Jean‐Hubert Caberg

1.4k total citations
16 papers, 383 citations indexed

About

Jean‐Hubert Caberg is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Jean‐Hubert Caberg has authored 16 papers receiving a total of 383 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Genetics and 4 papers in Genetics. Recurrent topics in Jean‐Hubert Caberg's work include Neurogenetic and Muscular Disorders Research (4 papers), RNA modifications and cancer (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Jean‐Hubert Caberg is often cited by papers focused on Neurogenetic and Muscular Disorders Research (4 papers), RNA modifications and cancer (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Jean‐Hubert Caberg collaborates with scholars based in Belgium, Rwanda and France. Jean‐Hubert Caberg's co-authors include Vincent Bours, Jacques Boniver, Pascale Hubert, Philippe Delvenne, Vinciane Dideberg, Laurent Servais, François Boemer, Christine Gilles, Latifa Bousarghin and Tamara Dangouloff and has published in prestigious journals such as Scientific Reports, The FASEB Journal and International Journal of Molecular Sciences.

In The Last Decade

Jean‐Hubert Caberg

16 papers receiving 373 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jean‐Hubert Caberg Belgium 10 195 87 86 70 60 16 383
Yong‐Min Lin China 13 155 0.8× 167 1.9× 33 0.4× 26 0.4× 8 0.1× 24 389
Fei Fei Gao China 10 106 0.5× 79 0.9× 45 0.5× 65 0.9× 52 0.9× 13 306
Ronan Bergin Ireland 8 195 1.0× 238 2.7× 52 0.6× 30 0.4× 37 0.6× 10 384
Paul Naumann United States 10 118 0.6× 58 0.7× 19 0.2× 54 0.8× 15 0.3× 12 334
Nicole Lucien France 11 245 1.3× 31 0.4× 19 0.2× 80 1.1× 57 0.9× 17 530
Darren Qiancheng Tan Singapore 9 242 1.2× 57 0.7× 43 0.5× 52 0.7× 19 0.3× 14 398
Nahoko Tomonobu Japan 9 184 0.9× 104 1.2× 29 0.3× 22 0.3× 33 0.6× 24 350
Chonghua Hao China 11 158 0.8× 42 0.5× 53 0.6× 6 0.1× 38 0.6× 16 281
Sara Lamorte Canada 7 226 1.2× 186 2.1× 29 0.3× 64 0.9× 33 0.6× 12 459

Countries citing papers authored by Jean‐Hubert Caberg

Since Specialization
Citations

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

Fields of papers citing papers by Jean‐Hubert Caberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jean‐Hubert Caberg. 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 Jean‐Hubert Caberg. The network helps show where Jean‐Hubert Caberg may publish in the future.

Co-authorship network of co-authors of Jean‐Hubert Caberg

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

All Works

16 of 16 papers shown
1.
Boemer, François, Claire Josse, Géraldine Luis, et al.. (2022). Novel Loss of Function Variant in BCKDK Causes a Treatable Developmental and Epileptic Encephalopathy. International Journal of Molecular Sciences. 23(4). 2253–2253. 5 indexed citations
2.
Caberg, Jean‐Hubert, Vinciane Dideberg, Tamara Dangouloff, et al.. (2021). Newborn screening of duchenne muscular dystrophy specifically targeting deletions amenable to exon-skipping therapy. Scientific Reports. 11(1). 3011–3011. 13 indexed citations
3.
Uwineza, Annette, Jean‐Hubert Caberg, Stéphane Wenric, et al.. (2019). VPS51 biallelic variants cause microcephaly with brain malformations: A confirmatory report. European Journal of Medical Genetics. 62(8). 103704–103704. 14 indexed citations
4.
Boemer, François, Jean‐Hubert Caberg, Vinciane Dideberg, et al.. (2019). Newborn screening for SMA in Southern Belgium. Neuromuscular Disorders. 29(5). 343–349. 57 indexed citations
5.
Boemer, François, Jean‐Hubert Caberg, Vinciane Dideberg, et al.. (2019). [(S)un (M)ay (A)rise on SMA : the hope of a region without spinal muscular atrophy].. PubMed. 74(9). 461–464. 6 indexed citations
6.
Wenric, Stéphane, Jean‐Hubert Caberg, Corinne Fasquelle, et al.. (2017). Transcriptome-wide analysis of natural antisense transcripts shows their potential role in breast cancer. Scientific Reports. 7(1). 17452–17452. 32 indexed citations
7.
Rostomyan, Liliya, Emilie Castermans, Jean‐Hubert Caberg, et al.. (2016). Combined treatment with octreotide LAR and pegvisomant in patients with pituitary gigantism: clinical evaluation and genetic screening. Pituitary. 19(5). 507–514. 14 indexed citations
8.
Caberg, Jean‐Hubert, Stéphane Wenric, Christophe Poulet, et al.. (2016). Genomic studies of multiple myeloma reveal an association between X chromosome alterations and genomic profile complexity. Genes Chromosomes and Cancer. 56(1). 18–27. 3 indexed citations
9.
Uwineza, Annette, et al.. (2015). Cytogenetic Studies of Rwandan Pediatric Patients Presenting with Global Developmental Delay, Intellectual Disability and/or Multiple Congenital Anomalies. Journal of Tropical Pediatrics. 62(1). 38–45. 4 indexed citations
10.
Debray, François‐Guillaume, Arnaud Vanlander, Vinciane Dideberg, et al.. (2015). Mutation of the iron‐sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy. Journal of Inherited Metabolic Disease. 38(6). 1147–1153. 38 indexed citations
11.
Uwineza, Annette, Yvan Butera, Anne‐Cecile Hellin, et al.. (2014). Pattern of congenital heart diseases in Rwandan children with genetic defects. Pan African Medical Journal. 19. 85–85. 7 indexed citations
12.
Dorboz, Imen, Marie Coutelier, A. Bertrand, et al.. (2014). Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1. Orphanet Journal of Rare Diseases. 9(1). 174–174. 39 indexed citations
13.
Uwineza, Annette, Jean‐Hubert Caberg, Mauricette Jamar, et al.. (2014). Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies. BMC Medical Genetics. 15(1). 11 indexed citations
14.
Uwineza, Annette, et al.. (2013). Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13.. PubMed. 24(2). 193–200. 6 indexed citations
15.
Hubert, Pascale, Catherine Maillard, Jean‐Hubert Caberg, et al.. (2007). Defensins induce the recruitment of dendritic cells in cervical human papillomavirus‐associated (pre)neoplastic lesions formed in vitro and transplanted in vivo. The FASEB Journal. 21(11). 2765–2775. 57 indexed citations
16.
Hubert, Pascale, Jean‐Hubert Caberg, Christine Gilles, et al.. (2005). E‐cadherin‐dependent adhesion of dendritic and Langerhans cells to keratinocytes is defective in cervical human papillomavirus‐associated (pre)neoplastic lesions. The Journal of Pathology. 206(3). 346–355. 77 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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