₁Christie Ballantyne

Summary for 2002 [at-glance overview of Christie Ballantyne work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Christie Ballantyne. According to available data, in 2002 Christie Ballantyne published at least 1 articles. This work was completed in collaboration with several authors including Beaudet, Arthur L and Bodamer, Olaf A. At least 3 different grants are awarded to Christie Ballantyne to support this work. All time total of the grant awards on file exceeds $3,250,391.

Analysis of the article abstracts and the titles suggests that Christie Ballantyne professional interests are focused around "hplc provide efficient", "causing familial hypercholesterolemia" and "efficient detection mutations". These might also be referred to as "mutations causing", "denaturing hplc" or "ldlr gene". Statistical analysis shows that Christie Ballantyne's writing is likely to contains terms "fh", "mutations", "individuals", "diagnosis", "causing" and "denaturing".

The majority of Christie Ballantyne articles are affiliated with Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA. Luckily, one email address is on file.

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Alternative names (0) [other authors with names similar to Christie Ballantyne]

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Year 2002 Charts [Christie Ballantyne frequent coauthors and the most common unique vocabulary terms for the selected year]

Historical Performance Charts [graphical overview of Christie Ballantyne publication and funding history for the range of years]

Emails (1) [email addresses extracted from Christie Ballantyne affiliations]

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Christie Ballantyne Coauthors (2) [all coauthors with the number of joint publications]

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1

₁₃Beaudet, Arthur L

1

₅Bodamer, Olaf A

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Affiliations (1) [condensed summary of the Christie Ballantyne affiliations, the leading number and the color conveys importance]

₁Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

Key Opinion Leader In [Christie Ballantyne 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]

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Keywords (15) [keywords assigned to Christie Ballantyne articles by PubMed, the leading number and the color conveys importance]

₁Chromatography, High Pressure Liquid | ₁Adult | ₁Receptors, LDL | ₁Exons | ₁Middle Aged | ₁Hyperlipoproteinemia Type II | ₁Polymorphism, Genetic | ₁Sensitivity and Specificity | ₁Female | ₁Male | ₁Polymerase Chain Reaction | ₁Mutation | ₁Cell Line | ₁DNA Mutational Analysis | ₁Humans

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

₈fh | ₆mutations | ₄individuals | ₄diagnosis | ₄causing | ₃denaturing | ₃hplc | ₃hypercholesterolemia | ₃efficient | ₃previously | ₃dhplc | ₃familial | ₃gene | ₃ldlr | ₂found | ₂controls | ₂detection | ₂exons | ₂identified | ₂sequencing | ₂provide | ₂clinical | ₂use | ₂lines | ₂cell | ₂reported | ₂nine | ₂disease | ₂heterozygous | ₂used | ₁unreported | ₁aberrantly
₃mutations causing | ₃denaturing hplc | ₃ldlr gene | ₃familial hypercholesterolemia | ₂use denaturing | ₂individuals fh | ₂fh cell | ₂clinical diagnosis | ₂hplc provide | ₂nine individuals | ₂provide efficient | ₂causing familial | ₂detection mutations | ₂cell lines | ₂efficient detection | ₂previously reported | ₂heterozygous fh | ₁unknown significance | ₁promoter ldlr | ₁imprecise molecular | ₁autosomal dominant | ₁diagnosis heterozygous | ₁intron boundaries | ₁conclusions dhplc | ₁background autosomal | ₁migrating fragments | ₁boundaries promoter | ₁prevent premature | ₁causing identified | ₁controls individuals | ₁fragments methods | ₁diagnosis help
₂hplc provide efficient | ₂causing familial hypercholesterolemia | ₂efficient detection mutations | ₂provide efficient detection | ₂use denaturing hplc | ₂fh cell lines | ₂detection mutations causing | ₂mutations causing familial | ₂denaturing hplc provide | ₁diagnosis fh imprecise | ₁hypercholesterolemia background autosomal | ₁including exon intron | ₁detect mutations causing | ₁significant morbidity mortality | ₁morbidity mortality currently | ₁clinical diagnosis heterozygous | ₁likely sensitive efficient | ₁familial hypercholesterolemia fh | ₁size ldlr gene | ₁heterozygous fh cell | ₁ldlr gene common | ₁aberrantly migrating fragments | ₁migrating fragments methods | ₁eight nine individuals | ₁unreported change 5'-untranslated | ₁clinical diagnosis fh | ₁nine individuals families | ₁results mutations previously | ₁hypercholesterolemia definitive diagnosis | ₁screened mutations denaturing | ₁control individuals screened | ₁c646y delg197 none

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