Nadia Chuzhanova

7.5k citations

83 papers · 5.1k indexed · 2 hit papers · h-index 35

Molecular Biology top 2%
Genetics top 1%
Ecology top 2%
Plant Science top 5%
Neurology top 2%

Co-authors: D.N. Cooper John C. Fry Kevin E. Ashelford Antonia J. Jones Andrew J. Weightman Jian‐Min Chen Claude Férec Michael Krawczak
Topics: Genomic variations and chromosomal abnormalities (22 papers)Chromosomal and Genetic Variations (13 papers)Genomics and Chromatin Dynamics (11 papers)
Cited by: Genetics Molecular Biology Neurology
Journals: Proceedings of the National Academy of Sciences Nucleic Acids Research Journal of Biological Chemistry
Partner nations: United Kingdom Germany France

In The Last Decade

Nadia Chuzhanova

82 papers receiving 5.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

At Least 1 in 20 16S rRNA Sequence Records Currently Held in Public Repositories Is Estimated To Contain Substantial Anomalies

2005 645 citations Nadia Chuzhanova et al. profile →
New Screening Software Shows that Most Recent Large 16S rRNA Gene Clone Libraries Contain Chimeras

2006 598 citations Nadia Chuzhanova et al. profile →

Peers

Countries citing papers authored by Nadia Chuzhanova

Since Specialization

Citations

This map shows the geographic impact of Nadia Chuzhanova's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Nadia Chuzhanova with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nadia Chuzhanova more than expected).

Fields of papers citing papers by Nadia Chuzhanova

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nadia Chuzhanova. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Nadia Chuzhanova. The network helps show where Nadia Chuzhanova may publish in the future.

