Laurence Colleaux

10.2k citations

93 papers · 5.1k indexed · 1 hit paper · h-index 41

Molecular Biology top 2%
Genetics top 0.5%
Cellular and Molecular Neuroscience top 5%
Cognitive Neuroscience top 5%
Cancer Research top 5%

Co-authors: Arnold Münnich Bernard Dujon Marlène Rio Francis Galibert L d'Auriol Florence Molinari Valérie Cormier‐Daire Nathalie Boddaert
Topics: Genetics and Neurodevelopmental Disorders (37 papers)Genomic variations and chromosomal abnormalities (24 papers)RNA modifications and cancer (12 papers)
Cited by: Genetics Molecular Biology Cellular and Molecular Neuroscience
Journals: Science Cell Proceedings of the National Academy of Sciences
Partner nations: France United Kingdom Germany

In The Last Decade

Laurence Colleaux

91 papers receiving 5.1k 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.

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

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

Peers

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

#	Work	Indexed citations
1	Between hope and reality: treatment of genetic diseases through nucleic acid-based drugs 2024 ·Communications Biology ·Virginie Baylot,Thi Khanh Le,David Taïeb,Palma Rocchi,Laurence Colleaux	14
2	Castration-Resistant Prostate Cancer: From Uncovered Resistance Mechanisms to Current Treatments 2023 ·Cancers ·Thi Khanh Le,(unknown),Virginie Baylot,(unknown),Michaël Baboudjian,Laurence Colleaux,David Taïeb,Palma Rocchi	48
3	A regulatory role for the cohesin loader NIPBL in nonhomologous end joining during immunoglobulin class switch recombination 2013 ·The Journal of Experimental Medicine ·(unknown),Likun Du,Torkild Visnes,Andrea Björkman,(unknown),Josephine Wincent,Guntram Borck,Laurence Colleaux,Valérie Cormier‐Daire,Dik C. van Gent,Juan Pié,Beatriz Puisac,Noel F.C.C. de Miranda,Sven Kracker,Lennart Hammarström,Jean‐Pierre de Villartay,Anne Durandy,Jacqueline Schoumans,Lena Ström,Qiang Pan‐Hammarström	29
4	Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth 2013 ·Human Molecular Genetics ·Lionel Van Maldergem,Qingming Hou,Vera M. Kalscheuer,Marlène Rio,Martine Doco‐Fenzy,Ana Medeira,Arjan P.M. de Brouwer,Christelle Cabrol,Stefan A. Haas,Pierre Cacciagli,Sébastien Moutton,Emilie Landais,Jacques Motté,Laurence Colleaux,Céline Bonnet,Laurent Villard,Juliette Dupont,Heng‐Ye Man	55
5	Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature 2011 ·The American Journal of Human Genetics ·Rami Abou Jamra,(unknown),Annick Raas‐Rothschild,Sebastian Eck,Elisabeth Graf,Rebecca Buchert,Guntram Borck,Arif B. Ekici,Felix F. Brockschmidt,Markus M. Nöthen,Arnold Münnich,Tim M. Strom,André Reis,Laurence Colleaux	167
6	Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family 2009 ·European Journal of Medical Genetics ·(unknown),Guntram Borck,Nathalie Boddaert,(unknown),(unknown),Arnold Münnich,Laurence Colleaux,Malika Chaouch	20
7	Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families 2009 ·Journal of Medical Genetics ·(unknown),(unknown),Guntram Borck,Clarisse Baumann,Geneviève Baujat,Éric Bieth,Patrick Edery,Chantal Farra,(unknown),Delphine Héron,Bruno Leheup,M Le Merrer,Stanislas Lyonnet,Dominique Martin‐Coignard,M Mathieu,Christel Thauvin‐Robinet,Alain Verloès,Laurence Colleaux,Arnold Münnich,Valérie Cormier‐Daire	79
8	Combination of Linkage Mapping and Microarray-Expression Analysis Identifies NF-κB Signaling Defect as a Cause of Autosomal-Recessive Mental Retardation 2009 ·The American Journal of Human Genetics ·(unknown),Marlène Rio,(unknown),Jean-Marc Plaza,Philippe Guigue,Florence Molinari,Nathalie Boddaert,Christine Bôle‐Feysot,Patrick Nitschké,Asma Smahi,Arnold Münnich,Laurence Colleaux	73
9	Clinical, cellular, and neuropathological consequences ofAP1S2mutations: further delineation of a recognizable X-linked mental retardation syndrome 2008 ·Human Mutation ·Guntram Borck,Anahi Molla‐Herman,Nathalie Boddaert,(unknown),Anne Philippe,Laurence Robel,Isabelle Desguerre,Françis Brunelle,Alexandre Benmerah,Arnold Münnich,Laurence Colleaux	36
