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
Molecular Biology D-index 65 Citations 13,100 252 World Ranking 1086 National Ranking 31

Overview

What is he best known for?

The fields of study Pascal Reynier is best known for:

  • Gene
  • Mitochondrion
  • Enzyme

In his work, Anatomy and Neuroscience is strongly intertwined with Optic nerve, which is a subfield of Optic neuropathy. Pascal Reynier connects Anatomy with Genetics in his research. His research links Mitochondrial disease with Genetics. His Neuroscience study frequently links to adjacent areas such as Optic nerve. Mitochondrial disease and mitochondrial fusion are inherently bound to his Mitochondrial DNA studies. Pascal Reynier performs integrative study on Gene and Mitochondrial biogenesis in his works. Pascal Reynier incorporates Mitochondrial biogenesis and Mitochondrial DNA in his studies. His work often combines Mitochondrion and mitochondrial fusion studies. Pascal Reynier integrates many fields in his works, including Mutation and Phenotype.

His most cited work include:

  • OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes (444 citations)
  • Mitochondrial DNA content affects the fertilizability of human oocytes (430 citations)
  • Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance (364 citations)

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

His Mitochondrial DNA study combines Mitochondrial disease and mitochondrial fusion studies. Pascal Reynier integrates several fields in his works, including mitochondrial fusion and Mitochondrial DNA. Borrowing concepts from Phenotype, he weaves in ideas under Gene. Genetics is closely attributed to Embryo in his work. He undertakes interdisciplinary study in the fields of Mitochondrion and Mitochondrial disease through his research. While working in this field, Pascal Reynier studies both Biochemistry and Enzyme. While working on this project, he studies both Enzyme and Biochemistry. In his research, he undertakes multidisciplinary study on Internal medicine and Endocrinology. While working in this field, he studies both Endocrinology and Internal medicine.

Pascal Reynier most often published in these fields:

  • Gene (70.19%)
  • Genetics (62.50%)
  • Mitochondrial DNA (43.75%)

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

Mitochondrial DNA content affects the fertilizability of human oocytes.

P Reynier;P May-Panloup;M F Chrétien;C J Morgan.
Molecular Human Reproduction (2001)

609 Citations

OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes

Patrizia Amati-Bonneau;Maria Lucia Valentino;Pascal Reynier;Maria Esther Gallardo.
Brain (2008)

516 Citations

Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.

Gavin Hudson;Patrizia Amati-Bonneau;Emma L. Blakely;Joanna D. Stewart.
Brain (2008)

507 Citations

Resveratrol Induces a Mitochondrial Complex I-dependent Increase in NADH Oxidation Responsible for Sirtuin Activation in Liver Cells

Valérie Desquiret-Dumas;Valérie Desquiret-Dumas;Naïg Gueguen;Naïg Gueguen;Géraldine Leman;Géraldine Leman;Stéphanie Baron.
Journal of Biological Chemistry (2013)

415 Citations

Multi-system neurological disease is common in patients with OPA1 mutations

Patrick Yu-Wai-Man;Philip G. Griffiths;Philip G. Griffiths;G. Gorman;C.-M. Lourenco.
Brain (2010)

384 Citations

Low oocyte mitochondrial DNA content in ovarian insufficiency

P. May-Panloup;M.F. Chrétien;C. Jacques;C. Vasseur.
Human Reproduction (2005)

327 Citations

Mitochondrial dynamics and disease, OPA1.

Aurélien Olichon;Emmanuelle Guillou;Cécile Delettre;Thomas Landes.
Biochimica et Biophysica Acta (2006)

253 Citations

Ovarian ageing: the role of mitochondria in oocytes and follicles

Pascale May-Panloup;Lisa Boucret;Juan Manuel Chao de la Barca;Valérie Desquiret-Dumas.
Human Reproduction Update (2016)

243 Citations

Dominant optic atrophy

Guy Lenaers;Christian P Hamel;Cecile Delettre;Patrizia Amati-Bonneau;Patrizia Amati-Bonneau.
Orphanet Journal of Rare Diseases (2012)

229 Citations

Increased sperm mitochondrial DNA content in male infertility

May-Panloup P;Chrétien Mf;Savagner F;Vasseur C.
Human Reproduction (2003)

219 Citations

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