Nathalie Bonello‐Palot

Author

Also Known As

Bonello, N., Bonello-Palot, Nathalie, Julia Bonastre, N Bonello, N. Bonello, N. Bonello-Palot, N. Bonello‐Palot, N. P. Bonello, Nathalie Bonello, Nathalie Bonello-Palot

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

Inserm Hôpital de la Timone Aix-Marseille Université Sorbonne Université Génétique Médicale & Génomique Fonctionelle

About

Nathalie Bonello‐Palot is an author at Inserm specializing in medicine, genetic epidemiology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	15	798
2	Cell Biology	4	4	381
3	Health Sciences	3	3	122
4	Natural Sciences	1	1	18
5	Public Health	1	1	19

Nathalie Bonello‐Palot

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype Cécile Rouzier, Sylvie Bannwarth, Annabelle Chaussenot, Brain Mitochondrial MyopathyGenome InstabilityMfn2 GeneMitochondrial FunctionOphthalmology	2011	234
Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation Annelies Rotthier, Jonathan Baets, Els De Vriendt, Brain	2009	165
Clopidogrel Loading Dose Adjustment According to Platelet Reactivity Monitoring in Patients Carrying the 2C19*2Loss of Function Polymorphism Laurent Bonello, Sebastien Arméro, Omar Aït Mokhtar, Journal of the American College of Cardiology ThrombopoiesisThrombosisPlatelet Reactivity MonitoringCardiovascular DiseaseBlood Platelet	2010	124
Relation of Body Mass Index to High On-Treatment Platelet Reactivity and of Failed Clopidogrel Dose Adjustment According to Platelet Reactivity Monitoring in Patients Undergoing Percutaneous Coronary Intervention Nathalie Bonello‐Palot, Sebastien Arméro, Franck Paganelli, The American Journal of Cardiology ThrombopoiesisThrombosisPercutaneous Coronary InterventionPlatelet Reactivity MonitoringCardiovascular Disease	2009	90
The XmnI Gγ polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 β-thalassemia intermedia patients Thi Khanh Tien Nguyen, Philippe Joly, Claire Bardel, Blood Cells Molecules and Diseases Immunohematologyβ-Thalassemia Intermedia PatientsGeneticsGenetic EpidemiologyImmunology	2010	61
Prelamin A accumulation in endothelial cells induces premature senescence and functional impairment Nathalie Bonello‐Palot, Stéphanie Simoncini, Stéphane Robert, Atherosclerosis AgingEndothelial CellsLongevityPhysiologyEndothelial Dysfunction	2014	60
Molecular diagnosis of inherited peripheral neuropathies by targeted next-generation sequencing: molecular spectrum delineation Juliette Bacquet, Tanya Stojkovic, Amandine Boyer, BMJ Open	2018	59
Loss of Neurological Disease HSAN-I-Associated Gene SPTLC2 Impairs CD8+ T Cell Responses to Infection by Inhibiting T Cell Metabolic Fitness Jingxia Wu, Sicong Ma, Roger Sandhoff, Immunity Autoimmune DiseaseMedicineT-regulatory CellImmunologyAutoimmunity	2019	51
A multicenter retrospective study of charcot‐marie‐tooth disease type 4B (CMT4B) associated with mutations in myotubularin‐related proteins (MTMRs) Davide Pareyson, Tanya Stojkovic, Mary M. Reilly, Annals of Neurology	2019	37
A Heterozygous ZMPSTE24 Mutation Associated with Severe Metabolic Syndrome, Ectopic Fat Accumulation, and Dilated Cardiomyopathy Damien Galant, Bénédicte Gaborit, Camille Desgrouas, Cells Metabolic DisorderPathologyLamina ArchitectureObesityMetabolic Syndrome	2016	36

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