₄Denise M Kirby

Summary for 2004 [at-glance overview of Denise M Kirby work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Denise M Kirby. According to available data, in 2004 Denise M Kirby published at least 4 articles. This work was completed in collaboration with several authors including Thorburn, David R and Ryan, Michael T. Many other authors have collaborated with Denise M Kirby as well. There is no information about the funding or the grants awarded to support this work.

Denise M Kirby has rank 132 when compared to all other authors using the keyword DNA, Mitochondrial. Analysis of the article abstracts and the titles suggests that Denise M Kirby professional interests are focused around "respiratory chain disorders", "de novo mutations" and "infantile mitochondrial encephalopathies". These might also be referred to as "respiratory chain", "complex deficiency" or "infantile mitochondrial". Statistical analysis shows that Denise M Kirby's writing is likely to contains terms "mitochondrial", "mutations", "complex", "gene", "mutation" and "human".

Unfortunately, there is not enough information to establish Denise M Kirby affiliation. Luckily, one email address is on file.

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Alternative names (0) [other authors with names similar to Denise M Kirby]

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Year 2004 Charts [Denise M Kirby frequent coauthors and the most common unique vocabulary terms for the selected year]

Historical Performance Charts [graphical overview of Denise M Kirby publication and funding history for the range of years]

Emails (1) [email addresses extracted from Denise M Kirby affiliations]

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Denise M Kirby Coauthors (19) [all coauthors with the number of joint publications]

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₁₄Turnbull, Douglass M

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Affiliations (3) [condensed summary of the Denise M Kirby affiliations, the leading number and the color conveys importance]

₂Murdoch Children's Childrens Research Institute, Royal Children's Hospital, Melbourne, Victoria 3052 Australia.
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 [Denise M Kirby 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]

₁₃₂DNA, Mitochondrial | ₇₀₄Mutation

Keywords (32) [keywords assigned to Denise M Kirby articles by PubMed, the leading number and the color conveys importance]

₄Humans | ₄Female | ₄Mutation | ₃DNA, Mitochondrial | ₃Male | ₂Electron Transport Complex I | ₂Genetic Complementation Test | ₁Infant, Newborn | ₁Gene Dosage | ₁Adolescent | ₁Reverse Transcriptase Polymerase Chain Reaction | ₁RNA, Messenger | ₁Chromosomes, Artificial, Bacterial | ₁Cell Fusion | ₁Genes, Lethal | ₁Mitochondrial Diseases | ₁Pedigree | ₁Mice | ₁Transgenes | ₁Molecular Diagnostic Techniques | ₁Prenatal Diagnosis | ₁In Situ Hybridization, Fluorescence | ₁Mice, Knockout | ₁Immunoblotting | ₁Blotting, Western | ₁Biochemistry | ₁Enzymes | ₁Animals | ₁Lactates | ₁Child, Preschool | ₁Pregnancy | ₁Friedreich Ataxia

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

₂₁mitochondrial | ₁₇mutations | ₁₆complex | ₁₄gene | ₁₂mutation | ₁₁human | ₁₀frda | ₉patients | ₈cause | ₈genes | ₈chain | ₈respiratory | ₈deficiency | ₇mouse | ₇lines | ₇disorders | ₆nuclear | ₆infantile | ₆mice | ₆expression | ₅transgene | ₅nd3 | ₅dna | ₄subunit | ₄unknown | ₄cases | ₄novo | ₄mtdna | ₄de | ₃novel | ₃can | ₃encephalopathies
₈respiratory chain | ₈complex deficiency | ₆infantile mitochondrial | ₅mitochondrial dna | ₅knockout mutation | ₄de novo | ₄human frda | ₄chain disorders | ₃novo mutations | ₃mitochondrial encephalopathies | ₃expression human | ₃human transgene | ₃transgenic mice | ₃cause infantile | ₃mutations mitochondrial | ₂mitochondrial encephalopathy | ₂caused mutations | ₂encephalopathy complex | ₂neonatal mitochondrial | ₂ndufs6 mutations | ₂nuclear mitochondrial | ₂mitochondrial nd3 | ₂tissues lines | ₂nd3 gene | ₂mutations novel | ₂mitochondrial complex | ₂subunit gene | ₂gene cause | ₂genes encoding | ₂lethal neonatal | ₂complex subunit | ₂complex assembly
₄respiratory chain disorders | ₃de novo mutations | ₃infantile mitochondrial encephalopathies | ₃cause infantile mitochondrial | ₃mitochondrial respiratory chain | ₃diagnosis mitochondrial respiratory | ₂novel cause lethal | ₂infantile mitochondrial encephalopathy | ₂lethal neonatal mitochondrial | ₂mitochondrial complex deficiency | ₂neonatal mitochondrial complex | ₂mitochondrial nd3 gene | ₂cause lethal neonatal | ₂mitochondrial dna mutations | ₂nuclear mitochondrial dna | ₂ndufs6 mutations novel | ₂different tissues lines | ₂nd3 gene cause | ₂mutations novel cause | ₂gene cause infantile | ₂complex deficiency common | ₂novo mutations mitochondrial | ₂encephalopathy complex deficiency | ₂mitochondrial encephalopathy complex | ₂mutations mitochondrial nd3 | ₂friedreich ataxia knockout | ₂respiratory chain subunits | ₂rescue friedreich ataxia | ₂mutation transgenic mice | ₂human bac-mediated rescue | ₂microarray expression analysis | ₂bac-mediated rescue friedreich

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