10	Oligosaccharyltransferase subunits mutations in non-syndromic mental retardation 2007 ·European Journal of Human Genetics ·Florence Molinari,S. Romano,François Foulquier,Willy Morelle,Pascale de Lonlay,(unknown),J. Teague,Sarah Edkins,PA Futreal,(unknown),(unknown),G. Turner,Gert Matthijs,Jozef Gécz,Arnold Münnich,Laurence Colleaux	4
11	Mutations in TCF4, Encoding a Class I Basic Helix-Loop-Helix Transcription Factor, Are Responsible for Pitt-Hopkins Syndrome, a Severe Epileptic Encephalopathy Associated with Autonomic Dysfunction 2007 ·The American Journal of Human Genetics ·Jeanne Amiel,Marlène Rio,Loïc de Pontual,Richard Redon,Valérie Malan,Nathalie Boddaert,Perrine Plouin,Nigel P. Carter,Stanislas Lyonnet,Arnold Münnich,Laurence Colleaux	212
12	Tequila, a Neurotrypsin Ortholog, Regulates Long-Term Memory Formation in Drosophila 2006 ·Science ·Gérard Didelot,Florence Molinari,P. Tchénio,Daniel Comas,(unknown),Arnold Munnich,Laurence Colleaux,Thomas Préat	67
13	Association of a Functional Deficit of the BK _Ca Channel, a Synaptic Regulator of Neuronal Excitability, With Autism and Mental Retardation 2006 ·American Journal of Psychiatry ·Frédéric Laumonnier,Sébastien Roger,Pascaline Guérin,Florence Molinari,Ridha Mrad,Dominique Cahard,A. Belhadj,(unknown),Antonio M. Persico,Maurizio Elia,Valentino Romano,Sébastien Holbert,Christian Andrés,Habiba Chaâbouni,Laurence Colleaux,Jacques Constant,Jean-Yves Le Guennec,Sylvain Briault	135
14	Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy 2005 ·The American Journal of Human Genetics ·Florence Molinari,Annick Raas‐Rothschild,Marlène Rio,Giuseppe Fiermonte,Férechté Encha‐Razavi,Luigi Palmieri,Ferdinando Palmieri,Ziva Ben‐Neriah,Noman Kadhom,Michel Vekemans,Tania Attié‐Bitach,Arnold Münnich,Pierre Rustin,Laurence Colleaux	115
15	Molecular karyotyping in human constitutional cytogenetics 2005 ·European Journal of Medical Genetics ·Damien Sanlaville,(unknown),C Turleau,(unknown),Guntram Borck,Laurence Colleaux,Michel Vekemans,Serge Romana	20
16	Paradoxical NSD1 Mutations in Beckwith-Wiedemann Syndrome and 11p15 Anomalies in Sotos Syndrome 2004 ·The American Journal of Human Genetics ·Geneviève Baujat,Marlène Rio,Sylvie Rossignol,Damien Sanlaville,Stanislas Lyonnet,Martine Le Merrer,Arnold Münnich,Christine Gicquel,Valérie Cormier‐Daire,Laurence Colleaux	88
17	Approche diagnostique du sujet présentant un retard mental sévère et syndromique 2004 ·Archives de Pédiatrie ·Marlène Rio,Laurence Colleaux,Damien Sanlaville,Guntram Borck,Florence Molinari,Arnold Münnich	1
18	Extracellular proteases and their inhibitors ingenetic diseases of the central nervous system 2003 ·Human Molecular Genetics ·Florence Molinari,(unknown),Arnold Münnich,P. Sonderegger,Laurence Colleaux	29
19	Construction of a YAC contig spanning the Xq13.3 subband 1995 ·Genomics ·Laurent Villard,Jozef Gécz,Laurence Colleaux,Anne-Marie Lossi,Jamel Chelly,Yumiko Ishikawa-Brush,Anthony P. Monaco,Michel Fontés	16
20	Purification and characterization of thein vitroactivity of I-SceI, a novel and highly specific endonuclease encoded by a group I intron 1990 ·Nucleic Acids Research ·Claude Monteilhet,Arnaud Perrin,Agnès Thierry,Laurence Colleaux,Bernard Dujon	140

About Laurence Colleaux

Laurence Colleaux is a scholar working on Genetics, Molecular Biology and Aging, having authored 93 papers that have together received 5.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (37 papers), Genomic variations and chromosomal abnormalities (24 papers) and RNA modifications and cancer (12 papers). The work is most often cited by research in Genetics (2.3k citations), Molecular Biology (3.3k citations) and Cellular and Molecular Neuroscience (551 citations). Laurence Colleaux has collaborated with scholars based in France, United Kingdom and Germany. Frequent 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. Their work appears in journals such as Science, Cell and Proceedings of the National Academy of Sciences.

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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