Judith Lopes

1.7k total citations
19 papers, 1.3k citations indexed

About

Judith Lopes is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Plant Science. According to data from OpenAlex, Judith Lopes has authored 19 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 4 papers in Plant Science. Recurrent topics in Judith Lopes's work include Hereditary Neurological Disorders (7 papers), DNA and Nucleic Acid Chemistry (5 papers) and DNA Repair Mechanisms (5 papers). Judith Lopes is often cited by papers focused on Hereditary Neurological Disorders (7 papers), DNA and Nucleic Acid Chemistry (5 papers) and DNA Repair Mechanisms (5 papers). Judith Lopes collaborates with scholars based in France, United States and Spain. Judith Lopes's co-authors include Alain Nicolas, Aurèle Piazza, Jean-Baptiste Boulé, Marie‐Paule Teulade‐Fichou, Cyril Ribeyre, Jean‐Louis Mergny, Virginia A. Zakian, Aurore Guédin, Rodrigo Bermejo and Marco Foiani and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and The EMBO Journal.

In The Last Decade

Judith Lopes

19 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Judith Lopes France 16 1.1k 159 150 137 69 19 1.3k
Kent E. Duncan Germany 16 1.0k 0.9× 66 0.4× 108 0.7× 52 0.4× 19 0.3× 23 1.1k
Minako Tateno Japan 9 421 0.4× 98 0.6× 135 0.9× 106 0.8× 30 0.4× 12 785
Patricia Combes France 15 567 0.5× 34 0.2× 89 0.6× 66 0.5× 28 0.4× 22 737
Gabriel Balmus United Kingdom 15 477 0.4× 93 0.6× 134 0.9× 77 0.6× 9 0.1× 26 784
Xinwen Zhang China 12 272 0.2× 92 0.6× 72 0.5× 58 0.4× 40 0.6× 41 494
Véronique Monnier France 15 567 0.5× 51 0.3× 138 0.9× 270 2.0× 59 0.9× 24 894
John K. Blackwood United Kingdom 12 675 0.6× 33 0.2× 156 1.0× 69 0.5× 31 0.4× 13 747
Melitta Dihanich Switzerland 13 549 0.5× 65 0.4× 46 0.3× 84 0.6× 11 0.2× 14 804
Nao Hosoda Japan 18 1.2k 1.1× 48 0.3× 45 0.3× 55 0.4× 11 0.2× 31 1.3k
Mary B. Comer United States 13 886 0.8× 465 2.9× 176 1.2× 160 1.2× 26 0.4× 17 1.1k

Countries citing papers authored by Judith Lopes

Since Specialization
Citations

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

Fields of papers citing papers by Judith Lopes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Judith Lopes

