Julien Buratti

2.4k total citations
22 papers, 324 citations indexed

About

Julien Buratti is a scholar working on Molecular Biology, Genetics and Food Science. According to data from OpenAlex, Julien Buratti has authored 22 papers receiving a total of 324 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Food Science. Recurrent topics in Julien Buratti's work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Probiotics and Fermented Foods (4 papers). Julien Buratti is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Probiotics and Fermented Foods (4 papers). Julien Buratti collaborates with scholars based in France, United States and Morocco. Julien Buratti's co-authors include Valentin Loux, Boris Keren, Anne Boland, Thomas Bourgeron, Emmanuelle Maguin, Benoît Quinquis, Nathalie Galleron, Sean P. Kennedy, Samira Boudebbouze and Bouziane Moumen and has published in prestigious journals such as International Journal of Molecular Sciences, Movement Disorders and BMC Genomics.

In The Last Decade

Julien Buratti

22 papers receiving 322 citations

Peers

Countries citing papers authored by Julien Buratti

Since Specialization

Citations

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

Fields of papers citing papers by Julien Buratti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julien Buratti

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Biallelic variants in ERLIN1: a series of 13 individuals with spastic paraparesis 2024 ·Human Genetics ·(unknown), Maha S. Zaki, Mahmoud Y. Issa, Boris Keren, (unknown), Florence Renaldo, Arnaud Isapof, (unknown), Giovanni Stévanin, Léna Guillot‐Noël, Thomas Courtin, Julien Buratti, (unknown), Joseph G. Gleeson, (unknown), Alexandra Durr, Jean‐Madeleine de Sainte Agathe, Cyril Mignot	1
2	Deep Characterization of a Greek Patient with Desmin-Related Myofibrillar Myopathy and Cardiomyopathy 2023 ·International Journal of Molecular Sciences ·Constantinos Papadopoulos, Edoardo Malfatti, Corinne Métay, Boris Keren, (unknown), Julien Buratti, Sophia Xirou, (unknown), George K. Papadimas	2
3	Loss of function of ADNP by an intragenic inversion 2023 ·European Journal of Human Genetics ·(unknown), (unknown), Julien Buratti, (unknown), E. Le Guern, Delphine Héron, Boris Keren, Jean‐Madeleine de Sainte Agathe	5
4	Patients with KCNH1 -related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome 2021 ·Journal of Medical Genetics ·(unknown), Olivier Patat, Sandra Whalen, Lionel Arnaud, Giulia Barcia, Julien Buratti, Benjamin Cogné, Diane Doummar, (unknown), (unknown), Éric Leguern, Gaëtan Lesca, Caroline Nava, Mathilde Nizon, Amélie Piton, Stéphanie Valence, Laurent Villard, Sarah Weckhuysen, Boris Keren, Cyril Mignot	8
5	SCN1A-related epilepsy with recessive inheritance: Two further families 2021 ·European Journal of Paediatric Neurology ·Raffaella Moretti, Lionel Arnaud, Delphine Bouteiller, Oriane Trouillard, (unknown), Julien Buratti, Agnès Rastetter, Boris Keren, Vincent des Portes, Joseph Toulouse, Isabelle Gourfinkel‐An, Eric Leguern, Christel Depienne, Cyril Mignot, Caroline Nava	4
6	Phenotype associated with TAF2 biallelic mutations: A clinical description of four individuals and review of the literature 2021 ·European Journal of Medical Genetics ·(unknown), Yline Capri, (unknown), Thomas Courtin, (unknown), Julien Thévenon, Julien Buratti, (unknown), Laurence Faivre, Boris Keren	4
7	Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity 2021 ·Haematologica ·Viviana Marin‐Esteban, (unknown), Blandine Beaupain, (unknown), Vincent Barlogis, Odile Fenneteau, Thierry Leblanc, (unknown), Philippe Pellet, Julien Buratti, Hélène Lapillonne, Françoise Bachelerie, Jean Donadieu, Christine Bellanné‐Chantelot	13
8	Involvement of ADGRV1 Gene in Familial Forms of Genetic Generalized Epilepsy 2021 ·Frontiers in Neurology ·(unknown), (unknown), (unknown), Sara Baldassari, Guillaume Achaz, (unknown), (unknown), Stéphanie Baulac, Julien Buratti, Omer Mohamed Abdalla, (unknown), (unknown), (unknown), Eric Noé, Liena E. O. Elsayed, Ammar Ahmed, Éric Leguern	9
9	Functional characterization of ABCC8 variants of unknown significance based on bioinformatics predictions, splicing assays, and protein analyses: Benefits for the accurate diagnosis of congenital hyperinsulinism 2021 ·Human Mutation ·Cécile Saint‐Martin, (unknown), Emily A. Rex, Omar Soukarieh, Jean‐Baptiste Arnoux, Julien Buratti, (unknown), Thierry Frébourg, Pascaline Gaildrat, Show‐Ling Shyng, Christine Bellanné‐Chantelot, Alexandra Martins	7
