Séverine Bacrot

428 total citations
7 papers, 126 citations indexed

About

Séverine Bacrot is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Séverine Bacrot has authored 7 papers receiving a total of 126 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Séverine Bacrot's work include RNA modifications and cancer (3 papers), Cancer-related molecular mechanisms research (2 papers) and Connective tissue disorders research (2 papers). Séverine Bacrot is often cited by papers focused on RNA modifications and cancer (3 papers), Cancer-related molecular mechanisms research (2 papers) and Connective tissue disorders research (2 papers). Séverine Bacrot collaborates with scholars based in France, Italy and Australia. Séverine Bacrot's co-authors include Arnold Münnich, Valérie Cormier‐Daire, Mathilde Doyard, Céline Huber, Olivier Alibeu, Patrick Nitschké, Alice Goldenberg, Pablo Lapunzina, Perrine Brunelle and Víctor L. Ruiz‐Pérez and has published in prestigious journals such as Journal of Medical Genetics, Human Mutation and Molecular Genetics and Metabolism.

In The Last Decade

Séverine Bacrot

7 papers receiving 126 citations

Peers

Countries citing papers authored by Séverine Bacrot

Since Specialization

Citations

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

Fields of papers citing papers by Séverine Bacrot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Séverine Bacrot

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Utility of genetic testing for prenatal presentations of hypophosphatasia 2021 ·Molecular Genetics and Metabolism ·(unknown), A. Taillandier, (unknown), (unknown), Estelle Colin, (unknown), Anya Rothenbühler, Jean‐Pierre Salles, Deborah Wenkert, Andreas Zankl, Christine Muti, Séverine Bacrot, Brigitte Simon‐Bouy, Étienne Mornet	4
2	Prenatal diagnosis of cerebro‐oculo‐facio‐skeletal syndrome: Report of three fetuses and review of the literature 2020 ·American Journal of Medical Genetics Part A ·(unknown), Nadège Calmels, Maryse Bonnière, Suzanne Chartier, Férechté Razavi, Jamel Chelly, Salima El Chehadeh, Sarah Baer, Lucile Boutaud, Séverine Bacrot, Cathy Obringer, R. Favre, Tania Attié‐Bitach, Vincent Laugel, Maria Cristina Antal	5
3	Pre and post-natal achondroplasia, retrospective series of 64 consecutives cases with analyze of the diagnostic methods and timing issues 2019 ·Bone Abstracts ·Geneviève Baujat, (unknown), Pascale Sonigo, Séverine Bacrot, (unknown), Caroline Michot, A. Millischer, (unknown), (unknown), Tania Attié‐Bitach, Bettina Bessières, Laurent Salomon, Y. Ville, Jean‐Paul Bonnefont, Julie Steffann, Valérie Cormier‐Daire	1
4	Whole exome sequencing diagnoses the first fetal case of Bainbridge‐Ropers syndrome presenting as pontocerebellar hypoplasia type 1 2018 ·Birth Defects Research ·Séverine Bacrot, Charlotte Mechler, (unknown), Dominique Martin‐Coignard, Philippe Roth, Caroline Michot, Amale Ichkou, Olivier Alibeu, Patrick Nitschké, Sophie Thomas, Michel Vekemans, Férechté Razavi, Lucile Boutaud, Tania Attié‐Bitach	11
5	FAM46A mutations are responsible for autosomal recessive osteogenesis imperfecta 2018 ·Journal of Medical Genetics ·Mathilde Doyard, Séverine Bacrot, Céline Huber, Maja Di Rocco, Alice Goldenberg, Mona Aglan, Perrine Brunelle, Samia A. Temtamy, Caroline Michot, Ghada A. Otaify, (unknown), Mireille Castanet, J. Leroux, Jean‐Paul Bonnefont, Arnold Münnich, Geneviève Baujat, Pablo Lapunzina, Sophie Monnot, Víctor L. Ruiz‐Pérez, Valérie Cormier‐Daire	53
6	Mutations inSNRPB, Encoding Components of the Core Splicing Machinery, Cause Cerebro-Costo-Mandibular Syndrome 2014 ·Human Mutation ·Séverine Bacrot, Mathilde Doyard, Céline Huber, Olivier Alibeu, Niklas Feldhahn, Daphné Lehalle, Didier Lacombe, Sandrine Marlin, Patrick Nitschké, Florence Petit, Marie‐Paule Vazquez, Arnold Münnich, Valérie Cormier‐Daire	36
7	Prenatal phenotype of Williams–Beuren syndrome and of the reciprocal duplication syndrome 2014 ·Clinical Case Reports ·(unknown), Licia Turolla, Eva Pompilii, Céline Dupont, Nicolas Gruchy, Simona De Toffol, Gabriella Bracalente, Séverine Bacrot, Enzo Troilo, Anne Claude Tabet, Sabrina Rossi, Anne Lise Delezoïde, (unknown), Nathalie Leporrier, Federico Maggi, Arnaud Molin, G. Pilu, Giuseppe Simoni, François Vialard, Francesca Romana Grati	16

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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