Thomas Guignard

664 total citations
15 papers, 228 citations indexed

About

Thomas Guignard is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Thomas Guignard has authored 15 papers receiving a total of 228 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Cancer Research. Recurrent topics in Thomas Guignard's work include Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cancer Genomics and Diagnostics (3 papers). Thomas Guignard is often cited by papers focused on Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cancer Genomics and Diagnostics (3 papers). Thomas Guignard collaborates with scholars based in France, United States and Finland. Thomas Guignard's co-authors include Jean‐Maurice Dura, Ana Boulanger, François Juge, M. Kœnig, Charles Van Goethem, David Baux, Anne‐Françoise Roux, Anne Bergougnoux, Vincent Gâtinois and Sophie Scheidecker and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Neuroscience.

In The Last Decade

Thomas Guignard

15 papers receiving 227 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Thomas Guignard France	8	131	95	45	26	22	15	228
Brice Ronsin France	10	159 1.2×	46 0.5×	69 1.5×	21 0.8×	31 1.4×	20	285
Dean Pasko United States	5	281 2.1×	112 1.2×	34 0.8×	24 0.9×	13 0.6×	5	340
Anneke T. Vulto‐van Silfhout Netherlands	8	174 1.3×	174 1.8×	17 0.4×	11 0.4×	20 0.9×	18	307
Jeffrey L. Pitman United States	8	270 2.1×	161 1.7×	64 1.4×	35 1.3×	21 1.0×	8	382
Carole Gautier‐Courteille France	13	376 2.9×	57 0.6×	37 0.8×	27 1.0×	32 1.5×	24	490
Aurélie Clément United States	9	204 1.6×	59 0.6×	18 0.4×	110 4.2×	15 0.7×	12	323
Sunit Dutta United States	9	258 2.0×	81 0.9×	42 0.9×	48 1.8×	15 0.7×	9	324
Inessa Grinberg United States	5	227 1.7×	141 1.5×	40 0.9×	17 0.7×	11 0.5×	7	386
Mathias S. Gierl Germany	7	309 2.4×	189 2.0×	47 1.0×	30 1.2×	16 0.7×	7	512

Countries citing papers authored by Thomas Guignard

Since Specialization

Citations

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

Fields of papers citing papers by Thomas Guignard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Guignard

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Guignard, Thomas, Jacques Puechberty, Simon Cabello‐Aguilar, et al.. (2024). Characterizing PALB2 intragenic duplication breakpoints in a triple-negative breast cancer case using long-read sequencing. Frontiers in Oncology. 14. 1355715–1355715. 1 indexed citations

Geoffroy, Véronique, Thomas Guignard, Arnaud Kress, et al.. (2023). The AnnotSV webserver in 2023: updated visualization and ranking. Nucleic Acids Research. 51(W1). W39–W45. 6 indexed citations

Yauy, Kévin, Charles Van Goethem, David Baux, et al.. (2023). Evaluating the Transition from Targeted to Exome Sequencing: A Guide for Clinical Laboratories. International Journal of Molecular Sciences. 24(8). 7330–7330. 2 indexed citations

Geoffroy, Véronique, Thomas Guignard, Arnaud Kress, et al.. (2021). AnnotSV and knotAnnotSV: a web server for human structural variations annotations, ranking and analysis. Nucleic Acids Research. 49(W1). W21–W28. 34 indexed citations

Baux, David, Charles Van Goethem, Thomas Guignard, et al.. (2020). Correction: MobiDetails: online DNA variants interpretation. European Journal of Human Genetics. 29(2). 361–361. 2 indexed citations

Baux, David, Charles Van Goethem, Thomas Guignard, et al.. (2020). MobiDetails: online DNA variants interpretation. European Journal of Human Genetics. 29(2). 356–360. 39 indexed citations

Yauy, Kévin, Anouck Schneider, Bee Ling Ng, et al.. (2019). Disruption of chromatin organisation causes MEF2C gene overexpression in intellectual disability: a case report. BMC Medical Genomics. 12(1). 116–116. 8 indexed citations

Baux, David, et al.. (2019). Abstracts from the 51st European Society of Human Genetics Conference: Posters. European Journal of Human Genetics. 27(S1). 1–688. 2 indexed citations

Mau‐Them, Frédéric Tran, Julien Thévenon, Thomas Guignard, et al.. (2018). LARP7 variants and further delineation of the Alazami syndrome phenotypic spectrum among primordial dwarfisms: 2 sisters. European Journal of Medical Genetics. 62(3). 161–166. 19 indexed citations

10.

Yauy, Kévin, David Baux, Charles Van Goethem, et al.. (2018). MoBiDiC Prioritization Algorithm, a Free, Accessible, and Efficient Pipeline for Single-Nucleotide Variant Annotation and Prioritization for Next-Generation Sequencing Routine Molecular Diagnosis. Journal of Molecular Diagnostics. 20(4). 465–473. 10 indexed citations

11.

Yauy, Kévin, Vincent Gâtinois, Thomas Guignard, et al.. (2018). Looking for Broken TAD Boundaries and Changes on DNA Interactions: Clinical Guide to 3D Chromatin Change Analysis in Complex Chromosomal Rearrangements and Chromothripsis. Methods in molecular biology. 1769. 353–361. 5 indexed citations

12.

Yauy, Kévin, Frédéric Tran Mau‐Them, Marjolaine Willems, et al.. (2017). B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation. Genetics in Medicine. 20(2). 269–274. 21 indexed citations

13.

Boulanger, Ana, et al.. (2010). ftz-f1 and Hr39 opposing roles on EcR expression during Drosophila mushroom body neuron remodeling. Nature Neuroscience. 14(1). 37–44. 64 indexed citations

14.

Guignard, Thomas, Minghao Jin, Marie O. Péquignot, et al.. (2010). FATP1 Inhibits 11-cis Retinol Formation via Interaction with the Visual Cycle Retinoid Isomerase RPE65 and Lecithin:Retinol Acyltransferase. Journal of Biological Chemistry. 285(24). 18759–18768. 13 indexed citations

15.

Guillon, P., et al.. (2008). Head-Related Transfer Function Customization by Frequency Scaling and Rotation Shift Based on a New Morphological Matching Method. Journal of the Audio Engineering Society. 2 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.

Explore authors with similar magnitude of impact