Nathalie Ronce

2.9k total citations · 1 hit paper
27 papers, 1.6k citations indexed

About

Nathalie Ronce is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Nathalie Ronce has authored 27 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 16 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Nathalie Ronce's work include Genetics and Neurodevelopmental Disorders (19 papers), RNA modifications and cancer (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Nathalie Ronce is often cited by papers focused on Genetics and Neurodevelopmental Disorders (19 papers), RNA modifications and cancer (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Nathalie Ronce collaborates with scholars based in France, Germany and United States. Nathalie Ronce's co-authors include Claude Moraine, Sylvain Briault, Martine Raynaud, Ben C.J. Hamel, Jamel Chelly, Frédéric Laumonnier, Jean‐Pierre Fryns, Marie‐Pierre Moizard, Hans‐Hilger Ropers and Marie Gomot and has published in prestigious journals such as Nature, The American Journal of Human Genetics and Molecular Psychiatry.

In The Last Decade

Nathalie Ronce

25 papers receiving 1.5k 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.

X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family

2004 553 citations Frédéric Laumonnier, Frédérique Bonnet‐Brilhault 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
Nathalie Ronce France	15	994	971	382	282	196	27	1.6k
Martine Raynaud France	25	1.9k 1.9×	2.1k 2.2×	757 2.0×	309 1.1×	186 0.9×	57	3.0k
Gabrielle Rudolf France	24	698 0.7×	592 0.6×	394 1.0×	708 2.5×	138 0.7×	69	2.1k
Francesca Zalfa Italy	19	1.8k 1.8×	1.2k 1.3×	502 1.3×	307 1.1×	198 1.0×	27	2.3k
Jennifer Skaug Canada	10	1.1k 1.1×	572 0.6×	319 0.8×	200 0.7×	238 1.2×	11	1.8k
Charlotte Kilstrup‐Nielsen Italy	26	1.4k 1.5×	1.5k 1.6×	402 1.1×	222 0.8×	189 1.0×	40	2.1k
Richard J. Schroer United States	24	976 1.0×	1.3k 1.3×	795 2.1×	208 0.7×	173 0.9×	39	2.0k
Yong-hui Jiang United States	10	823 0.8×	854 0.9×	406 1.1×	174 0.6×	80 0.4×	11	1.3k
Fabien Fauchereau France	13	606 0.6×	520 0.5×	356 0.9×	196 0.7×	183 0.9×	17	1.2k
Melissa B. Ramocki United States	19	1.1k 1.1×	1.2k 1.3×	497 1.3×	222 0.8×	160 0.8×	29	1.9k
Zhengmao Hu China	25	1000 1.0×	535 0.6×	295 0.8×	430 1.5×	207 1.1×	127	1.9k

Countries citing papers authored by Nathalie Ronce

Since Specialization

Citations

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

Fields of papers citing papers by Nathalie Ronce

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nathalie Ronce

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

Moizard, Marie‐Pierre, Nathalie Ronce, Paul Guéguen, et al.. (2025). Variant Update on ASCC1 : Characterization of the First Homozygous Missense Variant Involved in Prenatal‐Onset Spinal Muscular Atrophy With Congenital Bone Fractures 2. American Journal of Medical Genetics Part A. 200(3). 744–748.

Ronce, Nathalie, Benjamin Cogné, Thomas Besnard, et al.. (2024). Identification of a Rare Branch Point Variant in the SMS Gene in a Large Family With a Severe Form of Snyder–Robinson Syndrome. Clinical Genetics. 107(2). 231–233.

