Laurence Colleaux

10.2k total citations · 1 hit paper
93 papers, 5.1k citations indexed

About

Laurence Colleaux is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Laurence Colleaux has authored 93 papers receiving a total of 5.1k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Molecular Biology, 61 papers in Genetics and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in Laurence Colleaux's work include Genetics and Neurodevelopmental Disorders (37 papers), Genomic variations and chromosomal abnormalities (24 papers) and RNA modifications and cancer (12 papers). Laurence Colleaux is often cited by papers focused on Genetics and Neurodevelopmental Disorders (37 papers), Genomic variations and chromosomal abnormalities (24 papers) and RNA modifications and cancer (12 papers). Laurence Colleaux collaborates with scholars based in France, United Kingdom and Germany. Laurence Colleaux's co-authors include Arnold Münnich, Bernard Dujon, Marlène Rio, Francis Galibert, L d'Auriol, Florence Molinari, Valérie Cormier‐Daire, Nathalie Boddaert, Stanislas Lyonnet and Michel Vekemans and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Laurence Colleaux

91 papers receiving 5.1k citations

Hit Papers

align trajectories sort by overperformance

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.

Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations

2009 294 citations Sarah Boissel, Florence Molinari et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Laurence Colleaux France	41	3.3k	2.3k	551	504	379	93	5.1k
Michael E. Talkowski United States	32	2.7k 0.8×	1.9k 0.8×	324 0.6×	489 1.0×	323 0.9×	100	4.3k
Ronald G. Lafrenière Canada	22	2.9k 0.9×	2.0k 0.9×	351 0.6×	333 0.7×	948 2.5×	40	4.1k
Carl Baker United States	29	2.8k 0.9×	3.2k 1.4×	436 0.8×	993 2.0×	267 0.7×	34	5.0k
Kristen Brennand United States	38	4.4k 1.3×	1.4k 0.6×	1.1k 2.0×	495 1.0×	398 1.1×	106	6.1k
Nicoletta Landsberger Italy	30	4.4k 1.3×	2.9k 1.2×	275 0.5×	762 1.5×	278 0.7×	73	5.6k
Michel Guipponi Switzerland	32	2.1k 0.6×	931 0.4×	333 0.6×	258 0.5×	286 0.8×	87	3.7k
Barbara R. DuPont United States	25	1.9k 0.6×	1.3k 0.6×	675 1.2×	199 0.4×	105 0.3×	91	3.3k
Jonathan Sebat United States	32	4.3k 1.3×	4.7k 2.0×	570 1.0×	1.4k 2.8×	681 1.8×	62	7.7k
Dietrich Stephan United States	32	2.3k 0.7×	812 0.4×	520 0.9×	371 0.7×	280 0.7×	78	3.9k
Jonathan A. Bernstein United States	28	3.8k 1.1×	2.2k 1.0×	767 1.4×	507 1.0×	232 0.6×	116	5.6k

Countries citing papers authored by Laurence Colleaux

Since Specialization

Citations

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

Fields of papers citing papers by Laurence Colleaux

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laurence Colleaux

This figure shows the co-authorship network connecting the top 25 collaborators of Laurence Colleaux. A scholar is included among the top collaborators of Laurence Colleaux 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 Laurence Colleaux. Laurence Colleaux 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

Baylot, Virginie, Thi Khanh Le, David Taïeb, Palma Rocchi, & Laurence Colleaux. (2024). Between hope and reality: treatment of genetic diseases through nucleic acid-based drugs. Communications Biology. 7(1). 489–489. 14 indexed citations

Le, Thi Khanh, Virginie Baylot, Michaël Baboudjian, et al.. (2023). Castration-Resistant Prostate Cancer: From Uncovered Resistance Mechanisms to Current Treatments. Cancers. 15(20). 5047–5047. 48 indexed citations

Du, Likun, Torkild Visnes, Andrea Björkman, et al.. (2013). A regulatory role for the cohesin loader NIPBL in nonhomologous end joining during immunoglobulin class switch recombination. The Journal of Experimental Medicine. 210(12). 2503–2513. 29 indexed citations

