Mathilde Pacault

417 total citations
9 papers, 82 citations indexed

About

Mathilde Pacault is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Mathilde Pacault has authored 9 papers receiving a total of 82 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pediatrics, Perinatology and Child Health, 4 papers in Genetics and 3 papers in Molecular Biology. Recurrent topics in Mathilde Pacault's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (1 paper). Mathilde Pacault is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (1 paper). Mathilde Pacault collaborates with scholars based in France and Sweden. Mathilde Pacault's co-authors include Alison Eaton, Jérémy Fauconnier, Magnus Bäck, Edit Nagy, Thierry Bienvenu, France Leturcq, Juliette Nectoux, Dominique Vidaud, Emmanuelle Girodon and Laïla El Khattabi and has published in prestigious journals such as Blood, PLoS ONE and BJOG An International Journal of Obstetrics & Gynaecology.

In The Last Decade

Mathilde Pacault

8 papers receiving 80 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mathilde Pacault France	6	41	28	23	10	10	9	82
Mallory Owen United States	5	25 0.6×	66 2.4×	27 1.2×	7 0.7×	2 0.2×	8	103
H. Melanie Bedford Canada	5	22 0.5×	18 0.6×	26 1.1×	4 0.4×	4 0.4×	5	76
Claire Searle United Kingdom	4	9 0.2×	26 0.9×	28 1.2×	3 0.3×	4 0.4×	8	66
V. Reid Sutton United States	5	29 0.7×	36 1.3×	120 5.2×	19 1.9×	4 0.4×	11	167
Stavros Glentis Greece	4	12 0.3×	15 0.5×	31 1.3×	2 0.2×	2 0.2×	12	58
Bianca Berdel Germany	4	9 0.2×	16 0.6×	48 2.1×	6 0.6×	3 0.3×	7	105
Carol Gardiner United Kingdom	4	12 0.3×	18 0.6×	29 1.3×	3 0.3×	2 0.2×	7	59
Pierre Sinajon Canada	3	32 0.8×	26 0.9×	29 1.3×	7 0.7×	13 1.3×	3	71
Heleen Schuring‐Blom Netherlands	7	113 2.8×	117 4.2×	42 1.8×	3 0.3×	14 1.4×	8	178
Luis Daniel Campos-Acevedo Mexico	6	13 0.3×	37 1.3×	44 1.9×	2 0.2×	6 0.6×	16	80

Countries citing papers authored by Mathilde Pacault

Since Specialization

Citations

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

Fields of papers citing papers by Mathilde Pacault

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mathilde Pacault

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

Pacault, Mathilde, Marie‐Pierre Audrézet, Nathalie Couque, et al.. (2023). Vers une généralisation du diagnostic prénatal non-invasif des maladies monogéniques ? État des lieux et perspectives. Gynécologie Obstétrique Fertilité & Sénologie . 51(10). 463–470.

Pacault, Mathilde, Emmanuelle Girodon, France Leturcq, et al.. (2023). Non-invasive prenatal diagnosis of single gene disorders with enhanced relative haplotype dosage analysis for diagnostic implementation. PLoS ONE. 18(4). e0280976–e0280976. 6 indexed citations

Pacault, Mathilde, Nathalie Deburgrave, France Leturcq, et al.. (2023). Non-invasive Prenatal Diagnosis of Single Gene Disorders by Paternal Mutation Exclusion: 3 Years of Clinical Experience. Obstetrical & Gynecological Survey. 78(4). 204–206. 4 indexed citations

Pacault, Mathilde, Nathalie Deburgrave, France Leturcq, et al.. (2022). Non‐invasive prenatal diagnosis of single gene disorders by paternal mutation exclusion: 3 years of clinical experience. BJOG An International Journal of Obstetrics & Gynaecology. 129(11). 1879–1886. 8 indexed citations

Pacault, Mathilde, Marie Vincent, Thomas Besnard, et al.. (2018). New splicing pathogenic variant in EBP causing extreme familial variability of Conradi–Hünermann–Happle Syndrome. European Journal of Human Genetics. 26(12). 1784–1790. 5 indexed citations

Pacault, Mathilde, Mathilde Nizon, Olivier Pichon, et al.. (2018). A de novo 2q37.2 deletion encompassing AGAP1 and SH3BP4 in a patient with autism and intellectual disability. European Journal of Medical Genetics. 62(12). 103586–103586. 11 indexed citations

Pacault, Mathilde, Laïla El Khattabi, Thierry Bienvenu, et al.. (2018). Non-invasive prenatal diagnosis of paternally inherited disorders from maternal plasma: detection of NF1 and CFTR mutations using droplet digital PCR. Clinical Chemistry and Laboratory Medicine (CCLM). 56(5). 728–738. 27 indexed citations

Girodon, François, Fabrice Airaud, Céline Garrec, et al.. (2016). Next Generation Sequencing Is a Useful Tool for the Diagnosis of Congenital/Idiopathic Erythrocytoses. Blood. 128(22). 2434–2434. 1 indexed citations

Eaton, Alison, Edit Nagy, Mathilde Pacault, Jérémy Fauconnier, & Magnus Bäck. (2012). Cysteinyl leukotriene signaling through perinuclear CysLT1 receptors on vascular smooth muscle cells transduces nuclear calcium signaling and alterations of gene expression. Journal of Molecular Medicine. 90(10). 1223–1231. 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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