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Jean‐Hubert Caberg

Observed names: CABERG, Jean-Hubert, Caberg Jean Hubert, J H Caberg, J. Caberg, J.-H. Caberg, J.H. Caberg, J.‐H. Caberg, Jean Hubert Caberg, Jean- Hubert Caberg, Jean-Hubert Caberg, Jean-Hubert D. Caberg
Observed institutions: National Institutes of Health, University of Liège, Centre Hospitalier Universitaire Vaudois, University Hospital Münster, Centre Hospitalier Universitaire de Liège, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health Clinical Center, Hôpitaux universitaires Paris Sud, University of Lausanne
ORCID: 0000-0003-4083-3907
Observed ORCID: 0000-0003-4083-3907
OpenAlex ID: A5081616562
Gigantism and Acromegaly Due to Xq26 Microduplications and GPR101 Mutation
2014 · Giampaolo Trivellin, Adrian F. Daly, et al. · New England Journal of Medicine · 355
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Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients
2015 · Liliya Rostomyan, Adrian F Daly, et al. · Endocrine Related Cancer · 202
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Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants
2018 · Lucilla Pizzo, Matthew Jensen, et al. · Genetics in Medicine · 193
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X-linked acrogigantism syndrome: clinical profile and therapeutic responses
2015 · Albert Beckers, Maya Beth Lodish, et al. · Endocrine Related Cancer · 191
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Newborn screening for SMA in Southern Belgium
2019 · François Boemer, Jean-Hubert Caberg, et al. · Neuromuscular Disorders · 111
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E‐cadherin‐dependent adhesion of dendritic and Langerhans cells to keratinocytes is defective in cervical human papillomavirus‐associated (pre)neoplastic lesions
2005 · Pascale Hubert, Jean‐Hubert Caberg, et al. · The Journal of Pathology · 100
Implementation of genomic arrays in prenatal diagnosis: The Belgian approach to meet the challenges
2014 · Olivier Vanakker, Catheline Vilain, et al. · European Journal of Medical Genetics · 98
Somatic mosaicism underlies X-linked acrogigantism syndrome in sporadic male subjects
2016 · Adrian F Daly, Bo Yuan, et al. · Endocrine Related Cancer · 92
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Silencing of E7 oncogene restores functional E-cadherin expression in human papillomavirus 16-transformed keratinocytes
2008 · Jean-Hubert D. Caberg, Pascale M. Hubert, et al. · Carcinogenesis · 88
16p13.11 microduplication in 45 new patients: refined clinical significance and genotype–phenotype correlations
2018 · Laïla Allach El Khattabi, Solveig Heide, et al. · Journal of Medical Genetics · 85
Three years pilot of spinal muscular atrophy newborn screening turned into official program in Southern Belgium
2021 · François Boemer, Jean-Hubert Caberg, et al. · Scientific Reports · 75
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Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study
2018 · Sandra Martin-Brevet, Borja Rodríguez-Herreros, et al. · Biological Psychiatry · 75
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Estimating the effect size of the 15Q11.2 BP1–BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice
2019 · Aia Elise Jønch, Elise Douard, et al. · Journal of Medical Genetics · 74
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GHRH excess and blockade in X-LAG syndrome
2015 · Adrian F Daly, Philippe A Lysy, et al. · Endocrine Related Cancer · 74
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The cross-talk between dendritic and regulatory T cells: good or evil?
2007 · Pascale Hubert, Nathalie Jacobs, et al. · Journal of Leukocyte Biology · 74
Defensins induce the recruitment of dendritic cells in cervical human papillomavirus‐associated (pre)neoplastic lesions formed in vitro and transplanted in vivo
2007 · Pascale Hubert, Ludivine Herman, et al. · The FASEB Journal · 69
Increased migration of Langerhans cells in response to HPV16 E6 and E7 oncogene silencing: role of CCL20
2008 · Jean-Hubert Caberg, Pascale Hubert, et al. · Cancer Immunology Immunotherapy · 57
Mutation of the iron‐sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy
2015 · François‐Guillaume Debray, Claudia Stümpfig, et al. · Journal of Inherited Metabolic Disease · 54
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Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1
2014 · Imen Dorboz, Marie Coutelier, et al. · Orphanet Journal of Rare Diseases · 51
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Transcriptome-wide analysis of natural antisense transcripts shows their potential role in breast cancer
2017 · Stephane Wenric, Sonia ElGuendi, et al. · Scientific Reports · 47
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Role of hormone cofactors in the human papillomavirus-induced carcinogenesis of the uterine cervix
2006 · Philippe Delvenne, Ludivine Herman, et al. · Molecular and Cellular Endocrinology · 47
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Effects of eight neuropsychiatric copy number variants on human brain structure
2021 · Claudia Modenato, Kuldeep Kumar, et al. · Translational Psychiatry · 44
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Transforming Growth Factor-β1-Mediated Slug and Snail Transcription Factor Up-Regulation Reduces the Density of Langerhans Cells in Epithelial Metaplasia by Affecting E-Cadherin Expression
2008 · Michael Herfs, Pascale Hubert, et al. · American Journal Of Pathology · 41
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Diagnostic pitfall in antenatal manifestations of CPT II deficiency
2015 · F. Boemer, M. Deberg, et al. · Clinical Genetics · 33
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Combined treatment with octreotide LAR and pegvisomant in patients with pituitary gigantism: clinical evaluation and genetic screening
2016 · Ruth Mangupli, Liliya Rostomyan, et al. · Pituitary · 31
Works count: 79
Citation count: 2,625
H-index: 26
I10-index: 39
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