Cécile Cieuta‐Walti

Author

Cécile Cieuta‐Walti

Also Known As

C Cieuta-Walti, C. Cieuta-Walti, C. Cieuta‐Walti, Cecile Cieuta-Walti, Cecile Cieuta‐Walti, Cieuta-Walti, Cecile, Cécile Cieuta-Walti, Cécile Cieuta‐Walti, Jean-François Clément

Publications

671

Citations

H-Index

Concepts

All Affiliations

Fondation Jérôme-Lejeune Université de Sherbrooke Assistance Publique – Hôpitaux de Paris Pitié-Salpêtrière Hospital Hôpital Necker-Enfants Malades

About

Cécile Cieuta‐Walti is an author at Fondation Jérôme-Lejeune specializing in craniofacial growth, pediatrics, and child development.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	1	1	13
2	Child Development	1	1	13
3	Body Composition	1	1	13
4	Craniofacial Growth	1	1	13
5	Down Syndrome	1	1	13

Cécile Cieuta‐Walti

Publications

403

Citations

H-Index

Page 1

	Year	Citations
Opportunities, barriers, and recommendations in Down syndrome research James A. Hendrix, Angelika Amon, Leonard Abbeduto, Translational Science of Rare Diseases	2021	96
Acute Regression in Young People with Down Syndrome Clotilde Mircher, Cécile Cieuta‐Walti, Isabelle Marey, Brain Sciences	2017	67
Humanized mouse model of Rasmussen’s encephalitis supports the immune-mediated hypothesis Hania Kébir, Lionel Carmant, François Fontaine, Journal of Clinical Investigation	2018	40
Safety and preliminary efficacy on cognitive performance and adaptive functionality of epigallocatechin gallate (EGCG) in children with Down syndrome. A randomized phase Ib clinical trial (PERSEUS study) Cécile Cieuta‐Walti, Aida Cuenca‐Royo, Klaus Langohr, Genetics in Medicine	2022	31
Epileptiform Asymetries and Treatment Response in Juvenile Myoclonic Epilepsy Karine Létourneau, Cécile Cieuta‐Walti, Charles Deacon Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques	2010	27
Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer’s disease-related dysregulation Larissa Haertle, Tobias Müller, Roy Lardenoije, Clinical Epigenetics	2019	21
Molecular Rescue of Dyrk1A Overexpression Alterations in Mice with Fontup® Dietary Supplement: Role of Green Tea Catechins Yuchen Gu, Gautier Moroy, Jean‐Louis Paul, International Journal of Molecular Sciences	2020	20
Pathogenic variants in <scp><i>KCNQ2</i></scp> cause intellectual deficiency without epilepsy: Broadening the phenotypic spectrum of a potassium channelopathy Laura Mary, Elsa Nourisson, Claire Feger, American Journal of Medical Genetics Part A	2021	19
Early detection and treatment of obstructive sleep apnoea in infants with Down syndrome: a prospective, non-randomised, controlled, interventional study Brigitte Fauroux, Silvia Sacco, Vincent Couloigner, The Lancet Regional Health - Europe	2024	17
Anthropometric charts and congenital anomalies in newborns with Down syndrome Clotilde Mircher, Jeanne Toulas, Cécile Cieuta‐Walti, American Journal of Medical Genetics Part A	2017	14

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