Raymonda Varon

5.4k total citations · 1 hit paper
62 papers, 3.5k citations indexed

About

Raymonda Varon is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Raymonda Varon has authored 62 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 23 papers in Cancer Research and 17 papers in Genetics. Recurrent topics in Raymonda Varon's work include DNA Repair Mechanisms (32 papers), Carcinogens and Genotoxicity Assessment (22 papers) and Cancer-related Molecular Pathways (8 papers). Raymonda Varon is often cited by papers focused on DNA Repair Mechanisms (32 papers), Carcinogens and Genotoxicity Assessment (22 papers) and Cancer-related Molecular Pathways (8 papers). Raymonda Varon collaborates with scholars based in Germany, United States and Czechia. Raymonda Varon's co-authors include Karl Sperling, Markus Stümm, André Reis, E Seemanová, Martin Digweed, Patrick Concannon, Richard A. Gatti, Karen Cerosaletti, Krystyńa Chrzańowska and Mark O’Driscoll and has published in prestigious journals such as Cell, Molecular Cell and PLoS ONE.

In The Last Decade

Raymonda Varon

62 papers receiving 3.4k 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.

Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome

1998 811 citations Raymonda Varon, Christine Vissinga et al. Cell profile →

Peers

Countries citing papers authored by Raymonda Varon

Since Specialization

Citations

This map shows the geographic impact of Raymonda Varon'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 Raymonda Varon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Raymonda Varon more than expected).

Fields of papers citing papers by Raymonda Varon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Raymonda Varon. 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 Raymonda Varon. The network helps show where Raymonda Varon may publish in the future.

