₆David R Thorburn

Summary for 2004 [at-glance overview of David R Thorburn work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author David R Thorburn. According to available data, in 2004 David R Thorburn published at least 6 articles. This work was completed in collaboration with several authors including Kirby, Denise M and Taylor, Robert W. Many other authors have collaborated with David R Thorburn as well. There is no information about the funding or the grants awarded to support this work.

David R Thorburn has rank 52 when compared to all other authors using the keyword DNA, Mitochondrial. Analysis of the article abstracts and the titles suggests that David R Thorburn professional interests are focused around "respiratory chain disorders", "de novo mutations" and "risk developing mitochondrial". These might also be referred to as "mitochondrial dna", "respiratory chain" or "complex deficiency". Statistical analysis shows that David R Thorburn's writing is likely to contains terms "mitochondrial", "mutations", "complex", "gene", "mtdna" and "mutation".

Unfortunately, there is not enough information to establish David R Thorburn affiliation. Luckily, several email addresses are on file.

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Alternative names (1) [other authors with names similar to David R Thorburn]

₂₂Thorburn, D R

Year 2004 Charts [David R Thorburn frequent coauthors and the most common unique vocabulary terms for the selected year]

Historical Performance Charts [graphical overview of David R Thorburn publication and funding history for the range of years]

Emails (2) [email addresses extracted from David R Thorburn affiliations]

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David R Thorburn Coauthors (34) [all coauthors with the number of joint publications]

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₁₄Turnbull, Douglass M

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₂Fowler, Kerry J

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₁₉DiMauro, Salvatore

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Affiliations (4) [condensed summary of the David R Thorburn affiliations, the leading number and the color conveys importance]

₂Murdoch Children's Childrens Research Institute, Royal Children's Hospital, Melbourne, Victoria 3052 Australia.
₁Neurology, University of Newcastle upon Tyne, Newcastle upon Tyne, UK.
₁Cell and Gene Therapy Research Group, Murdoch Childrens Research Institute, University of Melbourne Department of Pediatrics, Royal Children's Hospital, Flemington Road, 3052, Melbourne, VIC, Australia.
₁Mitochondrial Research Group, School of Neurology, Neurobiology and Psychiatry, University of Newcastle upon Tyne, United Kingdom.

Key Opinion Leader In [David R Thorburn 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]

₅₂DNA, Mitochondrial | ₂₉₁Mutation

Keywords (32) [keywords assigned to David R Thorburn articles by PubMed, the leading number and the color conveys importance]

₅Humans | ₅Female | ₅Mutation | ₄DNA, Mitochondrial | ₄Male | ₂Mitochondrial Diseases | ₂Pedigree | ₂Mice | ₂Electron Transport Complex I | ₂Genetic Complementation Test | ₂Animals | ₂Adult | ₁Infant, Newborn | ₁Gene Dosage | ₁Brain | ₁Adolescent | ₁Reverse Transcriptase Polymerase Chain Reaction | ₁RNA, Messenger | ₁Chromosomes, Artificial, Bacterial | ₁Cell Fusion | ₁Genes, Lethal | ₁Child | ₁Transgenes | ₁Mitochondrial Proteins | ₁Kearns-Sayer Syndrome | ₁Kidney | ₁Molecular Diagnostic Techniques | ₁Gene Deletion | ₁Prenatal Diagnosis | ₁In Situ Hybridization, Fluorescence | ₁Mice, Knockout | ₁Immunoblotting

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

₂₄mitochondrial | ₁₈mutations | ₁₆complex | ₁₄gene | ₁₃mtdna | ₁₂mutation | ₁₁human | ₁₁patients | ₁₀frda | ₉disease | ₉disorders | ₉risk | ₈genes | ₈dna | ₈cause | ₈chain | ₈respiratory | ₇nuclear | ₇mouse | ₇deletion | ₆cases | ₆expression | ₆mice | ₅transgene | ₅knockout | ₄transgenic | ₄unknown | ₄disorder | ₃different | ₃rescue | ₃large | ₃common
₈mitochondrial dna | ₈respiratory chain | ₈complex deficiency | ₅knockout mutation | ₄mtdna deletion | ₄friedreich ataxia | ₄de novo | ₄human frda | ₃transgenic mice | ₃novo mutations | ₃expression human | ₃human transgene | ₃mtdna mutations | ₃unaffected mothers | ₃deletion disorder | ₃maternal age | ₂relation maternal | ₂risk unaffected | ₂chain subunits | ₂bac-mediated rescue | ₂neonatal mitochondrial | ₂rescue friedreich | ₂mtdna disease | ₂risk developing | ₂microarray expression | ₂ndufs6 mutations | ₂nuclear mitochondrial | ₂nd3 subunit | ₂tissues lines | ₂mutations novel | ₂genes including | ₂mitochondrial complex
₄respiratory chain disorders | ₃de novo mutations | ₂risk developing mitochondrial | ₂friedreich ataxia knockout | ₂novel cause lethal | ₂risk unaffected mothers | ₂age risk unaffected | ₂lethal neonatal mitochondrial | ₂mitochondrial complex deficiency | ₂neonatal mitochondrial complex | ₂respiratory chain subunits | ₂cause lethal neonatal | ₂mitochondrial dna mtdna | ₂rescue friedreich ataxia | ₂mitochondrial dna mutations | ₂mutation transgenic mice | ₂developing mitochondrial dna | ₂nuclear mitochondrial dna | ₂human bac-mediated rescue | ₂microarray expression analysis | ₂ndufs6 mutations novel | ₂different tissues lines | ₂mutations novel cause | ₂dna deletion disorder | ₂complex deficiency common | ₂mitochondrial dna deletion | ₂bac-mediated rescue friedreich | ₂relation maternal age | ₂ataxia knockout mutation | ₂encoding respiratory chain | ₂knockout mutation transgenic | ₂maternal age risk

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