citations)

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

Thomas Klopstock integrates Gene and Hereditary spastic paraplegia in his research. Thomas Klopstock combines Genetics and Mutation in his research. In his research, Thomas Klopstock performs multidisciplinary study on Mutation and Phenotype. His study on Phenotype is mostly dedicated to connecting different topics, such as Hereditary spastic paraplegia. Internal medicine is closely attributed to Disease in his study. He merges Disease with Gene in his study. Thomas Klopstock performs integrative study on Mitochondrial DNA and Mitochondrial myopathy in his works. By researching both Mitochondrial myopathy and Mitochondrial disease, Thomas Klopstock produces research that crosses academic boundaries. In his research, Thomas Klopstock undertakes multidisciplinary study on Mitochondrial disease and Mitochondrion.

Thomas Klopstock most often published in these fields:

  • Gene (67.65%)
  • Genetics (58.82%)
  • Internal medicine (50.00%)

What were the highlights of his more recent work (between 2014-2018)?

  • Internal medicine (100.00%)
  • Genetics (100.00%)
  • Spontaneous alternation (50.00%)

In recent works Thomas Klopstock was focusing on the following fields of study:

Thomas Klopstock regularly ties together related areas like Idebenone in his Internal medicine studies. His Idebenone study frequently draws connections between related disciplines such as Internal medicine. His Genetics study frequently draws connections between adjacent fields such as Amino acid. Thomas Klopstock merges many fields, such as Amino acid and Methionine, in his writings. As part of his studies on Methionine, Thomas Klopstock frequently links adjacent subjects like Genetics. His work on Spontaneous alternation is being expanded to include thematically relevant topics such as Endocrinology. His study in Hippocampal formation extends to Endocrinology with its themes. His multidisciplinary approach integrates Hippocampal formation and Hippocampus in his work. Thomas Klopstock carries out multidisciplinary research, doing studies in Hippocampus and Spontaneous alternation.

Between 2014 and 2018, his most popular works were:

  • A paternal methyl donor-rich diet altered cognitive and neural functions in offspring mice (44 citations)
  • Mitochondrial DNA mutation 14487T>C manifesting as Leber’s hereditary optic neuropathy (8 citations)

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

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Daniel J. Klionsky;Amal Kamal Abdel-Aziz;Sara Abdelfatah;Mahmoud Abdellatif.
Autophagy (2021)

8964 Citations

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease.

Andreas Bender;Kim J Krishnan;Christopher M Morris;Geoffrey A Taylor.
Nature Genetics (2006)

1606 Citations

Genome-wide, large-scale production of mutant mice by ENU mutagenesis

M. H. Hrabe de Angelis;H. Flaswinkel;H. Fuchs;B. Rathkolb.
Nature Genetics (2000)

775 Citations

A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice

Wolfgang Enard;Sabine Gehre;Kurt Hammerschmidt;Sabine M. Hölter.
Cell (2009)

615 Citations

A randomized placebo-controlled trial of idebenone in Leber’s hereditary optic neuropathy

Thomas Klopstock;Patrick Yu-Wai-Man;Patrick Yu-Wai-Man;Konstantinos Dimitriadis;Jacinthe Rouleau.
Brain (2011)

459 Citations

Post-stroke inhibition of induced NADPH oxidase type 4 prevents oxidative stress and neurodegeneration.

Christoph Kleinschnitz;Henrike Grund;Kirstin Wingler;Melanie Elise Armitage.
PLOS Biology (2010)

439 Citations

Phenotypic spectrum associated with mutations of the mitochondrial polymerase γ gene

R Horvath;G Hudson;G Ferrari;N Futterer.
Brain (2006)

430 Citations

Aberrant methylation of tRNAs links cellular stress to neuro‐developmental disorders

Sandra Blanco;Sabine Dietmann;Joana V Flores;Shobbir Hussain.
The EMBO Journal (2014)

407 Citations

Targeted next generation sequencing as a diagnostic tool in epileptic disorders

Johannes R. Lemke;Erik Riesch;Tim Scheurenbrand;Max Schubach.
Epilepsia (2012)

366 Citations

Rapamycin extends murine lifespan but has limited effects on aging

Frauke Neff;Diana Flores-Dominguez;Devon P. Ryan;Marion Horsch.
Journal of Clinical Investigation (2013)

348 Citations

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