10	Identification of biallelic germline variants of SRP68 in a sporadic case with severe congenital neutropenia 2020 ·Haematologica ·(unknown), Anne Pagnier, Séverine Clauin, Julien Buratti, Caroline Marty, Odile Fenneteau, Klaus Dieterich, Blandine Beaupain, Jean Donadieu, Isabelle Plo, Christine Bellanné-Chantelot	8
11	Congenital immobility and stiffness related to biallelic ATAD1 variants 2020 ·Neurology Genetics ·(unknown), Diane Doummar, Sandra Whalen, Boris Keren, Sandra Chantot‐Bastaraud, Kim Maincent, (unknown), M. Mayer, (unknown), Lydie Bürglen, Pierre‐Louis Léger, François Kieffer, Isabelle Martin, Delphine Héron, Julien Buratti, Arnaud Isapof, Alexandra Afenjar, Thierry Billette de Villemeur, Cyril Mignot	4
12	De novo variants in SIAH1, encoding an E3 ubiquitin ligase, are associated with developmental delay, hypotonia and dysmorphic features 2020 ·Journal of Medical Genetics ·Julien Buratti, Lei Ji, Boris Keren, Youngha Lee, (unknown), Serkan Erdin, Soo Yeon Kim, Timothy Blake Palculict, Vardiella Meiner, Jong‐Hee Chae, C. Geoffrey Woods, Allison Tam, Delphine Héron, Feng Cong, Tamar Harel	8
13	New evidence that biallelic loss of function in EEF1B2 gene leads to intellectual disability 2019 ·Clinical Genetics ·Lise Larcher, Julien Buratti, (unknown), Brigitte Benzacken, Eva Pipiras, Boris Keren, Andrée Delahaye‐Duriez	7
14	The complete loss of function of the SMS gene results in a severe form of Snyder-Robinson syndrome 2019 ·European Journal of Medical Genetics ·Lise Larcher, Joy Norris, (unknown), Julien Buratti, Cyril Mignot, Cathérine Garel, Boris Keren, Charles E. Schwartz, Sandra Whalen	21
15	Both rare and common genetic variants contribute to autism in the Faroe Islands 2019 ·npj Genomic Medicine ·Claire S. Leblond, Freddy Cliquet, (unknown), Guillaume Huguet, Alexandre Mathieu, Thomas Kergrohen, Julien Buratti, Nathalie Lemière, Laurence Cuisset, Thierry Bienvenu, Anne Boland, Jean‐François Deleuze, (unknown), (unknown), Jónrit Halling, Guðrið Andorsdóttir, Eva Billstedt, Christopher Gillberg, Thomas Bourgeron	52
16	Association of modifiers and other genetic factors explain Marfan syndrome clinical variability 2018 ·European Journal of Human Genetics ·Mélodie Aubart, Steven Gazal, Pauline Arnaud, Louise Benarroch, Marie‐Sylvie Gross, Julien Buratti, Anne Boland, Vincent Meyer, Habib Zouali, Nadine Hanna, Olivier Milleron, Chantal Stheneur, Thomas Bourgeron, Isabelle Desguerre, Marie‐Paule Jacob, Laurent Gouya, Emmanuelle Génin, Jean‐François Deleuze, Guillaume Jondeau, Cathérine Boileau	59
17	Permanent draft genome sequence of the probiotic strain Propionibacterium freudenreichii CIRM-BIA 129 (ITG P20) 2016 ·Standards in Genomic Sciences ·Hélène Falentin, Stéphanie‐Marie Deutsch, Valentin Loux, (unknown), Julien Buratti, Sandrine Parayre, Victoria Chuat, Valérie Barbe, Jean‐Marc Aury, Gwénaël Jan, Yves Le Loir	10
18	Mutations and genomic islands can explain the strain dependency of sugar utilization in 21 strains of Propionibacterium freudenreichii 2015 ·BMC Genomics ·Valentin Loux, Mahendra Mariadassou, S. Almeida, Hélène Chiapello, (unknown), Julien Buratti, (unknown), Valérie Barbe, Jean‐Marc Aury, Stéphanie‐Marie Deutsch, Sandrine Parayre, Marie‐Noëlle Madec, Victoria Chuat, Gwénaël Jan, Pierre Peterlongo, Vasco Azevedo, Yves Le Loir, Hélène Falentin	28
19	Lactobacillus delbrueckii ssp. lactis and ssp. bulgaricus: a chronicle of evolution in action 2014 ·BMC Genomics ·(unknown), Johan Binesse, Valentin Loux, Julien Buratti, Samira Boudebbouze, Rozenn Dervyn, Sean P. Kennedy, Nathalie Galleron, Benoît Quinquis, Jean-Michel Batto, Bouziane Moumen, Emmanuelle Maguin, Maarten van de Guchte	60
20	Genome Sequence of Lactobacillus delbrueckii subsp. lactis CNRZ327, a Dairy Bacterium with Anti-Inflammatory Properties 2014 ·Genome Announcements ·(unknown), Johan Binesse, Valentin Loux, Julien Buratti, Samira Boudebbouze, Rozenn Dervyn, (unknown), Emmanuelle Maguin, Maarten van de Guchte	5

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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