This figure shows the co-authorship network connecting the top 25 collaborators of Judith Lopes. A scholar is included among the top collaborators of Judith Lopes 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 Judith Lopes. Judith Lopes is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Loll, François, et al.. (2021). Epigenetic rewriting at centromeric DNA repeats leads to increased chromatin accessibility and chromosomal instability. Epigenetics & Chromatin. 14(1). 35–35. 9 indexed citations
2.
Piazza, Aurèle, Michael Adrian, Brahim Heddi, et al.. (2015). Short loop length and high thermal stability determine genomic instability induced by G‐quadruplex‐forming minisatellites. The EMBO Journal. 34(12). 1718–1734. 112 indexed citations
3.
Chung, Linda H., Zhigang Guo, Peiyao Jia, et al.. (2014). The FEN1 E359K germline mutation disrupts the FEN1–WRN interaction and FEN1 GEN activity, causing aneuploidy-associated cancers. Oncogene. 34(7). 902–911. 22 indexed citations
4.
Piazza, Aurèle, Alexandre Serero, Jean-Baptiste Boulé, et al.. (2012). Stimulation of Gross Chromosomal Rearrangements by the Human CEB1 and CEB25 Minisatellites in Saccharomyces cerevisiae Depends on G-Quadruplexes or Cdc13. PLoS Genetics. 8(11). e1003033–e1003033. 55 indexed citations
5.
Lopes, Judith, Aurèle Piazza, Rodrigo Bermejo, et al.. (2011). G‐quadruplex‐induced instability during leading‐strand replication. The EMBO Journal. 30(19). 4033–4046. 250 indexed citations
6.
Berger, Adeline, Jean-Baptiste Boulé, Claude Bobo, et al.. (2011). Assessment of human nter and cterBRCA1mutations using growth and localization assays in yeast. Human Mutation. 32(12). 1470–1480. 15 indexed citations
7.
Piazza, Aurèle, Jean-Baptiste Boulé, Judith Lopes, et al.. (2010). Genetic instability triggered by G-quadruplex interacting Phen-DC compounds in Saccharomyces cerevisiae. Nucleic Acids Research. 38(13). 4337–4348. 144 indexed citations
8.
Ribeyre, Cyril, Judith Lopes, Jean-Baptiste Boulé, et al.. (2009). The Yeast Pif1 Helicase Prevents Genomic Instability Caused by G-Quadruplex-Forming CEB1 Sequences In Vivo. PLoS Genetics. 5(5). e1000475–e1000475. 295 indexed citations
9.
Serero, Alexandre, Judith Lopes, Alain Nicolas, & Serge Boiteux. (2008). Yeast genes involved in cadmium tolerance: Identification of DNA replication as a target of cadmium toxicity. DNA repair. 7(8). 1262–1275. 44 indexed citations
10.
Lopes, Judith, Cyril Ribeyre, & Alain Nicolas. (2006). Complex Minisatellite Rearrangements Generated in the Total or Partial Absence of Rad27 / hFEN1 Activity Occur in a Single Generation and Are Rad51 and Rad52 Dependent. Molecular and Cellular Biology. 26(17). 6675–6689. 27 indexed citations
11.
Lopes, Judith. (2002). Instability of the human minisatellite CEB1 in rad27Delta and dna2-1 replication-deficient yeast cells. The EMBO Journal. 21(12). 3201–3211. 41 indexed citations
12.
Loeillet, Sophie, et al.. (2001). Links between replication and recombination in Saccharomyces cerevisiae : A hypersensitive requirement for homologous recombination in the absence of Rad27 activity. Proceedings of the National Academy of Sciences. 98(15). 8263–8269. 77 indexed citations
13.
Lopes, Judith, Sandrine Tardieu, Kaisa Silander, et al.. (1999). Homologous DNA Exchanges in Humans Can Be Explained by the Yeast Double-Strand Break Repair Model: A Study of 17p11.2 Rearrangements Associated with CMT1A and HNPP. Human Molecular Genetics. 8(12). 2285–2292. 47 indexed citations
14.
Lopes, Judith, N. Ravisé, A. Vandenberghe, et al.. (1998). Fine mapping of de novo CMT1A and HNPP rearrangements within CMTIA-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination. Human Molecular Genetics. 7(1). 141–148. 66 indexed citations
15.
Ravisé, N., Judith Lopes, N. Abbas, et al.. (1996). A de Novo Case of Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) of Maternal Origin: A New Mechanism for Deletion in 17p11.2?. Human Molecular Genetics. 5(1). 103–106. 27 indexed citations
16.
Leguern, Éric, Riadh Gouider, Michel Gugenheim, et al.. (1996). Microsatellite mapping of the deletion in patients with hereditary neuropathy with liability to pressure palsies (HNPP): new molecular tools for the study of the region 17p12→p11 and for diagnosis. Cytogenetic and Genome Research. 72(1). 20–25. 11 indexed citations
17.
Lopes, Judith, Éric Leguern, Riadh Gouider, et al.. (1996). Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.. PubMed. 58(6). 1223–30. 44 indexed citations
18.
Leguern, Éric, Nazha Birouk, A. Guilbot, et al.. (1996). La maladie de Charcot-Marie-Tooth. 7(3). 179–185. 1 indexed citations
19.
Leguern, Éric, Riadh Gouider, Judith Lopes, et al.. (1995). Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. Human Molecular Genetics. 4(9). 1673–1674. 15 indexed citations

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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