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 13,054 220 World Ranking 8312 National Ranking 605

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Enzyme
  • Internal medicine

His primary areas of investigation include Genetics, Phenotype, Mutation, Mutant and Endocrinology. His Phenotype research is multidisciplinary, incorporating elements of Gene knockout, Ribosomopathy, Genome-wide association study and Ribosomal protein. His Mutation study combines topics from a wide range of disciplines, such as Molecular biology, Hearing loss and Melanin.

His Mutant research is multidisciplinary, relying on both T cell, Autoimmunity, Immune system and Autoantibody. His biological study spans a wide range of topics, including Sphingosine, Sphingosine-1-phosphate and Internal medicine. His Gene research incorporates elements of Evolutionary biology and Sexual dimorphism.

His most cited work include:

  • Mutations in Dynein Link Motor Neuron Degeneration to Defects in Retrograde Transport (601 citations)
  • High-throughput discovery of novel developmental phenotypes (523 citations)
  • Cardioprotection and lifespan extension by the natural polyamine spermidine (403 citations)

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

Mutant, Genetics, Internal medicine, Phenotype and Endocrinology are his primary areas of study. His Mutant study combines topics from a wide range of disciplines, such as Mutation and Molecular biology. His study ties his expertise on Cell biology together with the subject of Mutation.

His Molecular biology research incorporates themes from Signal transduction and Knockout mouse. His research in Genetics intersects with topics in Hair cell and Hearing loss. The study incorporates disciplines such as Gene knockout, Regulation of gene expression, Neuroscience and Pathology in addition to Phenotype.

He most often published in these fields:

  • Mutant (27.14%)
  • Genetics (25.24%)
  • Internal medicine (21.90%)

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

  • Endocrinology (20.95%)
  • Internal medicine (21.90%)
  • Cell biology (17.14%)

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

His scientific interests lie mostly in Endocrinology, Internal medicine, Cell biology, Phenotype and Allele. His studies examine the connections between Endocrinology and genetics, as well as such issues in FGF21, with regards to Endogeny, Obesity and Brown adipose tissue. He has included themes like Diabetes mellitus, SNP and Sucrose in his Internal medicine study.

His Phenotype study combines topics in areas such as Mutation, Genetic traits, Neuroscience and Quantitative trait locus. His Retinal ganglion research focuses on subjects like Eye development, which are linked to Mutant. Gene and Genetics are inherently bound to his Methyltransferase studies.

Between 2018 and 2021, his most popular works were:

  • The rRNA m6A methyltransferase METTL5 is involved in pluripotency and developmental programs. (20 citations)
  • Alternative oxidase-mediated respiration prevents lethal mitochondrial cardiomyopathy (19 citations)
  • Endogenous FGF21-signaling controls paradoxical obesity resistance of UCP1-deficient mice. (13 citations)

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

  • Gene
  • Enzyme
  • Internal medicine

Helmut Fuchs mostly deals with Cell biology, Methyltransferase, Phenotype, Translation and Genetics. His study on Respiratory chain and Alternative oxidase is often connected to Metabolome and BCS1L as part of broader study in Cell biology. His Methyltransferase study incorporates themes from Intellectual disability, Messenger RNA, Immune system and Mutation.

His studies in Phenotype integrate themes in fields like Synaptic plasticity, Postsynaptic potential, Cognitive skill, SRC Family Tyrosine Kinase and Candidate gene. His work focuses on many connections between Translation and other disciplines, such as RNA, that overlap with his field of interest in Stem cell, Ribosomal RNA and Enzyme. His work on Genetics deals in particular with TRNA Methyltransferases, Gene, Genetic traits, Quantitative trait locus and Phenome.

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

Mutations in Dynein Link Motor Neuron Degeneration to Defects in Retrograde Transport

Majid Hafezparast;Rainer Klocke;Christiana Ruhrberg;Andreas Marquardt.
Science (2003)

801 Citations

High-throughput discovery of novel developmental phenotypes

Mary E. Dickinson;Ann M. Flenniken;Xiao Ji;Lydia Teboul.
Nature (2016)

776 Citations

Cardioprotection and lifespan extension by the natural polyamine spermidine

Tobias Eisenberg;Mahmoud Abdellatif;Sabrina Schroeder;Uwe Primessnig;Uwe Primessnig.
Nature Medicine (2016)

673 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

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

A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains

Michelle M Simon;Simon Greenaway;Jacqueline K White;Helmut Fuchs.
Genome Biology (2013)

399 Citations

Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects

Kelly A McGowan;Jun Z Li;Jun Z Li;Christopher Y Park;Veronica Beaudry.
Nature Genetics (2008)

391 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

An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice.

Morag A Lewis;Elizabeth Quint;Anne M Glazier;Helmut Fuchs.
Nature Genetics (2009)

343 Citations

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.

Sarah Vreugde;Alexandra Erven;Corné J. Kros;Walter Marcotti.
Nature Genetics (2002)

255 Citations

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