Mathilde Pacault
Impact in
-
- Cancer, Hypoxia, and Metabolism
-
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Myeloproliferative Neoplasms: Diagnosis and Treatment
- Genomics and Rare Diseases
Papers in
-
- Prenatal Screening and Diagnostics 5
-
- Cancer, Hypoxia, and Metabolism 2
- Co-authors
- Alison J. Eaton (1 shared paper)Edit Nagy (1 shared paper)Magnus Bäck (1 shared paper)Jérémy Fauconnier (1 shared paper)France Leturcq (5 shared papers)Juliette Nectoux (5 shared papers)Dominique Vidaud (4 shared papers)Thierry Bienvenu (5 shared papers)
- Journals
- The American Journal of Human Genetics (2 papers)Blood (2 papers)European Journal of Human Genetics (1 paper)Journal of Clinical Immunology (1 paper)Clinical Chemistry and Laboratory Medicine (CCLM) (1 paper)
- Partner nations
- FranceUnited StatesNetherlands
In The Last Decade
Mathilde Pacault
17 papers receiving 338 citations
Peers
Comparison fields: 5 of 57
- Cancer Research 57
- Genetics 97
- Genetics 28
- Pediatrics, Perinatology and Child Health 44
- Molecular Biology 149
Countries citing papers authored by Mathilde Pacault
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
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-authors
The 25 scholars most cited alongside Mathilde Pacault, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 90 | |
| 2 | 2018 | 75 | |
| 3 | 2018 | 42 | |
| 4 | 2018 | 32 | |
| 5 | 2012 | 23 | |
| 6 | 2017 | 15 | |
| 7 | 2018 | 12 | |
| 8 | 2018 | 10 | |
| 9 | 2023 | 10 | |
| 10 | 2022 | 9 | |
| 11 | 2023 | 7 | |
| 12 | 2023 | 5 | |
| 13 | NBEA: Developmental disease gene with early generalized epilepsy phenotypes | 2018 | 4 |
| 14 | 2024 | 4 | |
| 15 | 2016 | 1 | |
| 16 | 2023 | 1 | |
| 17 | Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis | 2023 | 1 |
About Mathilde Pacault
Mathilde Pacault is a scholar working on Pediatrics, Perinatology and Child Health, Cancer Research, Genetics, Physiology and Immunology and Allergy, having authored 17 papers that have together received 341 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Erythrocyte Function and Pathophysiology (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Cancer, Hypoxia, and Metabolism (2 papers), Ubiquitin and proteasome pathways (2 papers), Acute Myeloid Leukemia Research (1 paper) and Glycosylation and Glycoproteins Research (1 paper). The work is most often cited by research in Cancer Research (57 citations), Genetics (97 citations), Genetics (28 citations), Pediatrics, Perinatology and Child Health (44 citations) and Molecular Biology (149 citations). Mathilde Pacault has collaborated with scholars based in France, United States and Netherlands. Frequent co-authors include Alison J. Eaton, Edit Nagy, Magnus Bäck, Jérémy Fauconnier, France Leturcq, Juliette Nectoux, Dominique Vidaud, Thierry Bienvenu, Emmanuelle Girodon and Marie Vincent. Their work appears in journals such as The American Journal of Human Genetics, Blood, European Journal of Human Genetics, Journal of Clinical Immunology and Clinical Chemistry and Laboratory Medicine (CCLM).
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.