Ronce, Nathalie, Éric Bieth, Lydie Bürglen, et al.. (2010). Twenty-five novel mutations including duplications in the ATP7A gene. Clinical Genetics. 79(3). 243–253. 15 indexed citations

Laumonnier, Frédéric, Cheryl Shoubridge, Catherine Antar, et al.. (2009). Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism. Molecular Psychiatry. 15(7). 767–776. 89 indexed citations

Laumonnier, Frédéric, Frédérique Bonnet‐Brilhault, Marie Gomot, et al.. (2004). X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family. The American Journal of Human Genetics. 74(3). 552–557. 553 indexed citations breakdown →

Portes, Vincent des, Nathalie Boddaert, Silvia Sacco, et al.. (2003). Specific clinical and brain MRI features in mentally retarded patients with mutations in the Oligophrenin‐1 gene. American Journal of Medical Genetics Part A. 124A(4). 364–371. 45 indexed citations

Raynaud, Martine, Nathalie Ronce, John M. Opitz, et al.. (2003). Skewed X chromosome inactivation in carriers is not a constant finding in FG syndrome. European Journal of Human Genetics. 11(4). 352–356. 2 indexed citations

Laumonnier, Frédéric, Nathalie Ronce, Ben C.J. Hamel, et al.. (2002). Transcription Factor SOX3 Is Involved in X-Linked Mental Retardation with Growth Hormone Deficiency. The American Journal of Human Genetics. 71(6). 1450–1455. 232 indexed citations

Gomot, Marie, Nathalie Ronce, Ramzi Zemni, et al.. (2002). TM4SF2 gene involvement reconsidered in an XLMR family after neuropsychological assessment. American Journal of Medical Genetics. 112(4). 400–404. 9 indexed citations

10.

Toutain, Annick, Nathalie Ronce, Maria Immacolata Ferrante, et al.. (2002). Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genes. European Journal of Human Genetics. 10(9). 516–520. 15 indexed citations

11.

Gendrot, Chantal, Nathalie Ronce, Martine Raynaud, et al.. (1999). X‐linked nonspecific mental retardation (MRX16) mapping to distal Xq28: Linkage study and neuropsychological data in a large family. American Journal of Medical Genetics. 83(5). 411–418. 2 indexed citations

12.

Ronce, Nathalie, Martine Raynaud, Annick Toutain, et al.. (1999). Evidence for a new X-linked mental retardation gene in Xp21-Xp22: Clinical and molecular data in one family. American Journal of Medical Genetics. 83(2). 132–137. 10 indexed citations

13.

Walpole, Susannah M., Nathalie Ronce, Celene Grayson, et al.. (1999). Exclusion of RAI2 as the causative gene for Nance-Horan syndrome. Human Genetics. 104(5). 410–411. 9 indexed citations

14.

Billuart, Pierre, T. Bienvenu, Nathalie Ronce, et al.. (1998). Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardation.. PubMed. 46(9). 678–678. 33 indexed citations

15.

Billuart, Pierre, T Bienvenu, Nathalie Ronce, et al.. (1998). Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation. Nature. 392(6679). 923–926. 382 indexed citations

16.

Raynaud, Martine, et al.. (1998). X‐linked mental retardation with isolated growth hormone deficiency is mapped to Xq22–Xq27.2 in one family. American Journal of Medical Genetics. 76(3). 255–261. 2 indexed citations

17.

Toutain, Annick, Nathalie Ronce, Laura Robb, et al.. (1997). Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 region. Human Genetics. 99(2). 256–261. 25 indexed citations

18.

Briault, Sylvain, Ruth F. Hill, Antony E. Shrimpton, et al.. (1997). A gene for FG syndrome maps in the Xq12-q21.31 region. American Journal of Medical Genetics. 73(1). 87–90. 38 indexed citations

19.

Raynaud, Martine, Chantal Gendrot, Anne Moncla, et al.. (1996). X-linked mental retardation with neonatal hypotonia in a French family (MRX15): Gene assignment to Xp11.22-Xp21.1. American Journal of Medical Genetics. 64(1). 97–106. 12 indexed citations

20.

Gendrot, Chantal, Nathalie Ronce, Annick Toutain, et al.. (1994). X‐linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric region. Clinical Genetics. 45(3). 145–153. 14 indexed citations

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