Sarah Grotto

682 total citations
12 papers, 79 citations indexed

About

Sarah Grotto is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Sarah Grotto has authored 12 papers receiving a total of 79 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Genetics. Recurrent topics in Sarah Grotto's work include RNA regulation and disease (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Sarah Grotto is often cited by papers focused on RNA regulation and disease (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Sarah Grotto collaborates with scholars based in France, United Kingdom and Australia. Sarah Grotto's co-authors include Brigitte Benzacken, Valérie Drouin‐Garraud, Cyril Mignot, Jonathan Lévy, Boris Keren, Alain Verloès, A. Maruani, Céline Dupont, Anne‐Claude Tabet and Andrée Delahaye‐Duriez and has published in prestigious journals such as Clinical Chemistry, Annals of the Rheumatic Diseases and Journal of Medical Genetics.

In The Last Decade

Sarah Grotto

12 papers receiving 78 citations

Peers

Sarah Grotto

GENET

CMN

CCM

PPCH

Girolamo Aurelio Vitello Italy

Christina Q. Nguyen Australia

Jessica Sebastian United States

Agnès Guët France

Miriam Bloom United States

Maria Antonietta Pisanti Italy

Danielle Nolan United States

Martin Chevarin France

Eva Maria Christina Schwaibold Germany

Kimberly Foss United States

Girolamo Aurelio Vitello Italy

Sarah Grotto

43 ×0.8

25 ×1.0

GENET

19 ×1.1

CMN

5 ×0.6

CCM

6 ×0.7

PPCH

Citations per year, relative to Sarah Grotto Sarah Grotto (= 1×) peers Girolamo Aurelio Vitello

Countries citing papers authored by Sarah Grotto

Since Specialization

Citations

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

Fields of papers citing papers by Sarah Grotto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarah Grotto

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

All Works

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12 of 12 papers shown

Grangé, G., et al.. (2023). Neu Laxova syndrome and megacystis in the first trimester: Broadening the fetal phenotype. Prenatal Diagnosis. 43(13). 1666–1670. 2 indexed citations

Capri, Yline, Céline Dupont, Fabien Guimiot, et al.. (2023). DST variants are responsible for neurogenic arthrogryposis multiplex congenita enlarging the spectrum of type VI hereditary sensory autonomic neuropathy. Clinical Genetics. 104(5). 587–592. 2 indexed citations

Grotto, Sarah, Corinne Fouveaut, Sophie Christin‐Maître, et al.. (2023). NOBOX gene variants in premature ovarian insufficiency: ethnicity-dependent insights. Journal of Assisted Reproduction and Genetics. 41(1). 135–146. 4 indexed citations

Cuisset, Laurence, Sarah Grotto, Corinne Fouveaut, et al.. (2023). Stratification of the risk of ovarian dysfunction by studying the complexity of intermediate and premutation alleles of the FMR1 gene. American Journal of Medical Genetics Part A. 194(4). e63479–e63479. 2 indexed citations

Plaisancié, Julie, Jelena Martinović, Sandra Whalen, et al.. (2023). Clinical, genetic and biochemical signatures of RBP4-related ocular malformations. Journal of Medical Genetics. 61(1). 84–92. 2 indexed citations

Lœuillet, Laurence, Juliette Nectoux, E. Pannier, et al.. (2022). Two novel variations p.(Ser1275Thr) and p.(Ser1275Arg) in FLT4 causing prenatal hereditary lymphedema type 1. Birth Defects Research. 115(5). 563–571. 1 indexed citations

Marouillat, Sylviane, Nicolas Chatron, Bénédicte Gérard, et al.. (2021). Novel missense mutations in PTCHD1 alter its plasma membrane subcellular localization and cause intellectual disability and autism spectrum disorder. Human Mutation. 42(7). 848–861. 9 indexed citations

Marey, Isabelle, Véronique Fressart, Caroline Rambaud, et al.. (2020). Clinical impact of post-mortem genetic testing in cardiac death and cardiomyopathy. Open Medicine. 15(1). 435–446. 12 indexed citations

Lévy, Jonathan, Sarah Grotto, Cyril Mignot, et al.. (2018). NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder. Clinical Genetics. 94(2). 264–268. 25 indexed citations

10.

Grotto, Sarah, Valérie Drouin‐Garraud, Bernadette Chadefaux-Vekemans, et al.. (2018). Dilated Cardiomyopathy and Premature Ovarian Failure Unveiling Propionic Aciduria. Clinical Chemistry. 64(4). 752–754. 6 indexed citations

11.

Fogel, O., A. Cantagrel, Kei Ikeda, et al.. (2017). OP0062 Assessment of biotherapies' efficacy in blau syndrome: data from an international retrospective cohort of 23 cases. Annals of the Rheumatic Diseases. 76. 77–77. 1 indexed citations

12.

Grotto, Sarah, Valérie Drouin‐Garraud, Katrin Õunap, et al.. (2014). Clinical assessment of five patients with BRWD3 mutation at Xq21.1 gives further evidence for mild to moderate intellectual disability and macrocephaly. European Journal of Medical Genetics. 57(5). 200–206. 13 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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