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Genetics

D-Index
41
Citations
8962
World Ranking
4325
National Ranking
490

Overview

Nadia Chuzhanova is affiliated with Nottingham Trent University in the United Kingdom. Their research spans multiple fields, primarily focusing on Neuroscience and Biochemistry, Genetics and Molecular Biology. Within these domains, Chuzhanova's work is concentrated on subfields including Cognitive Neuroscience, Molecular Biology, Hematology, Global and Planetary Change, and Computer Networks and Communications.

Their research topics cover a diverse range of areas such as Neural dynamics and brain function, Functional Brain Connectivity Studies, Bioinformatics and Genomic Networks, Acute Myeloid Leukemia Research, Gene expression and cancer classification, Ecosystem dynamics and resilience, and Nonlinear Dynamics and Pattern Formation.

Chuzhanova has contributed to the academic literature with recent publications, which include:

  • Modelling the impact of structural directionality on connectome-based models of neural activity, 2020, Journal of Complex Networks
  • Towards In Silico Identification of Genes Contributing to Similarity of Patients' Multi-Omics Profiles: A Case Study of Acute Myeloid Leukemia, 2023, Genes
  • Synchrony in directed connectomes, 2022, Europhysics Letters (EPL)

Frequent publication venues for Chuzhanova include Genes, Journal of Complex Networks, and Europhysics Letters (EPL).

Their frequent coauthors have been:

  • Jonathan J. Crofts
  • Amelia Padmore
  • M. R. Nelson
  • Declan J. Batten

Best Publications

  • 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 Christopher Fry;Antonia Jane Jones

  • New screening software shows that most recent large 16S rRNA gene clone libraries contain chimeras.

    Kevin E. Ashelford;Nadia A. Chuzhanova;John C. Fry;Antonia J. Jones

  • Gene conversion: mechanisms, evolution and human disease

    Jian-Min Chen;David Neil Cooper;Nadia Chuzhanova;Claude Férec

  • A meta‐analysis of nonsense mutations causing human genetic disease

    Matthew Edwin Mort;Dobril Kirilov Ivanov;David Neil Cooper;Nadia Chuzhanova

  • 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

    M. Upadhyaya;S. M. Huson;M. Davies;N. Thomas

  • Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination‐associated motifs

    Shaun Shihantha Abeysinghe;Nadia Chuzhanova;Nadia Chuzhanova;Michael Krawczak;Edward Vincent Ball

  • Gains of glycosylation comprise an unexpectedly large group of pathogenic mutations

    Guillaume Vogt;Ariane Chapgier;Kun Yang;Kun Yang;Nadia Chuzhanova

  • Breakpoints of gross deletions coincide with non-B DNA conformations

    Albino Bacolla;Adam Jaworski;Adam Jaworski;Jacquelynn E. Larson;John P. Jakupciak

  • Genes, Mutations, and Human Inherited Disease at the Dawn of the Age of Personalized Genomics

    David Neil Cooper;Jian-Min Chen;Edward Vincent Ball;Katy Howells

  • Meta-Analysis of gross insertions causing human genetic disease: Novel mutational mechanisms and the role of replication slippage

    Jian-Min Chen;Nadia Chuzhanova;Peter D. Stenson;Claude Férec

  • On the complexity measures of genetic sequences

    Vladimir D.Gusev;Lubov A.Nemytikova;Nadia A.Chuzhanova

  • 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;Michael Krawczak

  • 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

    David Neil Cooper;Matthew Edwin Mort;Peter Daniel Stenson;Edward Vincent Ball

  • Genomic rearrangements in the CFTR gene: extensive allelic heterogeneity and diverse mutational mechanisms.

    Marie-Pierre Audrézet;Jian-Min Chen;Odile Raguénès;Nadia Chuzhanova

  • Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends.

    Nadia Chuzhanova;Shaun S. Abeysinghe;Michael Krawczak;David N. Cooper

  • Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer

    Clesson Turner;Christina Killoran;Nick S. T. Thomas;Marjorie Rosenberg

  • High-Resolution DNA Copy Number Profiling of Malignant Peripheral Nerve Sheath Tumors Using Targeted Microarray-Based Comparative Genomic Hybridization

    Kiran Kumar Mantripragada;Gillian Spurlock;Lan Kluwe;Nadia Chuzhanova

  • Feature selection for genetic sequence classification

    Nadia A. Chuzhanova;Antonia J. Jones;Steve Margetts

  • Comparative Analysis of Genome Sequences Covering the Seven Cronobacter Species

    Susan Joseph;Prerak Desai;Yongmei Ji;Craig A. Cummings

  • Complex gene rearrangements caused by serial replication slippage.

    Jian-Min Chen;Nadia Chuzhanova;Peter D. Stenson;Claude Férec

Frequent Co-Authors

David Neil Cooper
David Neil Cooper Cardiff University
Jian-Min Chen
Jian-Min Chen University of Western Brittany
Meena Upadhyaya
Meena Upadhyaya Cardiff University
Hildegard Kehrer-Sawatzki
Hildegard Kehrer-Sawatzki University of Ulm
Michael Krawczak
Michael Krawczak Kiel University
Claude Férec
Claude Férec University of Western Brittany
Peter D. Stenson
Peter D. Stenson Cardiff University
Matthew Mort
Matthew Mort Cardiff University
Ludwine Messiaen
Ludwine Messiaen University of Alabama at Birmingham
George P. Patrinos
George P. Patrinos University of Patras

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