Erika Launay

831 total citations
16 papers, 116 citations indexed

About

Erika Launay is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Erika Launay has authored 16 papers receiving a total of 116 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Erika Launay's work include Prenatal Screening and Diagnostics (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Chromosomal and Genetic Variations (3 papers). Erika Launay is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Chromosomal and Genetic Variations (3 papers). Erika Launay collaborates with scholars based in France, Australia and Brazil. Erika Launay's co-authors include P. Talley, Warren G. Sanger, Nyla A. Heerema, Alain Bernheim, Martine Raphaël, John Swansbury, A. Aupérin, S L Perkins, Catherine Patte and Mary Gerrard and has published in prestigious journals such as Blood, Leukemia and Human Genetics.

In The Last Decade

Erika Launay

14 papers receiving 115 citations

Peers

Erika Launay
Mara Andrés Spain
N. Peter Germany
Stephanie Mueller Germany
Ferran Vall‐Llovera Spain
Victor Enciso-Mora United Kingdom
Naïs Prade France
Matteo Leoncin Italy
Charmaine Smith Australia
Elen Oliveira Brazil
Andrei Coliţă Romania
Mara Andrés Spain
Erika Launay
Citations per year, relative to Erika Launay Erika Launay (= 1×) peers Mara Andrés

Countries citing papers authored by Erika Launay

Since Specialization
Citations

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

Fields of papers citing papers by Erika Launay

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erika Launay

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

All Works

16 of 16 papers shown
1.
Launay, Erika, et al.. (2025). Histopathology and immunohistochemistry findings in kidney and urinary bladder of rabies virus-infected mice. Acta Tropica. 263. 107550–107550. 1 indexed citations
2.
Dion, Ludivine, Maud Bidet, Chloé Quēlin, et al.. (2024). Optimizing care for MRKH patients: From malformation screening to uterus transplantation eligibility. Acta Obstetricia Et Gynecologica Scandinavica. 104(3). 514–521.
3.
Holtgrewe, Manuel, Andranik Ivanov, Christèle Dubourg, et al.. (2024). Loss-of-function variants affecting the STAGA complex component SUPT7L cause a developmental disorder with generalized lipodystrophy. Human Genetics. 143(5). 683–694. 2 indexed citations
4.
Bergougnoux, Anne, Nadège Servant, Linda Akloul, et al.. (2024). Identification and Characterization of Novel FSHR Copy Number Variations Causing Premature Ovarian Insufficiency. American Journal of Medical Genetics Part A. 197(3). e63924–e63924.
5.
Leclerc, Delphine, Sylvie Jaillard, Léna Damaj, et al.. (2023). Gene Editing Corrects In Vitro a G > A GLB1 Transition from a GM1 Gangliosidosis Patient. The CRISPR Journal. 6(1). 17–31. 2 indexed citations
6.
Barrois, Michel, Alexandre Vivanti, Jonathan Rosenblatt, et al.. (2023). Non‐invasive cell‐free DNA prenatal screening for trisomy 21 as part of primary screening strategy in twin pregnancy. Ultrasound in Obstetrics and Gynecology. 63(6). 807–814. 1 indexed citations
7.
Tucker, Elena J., Linda Akloul, Erika Launay, et al.. (2022). Pseudodicentric Chromosome Originating from an X-Autosome Translocation in a Male Patient with Cryptozoospermia. Cytogenetic and Genome Research. 162(3). 124–131. 1 indexed citations
8.
Lavillaureix, Alinoë, Philippe Loget, Erika Launay, et al.. (2022). Prenatal phenotype of 22q11 micro-duplications: A systematic review and report on 12 new cases. European Journal of Medical Genetics. 65(2). 104422–104422. 7 indexed citations
9.
Launay, Erika, et al.. (2021). Immunological impact of tetrahydrobiopterin on the central nervous system in a murine model of rabies virus infection. Revista do Instituto de Medicina Tropical de São Paulo. 63. e28–e28. 2 indexed citations
10.
Loget, Philippe, Sylvie Odent, G. Le Bouar, et al.. (2021). Multicolor-FISH Characterization of a Prenatal Mosaicism for a Chromosomal Rearrangement Undetected by Molecular Cytogenetics. Cytogenetic and Genome Research. 161(3-4). 143–152. 4 indexed citations
11.
Tucker, Elena J., Erika Launay, Linda Akloul, et al.. (2019). Pseudodicentric Chromosome Originating from Autosomes 9 and 21 in a Male Patient with Oligozoospermia. Cytogenetic and Genome Research. 159(4). 201–207. 3 indexed citations
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Dubourg, Christèle, Laurent Pasquier, Sylvie Odent, et al.. (2014). Postnatal diagnosis of 9q interstitial imbalances involving PTCH1, resulting from a familial intrachromosomal insertion. European Journal of Medical Genetics. 57(5). 195–199. 1 indexed citations
14.
Launay, Erika, Cathérine Henry, Claus Meyer, et al.. (2013). MLL-SEPT5fusion transcript in infant acute myeloid leukemia with t(11;22)(q23;q11). Leukemia & lymphoma. 55(3). 662–667. 7 indexed citations
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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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