Co-authorship network of co-authors of Nadia Chuzhanova

This figure shows the co-authorship network connecting the top 25 collaborators of Nadia Chuzhanova. A scholar is included among the top collaborators of Nadia Chuzhanova based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Nadia Chuzhanova. Nadia Chuzhanova is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Predicting novel genomic regions linked to genetic disorders using GWAS and chromosome conformation data – a case study of schizophrenia 2019 ·Scientific Reports ·(unknown),(unknown),Jonathan J. Crofts,Nadia Chuzhanova	6
2	A numerical simulation of neural fields on curved geometries 2018 ·Journal of Computational Neuroscience ·(unknown),David J. Chappell,Nadia Chuzhanova,Jonathan J. Crofts	6
3	Complexity and robustness in hypernetwork models of metabolism 2016 ·Journal of Theoretical Biology ·(unknown),Nadia Chuzhanova,Jonathan J. Crofts	15
4	Screening in silico predicted remotely acting NF1gene regulatory elements for mutations in patients with neurofibromatosis type 1 2013 ·Human Genomics ·Stephen E. Hamby,(unknown),D.N. Cooper,Meena Upadhyaya,Nadia Chuzhanova	3
5	Exploring the somatic NF1 mutational spectrum associated with NF1 cutaneous neurofibromas 2011 ·European Journal of Human Genetics ·Laura E. Thomas,Gill Spurlock,(unknown),(unknown),Matthew Mort,Stephen E. Hamby,Nadia Chuzhanova,Hilde Brems,Eric Legius,D.N. Cooper,Meena Upadhyaya	22
6	Comparative analysis of germline and somatic microlesion mutational spectra in 17 human tumor suppressor genes 2011 ·Human Mutation ·Dobril Ivanov,Stephen E. Hamby,Peter D. Stenson,(unknown),(unknown),D.N. Cooper,Nadia Chuzhanova	8
7	Non-B DNA-forming Sequences and WRN Deficiency Independently Increase the Frequency of Base Substitution in Human Cells 2011 ·Journal of Biological Chemistry ·Albino Bacolla,Guliang Wang,Aklank Jain,Nadia Chuzhanova,Regina Z. Cer,Jack Collins,D.N. Cooper,Vilhelm A. Bohr,Karen M. Vásquez	28
8	Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal loci 2010 ·Human Mutation ·(unknown),Jian‐Min Chen,Nadia Chuzhanova,Caroline Bénech,Teresa Casals,Milan Maçek,Thierry Bienvenu,Trudi McDevitt,Philip M. Farrell,(unknown),Taïeb Messaoud,Harry Cuppens,Garry R. Cutting,Peter D. Stenson,(unknown),Marie‐Pierre Audrézet,D.N. Cooper,Claude Férec	23
9	Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics 2010 ·Human Mutation ·D.N. Cooper,Jian‐Min Chen,Edward V. Ball,(unknown),Matthew Mort,Andrew D. Phillips,Nadia Chuzhanova,Michael Krawczak,Hildegard Kehrer‐Sawatzki,(unknown)	119
10	High-Resolution DNA Copy Number Profiling of Malignant Peripheral Nerve Sheath Tumors Using Targeted Microarray-Based Comparative Genomic Hybridization 2008 ·Clinical Cancer Research ·Kiran K. Mantripragada,Gillian Spurlock,Lan Kluwe,Nadia Chuzhanova,Rosalie E. Ferner,Ian M. Frayling,Jan P. Dumanski,Abhijit Guha,Victor Mautner,Meena Upadhyaya	94
11	Gene conversion: mechanisms, evolution and human disease 2007 ·Nature Reviews Genetics ·Jian‐Min Chen,D.N. Cooper,Nadia Chuzhanova,Claude Férec,George P. Patrinos	461
12	Type 2 NF1 Deletions Are Highly Unusual by Virtue of the Absence of Nonallelic Homologous Recombination Hotspots and an Apparent Preference for Female Mitotic Recombination 2007 ·The American Journal of Human Genetics ·Katharina Steinmann,D.N. Cooper,Lan Kluwe,Nadia Chuzhanova,(unknown),Eduard Serra,Conxi Lázaro,Montserrat Gilaberte,Katharina Wimmer,(unknown),Hildegard Kehrer‐Sawatzki	48
13	Long homopurinehomopyrimidine sequences are characteristic of genes expressed in brain and the pseudoautosomal region 2006 ·Nucleic Acids Research* ·Albino Bacolla,Jack Collins,Bert Gold,Nadia Chuzhanova,Ming Yi,Robert M. Stephens,Стефан Стефанов,(unknown),John P. Jakupciak,Michael Dean,Richard A. Lempicki,D.N. Cooper,Robert D. Wells	54
14	Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16 2005 ·Genome Research ·Violaine Goidts,(unknown),Pieter J. de Jong,D.N. Cooper,Nadia Chuzhanova,H. Hameister,Hildegard Kehrer‐Sawatzki	37
15	Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP‐B) deficiency 2005 ·American Journal of Medical Genetics Part A ·Mohammed Tredano,D.N. Cooper,Manfred Stuhrmann,John Christodoulou,Nadia Chuzhanova,Françoise Roudot‐Thoraval,Pierre‐Yves Boëlle,Jacques Élion,Marc Jeanpierre,Josué Feingold,Rémy Couderc,Michel Bahuau	16
16	THE EVOLUTION OF THE VERTEBRATE ?-GLOBIN GENE PROMOTER 2002 ·Evolution ·Nadia Chuzhanova,Michael Krawczak,Nick Thomas,(unknown),(unknown),D.N. Cooper	6
17	Meta-analysis of indels causing human genetic disease: mechanisms of mutagenesis and the role of local DNA sequence complexity 2002 ·Human Mutation ·Nadia Chuzhanova,(unknown),Edward V. Ball,Michael Krawczak,D.N. Cooper	88
18	Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regions 2000 ·Human Genetics ·Michael Krawczak,Nadia Chuzhanova,Peter D. Stenson,(unknown),Edward V. Ball,D.N. Cooper	11
19	Promoter shuffling has occurred during the evolution of the vertebrate growth hormone gene 2000 ·Gene ·Nadia Chuzhanova,Michael Krawczak,(unknown),(unknown),D.N. Cooper	18
20	The Algorithms of Recognition of the Functional Sites in Genetic Texts. 1990 ·(unknown),Nadia Chuzhanova	3

About Nadia Chuzhanova

Nadia Chuzhanova is a scholar working on Genetics, Molecular Biology and Neurology, having authored 83 papers that have together received 5.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (22 papers), Chromosomal and Genetic Variations (13 papers) and Genomics and Chromatin Dynamics (11 papers). The work is most often cited by research in Genetics (1.3k citations), Molecular Biology (2.9k citations) and Neurology (504 citations). Nadia Chuzhanova has collaborated with scholars based in United Kingdom, Germany and France. Frequent co-authors include D.N. Cooper, John C. Fry, Kevin E. Ashelford, Antonia J. Jones, Andrew J. Weightman, Jian‐Min Chen, Claude Férec, Michael Krawczak, Matthew Mort and Peter D. Stenson. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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