Bruno Delobel

4.4k total citations
37 papers, 804 citations indexed

About

Bruno Delobel is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Bruno Delobel has authored 37 papers receiving a total of 804 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 14 papers in Molecular Biology and 8 papers in Plant Science. Recurrent topics in Bruno Delobel's work include Genomic variations and chromosomal abnormalities (15 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Chromosomal and Genetic Variations (8 papers). Bruno Delobel is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Chromosomal and Genetic Variations (8 papers). Bruno Delobel collaborates with scholars based in France, United Kingdom and United States. Bruno Delobel's co-authors include Joris Andrieux, Marie‐Françoise Croquette, Serge Romana, Hélène De Leersnyder, Géraldine Viot, Jürgen‐Christoph von Kleist-Retzow, Stanislas Lyonnet, Urs Albrecht, Arnold Münnich and Bruno Claustrat and has published in prestigious journals such as Journal of The Electrochemical Society, The Journal of Pediatrics and Fertility and Sterility.

In The Last Decade

Bruno Delobel

35 papers receiving 733 citations

Peers

Bruno Delobel

GENET

Moritz Meins Germany

Ken‐Shiung Chen United States

Romeo Carrozzo Italy

Patricia Blanchet France

Matteo Della Monica Italy

Britt‐Marie Anderlid Sweden

Katherine Lachlan United Kingdom

Audrey Labalme France

Katrien Storm Belgium

Masayuki Anzai Japan

Moritz Meins Germany

Bruno Delobel

394 ×0.8

GENET

615 ×1.7

75 ×0.6

71 ×0.8

168 ×1.8

Citations per year, relative to Bruno Delobel Bruno Delobel (= 1×) peers Moritz Meins

Countries citing papers authored by Bruno Delobel

Since Specialization

Citations

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

Fields of papers citing papers by Bruno Delobel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bruno Delobel

This figure shows the co-authorship network connecting the top 25 collaborators of Bruno Delobel. A scholar is included among the top collaborators of Bruno Delobel 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 Bruno Delobel. Bruno Delobel 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

Caumes, Roseline, C. Thuillier, Odile Boute‐Bénéjean, et al.. (2024). NONO-related X-linked intellectual disability syndrome: Further clinical and molecular delineation. European Journal of Medical Genetics. 73. 104987–104987.

Bourrat, E., Dan Lipsker, B Taillan, et al.. (2022). Novel pathogenic variants in SLCO2A1 causing autosomal dominant primary hypertrophic osteoarthropathy. European Journal of Medical Genetics. 66(2). 104689–104689. 3 indexed citations

Pennamen, Perrine, Linh Le, Angèle Tingaud‐Sequeira, et al.. (2020). BLOC1S5 pathogenic variants cause a new type of Hermansky–Pudlak syndrome. Genetics in Medicine. 22(10). 1613–1622. 55 indexed citations

Arnaud, Pauline, Nadine Hanna, Julien Thévenon, et al.. (2020). A new mutational hotspot in the SKI gene in the context of MFS/TAA molecular diagnosis. Human Genetics. 139(4). 461–472. 6 indexed citations

Thuillier, C., et al.. (2018). A heterozygous microdeletion of 20q13.13 encompassing ADNP gene in a child with Helsmoortel–van der Aa syndrome. European Journal of Human Genetics. 26(10). 1497–1501. 8 indexed citations

Dharmadhikari, Avinash V., Tomasz Gambin, Przemysław Szafrański, et al.. (2014). Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite. BMC Medical Genetics. 15(1). 128–128. 21 indexed citations

Perrin, Aurore, Bruno Delobel, Audrey Basinko, et al.. (2012). Characterization and meiotic segregation of a supernumerary marker chromosome in sperm of infertile males: Case report and literature review. European Journal of Medical Genetics. 55(12). 743–746. 8 indexed citations

Sheth, Frenny, Joris Andrieux, Elisabeth Ewers, et al.. (2011). Characterization of sSMC by FISH and molecular techniques. European Journal of Medical Genetics. 54(3). 247–255. 14 indexed citations

Cossée, Mireille, Laurence Faivre, Christophe Philippe, et al.. (2010). ARX polyalanine expansions are highly implicated in familial cases of mental retardation with infantile epilepsy and/or hand dystonia. American Journal of Medical Genetics Part A. 155(1). 98–105. 21 indexed citations

10.

Andrieux, Joris, Christèle Dubourg, Marlène Rio, et al.. (2009). Genotype–phenotype correlation in four 15q24 deleted patients identified by array‐CGH. American Journal of Medical Genetics Part A. 149A(12). 2813–2819. 27 indexed citations

11.

Andrieux, Joris, Steven Richebourg, Bénédicte Duban‐Bedu, et al.. (2008). Characterization by array-CGH of an interstitial de novo tandem 6p21.2p22.1 duplication in a boy with epilepsy and developmental delay. European Journal of Medical Genetics. 51(4). 373–381. 11 indexed citations

12.

Andrieux, Joris, Frédéric Leprêtre, Jean‐Marie Cuisset, et al.. (2008). Deletion 18q21.2q21.32 involving TCF4 in a boy diagnosed by CGH-array. European Journal of Medical Genetics. 51(2). 172–177. 22 indexed citations

13.

Mignon‐Ravix, Cécile, D. Depétris, Judith Luciani, et al.. (2007). Recurrent rearrangements in the proximal 15q11–q14 region: a new breakpoint cluster specific to unbalanced translocations. European Journal of Human Genetics. 15(4). 432–440. 38 indexed citations

14.

Nicodème, Frédéric, Sandrine Geffroy, Massimo Conti, et al.. (2005). Familial occurrence of thymoma and autoimmune diseases with the constitutional translocation t(14;20)(q24.1;p12.3). Genes Chromosomes and Cancer. 44(2). 154–160. 14 indexed citations

15.

Giuliano, Fabienne, Sylvie Bannwarth, Sophie Monnot, et al.. (2004). Wolfram syndrome in French population: Characterization of novel mutations and polymorphisms in theWFS1 gene. Human Mutation. 25(1). 99–100. 46 indexed citations

16.

Feldmann, Delphine, Françoise Denoyelle, Natalie Loundon, et al.. (2003). Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 gene. European Journal of Human Genetics. 12(4). 279–284. 40 indexed citations

17.

Leersnyder, Hélène De, Marie‐Christine de Blois, Bruno Claustrat, et al.. (2001). Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome. The Journal of Pediatrics. 139(1). 111–116. 124 indexed citations

18.

Franke, Petra, Marion Leboyer, Jochen Hardt, et al.. (1999). Neuropsychological profiles of FMR-1 premutation and full-mutation carrier females. Psychiatry Research. 87(2-3). 223–231. 35 indexed citations

19.

Delobel, Bruno, O. Gabriel-Robez, Marie‐Françoise Croquette, et al.. (1998). Y-autosome translocation and infertility: usefulness of molecular, cytogenetic and meiotic studies. Human Genetics. 102(1). 98–98. 65 indexed citations

20.

Rousseaux‐Prévost, Roselyne, Jean-Marc Rigot, Bruno Delobel, et al.. (1996). Molecular mapping of a Yq deletion in a patient with normal stature. Human Genetics. 98(4). 505–507. 3 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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