Lucile Boutaud

736 total citations
20 papers, 233 citations indexed

About

Lucile Boutaud is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lucile Boutaud has authored 20 papers receiving a total of 233 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 12 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lucile Boutaud's work include Genetic and Kidney Cyst Diseases (8 papers), Fetal and Pediatric Neurological Disorders (6 papers) and Renal and related cancers (4 papers). Lucile Boutaud is often cited by papers focused on Genetic and Kidney Cyst Diseases (8 papers), Fetal and Pediatric Neurological Disorders (6 papers) and Renal and related cancers (4 papers). Lucile Boutaud collaborates with scholars based in France, United States and Tunisia. Lucile Boutaud's co-authors include Sophie Thomas, Michel Daudon, Delphine Guillemot, Bertrand Knebelmann, Guillaume Bollée, A Bensman, Irène Ceballos-Picot, Jérôme Harambat, P. Deteix and Tania Attié‐Bitach and has published in prestigious journals such as Journal of the American Society of Nephrology, PLoS Genetics and Journal of Medical Genetics.

In The Last Decade

Lucile Boutaud

19 papers receiving 230 citations

Peers

Lucile Boutaud
Shreya Raman United States
Nithiwat Vatanavicharn Thailand
Jonathan Z. Luo United States
Ludovic Jeanson France
Zeineb Bakey Germany
George Rebello South Africa
Hu Tan China
Rathi D. Thiagarajan Australia
Diana Fulmer United States
Barbara Logan United States
Shreya Raman United States
Lucile Boutaud
Citations per year, relative to Lucile Boutaud Lucile Boutaud (= 1×) peers Shreya Raman

Countries citing papers authored by Lucile Boutaud

Since Specialization
Citations

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

Fields of papers citing papers by Lucile Boutaud

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucile Boutaud

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

All Works

20 of 20 papers shown
1.
Boutaud, Lucile, Chloé Quēlin, Philippe Roth, et al.. (2025). Complete loss of IFT27 function leads to a phenotypic spectrum of fetal lethal ciliopathy associated with altered ciliogenesis. European Journal of Human Genetics. 33(3). 387–392. 2 indexed citations
2.
Hennocq, Quentin, Nicolas Garcelon, Sandrine Marlin, et al.. (2024). Artificial intelligence‐based diagnosis in fetal pathology using external ear shapes. Prenatal Diagnosis. 44(10). 1150–1158. 3 indexed citations
3.
Boutaud, Lucile, Virginie Hamel, Sophie Thomas, et al.. (2024). A Taybi-Linder syndrome-related RTTN variant impedes neural rosette formation in human cortical organoids. PLoS Genetics. 20(12). e1011517–e1011517.
4.
Tessier, Aude, Lucile Boutaud, Mélanie Parisot, et al.. (2023). Bi-allelic variations in CRB2, encoding the crumbs cell polarity complex component 2, lead to non-communicating hydrocephalus due to atresia of the aqueduct of sylvius and central canal of the medulla. Acta Neuropathologica Communications. 11(1). 29–29. 7 indexed citations
5.
Stos, Bertrand, Patrick Nitschké, Cécile Fourrage, et al.. (2023). Diagnosis of Menke‐Hennekam syndrome by prenatal whole exome sequencing and review of prenatal signs. Molecular Genetics & Genomic Medicine. 11(9). e2219–e2219. 1 indexed citations
6.
Boutaud, Lucile, Damelys Calderon, Nicolas Goudin, et al.. (2022). 2D and 3D Human Induced Pluripotent Stem Cell-Based Models to Dissect Primary Cilium Involvement during Neocortical Development. Journal of Visualized Experiments. 4 indexed citations
7.
Huber, Céline, Geneviève Baujat, Caroline Michot, et al.. (2022). Ellis-Van Creveld Syndrome: Clinical and Molecular Analysis of 50 Individuals. Journal of Medical Genetics. 60(4). 337–345. 8 indexed citations
8.
Boutaud, Lucile, Bettina Bessières, Christine Bole, et al.. (2022). Biallelic THOC6 pathogenic variants: Prenatal phenotype and review of the literature. Birth Defects Research. 114(10). 499–504. 5 indexed citations
9.
Devisme, Louise, Lucile Boutaud, Nadia Elkhartoufi, et al.. (2021). The first two non‐Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndrome. Clinical Genetics. 100(4). 462–467. 2 indexed citations
10.
Chartier, Suzanne, Lucile Boutaud, Caroline Alby, et al.. (2021). Prenatal‐onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation. Birth Defects Research. 113(18). 1324–1332. 2 indexed citations
11.
Calmels, Nadège, Maryse Bonnière, Suzanne Chartier, et al.. (2020). Prenatal diagnosis of cerebro‐oculo‐facio‐skeletal syndrome: Report of three fetuses and review of the literature. American Journal of Medical Genetics Part A. 182(5). 1236–1242. 5 indexed citations
12.
Thomas, Sophie, Lucile Boutaud, Madeline Louise Reilly, & Alexandre Benmerah. (2019). Cilia in hereditary cerebral anomalies. Biology of the Cell. 111(9). 217–231. 28 indexed citations
13.
Quēlin, Chloé, Philippe Loget, Lucile Boutaud, et al.. (2018). Loss of function IFT27 variants associated with an unclassified lethal fetal ciliopathy with renal agenesis. American Journal of Medical Genetics Part A. 176(7). 1610–1613. 11 indexed citations
14.
Bacrot, Séverine, Charlotte Mechler, Dominique Martin‐Coignard, et al.. (2018). Whole exome sequencing diagnoses the first fetal case of Bainbridge‐Ropers syndrome presenting as pontocerebellar hypoplasia type 1. Birth Defects Research. 110(6). 538–542. 11 indexed citations
15.
Cushion, Thomas D., Heather E. Olson, P. Ellen Grant, et al.. (2018). Clinical and Functional Characterization of the Recurrent TUBA1A p.(Arg2His) Mutation. Brain Sciences. 8(8). 145–145. 13 indexed citations
16.
Chartier, Suzanne, Caroline Alby, Lucile Boutaud, et al.. (2018). A neuropathological study of novel RTTN gene mutations causing a familial microcephaly with simplified gyral pattern. Birth Defects Research. 110(7). 598–602. 7 indexed citations
17.
Boutaud, Lucile, Bettina Bessières, Maryse Bonnière, et al.. (2017). Fetal Cerebral Ventricular Dilatation: Etiopathogenic Study of 130 Observations. Birth Defects Research. 109(19). 1586–1595. 2 indexed citations
18.
Alby, Caroline, Valérie Malan, Lucile Boutaud, et al.. (2015). Clinical, genetic and neuropathological findings in a series of 138 fetuses with a corpus callosum malformation. Birth Defects Research Part A Clinical and Molecular Teratology. 106(1). 36–46. 30 indexed citations
19.
Dupont, Céline, Clarisse Baumann, Élise Schaefer, et al.. (2013). COL2A1 gene disruption by a balanced translocation t(12;15)(q13;q22.2) in familial stickler syndrome. American Journal of Medical Genetics Part A. 161(10). 2663–2665. 3 indexed citations
20.
Bollée, Guillaume, Lucile Boutaud, Delphine Guillemot, et al.. (2010). Phenotype and Genotype Characterization of Adenine Phosphoribosyltransferase Deficiency. Journal of the American Society of Nephrology. 21(4). 679–688. 89 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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