B Delobel

1.7k total citations
18 papers, 451 citations indexed

About

B Delobel is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, B Delobel has authored 18 papers receiving a total of 451 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Plant Science. Recurrent topics in B Delobel's work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Chromosomal and Genetic Variations (4 papers). B Delobel is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Chromosomal and Genetic Variations (4 papers). B Delobel collaborates with scholars based in France, Italy and United States. B Delobel's co-authors include Fréderic Morel, V. Amice, Philippe Marchetti, Marc De Braekeleer, Nathalie Douet‐Guilbert, M. F. Croquette, M.‐J. Le Bris, J. Amice, M. Chery and Catherine Léonard and has published in prestigious journals such as Human Reproduction, Journal of Medical Genetics and Human Mutation.

In The Last Decade

B Delobel

17 papers receiving 434 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
B Delobel France 11 313 170 117 85 61 18 451
Caroline Schluth‐Bolard France 15 375 1.2× 434 2.6× 90 0.8× 125 1.5× 55 0.9× 43 786
Ilia V. Soloviev Russia 14 579 1.8× 356 2.1× 152 1.3× 160 1.9× 48 0.8× 26 788
M. G. Daker United Kingdom 13 333 1.1× 225 1.3× 82 0.7× 113 1.3× 37 0.6× 28 538
Françoise Devillard France 11 247 0.8× 152 0.9× 142 1.2× 78 0.9× 107 1.8× 27 431
Wayne Gottlieb United States 8 516 1.6× 394 2.3× 222 1.9× 63 0.7× 145 2.4× 11 770
M. Crippa Italy 12 145 0.5× 203 1.2× 43 0.4× 40 0.5× 72 1.2× 37 396
Vikram Jaswaney United States 7 424 1.4× 245 1.4× 154 1.3× 51 0.6× 16 0.3× 12 489
D Robinson United Kingdom 10 410 1.3× 269 1.6× 95 0.8× 105 1.2× 31 0.5× 14 534
Tiia Reimand Estonia 13 291 0.9× 229 1.3× 97 0.8× 19 0.2× 20 0.3× 41 488
Eric Crawford United States 7 343 1.1× 260 1.5× 57 0.5× 41 0.5× 195 3.2× 12 609

Countries citing papers authored by B Delobel

Since Specialization
Citations

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

Fields of papers citing papers by B Delobel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B Delobel

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

All Works

18 of 18 papers shown
1.
Petit, Florence, Muriel Holder‐Espinasse, Bénédicte Duban‐Bedu, et al.. (2010). Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell– Silver syndrome. Clinical Genetics. 81(3). 265–271. 28 indexed citations
2.
Némos, Christophe, Laëtitia Lambert, Fabienne Giuliano, et al.. (2009). Mutational spectrum of CDKL5 in early‐onset encephalopathies: a study of a large collection of French patients and review of the literature. Clinical Genetics. 76(4). 357–371. 83 indexed citations
3.
Caño, A., Cécile Rouzier, Sophie Monnot, et al.. (2007). Identification of novel mutations in WFS1 and genotype–phenotype correlation in Wolfram syndrome. American Journal of Medical Genetics Part A. 143A(14). 1605–1612. 60 indexed citations
4.
Douet‐Guilbert, Nathalie, M.‐J. Le Bris, V. Amice, et al.. (2005). Interchromosomal effect in sperm of males with translocations: report of 6 cases and review of the literature. International Journal of Andrology. 28(6). 372–379. 71 indexed citations
5.
Morel, Fréderic, Nathalie Douet‐Guilbert, Angèle Herry, et al.. (2004). Lack of intraindividual variation of unbalanced spermatozoa frequencies from a 46,XY,t(9;22)(q21;q11.2) carrier: Case report. Human Reproduction. 19(10). 2227–2230. 12 indexed citations
6.
Morel, Fréderic, Nathalie Douet‐Guilbert, A. Moerman, et al.. (2004). Chromosome aneuploidy in the spermatozoa of two men with globozoospermia. Molecular Human Reproduction. 10(11). 835–838. 30 indexed citations
7.
Durand, François, et al.. (2002). [Rothmund-Thomson syndrome, trisomy 8 mosaicism and RECQ4 gene mutation].. PubMed. 129(6-7). 892–5. 13 indexed citations
8.
Brèviere, Georges‐Marie, M. F. Croquette, B Delobel, P. Pellerin, & Christian Rey. (1999). Malformations conotroncales et autres aspects cliniques secondaires à la microdélétion 22q11. À propos d'une série de 111 patients. Archives de Pédiatrie. 6. S305–S307. 6 indexed citations
9.
Mignon, C., B Delobel, A. Moncla, et al.. (1998). Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication study.. Journal of Medical Genetics. 35(11). 932–938. 10 indexed citations
10.
Delobel, B, Valérie Delannoy, Giorgio Pini, et al.. (1998). Identification and molecular characterization of a small 11q23.3 de novo duplication in a patient with Rett syndrome manifestations.. PubMed. 80(3). 273–80. 22 indexed citations
11.
Cossée, Mireille, Céline Moutou, Valérie Biancalana, et al.. (1997). Le syndrome X fragile est encore méconnu: efficacité du diagnostic moléculaire chez les proposants avec retard mental. Archives de Pédiatrie. 4(3). 227–236. 1 indexed citations
12.
Moncla, A., et al.. (1997). Le syndrome de Smith-Magenis. Archives de Pédiatrie. 4(12). 1231–1237.
13.
Crépieux, Pascale, Brigitte Quatannens, B Delobel, et al.. (1997). Homologous T and B cells immortalized in vitro by the Epstein-Barr virus exhibit differential genetical and functional features. International Journal of Oncology. 11(1). 87–96. 5 indexed citations
14.
Birot, Anne‐Marie, et al.. (1996). A 5-megabase familial deletion removes the IDS and FMR-1 genes in a male Hunter patient. Human Mutation. 7(3). 266–268. 21 indexed citations
15.
Gabriel-Robez, O., et al.. (1996). Synaptic behaviour of sex chromosome in two XYY men.. PubMed. 39(3). 129–32. 16 indexed citations
16.
Chettouh, Zoubida, M. F. Croquette, B Delobel, et al.. (1995). Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.. PubMed. 57(1). 62–71. 66 indexed citations
17.
Delobel, B, et al.. (1995). Antley-Bixler syndrome: case report and review of the literature.. PubMed. 6(3). 241–6. 6 indexed citations
18.
Bonnot, G., B Delobel, & J. Guillaud. (1970). DÉTERMINATION DES PARAMÈTRES D'IDENTIFICATION ET DE DOSAGE PAR CHROMATOGRAPHIE D'ÉCHANGE D'IONS, DE 61 ACIDES AMINÉS ET COMPOSÉS APPARENTÉS. annales de biologie animale biochimie biophysique. 10(3). 357–367. 1 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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