Hélène Moirot

440 total citations
13 papers, 198 citations indexed

About

Hélène Moirot is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hélène Moirot has authored 13 papers receiving a total of 198 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hélène Moirot's work include Genomic variations and chromosomal abnormalities (5 papers), Chromosomal and Genetic Variations (3 papers) and Prenatal Screening and Diagnostics (3 papers). Hélène Moirot is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Chromosomal and Genetic Variations (3 papers) and Prenatal Screening and Diagnostics (3 papers). Hélène Moirot collaborates with scholars based in France and Pakistan. Hélène Moirot's co-authors include Nathalie Le Meur, Thierry Frébourg, Annick Rossi, Pascale Saugier-Véber, Géraldine Joly‐Hélas, François Vialard, Cécile Mignon‐Ravix, Bertrand Macé, Marie‐France Portnoï and D. Parain and has published in prestigious journals such as Human Reproduction, European Journal of Human Genetics and Molecular Genetics and Metabolism.

In The Last Decade

Hélène Moirot

12 papers receiving 185 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hélène Moirot France 9 119 76 59 45 26 13 198
Brian D. Kuchinka Canada 7 162 1.4× 84 1.1× 151 2.6× 22 0.5× 12 0.5× 8 237
Anne Bazin France 8 119 1.0× 74 1.0× 90 1.5× 42 0.9× 6 0.2× 16 195
Stefano Petrocchi Italy 8 129 1.1× 84 1.1× 16 0.3× 19 0.4× 16 0.6× 15 236
Drew Duckett United Kingdom 9 249 2.1× 142 1.9× 128 2.2× 63 1.4× 14 0.5× 23 353
Imma Rost Germany 9 212 1.8× 157 2.1× 45 0.8× 74 1.6× 8 0.3× 24 322
Maria Paola Recalcati Italy 11 240 2.0× 191 2.5× 89 1.5× 46 1.0× 14 0.5× 21 378
M. Elizabeth McCready Canada 10 120 1.0× 80 1.1× 39 0.7× 14 0.3× 22 0.8× 25 254
M. Crocker United Kingdom 9 183 1.5× 88 1.2× 68 1.2× 52 1.2× 8 0.3× 16 245
Daniele Caufin Italy 8 181 1.5× 85 1.1× 83 1.4× 85 1.9× 14 0.5× 8 222
Cynthia Lim United States 5 145 1.2× 126 1.7× 39 0.7× 34 0.8× 11 0.4× 9 231

Countries citing papers authored by Hélène Moirot

Since Specialization
Citations

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

Fields of papers citing papers by Hélène Moirot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hélène Moirot

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

All Works

13 of 13 papers shown
1.
Gruchy, Nicolas, François Vialard, Matthieu Décamp, et al.. (2011). Pregnancy outcomes in 188 French cases of prenatally diagnosed Klinefelter syndrome. Human Reproduction. 26(9). 2570–2575. 19 indexed citations
2.
Guimiot, Fabien, Pascale Marcorelles, Azzedine Aboura, et al.. (2009). Giant diencephalic harmartoma and related anomalies: A newly recognized entity distinct from the Pallister–Hall syndrome. American Journal of Medical Genetics Part A. 149A(6). 1108–1115. 9 indexed citations
3.
Joly‐Hélas, Géraldine, Nathalie Mousset‐Siméon, Hélène Moirot, et al.. (2007). Complex chromosomal rearrangement and intracytoplasmic sperm injection: A Case Report. Human Reproduction. 22(5). 1292–1297. 34 indexed citations
4.
Saugier-Véber, Pascale, Alice Goldenberg, Valérie Drouin‐Garraud, et al.. (2006). Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation. European Journal of Human Genetics. 14(9). 1009–1017. 27 indexed citations
5.
Bouchet, C, Sandrine Vuillaumier‐Barrot, M. Gonzalés, et al.. (2006). Detection of an Alu insertion in the POMT1 gene from three French Walker Warburg syndrome families. Molecular Genetics and Metabolism. 90(1). 93–96. 17 indexed citations
6.
Meur, Nathalie Le, Alice Goldenberg, Valérie Drouin‐Garraud, et al.. (2005). Molecular characterization of a 14q deletion in a boy with features of Holt–Oram syndrome. American Journal of Medical Genetics Part A. 134A(4). 439–442. 11 indexed citations
7.
Meur, Nathalie Le, Cosette Martin, Pascale Saugier-Véber, et al.. (2004). Complete germline deletion of the STK11 gene in a family with Peutz–Jeghers syndrome. European Journal of Human Genetics. 12(5). 415–418. 32 indexed citations
8.
Vialard, François, Cécile Mignon‐Ravix, D. Parain, et al.. (2003). Mechanism of intrachromosomal triplications 15q11‐q13: A new clinical report. American Journal of Medical Genetics Part A. 118A(3). 229–234. 25 indexed citations
9.
Delezoide, A. L., et al.. (1998). Oligo-amnios et grossesse: expérience des fœtopathologistes. Revue Française des Laboratoires. 1998(301). 47–52. 1 indexed citations
10.
Moirot, Hélène, et al.. (1992). [Nephroblastoma and fragile X syndrome].. PubMed. 49(5). 477–477. 5 indexed citations
11.
Gaillard, Dominique, et al.. (1990). Fetal Adrenal Development During the Second Trimester of Gestation. Pediatric Pathology. 10(3). 335–350. 14 indexed citations
12.
Moirot, Hélène, et al.. (1983). [Polysyndactyly with complex cardiopathy. Apropos of 3 cases in the same family].. PubMed. 31(2). 93–105.
13.
Moirot, Hélène, et al.. (1977). [Trisomy 9p by mat. t(2;9)(q36;q31)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 20(1). 45–51. 4 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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