Co-authorship network of co-authors of Raymonda Varon

This figure shows the co-authorship network connecting the top 25 collaborators of Raymonda Varon. A scholar is included among the top collaborators of Raymonda Varon 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 Raymonda Varon. Raymonda Varon 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	Two Missense Mutations in the Primary Autosomal Recessive Microcephaly Gene MCPH1 Disrupt the Function of the Highly Conserved N-Terminal BRCT Domain of Microcephalin 2012 ·Molecular Syndromology ·Mahdi Ghani, Peter N. Robinson, Susanne Morlot, Diana Mitter, Marc Trimborn, (unknown), Raymonda Varon, Karl Sperling, Heidemarie Neitzel	15
2	Identification of a novel candidate gene for non-syndromic autosomal recessive intellectual disability: the WASH complex member SWIP 2011 ·Human Molecular Genetics ·(unknown), Emmanuel Derivery, Hongbo Hu, Masoud Garshasbi, Mohsen Karbasiyan, Marco J. Herold, Gudrun Nürnberg, Reinhard Ullmann, Alexis Gautreau, Karl Sperling, Raymonda Varon, Anna Rajab	62
3	Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotype 2010 ·Human Mutation ·(unknown), Ilja Demuth, Ulrich Baumann, Detlev Schindler, (unknown), Heidemarie Neitzel, Gabriele Gillessen-Kaesbach, (unknown), (unknown), (unknown), Gudrun Nürnberg, Peter Nürnberg, Keng Wee Teik, Revathy Nallusamy, André Reis, (unknown), Martin Digweed, Raymonda Varon	22
4	Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New Form of Congenital Generalized Lipodystrophy with Muscle Rippling (CGL4) Due to PTRF-CAVIN Mutations 2010 ·PLoS Genetics ·Anna Rajab, Volker Straub, Liza McCann, Dominik Seelow, Raymonda Varon, Rita Barresi, (unknown), Barbara Lucke, Susanne Lützkendorf, Mohsen Karbasiyan, Sebastian Bachmann, Simone Spuler, Markus Schuelke	181
5	A mutation in GJA8 (p.P88Q) is associated with "balloon-like" cataract with Y-sutural opacities in a family of Indian origin. 2008 ·PubMed ·Vanita Vanita, Jai Rup Singh, Daljit Singh, Raymonda Varon, Karl Sperling	24
6	A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin. 2008 ·PubMed ·Vanita Vanita, Jai Rup Singh, Daljit Singh, Raymonda Varon, Karl Sperling	36
7	Clinical variability in distal spinal muscular atrophy type 1 (DSMA1): determination of steady-state IGHMBP2 protein levels in five patients with infantile and juvenile disease 2008 ·Journal of Molecular Medicine ·Ulf‐Peter Guenther, Lusy Handoko, Raymonda Varon, Ulrich Stephani, Chang‐Yong Tsao, Jerry R. Mendell, Susanne Lützkendorf, Christoph Hübner, Katja von Au, Sibylle Jablonka, Gunnar Dittmar, Udo Heinemann, A. Schuetz, Markus Schuelke	45
8	A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian origin. 2007 ·PubMed ·(unknown), (unknown), Dilbag Singh, Raymonda Varon, Peter N. Robinson, Karl Sperling	9
9	Clinical and mutational profile in spinal muscular atrophy with respiratory distress (SMARD): defining novel phenotypes through hierarchical cluster analysis 2007 ·Human Mutation ·Ulf‐Peter Guenther, Raymonda Varon, (unknown), (unknown), Alexander E. Volk, Christoph Hübner, Katja von Au, Markus Schuelke	58
10	Cancer Risk of Heterozygotes With the NBN Founder Mutation 2007 ·JNCI Journal of the National Cancer Institute ·E Seemanová, Petr Jarolı́m, Pavel Seeman, Raymonda Varon, Martin Digweed, M Swift, Karl Sperling	66
11	Nijmegen breakage syndrome (NBS) due to maternal isodisomy of chromosome 8 2006 ·American Journal of Medical Genetics Part A ·Raymonda Varon, (unknown), Klaus Wagner, (unknown), (unknown), (unknown), Erwin Petek, Holger Tönnies, (unknown), Karl Sperling, Peter M. Kroisel	7
12	Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability 2005 ·Journal of Medical Genetics ·E Seemanová, (unknown), Heidemarie Neitzel, Raymonda Varon, Jan Hadač, (unknown), Evelin Schröck, Pavel Seeman, Martin Digweed	37
13	Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader?Willi syndrome 2004 ·Human Genetics ·Maren Runte, Raymonda Varon, Denise Horn, Bernhard Horsthemke, Karin Buiting	78
14	Seckel syndrome exhibits cellular features demonstrating defects in the ATR-signalling pathway 2004 ·Human Molecular Genetics ·Gemma Alderton, Hans Joenje, Raymonda Varon, Anders D. Børglum, Penny A. Jeggo, Mark O’Driscoll	140
15	An inducible null mutant murine model of Nijmegen breakage syndrome proves the essential function of NBS1 in chromosomal stability and cell viability 2004 ·Human Molecular Genetics ·Ilja Demuth, Pierre‐Olivier Frappart, (unknown), Anna Melchers, Stephan Lobitz, (unknown), Raymonda Varon, Zdenko Herceg, Karl Sperling, Zhao‐Qi Wang, Martin Digweed	56
16	Increased cancer risk of heterozygotes with NBS1 germline mutations in poland 2004 ·International Journal of Cancer ·Jan Steffen, Raymonda Varon, Maria Mosor, (unknown), Martin Maurer, Markus Stümm, Dorota Nowakowska, (unknown), Ewa Kosakowska, W. Ruka, Zbigniew Nowecki, Piotr Rutkowski, Tomasz Demkow, (unknown), Mariusz Bidziński, (unknown), Karl Sperling	98
17	Radiosensitivity of Ataxia Telangiectasia and Nijmegen Breakage Syndrome Homozygotes and Heterozygotes as Determined by Three-Color FISH Chromosome Painting 2002 ·Radiation Research ·Susann Neubauer, Rouben Arutyunyan, Markus Stümm, Thilo Dörk, (unknown), Michael Bremer, Raymonda Varon, Rolf Sauer, Erich Gebhart	68
18	Clinical presentation and mutation identification in the NBS1 gene in a boy with Nijmegen breakage syndrome 2000 ·Clinical Genetics ·(unknown), Martin Herrmann, B Wittwer, Raymonda Varon, André Reis, J. Horst	9
19	Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome breakdown → 1998 ·Cell ·Raymonda Varon, Christine Vissinga, Matthias Platzer, Karen Cerosaletti, Krystyńa Chrzańowska, Kathrin Saar, Georg Beckmann, E Seemanová, Paul R. Cooper, Norma J. Nowak, Markus Stümm, Corry M.R. Weemaes, Richard A. Gatti, Richard K. Wilson, Martin Digweed, André Rosenthal, Karl Sperling, Patrick Concannon, André Reis	811
20	Recurrent nasal polyps as a monosymptomatic form of cystic fibrosis associated with a novel in-frame deletion (591del18) in the CFTR gene 1995 ·Human Molecular Genetics ·Raymonda Varon, K. Magdorf, Doris Staab, (unknown), (unknown), (unknown), André Reis	16

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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