Laurence Duplomb - Concepedia

Author

Laurence Duplomb

Inserm ORCID

Also Known As

L Duplomb, L. Duplomb, L. Duplomb‐Jego, Laurence Duplomb, Laurence Duplomb-Jego, Laurence Duplomb‐Jego

Publications

3.7K

Citations

H-Index

Concepts

All Affiliations

Inserm Université de Bourgogne CHU Dijon Bourgogne Centre National de la Recherche Scientifique Hôpital d'Enfants

About

Laurence Duplomb is an author at Inserm specializing in medicine, cell biology, and immunology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	23	29	1.5K
2	Health Sciences	3	3	288
3	Natural Sciences	2	2	143
4	Biochemistry	2	2	254
5	Social Sciences	1	1	25

Laurence Duplomb

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
PIK3R1 Mutations Cause Syndromic Insulin Resistance with Lipoatrophy Christel Thauvin‐Robinet, Martine Auclair, Laurence Duplomb, The American Journal of Human Genetics Metabolic SyndromeGeneticsDiabetesMedicineInsulin Signaling	2013	199
Interleukin‐34 is expressed by giant cell tumours of bone and plays a key role in RANKL‐induced osteoclastogenesis Marc Baud’huin, Romain Renault, Céline Charrier, The Journal of Pathology	2010	151
Hyperleptinemia prevents lipotoxic cardiomyopathy in acyl CoA synthase transgenic mice Young Lee, R. Haris Naseem, Laurence Duplomb, Proceedings of the National Academy of Sciences Heart FailureMetabolic DisorderHyperleptinemia PreventsImmunologyLeptin Cdna	2004	145
Interleukin-6 Inhibits Receptor Activator of Nuclear Factor κB Ligand-Induced Osteoclastogenesis by Diverting Cells into the Macrophage Lineage: Key Role of Serine727 Phosphorylation of Signal Transducer and Activator of Transcription 3 Laurence Duplomb, Marc Baud’huin, Céline Charrier, Endocrinology	2008	135
The <i>DYRK1A</i> gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy Jean‐Benoît Courcet, Laurence Faivre, Perrine Malzac, Journal of Medical Genetics	2012	123
In-Frame Mutations in Exon 1 of SKI Cause Dominant Shprintzen-Goldberg Syndrome Virginie Carmignac, Julien Thevenon, Lesley C. Adès, The American Journal of Human Genetics Developmental AnomalyIn-frame MutationsMendelian DisorderExon 1Genetic Disorder	2012	110
Hepatic insig-1 or -2 overexpression reduces lipogenesis in obese Zucker diabetic fatty rats and in fasted/refed normal rats Kiyosumi Takaishi, Laurence Duplomb, May-Yun Wang, Proceedings of the National Academy of Sciences Fasted/refed Normal RatsHepatic Insig-1Fatty Liver DiseaseInsulin SignalingOxidative Stress	2004	109
Lysosomal Signaling Licenses Embryonic Stem Cell Differentiation via Inactivation of Tfe3 Florian Villegas, Daphné Lehalle, Daniela Mayer, Cell stem cell Cell LineageLineage PlasticityDevelopmental BiologyCell SpecializationMedicine	2018	109
Cohen syndrome is associated with major glycosylation defects Laurence Duplomb, Sandrine Duvet, Damien Picot, Human Molecular Genetics GlycobiologyMolecular BiologyPathologyGlycosylation StatusGlycoproteomics	2013	96
Oncostatin M Regulates the Synthesis and Turnover of gp130, Leukemia Inhibitory Factor Receptor α, and Oncostatin M Receptor β by Distinct Mechanisms Frédéric Blanchard, Yanping Wang, Erin Kinzie, Journal of Biological Chemistry	2001	95

Page 1