Nadia Elkhartoufi

1.6k total citations
10 papers, 155 citations indexed

About

Nadia Elkhartoufi is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Nadia Elkhartoufi has authored 10 papers receiving a total of 155 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Nadia Elkhartoufi's work include Genetic and Kidney Cyst Diseases (9 papers), Fetal and Pediatric Neurological Disorders (5 papers) and Genetic Syndromes and Imprinting (3 papers). Nadia Elkhartoufi is often cited by papers focused on Genetic and Kidney Cyst Diseases (9 papers), Fetal and Pediatric Neurological Disorders (5 papers) and Genetic Syndromes and Imprinting (3 papers). Nadia Elkhartoufi collaborates with scholars based in France, United Kingdom and Morocco. Nadia Elkhartoufi's co-authors include Tania Attié‐Bitach, Sophie Thomas, Michel Vekemans, Lucile Boutaud, Arnold Münnich, Amale Ichkou, Nathalie Boddaert, Caroline Alby, Férechté Encha‐Razavi and Jieun Lee and has published in prestigious journals such as Journal of Medical Genetics, European Journal of Human Genetics and Clinical Genetics.

In The Last Decade

Nadia Elkhartoufi

10 papers receiving 154 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nadia Elkhartoufi France 8 107 103 50 21 11 10 155
Hannaleena Kokkonen Finland 8 173 1.6× 152 1.5× 83 1.7× 7 0.3× 10 0.9× 20 238
Matthieu Décamp France 7 89 0.8× 60 0.6× 55 1.1× 7 0.3× 8 0.7× 9 132
Amale Ichkou France 5 36 0.3× 42 0.4× 37 0.7× 9 0.4× 6 0.5× 6 79
Martin Chevarin France 7 72 0.7× 61 0.6× 8 0.2× 13 0.6× 8 0.7× 14 125
Laura Davis‐Keppen United States 5 58 0.5× 105 1.0× 32 0.6× 4 0.2× 32 2.9× 12 155
Mylène Béri France 7 150 1.4× 79 0.8× 65 1.3× 3 0.1× 13 1.2× 8 175
Ricarda Flöttmann Germany 8 95 0.9× 111 1.1× 19 0.4× 4 0.2× 4 0.4× 12 163
Muhsin Elmas Türkiye 6 32 0.3× 47 0.5× 10 0.2× 11 0.5× 9 0.8× 25 89
Céline Pebrel‐Richard France 7 91 0.9× 69 0.7× 39 0.8× 6 0.3× 2 0.2× 20 138
Pierre Sinajon Canada 3 26 0.2× 29 0.3× 32 0.6× 8 0.4× 3 0.3× 3 71

Countries citing papers authored by Nadia Elkhartoufi

Since Specialization
Citations

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

Fields of papers citing papers by Nadia Elkhartoufi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nadia Elkhartoufi

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

All Works

10 of 10 papers shown
1.
Tessier, Aude, Lucile Boutaud, Mélanie Parisot, et al.. (2023). Bi-allelic variations in CRB2, encoding the crumbs cell polarity complex component 2, lead to non-communicating hydrocephalus due to atresia of the aqueduct of sylvius and central canal of the medulla. Acta Neuropathologica Communications. 11(1). 29–29. 7 indexed citations
2.
Devisme, Louise, Lucile Boutaud, Nadia Elkhartoufi, et al.. (2021). The first two non‐Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome. Clinical Genetics. 100(4). 462–467. 2 indexed citations
3.
Quēlin, Chloé, Philippe Loget, Lucile Boutaud, et al.. (2018). Loss of function IFT27 variants associated with an unclassified lethal fetal ciliopathy with renal agenesis. American Journal of Medical Genetics Part A. 176(7). 1610–1613. 11 indexed citations
4.
Chartier, Suzanne, Caroline Alby, Lucile Boutaud, et al.. (2018). A neuropathological study of novel RTTN gene mutations causing a familial microcephaly with simplified gyral pattern. Birth Defects Research. 110(7). 598–602. 7 indexed citations
5.
Attié‐Bitach, Tania, et al.. (2015). [HIGH INCIDENCE AND BROAD GENETIC VARIABILITY OF MECKEL-GRUBER SYNDROME IN THE ARAB POPULATION RESIDING IN NORTH-EAST ISRAEL].. PubMed. 154(10). 632–6, 676. 2 indexed citations
6.
Elkhartoufi, Nadia, et al.. (2015). A homozygous AHI1 gene mutation (p.Thr304AsnfsX6) in a consanguineous Moroccan family with Joubert syndrome: a case report. Journal of Medical Case Reports. 9(1). 254–254. 7 indexed citations
7.
Alby, Caroline, Valérie Malan, Lucile Boutaud, et al.. (2015). Clinical, genetic and neuropathological findings in a series of 138 fetuses with a corpus callosum malformation. Birth Defects Research Part A Clinical and Molecular Teratology. 106(1). 36–46. 30 indexed citations
8.
Thomas, Sophie, Vincent Cantagrel, Laura Mariani, et al.. (2014). Identification of a novel ARL13B variant in a Joubert syndrome-affected patient with retinal impairment and obesity. European Journal of Human Genetics. 23(5). 621–627. 43 indexed citations
9.
Putoux, Audrey, Sheela Nampoothiri, Nicole Laurent, et al.. (2012). Novel KIF7 mutations extend the phenotypic spectrum of acrocallosal syndrome. Journal of Medical Genetics. 49(11). 713–720. 26 indexed citations
10.
Putoux, Audrey, Soumaya Mougou-Zerelli, Sophie Thomas, et al.. (2010). BBS10 mutations are common in ‘Meckel’-type cystic kidneys. Journal of Medical Genetics. 47(12). 848–852. 20 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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