₄H Ogier de Baulny

Summary for 2001 [at-glance overview of H Ogier de Baulny work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author H Ogier de Baulny. According to available data, in 2001 H Ogier de Baulny published at least 4 articles. This work was completed in collaboration with several authors including Callebaut, I and Elion, J. Many other authors have collaborated with H Ogier de Baulny as well. There is no information about the funding or the grants awarded to support this work.

Analysis of the article abstracts and the titles suggests that H Ogier de Baulny professional interests are focused around "frequent mutation among", "dna depletion dna" and "degree forms methylmalonic". These might also be referred to as "novel mutations", "complex iii" or "cytochrome gene". Statistical analysis shows that H Ogier de Baulny's writing is likely to contains terms "mutations", "patients", "mtdna", "mut", "mutation" and "depletion".

Unfortunately, there is not enough information to establish H Ogier de Baulny affiliation. Luckily, one email address is on file.

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Alternative names (1) [other authors with names similar to H Ogier de Baulny]

₈Ogier de Baulny, Hélène

Year 2001 Charts [H Ogier de Baulny frequent coauthors and the most common unique vocabulary terms for the selected year]

Historical Performance Charts [graphical overview of H Ogier de Baulny publication and funding history for the range of years]

Emails (1) [email addresses extracted from H Ogier de Baulny affiliations]

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H Ogier de Baulny Coauthors (19) [all coauthors with the number of joint publications]

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Affiliations (4) [condensed summary of the H Ogier de Baulny affiliations, the leading number and the color conveys importance]

₁Service de Biochimie-Génétique/INSERM U458, Assistance Publique-Hôpitaux de Paris, Hôpital Robert Debré, Paris, France.
₁INSERM U523, Institut de Myologie, Hôpital de la Salpêtrière, 75651 Paris cedex 13, France.
₁INSERM UR523, Institut de Myologie, H pital de La Salpêtrière, Paris, France.
₁Service de Biochimie-Hormonologie, Assitanace Publique-Hôpitaux de Paris, Hôpital Robert Debré, 48 Bd Sérurier, 75019 Paris, France.

Key Opinion Leader In [H Ogier de Baulny is considered a key opinion leader in any keyword where the rank of 5 is achieved, the leading number before the keyword shows the author's rank as compared to all other authors]

no keywords assigned

Keywords (32) [keywords assigned to H Ogier de Baulny articles by PubMed, the leading number and the color conveys importance]

₄Humans | ₃Female | ₂DNA, Mitochondrial | ₂Child, Preschool | ₂Molecular Sequence Data | ₂Child | ₂Male | ₂Amino Acid Substitution | ₂Mutation | ₂Mutation, Missense | ₁Mutagenesis | ₁Blotting, Southern | ₁Gene Dosage | ₁Antimycin A | ₁Dosage Compensation, Genetic | ₁Genetic Variation | ₁Cytochrome b Group | ₁Point Mutation | ₁Genotype | ₁Tyrosine | ₁Propionibacterium | ₁DNA Mutational Analysis | ₁Asparagine | ₁Protein Structure, Tertiary | ₁Acyl Coenzyme A | ₁Gene Frequency | ₁Infant | ₁European Continental Ancestry Group | ₁Amino Acid Sequence | ₁Age of Onset | ₁Phenotype | ₁Heterozygote

H Ogier de Baulny Unique Vocabulary (96) [single words, word pairs and phrases obtained by analysis of abstracts and titles, the leading number and the color conveys importance; H Ogier de Baulny might be a good expert witness on these terms]

₁₅mutations | ₁₁patients | ₁₁mtdna | ₁₀mut | ₇mutation | ₇depletion | ₆found | ₆dna | ₅cytochrome | ₅novel | ₅gene | ₅analysis | ₅human | ₅mitochondrial | ₅n219y | ₄iii | ₄complex | ₄degree | ₄patient | ₄using | ₃phenotype | ₃sequence | ₃number | ₃forms | ₃controls | ₃functional | ₃frequent | ₃clinical | ₃late-onset | ₃structure | ₃caucasian | ₃severity
₅novel mutations | ₄complex iii | ₄cytochrome gene | ₄mut degree | ₄mitochondrial dna | ₃n219y frequent | ₃forms methylmalonic | ₃mtdna depletion | ₂degree forms | ₂depletion dna | ₂deletions compensation | ₂analysis cytochrome | ₂overt complex | ₂iii defect | ₂deleterious mutations | ₂multiple deletions | ₂among mut | ₂mutation among | ₂methylmalonic acidemia | ₂late-onset mitochondrial | ₂caucasian patients | ₂dna depletion | ₂acidemia caucasian | ₂frequent mutation | ₂degree phenotype | ₂copy number | ₂number multiple | ₂dna copy | ₂mutations human | ₂molecular structural | ₂dna mtdna | ₂analysis novel
₂frequent mutation among | ₂dna depletion dna | ₂degree forms methylmalonic | ₂complex iii defect | ₂mitochondrial dna depletion | ₂mut degree phenotype | ₂overt complex iii | ₂methylmalonic acidemia caucasian | ₂mutation among mut | ₂copy number multiple | ₂among mut degree | ₂depletion dna copy | ₂analysis cytochrome gene | ₂dna copy number | ₂mut degree forms | ₂n219y frequent mutation | ₂multiple deletions compensation | ₂acidemia caucasian patients | ₂forms methylmalonic acidemia | ₂number multiple deletions | ₂late-onset mitochondrial dna | ₂structural analysis novel | ₂functional characterization novel | ₂propionibacterium shermanii enzyme | ₂patient mut methylmalonyl-coa | ₂mitochondrial dna mtdna | ₂mutations patient mut | ₂molecular structural analysis | ₂analysis novel mutations | ₂human cytochrome gene | ₂novel mutations patient | ₂mut methylmalonyl-coa deficiency

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