Nadia Chuzhanova

7.5k citations

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

Genetics top 1%
- Genomic variations and chromosomal abnormalities 22
- Genomics and Rare Diseases 9
Molecular Biology top 2%
- Genomics and Chromatin Dynamics 11
- RNA and protein synthesis mechanisms 9
- RNA modifications and cancer 9
- DNA Repair Mechanisms 6
Neurology top 2%
- Neurofibromatosis and Schwannoma Cases 11
Ecology top 2%
Endocrinology top 5%
Plant Science
- Chromosomal and Genetic Variations 13

Co-authors: D.N. Cooper John C. Fry Kevin E. Ashelford Antonia J. Jones Andrew J. Weightman Jian‐Min Chen Claude Férec Michael Krawczak
Cited by: Genetics Molecular Biology Neurology
Journals: Proceedings of the National Academy of Sciences (1 paper)Nucleic Acids Research (1 paper)Journal of Biological Chemistry (1 paper)
Partner nations: United Kingdom Germany France

In The Last Decade

Nadia Chuzhanova

82 papers receiving 5.0k citations

Hit Papers

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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

The 25 scholars most cited alongside Nadia Chuzhanova, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Nadia Chuzhanova Line = papers co-authored together Nadia Chuzhanova links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Predicting novel genomic regions linked to genetic disorders using GWAS and chromosome conformation data – a case study of schizophrenia Scientific Reports ·Daniel Buxton,Declan J. Batten,Jonathan J. Crofts,Nadia Chuzhanova	2019	6
2	A numerical simulation of neural fields on curved geometries Journal of Computational Neuroscience ·Rebecca L. Martin,David J. Chappell,Nadia Chuzhanova,Jonathan J. Crofts	2018	6
3	Complexity and robustness in hypernetwork models of metabolism Journal of Theoretical Biology ·Nicole Pearcy,Nadia Chuzhanova,Jonathan J. Crofts	2016	15
4	Screening in silico predicted remotely acting NF1gene regulatory elements for mutations in patients with neurofibromatosis type 1 Human Genomics ·Stephen E. Hamby,Pablo Reviriego,D.N. Cooper,Meena Upadhyaya,Nadia Chuzhanova	2013	3
5	Exploring the somatic NF1 mutational spectrum associated with NF1 cutaneous neurofibromas European Journal of Human Genetics ·Laura E. Thomas,Gill Spurlock,Claire Eudall,Nick S Thomas,Matthew Mort,Stephen E. Hamby,Nadia Chuzhanova,Hilde Brems,Eric Legius,D.N. Cooper,Meena Upadhyaya	2011	22
6	Comparative analysis of germline and somatic microlesion mutational spectra in 17 human tumor suppressor genes Human Mutation ·Dobril Ivanov,Stephen E. Hamby,Peter D. Stenson,Andrew D. Phillips,Hildegard Kehrer-Sawatzki,D.N. Cooper,Nadia Chuzhanova	2011	8
7	Non-B DNA-forming Sequences and WRN Deficiency Independently Increase the Frequency of Base Substitution in Human Cells 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	2011	28
8	Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal loci Human Mutation ·Sylvia Quéméner,Jian‐Min Chen,Nadia Chuzhanova,Caroline Bénech,Teresa Casals,Milan Maçek,Thierry Bienvenu,Trudi McDevitt,Philip M. Farrell,Ourida Loumi,Taïeb Messaoud,Harry Cuppens,Garry R. Cutting,Peter D. Stenson,K. Giteau,Marie‐Pierre Audrézet,D.N. Cooper,Claude Férec	2010	23
9	Genes, mutations, and human inherited disease at the dawn of the age of personalized genomics Human Mutation ·D.N. Cooper,Jian‐Min Chen,Edward V. Ball,Katy Howells,Matthew Mort,Andrew D. Phillips,Nadia Chuzhanova,Michael Krawczak,Hildegard Kehrer‐Sawatzki,Peter D. Stenson	2010	119
10	High-Resolution DNA Copy Number Profiling of Malignant Peripheral Nerve Sheath Tumors Using Targeted Microarray-Based Comparative Genomic Hybridization 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	2008	94
11	Gene conversion: mechanisms, evolution and human disease Nature Reviews Genetics ·Jian‐Min Chen,D.N. Cooper,Nadia Chuzhanova,Claude Férec,George P. Patrinos	2007	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 The American Journal of Human Genetics ·Katharina Steinmann,D.N. Cooper,Lan Kluwe,Nadia Chuzhanova,Cornelia Senger,Eduard Serra,Conxi Lázaro,Montserrat Gilaberte,Katharina Wimmer,Viktor-Felix Mautner,Hildegard Kehrer‐Sawatzki	2007	48
13	Long homopurinehomopyrimidine sequences are characteristic of genes expressed in brain and the pseudoautosomal region Nucleic Acids Research* ·Albino Bacolla,Jack Collins,Bert Gold,Nadia Chuzhanova,Ming Yi,Robert M. Stephens,Стефан Стефанов,Adam Olsh,John P. Jakupciak,Michael Dean,Richard A. Lempicki,D.N. Cooper,Robert D. Wells	2006	54
14	Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16 Genome Research ·Violaine Goidts,Justyna M. Szamalek,Pieter J. de Jong,D.N. Cooper,Nadia Chuzhanova,H. Hameister,Hildegard Kehrer‐Sawatzki	2005	37
15	Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP‐B) deficiency 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	2005	16
16	THE EVOLUTION OF THE VERTEBRATE ?-GLOBIN GENE PROMOTER Evolution ·Nadia Chuzhanova,Michael Krawczak,Nick Thomas,Lubov A. Nemytikova,Vladimir D. Gusev,D.N. Cooper	2002	6
17	Meta-analysis of indels causing human genetic disease: mechanisms of mutagenesis and the role of local DNA sequence complexity Human Mutation ·Nadia Chuzhanova,Emmanuel J. Anassis,Edward V. Ball,Michael Krawczak,D.N. Cooper	2002	88
18	Changes in primary DNA sequence complexity influence the phenotypic consequences of mutations in human gene regulatory regions Human Genetics ·Michael Krawczak,Nadia Chuzhanova,Peter D. Stenson,Bent Johansen,Edward V. Ball,D.N. Cooper	2000	11
19	Promoter shuffling has occurred during the evolution of the vertebrate growth hormone gene Gene ·Nadia Chuzhanova,Michael Krawczak,Lubov A. Nemytikova,Vladimir D. Gusev,D.N. Cooper	2000	18
20	The Algorithms of Recognition of the Functional Sites in Genetic Texts. Vladimir D. Gusev,Nadia Chuzhanova	1990	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), Genomics and Chromatin Dynamics (11 papers), Neurofibromatosis and Schwannoma Cases (11 papers), Genomics and Rare Diseases (9 papers), RNA and protein synthesis mechanisms (9 papers), RNA modifications and cancer (9 papers) and DNA Repair Mechanisms (6 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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