Asma Chaoui

423 total citations
8 papers, 320 citations indexed

About

Asma Chaoui is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, Asma Chaoui has authored 8 papers receiving a total of 320 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Surgery, 6 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Asma Chaoui's work include Congenital gastrointestinal and neural anomalies (6 papers), RNA regulation and disease (4 papers) and Digestive system and related health (2 papers). Asma Chaoui is often cited by papers focused on Congenital gastrointestinal and neural anomalies (6 papers), RNA regulation and disease (4 papers) and Digestive system and related health (2 papers). Asma Chaoui collaborates with scholars based in France, Spain and United States. Asma Chaoui's co-authors include Nadège Bondurand, Véronique Pingault, Viviane Baral, Yuli Watanabe, Michel Goossens, Renaud Touraine, Sandrine Marlin, Chrystel Leroy, F. Archambeaud and Christine Francannet and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Asma Chaoui

8 papers receiving 317 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Asma Chaoui France	8	173	103	80	68	49	8	320
Echaieb Anis France	2	137 0.8×	41 0.4×	19 0.2×	52 0.8×	29 0.6×	3	232
Cynthia C. Morton United States	8	178 1.0×	81 0.8×	58 0.7×	12 0.2×	33 0.7×	8	407
Mary Anne Potok United States	10	397 2.3×	193 1.9×	31 0.4×	54 0.8×	59 1.2×	13	561
Kemal O. Yariz United States	8	212 1.2×	90 0.9×	45 0.6×	25 0.4×	11 0.2×	9	346
Steven E. Boyden United States	9	218 1.3×	58 0.6×	17 0.2×	10 0.1×	8 0.2×	15	356
Julie Batut France	11	274 1.6×	35 0.3×	12 0.1×	13 0.2×	30 0.6×	22	338
Olivier Goupille France	12	175 1.0×	54 0.5×	16 0.2×	17 0.3×	32 0.7×	18	331
Robert Maiwald Germany	8	253 1.5×	214 2.1×	13 0.2×	45 0.7×	13 0.3×	13	460
Leonard Cheung United States	10	219 1.3×	128 1.2×	39 0.5×	41 0.6×	51 1.0×	18	394
Caroline Abadie France	8	265 1.5×	94 0.9×	10 0.1×	13 0.2×	43 0.9×	21	358

Countries citing papers authored by Asma Chaoui

Since Specialization

Citations

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

Fields of papers citing papers by Asma Chaoui

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Asma Chaoui

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

All Works

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8 of 8 papers shown

1.

Chaoui, Asma, Viviane Baral, Yuli Watanabe, et al.. (2015). Subnuclear re-localization of SOX10 and p54NRB correlates with a unique neurological phenotype associated with SOX10 missense mutations. Human Molecular Genetics. 24(17). 4933–4947. 11 indexed citations

2.

Pingault, Véronique, Asma Chaoui, Alain Verloès, et al.. (2014). Phenotypic similarities and differences in patients with a p.Met112Ile mutation in SOX10. American Journal of Medical Genetics Part A. 164(9). 2344–2350. 16 indexed citations

3.

Becdelièvre, Alix de, Lisa Golmard, Christian Vasseur, et al.. (2013). Combined Computational-Experimental Analyses ofCFTRExon Strength Uncover Predictability of Exon-Skipping Level. Human Mutation. 34(6). 873–881. 25 indexed citations

4.

Pingault, Véronique, Viviane Baral, Séverine Marcos, et al.. (2013). Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness. The American Journal of Human Genetics. 92(5). 707–724. 142 indexed citations

5.

Jannot, Anne‐Sophie, Anna Pelet, Alexandra Henrion‐Caude, et al.. (2013). Chromosome 21 Scan in Down Syndrome Reveals DSCAM as a Predisposing Locus in Hirschsprung Disease. PLoS ONE. 8(5). e62519–e62519. 18 indexed citations

6.

Lecerf, Laure, Macarena Ruiz‐Ferrer, Viviane Baral, et al.. (2013). An Impairment of Long Distance SOX10 Regulatory Elements Underlies Isolated Hirschsprung Disease. Human Mutation. 35(3). 303–307. 30 indexed citations

7.

Baral, Viviane, Asma Chaoui, Yuli Watanabe, et al.. (2012). Screening of MITF and SOX10 Regulatory Regions in Waardenburg Syndrome Type 2. PLoS ONE. 7(7). e41927–e41927. 11 indexed citations

8.

Chaoui, Asma, Yuli Watanabe, Renaud Touraine, et al.. (2011). Identification and functional analysis ofSOX10missense mutations in different subtypes of waardenburg syndrome. Human Mutation. 32(12). 1436–1449. 67 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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