Marie Deprez

2.6k total citations · 1 hit paper
9 papers, 544 citations indexed

About

Marie Deprez is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Marie Deprez has authored 9 papers receiving a total of 544 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Marie Deprez's work include Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). Marie Deprez is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). Marie Deprez collaborates with scholars based in France, Belgium and United States. Marie Deprez's co-authors include Pascal Barbry, Agnès Paquet, Laure‐Emmanuelle Zaragosi, Kévin Lebrigand, Virginie Magnone, Charles‐Hugo Marquette, Marin Truchi, Sandra Ruiz García, Marie‐Jeanne Arguel and Sylvie Leroy and has published in prestigious journals such as Nature Communications, Development and American Journal of Respiratory and Critical Care Medicine.

In The Last Decade

Marie Deprez

9 papers receiving 539 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.

A Single-Cell Atlas of the Human Healthy Airways

2020 255 citations Marie Deprez, Laure‐Emmanuelle Zaragosi et al. American Journal of Respiratory and Critical Care Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marie Deprez France	6	238	218	92	87	82	9	544
Sandra Ruiz García France	4	211 0.9×	165 0.8×	68 0.7×	33 0.4×	78 1.0×	5	444
Alisha M. Gruntman United States	14	189 0.8×	360 1.7×	138 1.5×	259 3.0×	35 0.4×	34	699
Nicholas W. Keiser United States	12	290 1.2×	387 1.8×	51 0.6×	206 2.4×	156 1.9×	17	799
Jenny L. Kerschner United States	16	256 1.1×	463 2.1×	59 0.6×	133 1.5×	52 0.6×	32	682
Sue O’Shea United States	7	73 0.3×	254 1.2×	40 0.4×	26 0.3×	51 0.6×	11	494
Stephen J. Delaney United Kingdom	13	328 1.4×	521 2.4×	58 0.6×	103 1.2×	93 1.1×	21	834
Romulo Hurtado United States	14	95 0.4×	410 1.9×	87 0.9×	52 0.6×	26 0.3×	17	550
Nicholas A. Robinson United States	10	59 0.2×	83 0.4×	38 0.4×	47 0.5×	32 0.4×	31	313
Virginia P. Van Keulen United States	10	78 0.3×	137 0.6×	49 0.5×	33 0.4×	168 2.0×	24	472
Grace Athas United States	10	151 0.6×	293 1.3×	41 0.4×	106 1.2×	82 1.0×	12	588

Countries citing papers authored by Marie Deprez

Since Specialization

Citations

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

Fields of papers citing papers by Marie Deprez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marie Deprez

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

All Works

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9 of 9 papers shown

1.

Cavard, Amélie, Olivier Mercey, Sophie Abélanet, et al.. (2023). The MIR34B/C genomic region contains multiple potential regulators of multiciliogenesis. FEBS Letters. 597(12). 1623–1637. 1 indexed citations

2.

Destrèe, Anne, Marie Deprez, Hazim Kadhim, et al.. (2022). ASC1 complex related conditions: Two novel paediatric patients with TRIP4 pathogenic variants and review of literature. European Journal of Medical Genetics. 65(4). 104469–104469. 1 indexed citations

3.

Deprez, Marie, Laure‐Emmanuelle Zaragosi, Marin Truchi, et al.. (2020). A Single-Cell Atlas of the Human Healthy Airways. American Journal of Respiratory and Critical Care Medicine. 202(12). 1636–1645. 255 indexed citations breakdown →

4.

García, Sandra Ruiz, Marie Deprez, Kévin Lebrigand, et al.. (2019). Novel dynamics of human mucociliary differentiation revealed by single-cell RNA sequencing of nasal epithelial cultures. Development. 146(20). 162 indexed citations

5.

Zaragosi, Laure‐Emmanuelle, Camille Boutin, Marie Deprez, et al.. (2018). CDC20B is required for deuterosome-mediated centriole production in multiciliated cells. Nature Communications. 9(1). 4668–4668. 51 indexed citations

6.

Moortgat, Stéphanie, Damien Lederer, Marie Deprez, et al.. (2018). Expanding the phenotypic spectrum associated with OPHN1 mutations: Report of 17 individuals with intellectual disability but no cerebellar hypoplasia. European Journal of Medical Genetics. 61(8). 442–450. 8 indexed citations

7.

Smogavec, Mateja, Juliane Hoyer, Damien Lederer, et al.. (2016). Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum. Journal of Medical Genetics. 53(12). 820–827. 41 indexed citations

8.

Moortgat, Stéphanie, et al.. (2014). A new Turkish infant with clinical features of CS/CISS1 syndrome and homozygous CRLF1 mutation. European Journal of Medical Genetics. 57(5). 212–215. 4 indexed citations

9.

Lessin, Marc S., et al.. (1995). Congenital diaphragmatic hernia with or without extracorporeal membrane oxygenation: are we making progress?. PubMed. 181(1). 65–71. 21 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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