Nadia Chuzhanova - Concepedia

Author

Nadia Chuzhanova

Also Known As

A. Chuzhanova, Chuzhanova, N, Chuzhanova, NA, Chuzhanova, Nadia, N A Chuzhanova, N CHUZHANOVA, N Chuzhanova, N. A. Chuzhanova, N. Chuzhanova, Nadia A Chuzhanova

115

Publications

7.5K

Citations

H-Index

Concepts

All Affiliations

Cardiff University Nottingham Trent University University of Lancashire Inserm Universität Ulm

About

Nadia Chuzhanova is an author at Cardiff University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	30	3.4K
2	Natural Sciences	9	9	1.5K
3	Engineering	1	1	21
4	Health Sciences	1	1	15
5	Public Health	1	1	20

Nadia Chuzhanova

Publications

6.1K

Citations

H-Index

Page 1

	Year	Citations
At Least 1 in 20 16S rRNA Sequence Records Currently Held in Public Repositories Is Estimated To Contain Substantial Anomalies Kevin E. Ashelford, Nadia Chuzhanova, John C. Fry, Applied and Environmental Microbiology Substantial AnomaliesPublic Repositories IsGeneticsGenomicsDna Barcoding	2005	800
New Screening Software Shows that Most Recent Large 16S rRNA Gene Clone Libraries Contain Chimeras Kevin E. Ashelford, Nadia Chuzhanova, John C. Fry, Applied and Environmental Microbiology	2006	680
A meta-analysis of nonsense mutations causing human genetic disease Matthew Mort, Dobril Ivanov, D.N. Cooper, Human Mutation Gene LesionsSomatic VariantGenetic DisorderGeneticsPathology	2008	482
An Absence of Cutaneous Neurofibromas Associated with a 3-bp Inframe Deletion in Exon 17 of the NF1 Gene (c.2970-2972 delAAT): Evidence of a Clinically Significant NF1 Genotype-Phenotype Correlation Meena Upadhyaya, Susan Huson, D. M. Davies, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGenetic EpidemiologyNf1 GenePathology	2006	360
Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs Shaun S. Abeysinghe, Nadia Chuzhanova, Michael Krawczak, Human Mutation Human Inherited DiseaseGeneticsMolecular BiologyNucleotide CompositionDeletion Breakpoints	2003	228
Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations Guillaume Vogt, Ariane Chapgier, Kun Yang, Nature Genetics Glycosylation CompriseBiosynthesisSomatic VariantLarge GroupPathogenesis	2005	209
Breakpoints of gross deletions coincide with non-B DNA conformations Albino Bacolla, Adam Jaworski, Jacquelynn E. Larson, Proceedings of the National Academy of Sciences	2004	193
Microdeletions and microinsertions causing human genetic disease: common mechanisms of mutagenesis and the role of local DNA sequence complexity Edward V. Ball, Peter D. Stenson, Shaun S. Abeysinghe, Human Mutation GeneticsMolecular BiologyPathologyMolecular GeneticsInherited Disease	2005	163
Methylation-mediated deamination of 5-methylcytosine appears to give rise to mutations causing human inherited disease in CpNpG trinucleotides, as well as in CpG dinucleotides D.N. Cooper, Matthew Mort, Peter D. Stenson, Human Genomics	2010	155
On the complexity measures of genetic sequences Vladimir D. Gusev, Lubov A. Nemytikova, Nadia Chuzhanova Bioinformatics	1999	154

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