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 42 Citations 7,101 71 World Ranking 15476 National Ranking 1132

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • DNA
  • Mutation

Her main research concerns Paraplegin, Cell biology, Mitochondrion, Hereditary spastic paraplegia and Biochemistry. Her Paraplegin study incorporates themes from Oculomotor apraxia, Exome sequencing, Spinal cord and Pathology. Her work deals with themes such as Respiratory Chain Deficiency, Mitochondrial protein synthesis and Skeletal muscle, which intersect with Cell biology.

Her study looks at the relationship between Mitochondrion and fields such as mitochondrial fusion, as well as how they intersect with chemical problems. Her Hereditary spastic paraplegia study necessitates a more in-depth grasp of Genetics. Her study in the field of Tissue specific also crosses realms of AAA proteins, Protease, Proteases and FGF21.

Her most cited work include:

  • Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1 (383 citations)
  • The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission (380 citations)
  • Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22 (315 citations)

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

Her primary scientific interests are in Cell biology, Mitochondrion, Genetics, Hereditary spastic paraplegia and Spastin. Her research in the fields of Mitochondrial biogenesis overlaps with other disciplines such as Kallmann syndrome. In general Mitochondrion study, her work on Inner mitochondrial membrane often relates to the realm of Proteases, thereby connecting several areas of interest.

She is studying Paraplegin, which is a component of Hereditary spastic paraplegia. Elena I. Rugarli works mostly in the field of Spastin, limiting it down to topics relating to Microtubule and, in certain cases, Lipid droplet. Her Neurodegeneration research incorporates elements of Kinase and Spinocerebellar ataxia.

She most often published in these fields:

  • Cell biology (54.76%)
  • Mitochondrion (32.14%)
  • Genetics (32.14%)

What were the highlights of her more recent work (between 2013-2021)?

  • Cell biology (54.76%)
  • Mitochondrion (32.14%)
  • Spastin (15.48%)

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

Elena I. Rugarli mainly focuses on Cell biology, Mitochondrion, Spastin, Mitochondrial biogenesis and Biochemistry. Elena I. Rugarli is interested in Respiratory chain, which is a field of Cell biology. Her Mitochondrion research incorporates themes from Translation, mitochondrial fusion, Neurodegeneration and Function.

Her mitochondrial fusion study combines topics from a wide range of disciplines, such as HEK 293 cells, ATP–ADP translocase and Mitochondrial fission. Her Spastin research includes themes of Evolutionary biology, Microtubule, Lipid droplet and Endogeny. Her work on Proteostasis, Interactome, Cell growth and Inner membrane as part of general Biochemistry research is frequently linked to Tafazzin, thereby connecting diverse disciplines of science.

Between 2013 and 2021, her most popular works were:

  • The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission (380 citations)
  • Tissue-specific loss of DARS2 activates stress responses independently of respiratory chain deficiency in the heart. (111 citations)
  • DNAJC19, a Mitochondrial Cochaperone Associated with Cardiomyopathy, Forms a Complex with Prohibitins to Regulate Cardiolipin Remodeling (108 citations)

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

  • Gene
  • DNA
  • Mutation

The scientist’s investigation covers issues in Cell biology, Mitochondrion, Biochemistry, mitochondrial fusion and Neurodegeneration. Her Cell biology research is multidisciplinary, incorporating perspectives in Respiratory Chain Deficiency, Optic Atrophy 1 and Tissue specific. Her work carried out in the field of Mitochondrion brings together such families of science as HEK 293 cells, Cell growth and DNAJA3.

Her work on Proteostasis and Interactome as part of general Biochemistry research is frequently linked to DNAJC19, Barth syndrome and Tafazzin, bridging the gap between disciplines. Her Proteostasis research includes themes of Protein subunit and Mitochondrial permeability transition pore. Her mitochondrial fusion research is multidisciplinary, incorporating elements of Axoplasmic transport, Inner mitochondrial membrane, Mitochondrial Size, Spinocerebellar ataxia and 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

Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1

Sarah Ehses;Ines Raschke;Giuseppe Mancuso;Andrea Bernacchia.
Journal of Cell Biology (2009)

472 Citations

The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission

Ruchika Anand;Timothy Wai;Michael J. Baker;Nikolay Kladt.
Journal of Cell Biology (2014)

467 Citations

The m-AAA Protease Defective in Hereditary Spastic Paraplegia Controls Ribosome Assembly in Mitochondria

Mark Nolden;Sarah Ehses;Mirko Koppen;Andrea Bernacchia.
Cell (2005)

463 Citations

Mitochondrial quality control: a matter of life and death for neurons

Elena I Rugarli;Thomas Langer;Thomas Langer.
The EMBO Journal (2012)

418 Citations

Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport

Fatima Ferreirinha;Angelo Quattrini;Marinella Pirozzi;Valentina Valsecchi.
Journal of Clinical Investigation (2004)

323 Citations

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

Nandita A. Quaderi;Susann Schweiger;Karin Gaudenz;Brunella Franco.
Nature Genetics (1997)

315 Citations

Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics

Alessia Errico;Andrea Ballabio;Elena I. Rugarli.
Human Molecular Genetics (2002)

277 Citations

Variable and Tissue-Specific Subunit Composition of Mitochondrial m-AAA Protease Complexes Linked to Hereditary Spastic Paraplegia

Mirko Koppen;Metodi D. Metodiev;Giorgio Casari;Elena I. Rugarli.
Molecular and Cellular Biology (2007)

219 Citations

OPA1 Processing Reconstituted in Yeast Depends on the Subunit Composition of the m-AAA Protease in Mitochondria

Stéphane Duvezin-Caubet;Mirko Koppen;Johannes Wagener;Michael Zick.
Molecular Biology of the Cell (2007)

199 Citations

Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targeting

Elena I. Rugarli;Beat Lutz;Shigeru C. Kuratani;Stefan Wawersik.
Nature Genetics (1993)

176 Citations

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