Philippe, Anne, Valérie Malan, Marie‐Line Jacquemont, et al.. (2013). Xq25 duplications encompassing GRIA3 and STAG2 genes in two families convey recognizable X‐linked intellectual disability with distinctive facial appearance. American Journal of Medical Genetics Part A. 161(6). 1370–1375. 19 indexed citations

Jamra, Rami Abou, Annick Raas‐Rothschild, Sebastian Eck, et al.. (2011). Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature. The American Journal of Human Genetics. 88(6). 788–795. 167 indexed citations

Rio, Marlène, Valérie Malan, Sarah Boissel, et al.. (2009). Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition. European Journal of Human Genetics. 18(3). 285–290. 29 indexed citations

Borck, Guntram, et al.. (2009). Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family. European Journal of Medical Genetics. 52(4). 180–184. 20 indexed citations

Borck, Guntram, Anahi Molla‐Herman, Nathalie Boddaert, et al.. (2008). Clinical, cellular, and neuropathological consequences ofAP1S2mutations: further delineation of a recognizable X-linked mental retardation syndrome. Human Mutation. 29(7). 966–974. 36 indexed citations

Molinari, Florence, S. Romano, François Foulquier, et al.. (2007). Oligosaccharyltransferase subunits mutations in non-syndromic mental retardation. European Journal of Human Genetics. 16. 25. 4 indexed citations

10.

Didelot, Gérard, Florence Molinari, P. Tchénio, et al.. (2006). Tequila, a Neurotrypsin Ortholog, Regulates Long-Term Memory Formation in Drosophila. Science. 313(5788). 851–853. 67 indexed citations

11.

Redon, Richard, Geneviève Baujat, Damien Sanlaville, et al.. (2006). Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndrome. European Journal of Human Genetics. 14(6). 759–767. 56 indexed citations

12.

Laumonnier, Frédéric, Sébastien Roger, Pascaline Guérin, et al.. (2006). Association of a Functional Deficit of the BK _Ca Channel, a Synaptic Regulator of Neuronal Excitability, With Autism and Mental Retardation. American Journal of Psychiatry. 163(9). 1622–1629. 135 indexed citations

13.

Molinari, Florence, Annick Raas‐Rothschild, Marlène Rio, et al.. (2005). Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy. The American Journal of Human Genetics. 76(2). 334–339. 115 indexed citations

14.

Baujat, Geneviève, Marlène Rio, Sylvie Rossignol, et al.. (2004). Paradoxical NSD1 Mutations in Beckwith-Wiedemann Syndrome and 11p15 Anomalies in Sotos Syndrome. The American Journal of Human Genetics. 74(4). 715–720. 88 indexed citations

15.

Molinari, Florence, et al.. (2003). Extracellular proteases and their inhibitors ingenetic diseases of the central nervous system. Human Molecular Genetics. 12(suppl 2). R195–R200. 29 indexed citations

16.

Rio, Marlène, Florence Molinari, S. Heuertz, et al.. (2002). Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation. Journal of Medical Genetics. 39(4). 266–270. 54 indexed citations

17.

Billett, Michael A., et al.. (1995). Developmental Changes of the 26 S Proteasome in Abdominal Intersegmental Muscles of Manduca sexta during Programmed Cell Death. Journal of Biological Chemistry. 270(4). 1850–1858. 129 indexed citations

18.

Pascolo, Steve, et al.. (1992). XI. Yeast sequencing reports. The sequence of a 9·3 kb segment located on the left arm of the yeast chromosome XI reveals five open reading frames including the CCE1 gene and putative products related to MYO2 and to the ribosomal protein L10. Yeast. 8(11). 987–995. 13 indexed citations

19.

Michel-Wolwertz, M.-R., Laurence Colleaux, Didier Breyer, et al.. (1992). Biochemical, genetic and molecular characterization of new respiratory-deficient mutants inChlamydomonas reinhardtii. Plant Molecular Biology. 18(4). 759–772. 49 indexed citations

20.

Monteilhet, Claude, Arnaud Perrin, Agnès Thierry, Laurence Colleaux, & Bernard Dujon. (1990). Purification and characterization of thein vitroactivity of I-SceI, a novel and highly specific endonuclease encoded by a group I intron. Nucleic Acids Research. 18(6). 1407–1413. 140 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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