Jean‐Marie Cuisset

Author

Jean‐Marie Cuisset

Also Known As

Cuisset, Jean-Marie, Guy Leverger, Günther Bernert, J M Cuisset, J M. Cuisset, J. -M. Cuisset, J. Cuisset, J. M. Cuisset, J.-M. Cuisset, J.M Cuisset

117

Publications

5.2K

Citations

H-Index

104

Concepts

All Affiliations

Inserm Centre Hospitalier Universitaire de Lille Hôpital Roger Salengro Assistance Publique – Hôpitaux de Paris Sorbonne Université

About

Jean‐Marie Cuisset is an author at Inserm specializing in medicine, health sciences, and applied physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	19	2K
2	Health Sciences	10	10	615
3	Public Health	2	2	92
4	Natural Sciences	1	1	35
5	Nursing	1	1	27

Jean‐Marie Cuisset

Publications

4.4K

Citations

H-Index

Page 1

	Year	Citations
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2 Robin Walters, Sébastien Jacquemont, Armand Valsesia, Nature ObesityMetabolic SyndromeChildhood ObesityDevelopmental BiologyMetabolic Disorder	2010	554
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Nature Gene DosageGeneticsHuman PolymorphismMolecular GeneticsChromosome 16P11.2	2011	474
De novo <i>LMNA</i> mutations cause a new form of congenital muscular dystrophy Susana Quijano‐Roy, Blaise Mbieleu, Carsten G. Bönnemann, Annals of Neurology	2008	281
Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies Karim Wahbi, Rabah Ben Yaou, Estelle Gandjbakhch, Circulation	2019	245
Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: Array CGH study of 47 unrelated cases Caroline Schluth‐Bolard, Bruno Delobel, Damien Sanlaville, European Journal of Medical Genetics Genetic DisorderGeneticsEvolutionary BiologyChromosomal RearrangementsArray Cgh Study	2009	173
Prospective and longitudinal natural history study of patients with Type 2 and 3 spinal muscular atrophy: Baseline data NatHis-SMA study A. Chabanon, A. Seferian, Aurore Daron, PLoS ONE	2018	146
Motor and respiratory heterogeneity in Duchenne patients: Implication for clinical trials Véronique Humbertclaude, Dalil Hamroun, Kamel Bezzou, European Journal of Paediatric Neurology MedicineRespiratory NeurobiologyPhysiologyClinical TrialsMotor Control	2011	138
ISPD produces CDP-ribitol used by FKTN and FKRP to transfer ribitol phosphate onto α-dystroglycan Isabelle Gerin, Benoît Ury, Isabelle Breloy, Nature Communications	2016	135
Comparison of seizure reduction and serum fatty acid levels after receiving the ketogenic and modified Atkins diet Natacha Porta, Louis Vallée, Elisabeth Boutry, Seizure NutritionClinical NutritionDietary TherapySeizure Reduction	2009	130
15q11.2 microdeletion (BP1–BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: A series of 52 patients Clémence Vanlerberghe, Florence Petit, Valérie Malan, European Journal of Medical Genetics Cardiovascular DiseaseBehaviour IssuesPediatric Heart DiseasePediatricsCongenital Heart Defect	2015	120

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